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Effects of bisphenol A and its analogs on reproductive health: A mini review
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bdrb.20336openalex-snapshot
Effects of in utero exposure to Bisphenol A or diethylstilbestrol on the adult male reproductive system
inferredcites →https://doi.org/10.1002/bmc.1241openalex-snapshot
Measurement of bisphenol A and bisphenol B levels in human blood sera from healthy and endometriotic women
inferredcites →https://doi.org/10.1002/jat.3188openalex-snapshot
The toxic effects of Bisphenol A on the mouse spermatocyte GC‐2 cell line: the role of the Ca2+‐calmodulin‐Ca2+/calmodulin‐dependent protein kinase II axis
inferredcites →https://doi.org/10.1002/tox.22043openalex-snapshot
Exposure to Bisphenol AF disrupts sex hormone levels and vitellogenin expression in zebrafish
inferredcites →https://doi.org/10.1002/tox.22282openalex-snapshot
Mitochondrial Dysfunction and Ca2+ Overload in Injured Sertoli Cells Exposed to Bisphenol A
inferredcites →https://doi.org/10.1002/tox.22300openalex-snapshot
Prenatal bisphenol a exposure leads to reproductive hazards on male offspring via the Akt/mTOR and mitochondrial apoptosis pathways
inferredcites →https://doi.org/10.1002/tox.22339openalex-snapshot
Bisphenol a induces autophagy and apoptosis concurrently involving the Akt/mTOR pathway in testes of pubertal SD rats
inferredcites →https://doi.org/10.1007/s00204-006-0117-xopenalex-snapshot
Toxicity of tetrabromobisphenol A (TBBPA) in zebrafish (Danio rerio) in a partial life-cycle test
inferredcites →https://doi.org/10.1007/s00204-007-0223-4openalex-snapshot
Subacute oral toxicity study of bisphenol F based on the draft protocol for the “Enhanced OECD Test Guideline no. 407”
inferredcites →https://doi.org/10.1007/s00244-014-0016-8openalex-snapshot
A Survey of Alkylphenols, Bisphenols, and Triclosan in Personal Care Products from China and the United States
inferredcites →https://doi.org/10.1007/s00244-014-0078-7openalex-snapshot
Association of Serum Bisphenol-A Concentration and Male Reproductive Function Among Exposed Workers
inferredcites →https://doi.org/10.1007/s00244-015-0199-7openalex-snapshot
Maternal Transfer of Bisphenol A During Nursing Causes Sperm Impairment in Male Offspring
inferredcites →https://doi.org/10.1007/s00420-016-1171-1openalex-snapshot
Environmental and occupational exposure to bisphenol A and endometriosis: urinary and peritoneal fluid concentration levels
inferredcites →https://doi.org/10.1007/s00441-013-1723-6openalex-snapshot
Bisphenol A exposure at an environmentally relevant dose induces meiotic abnormalities in adult male rats
inferredcites →https://doi.org/10.1007/s11033-012-1716-7openalex-snapshot
Bisphenol A exposure modifies DNA methylation of imprint genes in mouse fetal germ cells
inferredcites →https://doi.org/10.1007/s11356-016-7573-5openalex-snapshot
Metabolic and endocrine effects of bisphenol A exposure in market seller women with polycystic ovary syndrome
inferredcites →https://doi.org/10.1007/s13105-013-0298-8openalex-snapshot
Low dose of bisphenol A impairs the reproductive axis of prepuberal male rats
inferredcites →https://doi.org/10.1007/s13530-014-0215-8openalex-snapshot
Gene expression analysis of uterine smooth muscle cells exposed to bisphenol A
inferredcites →https://doi.org/10.1016/j.aquatox.2014.01.009openalex-snapshot
Developmental exposure of zebrafish (Danio rerio) to bisphenol-S impairs subsequent reproduction potential and hormonal balance in adults
inferredcites →https://doi.org/10.1016/j.bbagen.2014.05.018openalex-snapshot
Signaling related with biphasic effects of bisphenol A (BPA) on Sertoli cell proliferation: A comparative proteomic analysis
inferredcites →https://doi.org/10.1016/j.chembiol.2014.03.013openalex-snapshot
Defining Estrogenic Mechanisms of Bisphenol A Analogs through High Throughput Microscopy-Based Contextual Assays
inferredcites →https://doi.org/10.1016/j.chemosphere.2009.05.024openalex-snapshot
Assessment of human exposure to Bisphenol-A, Triclosan and Tetrabromobisphenol-A through indoor dust intake in Belgium
inferredcites →https://doi.org/10.1016/j.chemosphere.2014.05.004openalex-snapshot
Urinary levels of bisphenol analogues in residents living near a manufacturing plant in south China
inferredcites →https://doi.org/10.1016/j.chemosphere.2015.01.060openalex-snapshot
Long-term effects of Bisphenol AF (BPAF) on hormonal balance and genes of hypothalamus-pituitary-gonad axis and liver of zebrafish (Danio rerio), and the impact on offspring
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.02.125openalex-snapshot
Effect of bisphenol S exposure on male reproductive system of rats: A histological and biochemical study
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.05.027openalex-snapshot
Influence of metabolism on endocrine activities of bisphenol S
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.08.059openalex-snapshot
Gestational and lactational exposure to bisphenol AF in maternal rats increases testosterone levels in 23-day-old male offspring
inferredcites →https://doi.org/10.1016/j.domaniend.2010.01.004openalex-snapshot
Bisphenol A disrupts granulosa cell function
inferredcites →https://doi.org/10.1016/j.ejogrb.2014.03.052openalex-snapshot
An evidence in vitro for the influence of bisphenol A on uterine leiomyoma
inferredcites →https://doi.org/10.1016/j.envpol.2010.09.004openalex-snapshot
Bisphenol A induces a rapid activation of Erk1/2 through GPR30 in human breast cancer cells
inferredcites →https://doi.org/10.1016/j.envres.2015.11.029openalex-snapshot
Urinary biomarkers of exposure to 57 xenobiotics and its association with oxidative stress in a population in Jeddah, Saudi Arabia
inferredcites →https://doi.org/10.1016/j.etap.2014.09.014openalex-snapshot
Increase in the expression of inducible nitric oxide synthase on exposure to bisphenol A: A possible cause for decline in steroidogenesis in male mice
inferredcites →https://doi.org/10.1016/j.etap.2014.10.015openalex-snapshot
Exposure to a low dose of bisphenol A impairs pituitary-ovarian axis in prepubertal rats
inferredcites →https://doi.org/10.1016/j.etap.2014.10.018openalex-snapshot
Mitochondrion-mediated apoptosis is involved in reproductive damage caused by BPA in male rats
inferredcites →https://doi.org/10.1016/j.etap.2015.03.007openalex-snapshot
Exposure to bisphenol-A and reproductive hormones among male adults
inferredcites →https://doi.org/10.1016/j.fct.2006.03.006openalex-snapshot
Effects of tetrabromobisphenol A, brominated flame retardant, in ICR mice after prenatal and postnatal exposure
inferredcites →https://doi.org/10.1016/j.fct.2011.11.041openalex-snapshot
Bisphenol A impairs insulin signaling and glucose homeostasis and decreases steroidogenesis in rat testis: An in vivo and in silico study
inferredcites →https://doi.org/10.1016/j.fct.2015.03.023openalex-snapshot
Tetrabromobisphenol A (TBBPA): Possible modes of action of toxicity and carcinogenicity in rodents
inferredcites →https://doi.org/10.1016/j.fct.2015.04.009openalex-snapshot
Effects of oral exposure to bisphenol A on gene expression and global genomic DNA methylation in the prostate, female mammary gland, and uterus of NCTR Sprague-Dawley rats
inferredcites →https://doi.org/10.1016/j.fertnstert.2010.09.026openalex-snapshot
Urine bisphenol-A (BPA) level in relation to semen quality
inferredcites →https://doi.org/10.1016/j.fertnstert.2011.06.063openalex-snapshot
Bisphenol A exposure reduces the estradiol response to gonadotropin stimulation during in vitro fertilization
inferredcites →https://doi.org/10.1016/j.fertnstert.2013.03.026openalex-snapshot
Bisphenol A and phthalates and endometriosis: the Endometriosis: Natural History, Diagnosis and Outcomes Study
inferredcites →https://doi.org/10.1016/j.fertnstert.2013.09.030openalex-snapshot
Are urinary bisphenol A levels in men related to semen quality and embryo development after medically assisted reproduction?
inferredcites →https://doi.org/10.1016/j.fertnstert.2014.11.005openalex-snapshot
A new chapter in the bisphenol A story: bisphenol S and bisphenol F are not safe alternatives to this compound
inferredcites →https://doi.org/10.1016/j.jchromb.2012.06.005openalex-snapshot
Determination of bisphenol AF (BPAF) in tissues, serum, urine and feces of orally dosed rats by ultra-high-pressure liquid chromatography–electrospray tandem mass spectrometry
inferredcites →https://doi.org/10.1016/j.jsbmb.2013.01.003openalex-snapshot
Zebrafish and steroids: What do we know and what do we need to know?
inferredcites →https://doi.org/10.1016/j.jsbmb.2015.11.016openalex-snapshot
Ovarian dysfunctions in adult female rat offspring born to mothers perinatally exposed to low doses of bisphenol A
inferredcites →https://doi.org/10.1016/j.lfs.2009.10.004openalex-snapshot
Perinatal exposure of rats to Bisphenol A affects the fertility of male offspring
inferredcites →https://doi.org/10.1016/j.mce.2013.04.025openalex-snapshot
Effects of estrogen and estrogenic compounds, 4-tert-octylphenol, and bisphenol A on the uterine contraction and contraction-associated proteins in rats
inferredcites →https://doi.org/10.1016/j.mrgentox.2007.10.014openalex-snapshot
Exposure of mouse oocytes to bisphenol A causes meiotic arrest but not aneuploidy
inferredcites →https://doi.org/10.1016/j.mrgentox.2007.10.017openalex-snapshot
Continuous exposure to bisphenol A during in vitro follicular development induces meiotic abnormalities
inferredcites →https://doi.org/10.1016/j.ntt.2014.01.002openalex-snapshot
Effects of perinatal bisphenol A exposure during early development on radial arm maze behavior in adult male and female rats
inferredcites →https://doi.org/10.1016/j.rbmo.2010.12.007openalex-snapshot
Effect of bisphenol A on human endometrial stromal fibroblasts in vitro
inferredcites →https://doi.org/10.1016/j.reprotox.2007.06.004openalex-snapshot
In vivo effects of bisphenol A in laboratory rodent studies
inferredcites →https://doi.org/10.1016/j.reprotox.2007.07.005openalex-snapshot
Chapel Hill bisphenol A expert panel consensus statement: Integration of mechanisms, effects in animals and potential to impact human health at current levels of exposure
inferredcites →https://doi.org/10.1016/j.reprotox.2007.07.010openalex-snapshot
Human exposure to bisphenol A (BPA)
inferredcites →https://doi.org/10.1016/j.reprotox.2009.06.011openalex-snapshot
Developmental toxicity of brominated flame retardants, tetrabromobisphenol A and 1,2,5,6,9,10-hexabromocyclododecane, in rat offspring after maternal exposure from mid-gestation through lactation
inferredcites →https://doi.org/10.1016/j.reprotox.2010.07.005openalex-snapshot
Semen quality and sperm DNA damage in relation to urinary bisphenol A among men from an infertility clinic
inferredcites →https://doi.org/10.1016/j.reprotox.2010.10.013openalex-snapshot
Administration of bisphenol A to dams during perinatal period modifies molecular and morphological reproductive parameters of the offspring
inferredcites →https://doi.org/10.1016/j.reprotox.2010.12.002openalex-snapshot
Effect of perinatal and postnatal bisphenol A exposure to the regulatory circuits at the hypothalamus–pituitary–gonadal axis of CD-1 mice
inferredcites →https://doi.org/10.1016/j.reprotox.2011.06.118openalex-snapshot
Neonatal exposure to bisphenol A or diethylstilbestrol alters the ovarian follicular dynamics in the lamb
inferredcites →https://doi.org/10.1016/j.reprotox.2012.05.095openalex-snapshot
Effect of tetrabrombisphenol A on induction of apoptosis in the testes and changes in expression of selected testicular genes in CD1 mice
inferredcites →https://doi.org/10.1016/j.reprotox.2013.03.008openalex-snapshot
Changes in steroid metabolism among girls with precocious puberty may not be associated with urinary levels of bisphenol A
inferredcites →https://doi.org/10.1016/j.reprotox.2013.07.022openalex-snapshot
Bisphenol A inhibits cultured mouse ovarian follicle growth partially via the aryl hydrocarbon receptor signaling pathway
inferredcites →https://doi.org/10.1016/j.reprotox.2013.08.008openalex-snapshot
Bisphenol A and human health: A review of the literature
inferredcites →https://doi.org/10.1016/j.reprotox.2013.09.002openalex-snapshot
Prepubertal bisphenol A exposure interferes with ovarian follicle development and its relevant gene expression
inferredcites →https://doi.org/10.1016/j.reprotox.2014.03.002openalex-snapshot
Bisphenol A affects human endometrial endothelial cell angiogenic activity in vitro
inferredcites →https://doi.org/10.1016/j.reprotox.2014.06.002openalex-snapshot
Prenatal and peripubertal phthalates and bisphenol A in relation to sex hormones and puberty in boys
inferredcites →https://doi.org/10.1016/j.reprotox.2014.09.003openalex-snapshot
Soy but not bisphenol A (BPA) induces hallmarks of polycystic ovary syndrome (PCOS) and related metabolic co-morbidities in rats
inferredcites →https://doi.org/10.1016/j.reprotox.2014.10.010openalex-snapshot
Egr1 is rapidly and transiently induced by estrogen and bisphenol A via activation of nuclear estrogen receptor-dependent ERK1/2 pathway in the uterus
inferredcites →https://doi.org/10.1016/j.reprotox.2014.10.013openalex-snapshot
BPA-induced apoptosis of rat Sertoli cells through Fas/FasL and JNKs/p38 MAPK pathways
inferredcites →https://doi.org/10.1016/j.reprotox.2014.11.003openalex-snapshot
Urinary bisphenol A and semen quality, the LIFE Study
inferredcites →https://doi.org/10.1016/j.reprotox.2015.01.011openalex-snapshot
Developmental exposure to bisphenol A alters the differentiation and functional response of the adult rat uterus to estrogen treatment
inferredcites →https://doi.org/10.1016/j.reprotox.2015.05.012openalex-snapshot
Bisphenol A exposure inhibits germ cell nest breakdown by reducing apoptosis in cultured neonatal mouse ovaries
inferredcites →https://doi.org/10.1016/j.reprotox.2015.08.001openalex-snapshot
Strain-specific induction of endometrial periglandular fibrosis in mice exposed during adulthood to the endocrine disrupting chemical bisphenol A
inferredcites →https://doi.org/10.1016/j.reprotox.2015.10.011openalex-snapshot
Bisphenol A-induced epithelial to mesenchymal transition is mediated by cyclooxygenase-2 up-regulation in human endometrial carcinoma cells
inferredcites →https://doi.org/10.1016/j.reprotox.2015.12.002openalex-snapshot
BPA exposure during in vitro oocyte maturation results in dose-dependent alterations to embryo development rates, apoptosis rate, sex ratio and gene expression
inferredcites →https://doi.org/10.1016/j.reprotox.2015.12.004openalex-snapshot
The effects of in utero bisphenol A exposure on the ovaries in multiple generations of mice
inferredcites →https://doi.org/10.1016/j.reprotox.2016.09.014openalex-snapshot
In vitro exposure of human spermatozoa to bisphenol A induces pro-oxidative/apoptotic mitochondrial dysfunction
inferredcites →https://doi.org/10.1016/j.scitotenv.2013.02.038openalex-snapshot
Levels of tetrabromobisphenol A, hexabromocyclododecanes and polybrominated diphenyl ethers in human milk from the general population in Beijing, China
inferredcites →https://doi.org/10.1016/j.taap.2013.03.016openalex-snapshot
Bisphenol A differentially activates protein kinase C isoforms in murine placental tissue
inferredcites →https://doi.org/10.1016/j.taap.2013.05.015openalex-snapshot
In vitro study on the agonistic and antagonistic activities of bisphenol-S and other bisphenol-A congeners and derivatives via nuclear receptors
inferredcites →https://doi.org/10.1016/j.taap.2015.10.010openalex-snapshot
Exposure to bisphenol A in young adult mice does not alter ovulation but does alter the fertilization ability of oocytes
inferredcites →https://doi.org/10.1016/j.taap.2016.11.013openalex-snapshot
The regulation of cellular apoptosis by the ROS-triggered PERK/EIF2α/chop pathway plays a vital role in bisphenol A-induced male reproductive toxicity
inferredcites →https://doi.org/10.1016/j.tiv.2008.01.015openalex-snapshot
Tetrabromobisphenol A (TBBPA), induces cell death in TM4 Sertoli cells by modulating Ca2+ transport proteins and causing dysregulation of Ca2+ homeostasis
inferredcites →https://doi.org/10.1016/j.tiv.2016.02.017openalex-snapshot
Regulatory and junctional proteins of the blood-testis barrier in human Sertoli cells are modified by monobutyl phthalate (MBP) and bisphenol A (BPA) exposure
inferredcites →https://doi.org/10.1016/j.tox.2006.06.009openalex-snapshot
Human exposure to bisphenol A
inferredcites →https://doi.org/10.1016/j.tox.2007.12.009openalex-snapshot
Endocrine effects of tetrabromobisphenol-A (TBBPA) in Wistar rats as tested in a one-generation reproduction study and a subacute toxicity study
inferredcites →https://doi.org/10.1016/j.tox.2009.09.012openalex-snapshot
Neonatal exposure of male rats to Bisphenol A impairs fertility and expression of sertoli cell junctional proteins in the testis
inferredcites →https://doi.org/10.1016/j.tox.2014.06.001openalex-snapshot
Involvement of CaM-CaMKII-ERK in bisphenol A-induced Sertoli cell apoptosis
inferredcites →https://doi.org/10.1016/j.tox.2014.12.013openalex-snapshot
A reproductive, developmental and neurobehavioral study following oral exposure of tetrabromobisphenol A on Sprague-Dawley rats
inferredcites →https://doi.org/10.1016/j.tox.2015.01.002openalex-snapshot
Adult exposure to bisphenol A (BPA) in Wistar rats reduces sperm quality with disruption of the hypothalamic–pituitary–testicular axis
inferredcites →https://doi.org/10.1016/j.tox.2015.01.003openalex-snapshot
Structural bisphenol analogues differentially target steroidogenesis in murine MA-10 Leydig cells as well as the glucocorticoid receptor
inferredcites →https://doi.org/10.1016/j.toxlet.2003.07.003openalex-snapshot
Comparative study of the uterotrophic potency of 14 chemicals in a uterotrophic assay and their receptor-binding affinity
inferredcites →https://doi.org/10.1016/j.toxlet.2010.02.002openalex-snapshot
Bisphenol A may cause testosterone reduction by adversely affecting both testis and pituitary systems similar to estradiol
inferredcites →https://doi.org/10.1016/j.toxlet.2012.03.802openalex-snapshot
Bisphenol AF may cause testosterone reduction by directly affecting testis function in adult male rats
inferredcites →https://doi.org/10.1016/j.toxlet.2013.03.011openalex-snapshot
Decreased androgen receptor expression may contribute to spermatogenesis failure in rats exposed to low concentration of bisphenol A
inferredcites →https://doi.org/10.1016/j.toxlet.2014.01.035openalex-snapshot
Involvement of activating ERK1/2 through G protein coupled receptor 30 and estrogen receptor α/β in low doses of bisphenol A promoting growth of Sertoli TM4 cells
inferredcites →https://doi.org/10.1016/j.toxlet.2015.08.009openalex-snapshot
Paternal BPA exposure in early life alters Igf2 epigenetic status in sperm and induces pancreatic impairment in rat offspring
inferredcites →https://doi.org/10.1016/j.ygcen.2010.03.030openalex-snapshot
Pre-natal exposure of mice to bisphenol A elicits an endometriosis-like phenotype in female offspring
inferredcites →https://doi.org/10.1016/j.yhbeh.2013.09.007openalex-snapshot
Transgenerational effects of prenatal bisphenol A on social recognition
inferredcites →https://doi.org/10.1016/j.yrtph.2015.04.009openalex-snapshot
Comparative endpoint sensitivity of in vitro estrogen agonist assays
inferredcites →https://doi.org/10.1016/s0303-7207(98)00084-7openalex-snapshot
Bisphenol A interacts with the estrogen receptor α in a distinct manner from estradiol
inferredcites →https://doi.org/10.1016/s0890-6238(03)00044-3openalex-snapshot
Estrogenic effects of food wrap packaging xenoestrogens and flavonoids in female Wistar rats: a comparative study
inferredcites →https://doi.org/10.1017/s0967199415000027openalex-snapshot
Comparison of the effects of BPA and BPAF on oocyte spindle assembly and polar body release in mice
inferredcites →https://doi.org/10.1021/acs.est.5b02135openalex-snapshot
Urinary Concentrations of Bisphenol A and Three Other Bisphenols in Convenience Samples of U.S. Adults during 2000–2014
inferredcites →https://doi.org/10.1021/es300876nopenalex-snapshot
Bisphenol S, a New Bisphenol Analogue, in Paper Products and Currency Bills and Its Association with Bisphenol A Residues
inferredcites →https://doi.org/10.1021/es301334jopenalex-snapshot
Bisphenol S in Urine from the United States and Seven Asian Countries: Occurrence and Human Exposures
inferredcites →https://doi.org/10.1021/es302004wopenalex-snapshot
Occurrence of Eight Bisphenol Analogues in Indoor Dust from the United States and Several Asian Countries: Implications for Human Exposure
inferredcites →https://doi.org/10.1021/es302638dopenalex-snapshot
Predictors of Tetrabromobisphenol-A (TBBP-A) and Hexabromocyclododecanes (HBCD) in Milk from Boston Mothers
inferredcites →https://doi.org/10.1021/es400329topenalex-snapshot
Effects of Bisphenol S Exposure on Endocrine Functions and Reproduction of Zebrafish
inferredcites →https://doi.org/10.1021/es9001604openalex-snapshot
Determinants of Plasma Concentrations of Perfluorooctanesulfonate and Brominated Organic Compounds in Nunavik Inuit Adults (Canada)
inferredcites →https://doi.org/10.1021/es9028292openalex-snapshot
Urinary Bisphenol A Concentrations in Relation to Serum Thyroid and Reproductive Hormone Levels in Men from an Infertility Clinic
inferredcites →https://doi.org/10.1021/jf062250qopenalex-snapshot
Disposition and Metabolic Profiling of Bisphenol F in Pregnant and Nonpregnant Rats
inferredcites →https://doi.org/10.1021/jf400445nopenalex-snapshot
Concentrations and Profiles of Bisphenol A and Other Bisphenol Analogues in Foodstuffs from the United States and Their Implications for Human Exposure
inferredcites →https://doi.org/10.1038/jes.2010.9openalex-snapshot
Daily intake of bisphenol A and potential sources of exposure: 2005–2006 National Health and Nutrition Examination Survey
inferredcites →https://doi.org/10.1038/srep05664openalex-snapshot
Profiling of the Tox21 10K compound library for agonists and antagonists of the estrogen receptor alpha signaling pathway
inferredcites →https://doi.org/10.1038/srep09169openalex-snapshot
Bisphenol-A Affects Male Fertility via Fertility-related Proteins in Spermatozoa
inferredcites →https://doi.org/10.1038/srep40337openalex-snapshot
Long-term exposure to a ‘safe’ dose of bisphenol A reduced protein acetylation in adult rat testes
inferredcites →https://doi.org/10.1039/c6tx00258gopenalex-snapshot
Signals involved in the effects of bisphenol A (BPA) on proliferation and motility of Leydig cells: a comparative proteomic analysis
inferredcites →https://doi.org/10.1073/pnas.1207854109openalex-snapshot
Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey
inferredcites →https://doi.org/10.1080/02652030701882999openalex-snapshot
Determination of brominated flame retardants in food by LC–MS/MS: diastereoisomer-specific hexabromocyclododecane and tetrabromobisphenol A
inferredcites →https://doi.org/10.1093/abbs/gmw039openalex-snapshot
Bisphenol A accelerates capacitation-associated protein tyrosine phosphorylation of rat sperm by activating protein kinase A
inferredcites →https://doi.org/10.1093/annweh/wxw006openalex-snapshot
Assessment of Occupational Exposure to Bisphenol A in Five Different Production Companies in Finland
inferredcites →https://doi.org/10.1093/annweh/wxw021openalex-snapshot
Urinary Bisphenol A (BPA) Concentrations among Workers in Industries that Manufacture and Use BPA in the USA
inferredcites →https://doi.org/10.1093/humrep/deg273openalex-snapshot
Human 'testicular dysgenesis syndrome': a possible model using in-utero exposure of the rat to dibutyl phthalate
inferredcites →https://doi.org/10.1093/humrep/deu011openalex-snapshot
Environmental toxicants perturb human Sertoli cell adhesive function via changes in F-actin organization mediated by actin regulatory proteins
inferredcites →https://doi.org/10.1093/humrep/deu227openalex-snapshot
A population-based case–control study of urinary bisphenol A concentrations and risk of endometriosis
inferredcites →https://doi.org/10.1093/humrep/dev183openalex-snapshot
Urinary bisphenol A concentrations and association within vitrofertilization outcomes among women from a fertility clinic
inferredcites →https://doi.org/10.1093/humrep/dew088openalex-snapshot
Does BPA alter steroid hormone synthesis in human granulosa cellsin vitro?
inferredcites →https://doi.org/10.1093/jb/mvm158openalex-snapshot
Structural Evidence for Endocrine Disruptor Bisphenol A Binding to Human Nuclear Receptor ERR
inferredcites →https://doi.org/10.1093/toxsci/kfi074openalex-snapshot
Comparative Study of the Endocrine-Disrupting Activity of Bisphenol A and 19 Related Compounds
inferredcites →https://doi.org/10.1093/toxsci/kfm306openalex-snapshot
Gestational and Lactational Exposure to Ethinyl Estradiol, but not Bisphenol A, Decreases Androgen-Dependent Reproductive Organ Weights and Epididymal Sperm Abundance in the Male Long Evans Hooded Rat
inferredcites →https://doi.org/10.1093/toxsci/kfq319openalex-snapshot
Bisphenol A Impairs Follicle Growth, Inhibits Steroidogenesis, and Downregulates Rate-Limiting Enzymes in the Estradiol Biosynthesis Pathway
inferredcites →https://doi.org/10.1093/toxsci/kft198openalex-snapshot
Endocrine Disruptors Differentially Target ATP-Binding Cassette Transporters in the Blood-Testis Barrier and Affect Leydig Cell Testosterone Secretion In Vitro
inferredcites →https://doi.org/10.1093/toxsci/kfu022openalex-snapshot
Toxicity Evaluation of Bisphenol A Administered by Gavage to Sprague Dawley Rats From Gestation Day 6 Through Postnatal Day 90
inferredcites →https://doi.org/10.1093/toxsci/kfu030openalex-snapshot
Are Structural Analogues to Bisphenol A Safe Alternatives?
inferredcites →https://doi.org/10.1093/toxsci/kfu081openalex-snapshot
A Short-term In Vivo Screen Using Fetal Testosterone Production, a Key Event in the Phthalate Adverse Outcome Pathway, to Predict Disruption of Sexual Differentiation
inferredcites →https://doi.org/10.1093/toxsci/kfw070openalex-snapshot
Bisphenol A Impairs Mature Sperm Functions by a CatSper-Relevant Mechanism
inferredcites →https://doi.org/10.1093/toxsci/kfw076openalex-snapshot
Bisphenol A-Induced Ovotoxicity Involves DNA Damage Induction to Which the Ovary Mounts a Protective Response Indicated by Increased Expression of Proteins Involved in DNA Repair and Xenobiotic Biotransformation
inferredcites →https://doi.org/10.1093/toxsci/kfw178openalex-snapshot
High-Content Analysis Provides Mechanistic Insights into the Testicular Toxicity of Bisphenol A and Selected Analogues in Mouse Spermatogonial Cells
inferredcites →https://doi.org/10.1095/biolreprod.102.010371openalex-snapshot
Sertoli Cell Tight Junction Dynamics: Their Regulation During Spermatogenesis1
inferredcites →https://doi.org/10.1095/biolreprod.104.037184openalex-snapshot
Exposure In Utero to Di(n-Butyl) Phthalate Alters the Vimentin Cytoskeleton of Fetal Rat Sertoli Cells and Disrupts Sertoli Cell-Gonocyte Contact1
inferredcites →https://doi.org/10.1095/biolreprod.109.078261openalex-snapshot
Neonatal Bisphenol-A Exposure Alters Rat Reproductive Development and Ovarian Morphology Without Impairing Activation of Gonadotropin-Releasing Hormone Neurons1
inferredcites →https://doi.org/10.1095/biolreprod.110.084814openalex-snapshot
Gene Expression in the Fetal Mouse Ovary Is Altered by Exposure to Low Doses of Bisphenol A1
inferredcites →https://doi.org/10.1095/biolreprod.111.095349openalex-snapshot
The Industrial Chemical Bisphenol A (BPA) Interferes with Proliferative Activity and Development of Steroidogenic Capacity in Rat Leydig Cells1
inferredcites →https://doi.org/10.1095/biolreprod42.3.399openalex-snapshot
Hormonal Regulation of Cytochrome P450 Enzymes, Cholesterol Side-Chain Cleavage and 17α-Hydroxylase/C17 – 20 Lyase in Leydig Cells1
inferredcites →https://doi.org/10.1096/fj.09-140533openalex-snapshot
Bisphenol‐A exposure in utero leads to epigenetic alterations in the developmental programming of uterine estrogen response
inferredcites →https://doi.org/10.1111/and.12182openalex-snapshot
Sperm impairments in adult vesper mice (Calomys laucha) caused byin uteroexposure to bisphenol A
inferredcites →https://doi.org/10.1111/andr.12176openalex-snapshot
Low‐dose effect of developmental bisphenol A exposure on sperm count and behaviour in rats
inferredcites →https://doi.org/10.1111/apa.12885openalex-snapshot
The endocrine disruptor bisphenol A may play a role in the aetiopathogenesis of polycystic ovary syndrome in adolescent girls
inferredcites →https://doi.org/10.1111/j.1365-2605.2009.01014.xopenalex-snapshot
Urinary bisphenol A concentrations and ovarian response among women undergoing IVF
inferredcites →https://doi.org/10.1111/j.1745-7262.2008.00292.xopenalex-snapshot
Effects of estradiol-17β and bisphenol A administered chronically to mice throughout pregnancy and lactation on the male pups’ reproductive system
inferredcites →https://doi.org/10.1111/j.2047-2927.2014.00257.xopenalex-snapshot
The effect of tetrabromobisphenol A on protamine content and DNA integrity in mouse spermatozoa
inferredcites →https://doi.org/10.1159/000381321openalex-snapshot
Bisphenol A Exposure during Oocyte Maturation in vitro Results in Spindle Abnormalities and Chromosome Misalignment in Bos taurus
inferredcites →https://doi.org/10.1177/0192623314557335openalex-snapshot
Environmental Chemical Exposure May Contribute to Uterine Cancer Development
inferredcites →https://doi.org/10.1177/0748233712446728openalex-snapshot
Lipoic acid mitigates bisphenol A-induced testicular mitochondrial toxicity in rats
inferredcites →https://doi.org/10.1186/1472-6823-14-86openalex-snapshot
Exploring the potential association between brominated diphenyl ethers, polychlorinated biphenyls, organochlorine pesticides, perfluorinated compounds, phthalates, and bisphenol a in polycystic ovary syndrome: a case–control study
inferredcites →https://doi.org/10.1210/en.2002-220710openalex-snapshot
Sertoli and Germ Cell Development in Hypogonadal (hpg) Mice Expressing Transgenic Follicle-Stimulating Hormone Alone or in Combination with Testosterone
inferredcites →https://doi.org/10.1210/en.2003-1174openalex-snapshot
Inhibition of Testicular Steroidogenesis by the Xenoestrogen Bisphenol A Is Associated with Reduced Pituitary Luteinizing Hormone Secretion and Decreased Steroidogenic Enzyme Gene Expression in Rat Leydig Cells
inferredcites →https://doi.org/10.1210/en.2006-0527openalex-snapshot
Acute and Long-Term Effects of in Utero Exposure of Rats to Di( n -Butyl) Phthalate on Testicular Germ Cell Development and Proliferation
inferredcites →https://doi.org/10.1210/en.2009-1037openalex-snapshot
Neonatal Exposure to Bisphenol A Alters Rat Uterine Implantation-Associated Gene Expression and Reduces the Number of Implantation Sites
inferredcites →https://doi.org/10.1210/en.2015-2031openalex-snapshot
Chronic Exposure to Bisphenol A Affects Uterine Function During Early Pregnancy in Mice
inferredcites →https://doi.org/10.1210/endo.139.10.6216openalex-snapshot
Interaction of Estrogenic Chemicals and Phytoestrogens with Estrogen Receptor β
inferredcites →https://doi.org/10.1210/jc.2010-1658openalex-snapshot
Endocrine Disruptors and Polycystic Ovary Syndrome (PCOS): Elevated Serum Levels of Bisphenol A in Women with PCOS
inferredcites →https://doi.org/10.1289/ehp.0800045openalex-snapshot
Prenatal Exposure to Bisphenol A at Environmentally Relevant Doses Adversely Affects the Murine Female Reproductive Tract Later in Life
inferredcites →https://doi.org/10.1289/ehp.0901257openalex-snapshot
Neonatal Exposure to Bisphenol A and Reproductive and Endocrine Alterations Resembling the Polycystic Ovarian Syndrome in Adult Rats
inferredcites →https://doi.org/10.1289/ehp.0901819openalex-snapshot
Bisphenol AF Is a Full Agonist for the Estrogen Receptor ERα but a Highly Specific Antagonist for ERβ
inferredcites →https://doi.org/10.1289/ehp.1002037openalex-snapshot
Are Environmental Levels of Bisphenol A Associated with Reproductive Function in Fertile Men?
inferredcites →https://doi.org/10.1289/ehp.1002367openalex-snapshot
Daily Bisphenol A Excretion and Associations with Sex Hormone Concentrations: Results from the InCHIANTI Adult Population Study
inferredcites →https://doi.org/10.1289/ehp.10587openalex-snapshot
Direct Evidence Revealing Structural Elements Essential for the High Binding Ability of Bisphenol A to Human Estrogen-Related Receptor-γ
inferredcites →https://doi.org/10.1289/ehp.10753openalex-snapshot
Exposure of the U.S. Population to Bisphenol A and 4- tertiary -Octylphenol: 2003–2004
inferredcites →https://doi.org/10.1289/ehp.1104307openalex-snapshot
Urinary Bisphenol A Concentrations and Implantation Failure among Women Undergoing in Vitro Fertilization
inferredcites →https://doi.org/10.1289/ehp.1307309openalex-snapshot
Urinary Bisphenol A Levels in Young Men: Association with Reproductive Hormones and Semen Quality
inferredcites →https://doi.org/10.1289/ehp.1307728openalex-snapshot
Bisphenol A and Reproductive Health: Update of Experimental and Human Evidence, 2007–2013
inferredcites →https://doi.org/10.1289/ehp.1408605openalex-snapshot
Paternal Urinary Concentrations of Parabens and Other Phenols in Relation to Reproductive Outcomes among Couples from a Fertility Clinic
inferredcites →https://doi.org/10.1289/ehp.1408989openalex-snapshot
Bisphenol S and F: A Systematic Review and Comparison of the Hormonal Activity of Bisphenol A Substitutes
inferredcites →https://doi.org/10.1289/ehp.7505openalex-snapshot
Xenoestrogens at Picomolar to Nanomolar Concentrations Trigger Membrane Estrogen Receptor-α–Mediated Ca2+ Fluxes and Prolactin Release in GH3/B6 Pituitary Tumor Cells
inferredcites →https://doi.org/10.1289/ehp.9366openalex-snapshot
In Utero Exposure to Di( n -butyl) Phthalate and Testicular Dysgenesis: Comparison of Fetal and Adult End Points and Their Dose Sensitivity
inferredcites →https://doi.org/10.1289/ehp150openalex-snapshot
Serum Testosterone Concentrations and Urinary Bisphenol A, Benzophenone-3, Triclosan, and Paraben Levels in Male and Female Children and Adolescents: NHANES 2011–2012
inferredcites →https://doi.org/10.1289/ehp378openalex-snapshot
Gestational Exposure to Bisphenol A Affects the Function and Proteome Profile of F1 Spermatozoa in Adult Mice
inferredcites →https://doi.org/10.1292/jvms.11-0135openalex-snapshot
Bisphenol-A (BPA) Affects Reproductive Formation across Generations in Mice
inferredcites →https://doi.org/10.1371/journal.pgen.1004949openalex-snapshot
Estrogenic Exposure Alters the Spermatogonial Stem Cells in the Developing Testis, Permanently Reducing Crossover Levels in the Adult
inferredcites →https://doi.org/10.1371/journal.pgen.1006223openalex-snapshot
Exposure to the BPA-Substitute Bisphenol S Causes Unique Alterations of Germline Function
inferredcites →https://doi.org/10.1371/journal.pone.0083170openalex-snapshot
Biotransformation of Bisphenol AF to Its Major Glucuronide Metabolite Reduces Estrogenic Activity
inferredcites →https://doi.org/10.1371/journal.pone.0085894openalex-snapshot
Bisphenol A Exposure Alters Developmental Gene Expression in the Fetal Rhesus Macaque Uterus
inferredcites →https://doi.org/10.17877/de290r-127openalex-snapshot
Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats
inferredcites →https://doi.org/10.18632/oncotarget.8689openalex-snapshot
The toxic effects and possible mechanisms of Bisphenol A on oocyte maturation of porcine in vitro
inferredcites →https://doi.org/10.20883/jms.2016.5openalex-snapshot
Bisphenol A modifies human spermatozoa motility in vitro
inferredcites →https://doi.org/10.2131/jts.37.565openalex-snapshot
Lack of effects for dietary exposure of bisphenol A during in utero and lactational periods on reproductive development in rat offspring
inferredcites →https://doi.org/10.2164/jandrol.111.013706openalex-snapshot
Induction and Persistence of Abnormal Testicular Germ Cells Following Gestational Exposure to Di‐(n‐Butyl) Phthalate in p53‐Null Mice
inferredcites →https://doi.org/10.3109/10715762.2010.510523openalex-snapshot
Generation of reactive oxygen species in sperms of rats as an earlier marker for evaluating the toxicity of endocrine-disrupting chemicals
inferredcites →https://doi.org/10.3390/ijerph121013240openalex-snapshot
Associations between Bisphenol A Exposure and Reproductive Hormones among Female Workers
inferredcites →https://doi.org/10.3390/ijerph14010018openalex-snapshot
Bisphenol A and Ovarian Reserve among Infertile Women with Polycystic Ovarian Syndrome
inferredcites →https://doi.org/10.4236/asm.2016.64006openalex-snapshot
Effects of Bisphenol A on Testosterone Levels and Sexual Behaviors of Male Mice
inferredcites →https://doi.org/10.7150/ijms.11957openalex-snapshot
Bisphenol A, Dichlorodiphenyltrichloroethane (DDT) and Vinclozolin Affect ex-vivo Uterine Contraction in Rats via Uterotonin (Prostaglandin F2α, Acetylcholine and Oxytocin) Related Pathways
inferredcites →https://doi.org/10.7669/j.issn.1001-7844.2015.01.0014openalex-snapshot
Pubertal exposure to bisphenol A affects the reproduction of male mice and sex ratio of offspring
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4648934openalex-extracted
The Effect of Bisphenol a Training on the Knowledge Levels of Women: A Quasi-Experimental Study
inferred← citeshttps://doi.org/10.1002/ijgo.15349openalex-snapshot
Bisphenol A and polycystic ovary syndrome in human: A systematic review
inferred← citeshttps://doi.org/10.1002/jat.4514openalex-snapshot
Neurodevelopmental toxicity of bisphenol AF in zebrafish larvae and the protective effects of curcumin
inferred← citeshttps://doi.org/10.1002/jat.4685openalex-snapshot
In silico analysis of endocrine‐disrupting potential of triclosan, bisphenol A, and their analogs and derivatives
inferred← citeshttps://doi.org/10.1002/jat.70302openalex-snapshot
A Systematic Review of Genotoxicity and Mutagenicity Affecting Reproductive and Neurocognitive Health: Bridging Siloed Disciplines
inferred← citeshttps://doi.org/10.1002/jat.70320openalex-snapshot
BPA and Male Reproductive Health: Mechanistic Insights, Toxicological Implications, and the Protective Role of Antioxidants
inferred← citeshttps://doi.org/10.1002/macp.202100449openalex-snapshot
Synthesis and Characterization of Partially Biobased Aromatic (Co)polycarbonates Containing Biphenylene Units and Pendant Pentadecyl Chains
inferred← citeshttps://doi.org/10.1002/slct.202202919openalex-snapshot
Transition Metal Catalysed C‐S Cross‐Coupling Reactions at Room Temperature.
inferred← citeshttps://doi.org/10.1002/tox.70171openalex-snapshot
The Reproductive Toxicity of Microplastics: From Environmental Contamination to Organ Distribution and Reproductive Hazards
inferred← citeshttps://doi.org/10.1002/vms3.70322openalex-snapshot
Therapeutic Effects of Naringin on Bisphenol A‐Induced Oxidative Stress Damage in Nervous and Reproductive Systems of Cockerel Chickens
inferred← citeshttps://doi.org/10.1007/16833_2024_399openalex-snapshot
Micro(Nano)Plastics and the Risk of Cancer Development: Calling for Attention to a Macro Issue
inferred← citeshttps://doi.org/10.1007/978-3-030-38366-4_9-1openalex-snapshot
Environmental Impact on Semen Quality and Male Fertility
inferred← citeshttps://doi.org/10.1007/978-3-030-39044-0_9openalex-snapshot
Environmental Impact on Semen Quality and Male Fertility
inferred← citeshttps://doi.org/10.1007/978-3-030-83160-8_13openalex-snapshot
Endocrine Disruptors and Human Reproduction
inferred← citeshttps://doi.org/10.1007/978-3-031-31501-5_22openalex-snapshot
Influence of Endocrine Disruptors on Male Reproductive Tract
inferred← citeshttps://doi.org/10.1007/978-3-031-65245-5_22openalex-snapshot
Einfluss von endokrinen Disruptoren auf den männlichen Fortpflanzungstrakt
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Addressing the Challenges and Strategies for Improving Micropollutant Degradation in Biological Wastewater Treatment
inferred← citeshttps://doi.org/10.1007/978-3-032-28619-2_13openalex-snapshot
The Toxicological Impact of Xenobiotics on Terrestrial and Aquatic Ecosystems
inferred← citeshttps://doi.org/10.1007/978-981-15-0520-1_16openalex-snapshot
Bisphenols and Alkylphenols
inferred← citeshttps://doi.org/10.1007/978-981-15-0540-9_20openalex-snapshot
Measurement, Analysis, and Remediation of Bisphenol-A from Environmental Matrices
inferred← citeshttps://doi.org/10.1007/978-981-32-9535-3_4openalex-snapshot
Plasticizer Exposure and Reproductive Health: Phthalates and Bisphenol A
inferred← citeshttps://doi.org/10.1007/978-981-95-0575-3_13openalex-snapshot
Environmental Chemical-Induced Heat Shock Proteins in Toxicology: Past, Present, and Future Trends
inferred← citeshttps://doi.org/10.1007/s00129-023-05125-6openalex-snapshot
Gefährdung durch Alltagschemikalien
inferred← citeshttps://doi.org/10.1007/s00204-023-03523-2openalex-snapshot
Effects of bisphenol F, bisphenol S, and bisphenol AF on cultured human osteoblasts
inferred← citeshttps://doi.org/10.1007/s00204-025-04025-zopenalex-snapshot
Mechanisms of bisphenol A and its analogs as endocrine disruptors via nuclear receptors and related signaling pathways
inferred← citeshttps://doi.org/10.1007/s00204-025-04133-wopenalex-snapshot
From toxicogenomics data to cumulative assessment groups: a framework for chemical grouping
inferred← citeshttps://doi.org/10.1007/s00216-019-01996-8openalex-snapshot
Surface plasmon resonance biosensor for the ultrasensitive detection of bisphenol A
inferred← citeshttps://doi.org/10.1007/s10562-024-04745-4openalex-snapshot
Degradation of Bisphenols by Micro-Nano Bubbles Assisted Laccase: Kinetics, Michaelis–Menten Kinetics, Degradation Pathway, and Transformation Relationship
inferred← citeshttps://doi.org/10.1007/s10811-022-02704-3openalex-snapshot
Toxicity of bisphenol A and its structural congeners to microalgae Chlorella vulgaris and Desmodesmus armatus
inferred← citeshttps://doi.org/10.1007/s11356-020-10498-5openalex-snapshot
Molecular and cellular responses to short exposure to bisphenols A, F, and S and eluates of microplastics in C. elegans
inferred← citeshttps://doi.org/10.1007/s11356-021-14496-zopenalex-snapshot
Effects of prenatal exposure to bisphenols on newborn leucocyte telomere length: a prospective birth cohort study in China
inferred← citeshttps://doi.org/10.1007/s11356-021-15166-wopenalex-snapshot
Tetrabromobisphenol A: a neurotoxicant or not?
inferred← citeshttps://doi.org/10.1007/s11356-022-18812-zopenalex-snapshot
Toxicity screening of bisphenol A replacement compounds: cytotoxicity and mRNA expression in LMH 3D spheroids
inferred← citeshttps://doi.org/10.1007/s11356-022-21817-3openalex-snapshot
Associations of bisphenol exposure with thyroid hormones in pregnant women: a prospective birth cohort study in China
inferred← citeshttps://doi.org/10.1007/s11356-022-23089-3openalex-snapshot
Ten bisphenol analogs were abundantly found in swine and bovine urines collected from two Chinese farms: concentration profiles and risk evaluation
inferred← citeshttps://doi.org/10.1007/s11356-022-24920-7openalex-snapshot
The antioxidant effects of coenzyme Q10 on albino rat testicular toxicity and apoptosis triggered by bisphenol A
inferred← citeshttps://doi.org/10.1007/s11356-023-26421-7openalex-snapshot
Associations between exposure to a mixture of phenols and sex steroid hormones among pre- and postmenopausal women: evidence from NHANES 2015–2016
inferred← citeshttps://doi.org/10.1007/s11356-023-27915-0openalex-snapshot
Identification of aquatic ecological risk of bisphenol S in four Asian countries based on the SSD and alternative toxicity data of model species Danio rerio
inferred← citeshttps://doi.org/10.1007/s11356-023-30306-0openalex-snapshot
A lipidomic approach to bisphenol F-induced non-alcoholic fatty liver disease-like changes: altered lipid components in a murine model
inferred← citeshttps://doi.org/10.1007/s12020-020-02502-2openalex-snapshot
Nonfunctional adrenal incidentalomas may be related to bisphenol-A
inferred← citeshttps://doi.org/10.1007/s12020-025-04521-3openalex-snapshot
Bisphenols and their role in female infertility and hormone-related cancer
inferred← citeshttps://doi.org/10.1007/s13205-019-1648-1openalex-snapshot
Simultaneous laccase production and transformation of bisphenol-A and triclosan using Trametes versicolor
inferred← citeshttps://doi.org/10.1007/s13530-024-00236-6openalex-snapshot
In utero and lactational bisphenol A exposure alters testicular function in adult Wistar rats
inferred← citeshttps://doi.org/10.1007/s13596-024-00803-9openalex-snapshot
Protective effects of Sphaeranthus indicus floral extract against BPS-induced testicular damage in rats occurs through downregulation of RIPK1/3-MLK-driven necroptosis and Fas-FasL-mediated apoptosis
inferred← citeshttps://doi.org/10.1007/s42000-025-00638-2openalex-snapshot
The deleterious effect of bisphenol S on early embryo development of mice
inferred← citeshttps://doi.org/10.1007/s43032-024-01521-yopenalex-snapshot
Toxicological Impact of Bisphenol A on Females’ Reproductive System: Review Based on Experimental and Epidemiological Studies
inferred← citeshttps://doi.org/10.1007/s44206-023-00078-8openalex-snapshot
From Seller Screens to Buyer Screens: Toward a Smart Digital Receipt Solution for Sustainability and Greenhouse Gas Mitigation by Million Tons
inferred← citeshttps://doi.org/10.1007/s44339-025-00046-6openalex-snapshot
Effects of Bisphenol-A on human endocrine function and health outcomes: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-820480-1.00162-5openalex-snapshot
Environmental pollution and brain function
inferred← citeshttps://doi.org/10.1016/b978-0-12-824315-2.00420-6openalex-snapshot
Reproductive system, female
inferred← citeshttps://doi.org/10.1016/b978-0-323-85126-8.00011-4openalex-snapshot
Engineering Thermoplastics: Acrylics, Polycarbonates, Polyurethanes, Polyacetals, Polyesters, and Polyamides
inferred← citeshttps://doi.org/10.1016/b978-0-323-88653-6.00015-8openalex-snapshot
Impact of recycled plastic biocomposites on the economy and socioenvironment
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00209-6openalex-snapshot
Effects of Biotransformation on the Toxicity of Organic Chemicals
inferred← citeshttps://doi.org/10.1016/b978-0-443-13301-5.00007-xopenalex-snapshot
Challenges and applications of laccase in bioremediation
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00521-6openalex-snapshot
Environmental Effects on Developing Germ Cells
inferred← citeshttps://doi.org/10.1016/bs.agron.2020.06.005openalex-snapshot
Use of plastic mulch in agriculture and strategies to mitigate the associated environmental concerns
inferred← citeshttps://doi.org/10.1016/j.aquatox.2022.106190openalex-snapshot
Long-term exposure of zebrafish to bisphenol F: Adverse effects on parental reproduction and offspring neurodevelopment
inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106654openalex-snapshot
Metabolic and oxidative stress response of sea cucumber Apostichopus japonicus exposed to acute high concentration of bisphenol AF
inferred← citeshttps://doi.org/10.1016/j.aquatox.2025.107488openalex-snapshot
Mechanistic study of bisphenol A on the growth and microcystin production of Microcystis aeruginosa at different nitrogen levels revealed by the metabolomic analysis
inferred← citeshttps://doi.org/10.1016/j.arcmed.2026.103380openalex-snapshot
Role of Bisphenol A and its Analogues on Epigenetics and their Impact on the Developmental Origins of Female and Male Reproductive Disorders
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119505openalex-snapshot
Alterations induced by Bisphenol A on cellular organelles and potential relevance on human health
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109275openalex-snapshot
A critical review of presence, removal and potential impacts of endocrine disruptors bisphenol A
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109329openalex-snapshot
Sex-specific changes in oxidative stress parameters and longevity produced by Bisphenol F and S compared to Bisphenol A in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109467openalex-snapshot
Transcriptomic sequencing reveals the potential molecular mechanism by which Tetrabromobisphenol A bis (2-hydroxyethyl ether) exposure exerts developmental neurotoxicity in developing zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109527openalex-snapshot
A transcriptomic-based analysis predicts the neuroendocrine disrupting effect on adult male and female zebrafish (Danio rerio) following long-term exposure to tetrabromobisphenol A bis(2-hydroxyethyl) ether
inferred← citeshttps://doi.org/10.1016/j.cbpc.2026.110543openalex-snapshot
Developmental bisphenol A exposure modifies gene expression without altering stress or cognitive outcomes in offspring of a live-bearing fish
inferred← citeshttps://doi.org/10.1016/j.cbpc.2026.110600openalex-snapshot
Effects of long-term exposure to 2,6-di-tert-butylhydroxytoluene and its transformation product 2,6-di-tert-butylbenzoquinone on development and reproduction in zebrafish
inferred← citeshttps://doi.org/10.1016/j.cej.2022.138814openalex-snapshot
Enhanced degradation of organic contaminants by thermally activated peroxymonosulfate in the presence of chloride ion
inferred← citeshttps://doi.org/10.1016/j.ces.2026.124371openalex-snapshot
Oxygen vacancy-enhanced hydrogen spillover synergistically promotes the efficient hydrodeoxygenation of polycarbonate to sustainable aviation fuel over ultrasmall Ru nanoclusters
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.01.020openalex-snapshot
Long-term bisphenol S exposure induces fat accumulation in liver of adult male zebrafish (Danio rerio) and slows yolk lipid consumption in F1 offspring
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.01.065openalex-snapshot
Is bisphenol S a safer alternative to bisphenol A in terms of potential fetal exposure ? Placental transfer across the perfused human placenta
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.03.167openalex-snapshot
Regulation of TBBPA-induced oxidative stress on mitochondrial apoptosis in L02 cells through the Nrf2 signaling pathway
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.05.017openalex-snapshot
Chronic dietary administration of lower levels of diethyl phthalate induces murine testicular germ cell inflammation and sperm pathologies: Involvement of oxidative stress
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.06.073openalex-snapshot
Effects of bisphenol A on post-embryonic development of the cotton pest Spodoptera littoralis
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126422openalex-snapshot
Association of prenatal exposure to bisphenols and birth size in Zhuang ethnic newborns
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128019openalex-snapshot
Prenatal exposure to bisphenol S and altered newborn mitochondrial DNA copy number in a baby cohort study: Sex-specific associations
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.129624openalex-snapshot
Investigating the glucuronidation and sulfation pathways contribution and disposition kinetics of Bisphenol S and its metabolites using LC-MS/MS-based nonenzymatic hydrolysis method
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130118openalex-snapshot
Prenatal exposure to bisphenols affects pregnancy outcomes and offspring development in rats
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130213openalex-snapshot
Comparison of the materno-fetal transfer of fifteen structurally related bisphenol analogues using an ex vivo human placental perfusion model
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.131363openalex-snapshot
Role of cerium oxide nanoparticles in improving oxidative stress and developmental delays in Drosophila melanogaster as an in-vivo model for bisphenol a toxicity
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.132160openalex-snapshot
Analyzing the synergistic adverse effects of BPA and its substitute, BHPF, on ulcerative colitis through comparative metabolomics
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.133510openalex-snapshot
Bisphenol S exposure induces intestinal inflammation: An integrated metabolomic and transcriptomic study
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.134834openalex-snapshot
Exposure to phthalates, phenols, and parabens mixture and alterations in sex steroid hormones among adolescents
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.136259openalex-snapshot
Efficient removal of TBBPA with a Z-scheme BiVO4-(rGO-Cu2O) photocatalyst under sunlight irradiation
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.143297openalex-snapshot
Antioxidants in mitigating phthalate-induced male reproductive toxicity: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.chroma.2022.463489openalex-snapshot
Multi-residue determination of bisphenol analogues in organism tissues by ultra-high performance liquid chromatography-tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.chroma.2024.465096openalex-snapshot
Determination of nine bisphenol analogues in human urine by high-throughput solid-phase extraction and ultra-high performance liquid chromatography-tandem mass spectrometry analysis
inferred← citeshttps://doi.org/10.1016/j.cotox.2023.100391openalex-snapshot
Adverse outcome pathway network approach to identify endocrine disruptor-induced reproductive toxicity
inferred← citeshttps://doi.org/10.1016/j.cotox.2024.100465openalex-snapshot
Inter- and trans-generational impacts of environmental exposures on the germline resolved at the single-cell level
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112960openalex-snapshot
Prenatal exposure to bisphenols and risk of preterm birth: Findings from Guangxi Zhuang birth cohort in China
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113453openalex-snapshot
Bisphenol B disrupts testis differentiation partly via the estrogen receptor-mediated pathway and subsequently causes testicular dysgenesis in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113515openalex-snapshot
Tetramethyl bisphenol a inhibits leydig cell function in late puberty by inducing ferroptosis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.114079openalex-snapshot
Effect of bisphenol F on sexual performance and quality of offspring in Male Wistar rats
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.114565openalex-snapshot
The toxic effect of bisphenol AF and nanoplastic coexposure in parental and offspring generation zebrafish
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115320openalex-snapshot
TBBPA causes inflammation and cell death via the ROS/NF-κB pathway in the gastric mucosa
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115665openalex-snapshot
Effects of prenatal single and mixed bisphenol exposure on bone mineral density in preschool children: A population-based prospective cohort study
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116037openalex-snapshot
Mode of action exploration of reproductive toxicity induced by bisphenol S using human normal ovarian epithelial cells through ERβ-MAPK signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118428openalex-snapshot
Integrated lipidomics and metabolomics approach to assess sex-dependent effects of acute bisphenol A exposure on hepatic lipid metabolism in zebrafish
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118737openalex-snapshot
The role of endoplasmic reticulum stress in BPS-induced disruption of endometrial decidualization
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118747openalex-snapshot
Unveiling BPS-induced colonic inflammatory injury in female mice: Integrated evidence from colon microbiome and metabolomic analyses
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120447openalex-snapshot
Integrated multi-omics analyses reveal potential inflammatory, hepatic, and endocrine risks of the overlooked BPA isomer o,p’-BPA
inferred← citeshttps://doi.org/10.1016/j.electacta.2026.148842openalex-snapshot
Effects of disposable containers and syringes on electrochemical systems
inferred← citeshttps://doi.org/10.1016/j.envadv.2023.100444openalex-snapshot
Microplastics and plastic additives as contaminants of emerging concern: A multi-biomarker approach using Rhinella arenarum tadpoles
inferred← citeshttps://doi.org/10.1016/j.envint.2020.105828openalex-snapshot
A validated search filter for the identification of endocrine disruptors based on the ECHA/EFSA guidance recommendations
inferred← citeshttps://doi.org/10.1016/j.envint.2020.106305openalex-snapshot
Sex-specific associations of prenatal exposure to bisphenol A and its alternatives with fetal growth parameters and gestational age
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107225openalex-snapshot
Tyrosinase-functionalized polyhydroxyalkanoate bio-beads as a novel biocatalyst for degradation of bisphenol analogues
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107576openalex-snapshot
Lifestyle interventions to reduce endocrine-disrupting phthalate and phenol exposures among reproductive age men and women: A review and future steps
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107721openalex-snapshot
Adverse (geno)toxic effects of bisphenol A and its analogues in hepatic 3D cell model
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107722openalex-snapshot
Comparison of toxicokinetic properties of eleven analogues of Bisphenol A in pig after intravenous and oral administrations
inferred← citeshttps://doi.org/10.1016/j.envint.2023.107976openalex-snapshot
Estrogenic and non-estrogenic effects of bisphenol A and its action mechanism in the zebrafish model: An overview of the past two decades of work
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109372openalex-snapshot
Chemical risk assessment in food animals via physiologically based pharmacokinetic modeling – Part II: Environmental pollutants on animal and human health assessments
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110191openalex-snapshot
Assessment of Pergafast 201 absorption and metabolism in viable human skin: A comparative study with bisphenol A and bisphenol S
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.01.116openalex-snapshot
Effects of perinatal exposure to BPA, BPF and BPAF on liver function in male mouse offspring involving in oxidative damage and metabolic disorder
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.07.089openalex-snapshot
Urinary bisphenol analogues concentrations and biomarkers of oxidative DNA and RNA damage in Chinese school children in East China: A repeated measures study
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.113980openalex-snapshot
Evaluation of the effects of low concentrations of bisphenol AF on gonadal development using the Xenopus laevis model: A finding of testicular differentiation inhibition coupled with feminization
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114535openalex-snapshot
Long-term bisphenol S exposure aggravates non-alcoholic fatty liver by regulating lipid metabolism and inducing endoplasmic reticulum stress response with activation of unfolded protein response in male zebrafish
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.116380openalex-snapshot
Multisystemic alterations in humans induced by bisphenol A and phthalates: Experimental, epidemiological and clinical studies reveal the need to change health policies
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.116448openalex-snapshot
Adsorption of emerging contaminants from water and wastewater by modified biochar: A review
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.118825openalex-snapshot
Bisphenol AF blocks Leydig cell regeneration from stem cells in male rats
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.123549openalex-snapshot
Structural insight into the mechanisms and interacting features of endocrine disruptor Bisphenol A and its analogs with human estrogen-related receptor gamma
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.123600openalex-snapshot
Bisphenols and brominated bisphenols induced endothelial dysfunction via its disruption of endothelial nitric oxide synthase
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124064openalex-snapshot
Spatial distribution, source identification, and potential risks of 14 bisphenol analogues in soil under different land uses in the megacity of Chengdu, China
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124447openalex-snapshot
Emerging regulatory roles of noncoding RNAs induced by bisphenol a (BPA) and its alternatives in human diseases
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.125844openalex-snapshot
Embryonic BPF exposure induces neurodevelopmental and neurobehavioral toxicity by affecting neural stem cell proliferation in Drosophila
inferred← citeshttps://doi.org/10.1016/j.envres.2021.111459openalex-snapshot
The associations of birth outcome differences in twins with prenatal exposure to bisphenol A and its alternatives
inferred← citeshttps://doi.org/10.1016/j.envres.2021.112233openalex-snapshot
Regulatory and academic studies to derive reference values for human health: The case of bisphenol S
inferred← citeshttps://doi.org/10.1016/j.envres.2021.112293openalex-snapshot
Environmental exposure to bisphenol analogues and unexplained recurrent miscarriage: A case-control study
inferred← citeshttps://doi.org/10.1016/j.envres.2021.112594openalex-snapshot
Review of the environmental occurrence, analytical techniques, degradation and toxicity of TBBPA and its derivatives
inferred← citeshttps://doi.org/10.1016/j.envres.2022.114198openalex-snapshot
Multi-omics approaches for remediation of bisphenol A: Toxicity, risk analysis, road blocks and research perspectives
inferred← citeshttps://doi.org/10.1016/j.envres.2023.116900openalex-snapshot
Exposure to bisphenol A associated with multiple health-related outcomes in humans: An umbrella review of systematic reviews with meta-analyses
inferred← citeshttps://doi.org/10.1016/j.envres.2024.120086openalex-snapshot
Exploring the association between urinary bisphenol A, S, and F levels and semen quality parameters: Findings from Led-Fertyl cross-sectional study
inferred← citeshttps://doi.org/10.1016/j.envres.2024.120476openalex-snapshot
Prenatal bisphenol analogs exposure and placental DNA hypomethylation of genes in the PPAR signaling pathway: Insights for bisphenol analogs’ effects on infant anthropometry
inferred← citeshttps://doi.org/10.1016/j.envres.2025.120888openalex-snapshot
Perinatal exposure to bisphenol A or S alters differently sexual behavior and kisspeptin system in mice
inferred← citeshttps://doi.org/10.1016/j.envres.2026.123678openalex-snapshot
Transport of bisphenol analogues and their conjugated metabolites across human blood-cerebrospinal fluid barrier
inferred← citeshttps://doi.org/10.1016/j.envres.2026.125752openalex-snapshot
Associations between prenatal bisphenol S with gestational age and preterm birth: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.etap.2023.104300openalex-snapshot
Bisphenol S dysregulates thyroid hormone homeostasis; Testicular survival, redox and metabolic status: Ameliorative actions of melatonin
inferred← citeshttps://doi.org/10.1016/j.fct.2023.113701openalex-snapshot
Safer alternatives? Bisphenol F and Bisphenol S induce oxidative stress in Drosophila melanogaster larvae and trigger developmental damage
inferred← citeshttps://doi.org/10.1016/j.fct.2023.114416openalex-snapshot
Potential impacts of bisphenols on prostate cells: An overview of cytotoxicity, proliferation, oxidative stress, apoptosis, and ER-stress response activation
inferred← citeshttps://doi.org/10.1016/j.fct.2024.114485openalex-snapshot
Bisphenol chemicals in colostrum from Shanghai, China during 2006–2019: Concentration, temporal variation, and potential influence on birth parameters
inferred← citeshttps://doi.org/10.1016/j.fct.2025.115827openalex-snapshot
Assessing the role of bisphenol A in female reproductive cancers using network toxicology, molecular dynamics, and preliminary experimental validation
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2020.03.014openalex-snapshot
Heritability of subfertility among Danish twins
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.135642openalex-snapshot
Quantitative determination of BPA, BPB, BPF and BPS levels in canned legumes from Italian market
inferred← citeshttps://doi.org/10.1016/j.fshw.2022.03.020openalex-snapshot
The protective effects of Procyanidin C-1 on bisphenol a-induced testicular dysfunction in aged mice
inferred← citeshttps://doi.org/10.1016/j.hazl.2024.100110openalex-snapshot
Disruption of functions of primary human neonatal melanocytes cultured in the presence of bisphenol A and its analogs bisphenol F and bisphenol S
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e13003openalex-snapshot
High cytotoxicity of a degraded TBBPA, dibromobisphenol A, through apoptotic and necrosis pathways
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e18140openalex-snapshot
Origin, dietary exposure, and toxicity of endocrine-disrupting food chemical contaminants: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.jece.2025.119094openalex-snapshot
Advancement of electrochemical sensors in the detection of estrogen steroids in the environment: A critical review
inferred← citeshttps://doi.org/10.1016/j.jece.2026.125215openalex-snapshot
Visible-light bisphenol S removal by magnetically recoverable BiOBr/ZnFe2O4: Catalyst recovery and water-matrix effects
inferred← citeshttps://doi.org/10.1016/j.jes.2020.04.016openalex-snapshot
A simple fluorescence anisotropy assay for detection of bisphenol A using fluorescently labeled aptamer
inferred← citeshttps://doi.org/10.1016/j.jfca.2023.105366openalex-snapshot
Analysis of bisphenols and their derivatives in infant and toddler ready-to-feed milk and powdered milk by LC MS/MS
inferred← citeshttps://doi.org/10.1016/j.jfca.2024.106852openalex-snapshot
Occurrence and profiles of bisphenol A and its analogues in marine shrimps from Tianjin and their implications for human exposure
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.130945openalex-snapshot
Characterization of pregnant women exposure to halogenated parabens and bisphenols through water consumption
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131103openalex-snapshot
Efficient removal of organic contaminants in CuS-mediated solid-liquid-interfacial fenton-like system: Role of bimetallic cycle and sulfur species
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133935openalex-snapshot
Deciphering the mechanisms and interactions of the endocrine disruptor bisphenol A and its analogs with the androgen receptor
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.136770openalex-snapshot
Addressing data gaps in deriving aquatic life ambient water quality criteria for contaminants of emerging concern: Challenges and the potential of in silico methods
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.142403openalex-snapshot
Is BPA only the tip of the iceberg? Occurrence and risk assessment of 32 bisphenol analogues in landfill leachate
inferred← citeshttps://doi.org/10.1016/j.jmst.2021.03.071openalex-snapshot
Diatomite supported nano zero valent iron with 3D network for peroxymonosulfate activation in efficient degradation of bisphenol A
inferred← citeshttps://doi.org/10.1016/j.jwpe.2019.01.017openalex-snapshot
Pollutant removal and acute toxicity assessment (Artemia salina) of landfill leachate treated by photo-Fenton process mediated by oxalic acid
inferred← citeshttps://doi.org/10.1016/j.jwpe.2025.107777openalex-snapshot
Advanced landfill leachate treatment: Sequential electrocoagulation and electrooxidation system for efficient remediation
inferred← citeshttps://doi.org/10.1016/j.microc.2021.106413openalex-snapshot
HPLC-DAD and PARAFAC for the determination of bisphenol-A and another four bisphenols migrating from BPA-free polycarbonate glasses
inferred← citeshttps://doi.org/10.1016/j.neuro.2021.06.001openalex-snapshot
Behavioral changes and hyperglycemia in NODEF mice following bisphenol S exposure are affected by diets
inferred← citeshttps://doi.org/10.1016/j.ntt.2024.107331openalex-snapshot
Bisphenol F affects neurodevelopmental gene expression, mushroom body development, and behavior in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.polymdegradstab.2019.05.018openalex-snapshot
Epoxidized linseed oils based networks. Case of thermal degradation
inferred← citeshttps://doi.org/10.1016/j.reprotox.2019.08.001openalex-snapshot
BPA interferes with StAR-mediated mitochondrial cholesterol transport to induce germline dysfunctions
inferred← citeshttps://doi.org/10.1016/j.reprotox.2020.05.003openalex-snapshot
Developmental Exposure to Tetrabromobisphenol A Has Minimal Impact on Male Rat Reproductive Health
inferred← citeshttps://doi.org/10.1016/j.reprotox.2021.05.004openalex-snapshot
Bisphenol analogs AF, S and F: Effects on functional characteristics of porcine granulosa cells
inferred← citeshttps://doi.org/10.1016/j.reprotox.2021.11.007openalex-snapshot
Low-dose bisphenol S exposure induces hypospermatogenesis and mitochondrial dysfunction in rats: A possible implication of StAR protein
inferred← citeshttps://doi.org/10.1016/j.reprotox.2023.108380openalex-snapshot
The fate of bisphenol A, bisphenol S, and their respective glucuronide metabolites in ovarian cells
inferred← citeshttps://doi.org/10.1016/j.reprotox.2023.108456openalex-snapshot
Carvacrol showed a curative effect on reproductive toxicity caused by Bisphenol AF via antioxidant, anti-inflammatory and anti-apoptotic properties
inferred← citeshttps://doi.org/10.1016/j.reprotox.2024.108579openalex-snapshot
Molecular insights into the antioxidative and anti-inflammatory effects of P-coumaric acid against bisphenol A-induced testicular injury: In vivo and in silico studies
inferred← citeshttps://doi.org/10.1016/j.reprotox.2024.108723openalex-snapshot
Elucidating the molecular interactions and immune modulation of bisphenols exposure in the pathogenesis of polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1016/j.reprotox.2025.108857openalex-snapshot
The biological effects of bisphenol AF in reproduction and development: What do we know so far?
inferred← citeshttps://doi.org/10.1016/j.reprotox.2025.109000openalex-snapshot
Cell-free circulating epigenomic signatures: Non-invasive biomarkers of pregnancy-related outcomes associated with plasticizer exposure
inferred← citeshttps://doi.org/10.1016/j.reprotox.2025.109017openalex-snapshot
Reprotoxic effect of bisphenol F and bisphenol S on female Drosophila melanogaster exposed during development
inferred← citeshttps://doi.org/10.1016/j.saa.2022.121910openalex-snapshot
Potential toxicity of bisphenol A to α-chymotrypsin and the corresponding mechanisms of their binding
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.02.064openalex-snapshot
Photochemical degradation of BPF, BPS and BPZ in aqueous solution: Identification of transformation products and degradation kinetics
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.139190openalex-snapshot
Oxidative stress in bisphenol AF-induced cardiotoxicity in zebrafish and the protective role of N-acetyl N-cysteine
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.142854openalex-snapshot
Bisphenol A in Africa: A review of environmental and biological levels
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.144059openalex-snapshot
Bisphenol S perturbs Sertoli cell junctions in male rats via alterations in cytoskeletal organization mediated by an imbalance between mTORC1 and mTORC2
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.148796openalex-snapshot
The internal exposure of bisphenol analogues in South China adults and the associated health risks
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.148985openalex-snapshot
Accumulation and passive sampling of bisphenol analogues using triolein-embedded cellulose acetate membrane in waters
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.154444openalex-snapshot
Bisphenol chemicals disturb intestinal homeostasis via Notch/Wnt signaling and induce mucosal barrier dysregulation and inflammation
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.156590openalex-snapshot
Long-term exposure to bisphenol A and its analogues alters the behavior of marine medaka (Oryzias melastigma) and causes hepatic injury
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.160089openalex-snapshot
Transcriptomic profiling reveals the neuroendocrine-disrupting effect and toxicity mechanism of TBBPA-DHEE exposure in zebrafish (Danio rerio) during sexual development
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.160762openalex-snapshot
In vitro and in silico assessment of GPER-dependent neurocytotoxicity of emerging bisphenols
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.163122openalex-snapshot
Dermal exposure to bisphenols in pregnant women's and baby clothes: Risk characterization
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.163496openalex-snapshot
Risk assessment of bisphenol A (BPA) in Irish meat and meat products
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.165586openalex-snapshot
Associations among bisphenol A, its analogs, and chlorinated derivatives in placenta and risk for neural tube defects: A case-control study
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.167076openalex-snapshot
Exposure assessment to bisphenol A (BPA) and its analogues bisphenol S (BPS) and bisphenol F (BPF) in wild boars by hair analysis
inferred← citeshttps://doi.org/10.1016/j.scowo.2025.100161openalex-snapshot
Plant extract-mediated synthesis of rods-like tin oxide loaded on graphene oxide and its application for electrochemical sensor of bisphenol-A
inferred← citeshttps://doi.org/10.1016/j.seppur.2020.116924openalex-snapshot
Fabrication of Fe2O3/g-C3N4@N-TiO2 photocatalyst nanotube arrays that promote bisphenol A photodegradation under simulated sunlight irradiation
inferred← citeshttps://doi.org/10.1016/j.taap.2021.115634openalex-snapshot
Bisphenol analogs AF and S: Effects on cell status and production of angiogenesis-related factors by COV434 human granulosa cell line
inferred← citeshttps://doi.org/10.1016/j.taap.2024.116953openalex-snapshot
Cyanidin improves spatial memory and cognition in bisphenol A-induced rat model of Alzheimer's-like neuropathology by restoring canonical Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.08.023openalex-snapshot
Azanza garckeana ameliorates Bisphenol A-induced reproductive toxicities in rabbit bucks
inferred← citeshttps://doi.org/10.1016/j.tice.2021.101502openalex-snapshot
Structural and chemical role of mesenchymal stem cells and resveratrol in regulation of apoptotic -induced genes in Bisphenol-A induced uterine damage in adult female albino rats
inferred← citeshttps://doi.org/10.1016/j.tiv.2023.105589openalex-snapshot
High-content analysis of testicular toxicity of BPA and its selected analogs in mouse spermatogonial, Sertoli cells, and Leydig cells revealed BPAF induced unique multinucleation phenotype associated with the increased DNA synthesis
inferred← citeshttps://doi.org/10.1016/j.tox.2019.03.016openalex-snapshot
Bisphenol F has different effects on preadipocytes differentiation and weight gain in adult mice as compared with Bisphenol A and S
inferred← citeshttps://doi.org/10.1016/j.tox.2019.05.008openalex-snapshot
Use of connectivity mapping to support read across: A deeper dive using data from 186 chemicals, 19 cell lines and 2 case studies
inferred← citeshttps://doi.org/10.1016/j.tox.2022.153282openalex-snapshot
Bisphenols A, F, S and AF trigger apoptosis and/or endoplasmic reticulum stress in human endometrial stromal cells
inferred← citeshttps://doi.org/10.1016/j.tox.2024.154040openalex-snapshot
Bisphenol A and its potential mechanism of action for reproductive toxicity
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