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Bisphenol S instead of bisphenol A: a story of reproductive disruption by regretable substitution - a review
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/2012.jama.11461openalex-snapshot
Association Between Urinary Bisphenol A Concentration and Obesity Prevalence in Children and Adolescents
inferredcites →https://doi.org/10.1001/jama.2013.283735openalex-snapshot
Handling of Thermal Receipts as a Source of Exposure to Bisphenol A
inferredcites →https://doi.org/10.1001/jama.300.11.1303openalex-snapshot
Association of Urinary Bisphenol A Concentration With Medical Disorders and Laboratory Abnormalities in Adults
inferredcites →https://doi.org/10.1002/em.21847openalex-snapshot
Di‐(2‐ethylhexyl) phthalate and bisphenol A exposure impairs mouse primordial follicle assembly in vitro
inferredcites →https://doi.org/10.1002/tox.10035openalex-snapshot
Acute toxicity, mutagenicity, and estrogenicity of bisphenol‐A and other bisphenols
inferredcites →https://doi.org/10.1007/978-3-319-01619-1_3openalex-snapshot
Adverse Effects of Bisphenol A on Male Reproductive Function
inferredcites →https://doi.org/10.1007/s00204-016-1671-5openalex-snapshot
From bisphenol A to bisphenol F and a ban of mustard due to chronic low-dose exposures?
inferredcites →https://doi.org/10.1007/s002040050659openalex-snapshot
Metabolism and cytotoxicity of bisphenol A and other bisphenols in isolated rat hepatocytes
inferredcites →https://doi.org/10.1007/s00216-010-3464-7openalex-snapshot
Comparison of two derivatization-based methods for solid-phase microextraction–gas chromatography–mass spectrometric determination of bisphenol A, bisphenol S and biphenol migrated from food cans
inferredcites →https://doi.org/10.1007/s00420-012-0834-9openalex-snapshot
Bisphenol A concentrations in maternal breast milk and infant urine
inferredcites →https://doi.org/10.1007/s10646-012-0863-xopenalex-snapshot
Neonicotinoids in bees: a review on concentrations, side-effects and risk assessment
inferredcites →https://doi.org/10.1007/s10815-011-9634-5openalex-snapshot
Relationship between meiotic spindle characteristics in human oocytes and the timing of the first zygotic cleavage after intracytoplasmic sperm injection
inferredcites →https://doi.org/10.1007/s11033-011-1372-3openalex-snapshot
Fetal exposure to bisphenol A affects the primordial follicle formation by inhibiting the meiotic progression of oocytes
inferredcites →https://doi.org/10.1007/s40572-014-0025-9openalex-snapshot
Endocrine Disruptors: Time to Act
inferredcites →https://doi.org/10.1016/j.ajpath.2012.05.021openalex-snapshot
Respiratory and Olfactory Cytotoxicity of Inhaled 2,3-Pentanedione in Sprague-Dawley Rats
inferredcites →https://doi.org/10.1016/j.aquatox.2005.08.004openalex-snapshot
Effect of bisphenol A on maturation and quality of semen and eggs in the brown trout, Salmo trutta f. fario
inferredcites →https://doi.org/10.1016/j.aquatox.2011.10.013openalex-snapshot
Disruption of the hypothalamic-pituitary-thyroid axis in zebrafish embryo–larvae following waterborne exposure to BDE-47, TBBPA and BPA
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.cbi.2013.03.013openalex-snapshot
Bisphenol A affects androgen receptor function via multiple mechanisms
inferredcites →https://doi.org/10.1016/j.cbi.2015.05.012openalex-snapshot
Stress lowers the threshold dose at which bisphenol A disrupts blastocyst implantation, in conjunction with decreased uterine closure and e-cadherin
inferredcites →https://doi.org/10.1016/j.chemosphere.2006.06.073openalex-snapshot
Measurement of bisphenol A concentrations in human colostrum
inferredcites →https://doi.org/10.1016/j.chemosphere.2012.05.003openalex-snapshot
Bisphenol A in human placental and fetal liver tissues collected from Greater Montreal area (Quebec) during 1998–2008
inferredcites →https://doi.org/10.1016/j.chemosphere.2013.05.029openalex-snapshot
Genotoxic potentials and related mechanisms of bisphenol A and other bisphenol compounds: A comparison study employing chicken DT40 cells
inferredcites →https://doi.org/10.1016/j.chemosphere.2014.02.034openalex-snapshot
Chemical alternatives assessment: The case of flame retardants
inferredcites →https://doi.org/10.1016/j.chemosphere.2014.12.062openalex-snapshot
Occurrence of endocrine disrupting compounds in five estuaries of the northwest coast of Spain: Ecological and human health impact
inferredcites →https://doi.org/10.1016/j.chroma.2013.12.074openalex-snapshot
Simultaneous determination of seven bisphenols in environmental water and solid samples by liquid chromatography–electrospray tandem mass spectrometry
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.envint.2011.04.010openalex-snapshot
Bisphenol A (BPA) in China: A review of sources, environmental levels, and potential human health impacts
inferredcites →https://doi.org/10.1016/j.envint.2012.08.003openalex-snapshot
A novel abbreviation standard for organobromine, organochlorine and organophosphorus flame retardants and some characteristics of the chemicals
inferredcites →https://doi.org/10.1016/j.envint.2013.02.014openalex-snapshot
Dietary and sociodemographic determinants of bisphenol A urine concentrations in pregnant women and children
inferredcites →https://doi.org/10.1016/j.envpol.2013.11.023openalex-snapshot
Occurrence and profiles of bisphenol analogues in municipal sewage sludge in China
inferredcites →https://doi.org/10.1016/j.envres.2005.09.001openalex-snapshot
Large effects from small exposures. II. The importance of positive controls in low-dose research on bisphenol A
inferredcites →https://doi.org/10.1016/j.etap.2004.05.009openalex-snapshot
Estrogenic activity of alkylphenols, bisphenol S, and their chlorinated derivatives using a GFP expression system
inferredcites →https://doi.org/10.1016/j.etap.2011.06.003openalex-snapshot
Serum unconjugated bisphenol A concentrations in men may influence embryo quality indicators during in vitro fertilization
inferredcites →https://doi.org/10.1016/j.fct.2014.04.011openalex-snapshot
Comparative study of bisphenol A and its analogue bisphenol S on human hepatic cells: A focus on their potential involvement in nonalcoholic fatty liver disease
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.2013.08.021openalex-snapshot
Chronic exposure to a low concentration of bisphenol A during follicle culture affects the epigenetic status of germinal vesicles and metaphase II oocytes
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.ijdevneu.2013.03.004openalex-snapshot
Developmental regulation of neuronal genes by DNA methylation: Environmental influences
inferredcites →https://doi.org/10.1016/j.jchromb.2010.10.021openalex-snapshot
Determination of Bisphenol A and its chlorinated derivatives in placental tissue samples by liquid chromatography–tandem mass spectrometry
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.mrgentox.2007.10.009openalex-snapshot
Evaluation of aneugenic effects of bisphenol A in somatic and germ cells of the mouse
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.neuro.2009.02.010openalex-snapshot
Impact of neonatal exposure to the ERα agonist PPT, bisphenol-A or phytoestrogens on hypothalamic kisspeptin fiber density in male and female rats
inferredcites →https://doi.org/10.1016/j.rbmo.2014.06.013openalex-snapshot
Bisphenol A, oocyte maturation, implantation, and IVF outcome: review of animal and human data
inferredcites →https://doi.org/10.1016/j.reprotox.2007.05.010openalex-snapshot
In vitro molecular mechanisms of bisphenol A action
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.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.2011.08.010openalex-snapshot
Preimplantation exposure to bisphenol A (BPA) affects embryo transport, preimplantation embryo development, and uterine receptivity in mice
inferredcites →https://doi.org/10.1016/j.reprotox.2012.03.009openalex-snapshot
Fetal bisphenol A exposure: Concentration of conjugated and unconjugated bisphenol A in amniotic fluid in the second and third trimesters
inferredcites →https://doi.org/10.1016/j.reprotox.2013.02.002openalex-snapshot
Regulatory decisions on endocrine disrupting chemicals should be based on the principles of endocrinology
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.2014.06.001openalex-snapshot
Bidirectional placental transfer of Bisphenol A and its main metabolite, Bisphenol A-Glucuronide, in the isolated perfused human placenta
inferredcites →https://doi.org/10.1016/j.smim.2014.03.005openalex-snapshot
Functions of caspase 8: The identified and the mysterious
inferredcites →https://doi.org/10.1016/j.taap.2004.11.015openalex-snapshot
Toxicological awakenings: the rebirth of hormesis as a central pillar of toxicology
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.2014.07.025openalex-snapshot
Is bisphenol S a safe substitute for bisphenol A in terms of metabolic function? An in vitro study
inferredcites →https://doi.org/10.1016/j.taap.2015.03.003openalex-snapshot
The effects of in utero bisphenol A exposure on reproductive capacity in several generations of mice
inferredcites →https://doi.org/10.1016/j.tiv.2012.03.013openalex-snapshot
Weak estrogenic transcriptional activities of Bisphenol A and Bisphenol S
inferredcites →https://doi.org/10.1016/j.tox.2005.08.006openalex-snapshot
Evaluation of androgen receptor transcriptional activities of bisphenol A, octylphenol and nonylphenol in vitro
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.2006.08.012openalex-snapshot
Endocrine disruptor bisphenol A strongly binds to human estrogen-related receptor γ (ERRγ) with high constitutive activity
inferredcites →https://doi.org/10.1016/s0048-9697(98)00332-5openalex-snapshot
Amphibians as a model to study endocrine disruptors: II. Estrogenic activity of environmental chemicals in vitro and in vivo
inferredcites →https://doi.org/10.1016/s0140-6736(61)90927-8openalex-snapshot
THALIDOMIDE AND CONGENITAL ABNORMALITIES
inferredcites →https://doi.org/10.1016/s0890-6238(02)00005-9openalex-snapshot
Developmental effects of perinatal exposure to bisphenol-A and diethylstilbestrol on reproductive organs in female mice
inferredcites →https://doi.org/10.1016/s0890-6238(02)00051-5openalex-snapshot
Maternal serum and amniotic fluid bisphenol A concentrations in the early second trimester
inferredcites →https://doi.org/10.1016/s0960-9822(03)00189-1openalex-snapshot
Bisphenol A Exposure Causes Meiotic Aneuploidy in the Female Mouse
inferredcites →https://doi.org/10.1016/s1472-6483(10)60784-5openalex-snapshot
Meiotic spindle and zona pellucida characteristics as predictors of embryonic development: a preliminary study using PolScope imaging
inferredcites →https://doi.org/10.1017/s1751731112001140openalex-snapshot
Pyrethroids cypermethrin, deltamethrin and fenvalerate have different effects on in vitro maturation of pig oocytes at different stages of growth
inferredcites →https://doi.org/10.1021/es000198nopenalex-snapshot
Reproductive Effects of Long-Term Exposure to Bisphenol A in the Fathead Minnow ( Pimephales promelas )
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/es400329topenalex-snapshot
Effects of Bisphenol S Exposure on Endocrine Functions and Reproduction of Zebrafish
inferredcites →https://doi.org/10.1021/es505302copenalex-snapshot
Cell-Specific Biotransformation of Benzophenone-2 and Bisphenol-S in Zebrafish and Human in Vitro Models Used for Toxicity and Estrogenicity Screening
inferredcites →https://doi.org/10.1021/jp500404uopenalex-snapshot
Exploring the Interaction of Bisphenol-S with Serum Albumins: A Better or Worse Alternative for Bisphenol A?
inferredcites →https://doi.org/10.1021/tx7002382openalex-snapshot
Screening of 397 Chemicals and Development of a Quantitative Structure−Activity Relationship Model for Androgen Receptor Antagonism
inferredcites →https://doi.org/10.1038/137996a0openalex-snapshot
Synthetic strogenic Agents without the Phenanthrene Nucleus
inferredcites →https://doi.org/10.1073/pnas.0703739104openalex-snapshot
Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development
inferredcites →https://doi.org/10.1073/pnas.1107958108openalex-snapshot
Disruption of adult expression of sexually selected traits by developmental exposure to bisphenol A
inferredcites →https://doi.org/10.1073/pnas.1203574109openalex-snapshot
Structural and mechanistic insights into bisphenols action provide guidelines for risk assessment and discovery of bisphenol A substitutes
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/10.1073/pnas.1214056110openalex-snapshot
Sex-specific epigenetic disruption and behavioral changes following low-dose in utero bisphenol A exposure
inferredcites →https://doi.org/10.1073/pnas.1417731112openalex-snapshot
Low-dose exposure to bisphenol A and replacement bisphenol S induces precocious hypothalamic neurogenesis in embryonic zebrafish
inferredcites →https://doi.org/10.1080/02652030210146837openalex-snapshot
Survey of bisphenol A and bisphenol F in canned foods
inferredcites →https://doi.org/10.1080/19440049.2015.1110623openalex-snapshot
Natural occurrence of bisphenol F in mustard
inferredcites →https://doi.org/10.1080/20024091064291openalex-snapshot
Critical Review and Evaluation of the Uterotrophic Bioassay for the Identification of Possible Estrogen Agonists and Antagonists: In Support of the Validation of the OECD Uterotrophic Protocols for the Laboratory Rodent
inferredcites →https://doi.org/10.1093/humrep/17.11.2839openalex-snapshot
Determination of bisphenol A concentrations in human biological fluids reveals significant early prenatal exposure
inferredcites →https://doi.org/10.1093/humrep/der249openalex-snapshot
Human meiotic progression and recombination are affected by Bisphenol A exposure during in vitro human oocyte development
inferredcites →https://doi.org/10.1093/humrep/des328openalex-snapshot
Urinary bisphenol A concentrations and early reproductive health outcomes among women undergoing IVF
inferredcites →https://doi.org/10.1093/humrep/det312openalex-snapshot
Bisphenol-A and human oocyte maturation in 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/molehr/gah179openalex-snapshot
Bisphenol-A induces cell cycle delay and alters centrosome and spindle microtubular organization in oocytes during meiosis
inferredcites →https://doi.org/10.1093/molehr/gar074openalex-snapshot
Gene expression is altered after bisphenol A exposure in human fetal oocytes in vitro
inferredcites →https://doi.org/10.1093/occmed/52.8.467openalex-snapshot
Work with pesticides and organophosphate sheep dips
inferredcites →https://doi.org/10.1093/toxsci/62.2.330openalex-snapshot
The Frequency of U-Shaped Dose Responses in the Toxicological Literature
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/kfr061openalex-snapshot
Bisphenol A Disrupts Steroidogenesis in Human H295R Cells
inferredcites →https://doi.org/10.1093/toxsci/kfu023openalex-snapshot
AroER Tri-Screen Is a Biologically Relevant Assay for Endocrine Disrupting Chemicals Modulating the Activity of Aromatase and/or the Estrogen Receptor
inferredcites →https://doi.org/10.1093/toxsci/kfu030openalex-snapshot
Are Structural Analogues to Bisphenol A Safe Alternatives?
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/10.1097/ede.0b013e318280e02fopenalex-snapshot
Urinary Bisphenol A Concentration and Thyroid Function in Chinese Adults
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/10.1126/science.347.6227.1213-mopenalex-snapshot
Using chemical design to avoid regrets
inferredcites →https://doi.org/10.1126/science.aaa6736openalex-snapshot
Toward designing safer chemicals
inferredcites →https://doi.org/10.1136/oemed-2011-100529openalex-snapshot
High urinary bisphenol A concentrations in workers and possible laboratory abnormalities
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/10.1186/1476-069x-12-26openalex-snapshot
Mixtures of xenoestrogens disrupt estradiol-induced non-genomic signaling and downstream functions in pituitary cells
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.2008-0580openalex-snapshot
Persistent Impairment of Hypothalamic KiSS-1 System after Exposures to Estrogenic Compounds at Critical Periods of Brain Sex Differentiation
inferredcites →https://doi.org/10.1210/en.2012-1422openalex-snapshot
Endocrine-Disrupting Chemicals and Public Health Protection: A Statement of Principles from The Endocrine Society
inferredcites →https://doi.org/10.1210/en.2014-2027openalex-snapshot
Bisphenol A Exposure Disrupts Metabolic Health Across Multiple Generations in the Mouse
inferredcites →https://doi.org/10.1210/en.2015-1785openalex-snapshot
Actions of Bisphenol A and Bisphenol S on the Reproductive Neuroendocrine System During Early Development in Zebrafish
inferredcites →https://doi.org/10.1210/endo.132.6.8504731openalex-snapshot
Bisphenol-A: an estrogenic substance is released from polycarbonate flasks during autoclaving
inferredcites →https://doi.org/10.1210/er.2008-0021openalex-snapshot
Bisphenol-A and the Great Divide: A Review of Controversies in the Field of Endocrine Disruption
inferredcites →https://doi.org/10.1210/er.2009-0002openalex-snapshot
Endocrine-Disrupting Chemicals: An Endocrine Society Scientific Statement
inferredcites →https://doi.org/10.1210/er.2011-1050openalex-snapshot
Hormones and Endocrine-Disrupting Chemicals: Low-Dose Effects and Nonmonotonic Dose Responses
inferredcites →https://doi.org/10.1289/ehp.021100703openalex-snapshot
Parent Bisphenol A Accumulation in the Human Maternal-Fetal-Placental Unit
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.0901161openalex-snapshot
Peroxisome Proliferator–Activated Receptor-γ Mediates Bisphenol A Inhibition of FSH-Stimulated IGF-1, Aromatase, and Estradiol in Human Granulosa Cells
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.1103850openalex-snapshot
Chronic Oral Exposure to Bisphenol A Results in a Nonmonotonic Dose Response in Mammary Carcinogenesis and Metastasis in MMTV-erbB2 Mice
inferredcites →https://doi.org/10.1289/ehp.1104426openalex-snapshot
Bisphenol A and Its Analogues Activate Human Pregnane X Receptor
inferredcites →https://doi.org/10.1289/ehp.1205179openalex-snapshot
Environmental Chemicals: Evaluating Low-Dose Effects
inferredcites →https://doi.org/10.1289/ehp.1205826openalex-snapshot
Bisphenol S Disrupts Estradiol-Induced Nongenomic Signaling in a Rat Pituitary Cell Line: Effects on Cell Functions
inferredcites →https://doi.org/10.1289/ehp.121-a97openalex-snapshot
Assessing the Safety of a Replacement Chemical: Nongenomic Activity of Bisphenol S
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.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.6115openalex-snapshot
Children's health and the environment: public health issues and challenges for risk assessment.
inferredcites →https://doi.org/10.1289/ehp.7713openalex-snapshot
An Extensive New Literature Concerning Low-Dose Effects of Bisphenol A Shows the Need for a New Risk Assessment
inferredcites →https://doi.org/10.1289/ehp.93101378openalex-snapshot
Developmental effects of endocrine-disrupting chemicals in wildlife and humans.
inferredcites →https://doi.org/10.1289/ehp.9368openalex-snapshot
Endocrine-Disrupting Potential of Bisphenol A, Bisphenol A Dimethacrylate, 4- n -Nonylphenol, and 4- n -Octylphenol in Vitro : New Data and a Brief Review
inferredcites →https://doi.org/10.1289/ehp.98106167openalex-snapshot
The Estrogenicity of Bisphenol A-Related Diphenylalkanes with Various Substituents at the Central Carbon and the Hydroxy Groups
inferredcites →https://doi.org/10.1371/journal.pgen.0030005openalex-snapshot
Bisphenol A Exposure In Utero Disrupts Early Oogenesis in the Mouse
inferredcites →https://doi.org/10.1371/journal.pgen.1003401openalex-snapshot
Bisphenol A Exposure Disrupts Genomic Imprinting in the Mouse
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.pone.0010741openalex-snapshot
Bisphenol A in Oocytes Leads to Growth Suppression and Altered Stress Performance in Juvenile Rainbow Trout
inferredcites →https://doi.org/10.1371/journal.pone.0051579openalex-snapshot
Differential Effects of Bisphenol A and Diethylstilbestrol on Human, Rat and Mouse Fetal Leydig Cell Function
inferredcites →https://doi.org/10.1371/journal.pone.0055387openalex-snapshot
Plastics Derived Endocrine Disruptors (BPA, DEHP and DBP) Induce Epigenetic Transgenerational Inheritance of Obesity, Reproductive Disease and Sperm Epimutations
inferredcites →https://doi.org/10.1371/journal.pone.0117226openalex-snapshot
An Investigation of the Endocrine-Disruptive Effects of Bisphenol A in Human and Rat Fetal Testes
inferredcites →https://doi.org/10.14219/jada.archive.2006.0185openalex-snapshot
Exposure to bisphenol A from bis-glycidyl dimethacrylate–based dental sealants
inferredcites →https://doi.org/10.1507/endocrj.49.465openalex-snapshot
The Activity of Bisphenol A Depends on Both the Estrogen Receptor Subtype and the Cell Type.
inferredcites →https://doi.org/10.1530/rep-06-0318openalex-snapshot
Physiological temperature variants and culture media modify meiotic progression and developmental potential of pig oocytes in vitro
inferredcites →https://doi.org/10.15430/jcp.2015.20.1.12openalex-snapshot
Endocrine-disrupting Chemicals: Review of Toxicological Mechanisms Using Molecular Pathway Analysis
inferredcites →https://doi.org/10.17221/6994-cjasopenalex-snapshot
The role of nitric oxide synthase isoforms in aged porcine oocytes
inferredcites →https://doi.org/10.17221/7088-cjasopenalex-snapshot
Inhibition of c-Jun N-terminal kinase (JNK) suppresses porcine oocyte ageing in vitro
inferredcites →https://doi.org/10.2131/jts.38.285openalex-snapshot
Gene expression of epigenetic regulatory factors related to primary silencing mechanism is less susceptible to lower doses of bisphenol A in embryonic hypothalamic cells
inferredcites →https://doi.org/10.2166/wst.2006.189openalex-snapshot
Biodegradation of a variety of bisphenols under aerobic and anaerobic conditions
inferredcites →https://doi.org/10.2203/dose-response.13-020.vandenbergopenalex-snapshot
Non-Monotonic Dose Responses in Studies of Endocrine Disrupting Chemicals: Bisphenol a as a Case Study
inferredcites →https://doi.org/10.2478/10004-1254-64-2013-2319openalex-snapshot
Mutagenicity and DNA Damage of Bisphenol a and its Structural Analogues in Hepg2 Cells
inferredcites →https://doi.org/10.2754/avb200574020287openalex-snapshot
Effect of Exposure to Bisphenol A on the Sex Differentiation in Zebrafish (Danio rerio)
inferredcites →https://doi.org/10.33549/physiolres.933090openalex-snapshot
Differences in Bisphenol A and Estrogen Levels in the Plasma and Seminal Plasma of Men With Different Degrees of Infertility
inferredcites →https://doi.org/10.3389/fendo.2015.00091openalex-snapshot
Epigenetic Regulation of Non-Lymphoid Cells by Bisphenol A, a Model Endocrine Disrupter: Potential Implications for Immunoregulation
inferredcites →https://doi.org/10.3390/ijerph110707537openalex-snapshot
Bisphenol-A: Epigenetic Reprogramming and Effects on Reproduction and Behavior
inferredcites →https://doi.org/10.3390/ijerph6041472openalex-snapshot
Biodegradation of Bisphenol A, Bisphenol F and Bisphenol S in Seawater
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.4681972openalex-extracted
High Tg Catalyst-Free Self-Healing Vitrimer Derived from Turpentine and its Application in Glass Fiber Reinforced Composites
inferred← citeshttps://doi.org/10.2139/ssrn.4812445openalex-extracted
High Tg Catalyst-Free Self-Healing Vitrimer Derived from Turpentine and its Application in Glass Fiber Reinforced Composites
inferred← citeshttps://doi.org/10.1002/ieam.4611openalex-snapshot
An overview of the occurrence, fate, and human risks of the bisphenol-A present in plastic materials, components, and products
inferred← citeshttps://doi.org/10.1002/jat.4170openalex-snapshot
Oxidative stress‐mediated apoptosis is involved in bisphenol S‐induced reproductive toxicity in male C57BL/6 mice
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/s10126-026-10694-3openalex-snapshot
Dietary Myo-Inositol Improves Growth, Antioxidant and Immune Responses in Bisphenol S-Exposed Procambarus clarkii
inferred← citeshttps://doi.org/10.1007/s10337-022-04149-9openalex-snapshot
Development and Validation of a Modified QuEChERS Method for the Analysis of Bisphenols in Meats by UPLC-MS/MS
inferred← citeshttps://doi.org/10.1007/s11082-023-05601-2openalex-snapshot
Design and simulation of photonic crystal fibre sensor for harmful chemicals detection in polycarbonate plastics
inferred← citeshttps://doi.org/10.1007/s11270-019-4096-yopenalex-snapshot
Importance of Organic Matter to the Retention and Transport of Bisphenol A and Bisphenol S in Saturated Soils
inferred← citeshttps://doi.org/10.1007/s11270-019-4238-2openalex-snapshot
Effect of Residual NAPLs on the Transport of Bisphenol A and Bisphenol S in Saturated Porous Media
inferred← citeshttps://doi.org/10.1007/s11356-022-21888-2openalex-snapshot
Cytotoxic and genotoxic evaluation of bisphenol S on onion root tips by Allium cepa and comet tests
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/s11356-024-34666-zopenalex-snapshot
Effect of thyroid disruption on ovarian development following maternal exposure to Bisphenol S
inferred← citeshttps://doi.org/10.1007/s12403-021-00397-6openalex-snapshot
Distribution and Potential Transdermal Human Intake of Bisphenol A and Bisphenol S from Thermal Receipt Papers in Korea Market
inferred← citeshttps://doi.org/10.1007/s12403-021-00444-2openalex-snapshot
Comprehensive Assessment of Local Population Chemical Exposome by Combination of Organic Pollutant- and Metal-Multi-Residue Analysis in Hair
inferred← citeshttps://doi.org/10.1007/s44274-026-00764-7openalex-snapshot
Navigating endocrine disrupting compounds in aquatic ecosystems through sources, biological implications, and sustainable remediation techniques
inferred← citeshttps://doi.org/10.1016/j.aquatox.2024.106957openalex-snapshot
Bisphenol S exposed changes in intestinal microflora and metabolomics of freshwater crayfish, Procambarus clarkii
inferred← citeshttps://doi.org/10.1016/j.bpobgyn.2023.102347openalex-snapshot
Effects of endocrine disrupting compounds on female fertility
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111891openalex-snapshot
Implications of early-life BPS-induced thyroid disruption on adult female reproductive disorders
inferred← citeshttps://doi.org/10.1016/j.cbpc.2023.109811openalex-snapshot
The effects of bisphenol S exposure on the growth, physiological and biochemical indices, and ecdysteroid receptor gene expression in red swamp crayfish, Procambarus clarkii
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.126525openalex-snapshot
Human in vitro percutaneous absorption of bisphenol S and bisphenol A: A comparative study
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130711openalex-snapshot
Intestinal toxicity and microbial community disorder induced by bisphenol F and bisphenol S in zebrafish
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2019.110670openalex-snapshot
The impact of toxic bisphenols on model human erythrocyte membranes
inferred← citeshttps://doi.org/10.1016/j.envc.2022.100552openalex-snapshot
Removing imidacloprid, bisphenol-S and azithromycin by ferrate (Fe(VI)): efficiency, oxidation products, toxicity and kinetics
inferred← citeshttps://doi.org/10.1016/j.envint.2019.105050openalex-snapshot
Urinary bisphenol S concentrations: Potential predictors of and associations with semen quality parameters among men attending a fertility center
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.03.100openalex-snapshot
Short and long-term effects of bisphenol S (BPS) exposure during pregnancy and lactation on plasma lipids, hormones, and behavior in rats
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120114openalex-snapshot
Effect of Bisphenol S on testicular tissue after low-dose lactation exposure
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120375openalex-snapshot
Assessment of BPA and BPS exposure in the general population in Guangzhou, China - Estimation of daily intakes based on urinary metabolites
inferred← citeshttps://doi.org/10.1016/j.envres.2019.108576openalex-snapshot
Quantification of eight bisphenol analogues in blood and urine samples of workers in a hazardous waste incinerator
inferred← citeshttps://doi.org/10.1016/j.envres.2020.110336openalex-snapshot
Bisphenol A, bisphenol S and their glucuronidated metabolites modulate glycolysis and functional responses of human neutrophils
inferred← citeshttps://doi.org/10.1016/j.foodchem.2018.08.109openalex-snapshot
Development and validation of a LC–MS/MS method for the analysis of bisphenol a in polyethylene terephthalate
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120596openalex-snapshot
High Tg catalyst-free self-healing vitrimer derived from turpentine and its application in glass fiber reinforced composites
inferred← citeshttps://doi.org/10.1016/j.jclepro.2022.132637openalex-snapshot
REACH authorisation and the substitution of hazardous chemicals: The case of trichloroethylene
inferred← citeshttps://doi.org/10.1016/j.jece.2023.111601openalex-snapshot
Photochemical degradation of bisphenols and fluconazole by UV-activated persulfate – Benefits for cost-efficient removal in wastewater treatment plants
inferred← citeshttps://doi.org/10.1016/j.jwpe.2020.101490openalex-snapshot
Adsorption of Bisphenol S from aqueous solution on powdered activated carbon and chronic toxicity evaluation with microcrustacean Ceriodaphnia dubia
inferred← citeshttps://doi.org/10.1016/j.microc.2020.104964openalex-snapshot
Extraction of four endocrine-disrupting chemicals using a Fe3O4/graphene oxide/di-(2-ethylhexyl) phosphoric acid nano-composite, and their quantification by HPLC-UV
inferred← citeshttps://doi.org/10.1016/j.reprotox.2019.08.014openalex-snapshot
Male exposure to bisphenol A (BPA) and semen quality in the Home Observation of Periconceptional Exposures (HOPE) cohort
inferred← citeshttps://doi.org/10.1016/j.reprotox.2019.12.005openalex-snapshot
Acute low-dose bisphenol S exposure affects mouse oocyte quality
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.09.194openalex-snapshot
Occurrence of bisphenol S in the environment and implications for human exposure: A short review
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.152734openalex-snapshot
Determination of contamination levels for multiple endocrine disruptors in hair from a non-occupationally exposed population living in Liege (Belgium)
inferred← citeshttps://doi.org/10.1016/j.taap.2021.115409openalex-snapshot
Exposure to alternative bisphenols BPS and BPF through breast milk: Noxious heritage effect during nursing associated with idiopathic infertility
inferred← citeshttps://doi.org/10.1016/j.talanta.2017.05.070openalex-snapshot
Determination of selected bisphenols, parabens and estrogens in human plasma using LC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.wasman.2020.04.017openalex-snapshot
Challenges of plastic waste generation and management in sub-Saharan Africa: A review
inferred← citeshttps://doi.org/10.1038/s41545-020-00095-xopenalex-snapshot
Preliminarily comparative performance of removing bisphenol-S by ferrate oxidation and ozonation
inferred← citeshttps://doi.org/10.1038/s41598-017-00570-5openalex-snapshot
Bisphenol S negatively affects the meotic maturation of pig oocytes
inferred← citeshttps://doi.org/10.1038/s41598-025-91984-zopenalex-snapshot
Bisphenol-S exposure of zebrafish unveils the hidden risks of bisphenol paradigm with growth, developmental, and behavioral impacts similar to bisphenol-A
inferred← citeshttps://doi.org/10.1039/c8tx00064fopenalex-snapshot
The state of bisphenol research in the lesser developed countries of the EU: a mini-review
inferred← citeshttps://doi.org/10.1039/c9tx00055kopenalex-snapshot
Toxicity and multigenerational effects of bisphenol S exposure to Caenorhabditis elegans on developmental, biochemical, reproductive and oxidative stress
inferred← citeshttps://doi.org/10.1051/bioconf/202518301007openalex-snapshot
Wing Damage and Size Reduction in Drosophila melanogaster Caused by Bisphenol A
inferred← citeshttps://doi.org/10.1057/s41285-018-00084-8openalex-snapshot
Routine exposure: social practices and environmental health risks in the home
inferred← citeshttps://doi.org/10.1080/00498254.2018.1480818openalex-snapshot
Bisphenol S modulates concentrations of bisphenol A and oestradiol in female and male mice
inferred← citeshttps://doi.org/10.1088/1755-1315/1439/1/012010openalex-snapshot
Negative Geotaxis Assay in Three Drosophila Strains Consuming Bisphenol A: Duration and Number of Climbing Successes
inferred← citeshttps://doi.org/10.1093/biolre/ioab139openalex-snapshot
Comparing effects and action mechanisms of BPA and BPS on HTR-8/SVneo placental cells
inferred← citeshttps://doi.org/10.1101/2025.01.24.634648openalex-snapshot
From Toxicogenomics Data to Cumulative Assessment Groups: A Mechanistic Framework for Chemical Grouping
inferred← citeshttps://doi.org/10.1128/msystems.00912-24openalex-snapshot
Bisphenol S impairs oocyte quality by inducing gut microbiota dysbiosis
inferred← citeshttps://doi.org/10.1186/s12302-024-00919-4openalex-snapshot
Grouping strategies for assessing and managing persistent and mobile substances
inferred← citeshttps://doi.org/10.17221/90/2023-cjasopenalex-snapshot
The occurrence and risk assessment of bisphenol A and its analogues - bisphenol B, F, S, Z and AF in the urine of lactating sows
inferred← citeshttps://doi.org/10.22271/tpi.2021.v10.i8sh.7340openalex-snapshot
Bisphenol A and cattle fertility
inferred← citeshttps://doi.org/10.2478/acb-2018-0021openalex-snapshot
Endocrine disruptive compounds and male reproduction
inferred← citeshttps://doi.org/10.2478/acb-2021-0023openalex-snapshot
Endocrine disrupting chemicals and their detection in an IVF laboratory
inferred← citeshttps://doi.org/10.2903/sp.efsa.2025.en-9335openalex-snapshot
Inference of chemical grouping from processed OMICS data in Comparative Toxicogenomics Database
inferred← citeshttps://doi.org/10.33263/briac95.433438openalex-snapshot
Detection of imidacloprid and Bisphenol-S by Solid Phase Extraction (SPE) coupled with UV-VIS spectrometer and LC-MS
inferred← citeshttps://doi.org/10.33549/physiolres.933723openalex-snapshot
Prenatal Exposure to Bisphenols and Parabens and Impacts on Human Physiology
inferred← citeshttps://doi.org/10.33549/physiolres.934521openalex-snapshot
Endocrine Disruptors, Obesity, and Cytokines - How Relevant Are They to PCOS?
inferred← citeshttps://doi.org/10.3389/fgene.2021.692897openalex-snapshot
Overview of the Mechanisms of Action of Selected Bisphenols and Perfluoroalkyl Chemicals on the Male Reproductive Axes
inferred← citeshttps://doi.org/10.3389/fnmol.2023.1234841openalex-snapshot
Influence of bisphenol A and its analog bisphenol S on cocaine- and amphetamine-regulated transcript peptide–positive enteric neurons in the mouse gastrointestinal tract
inferred← citeshttps://doi.org/10.3389/fphys.2022.725442openalex-snapshot
Nursing Exposure to Bisphenols as a Cause of Male Idiopathic Infertility
inferred← citeshttps://doi.org/10.3390/genes13010142openalex-snapshot
Effects of BPA, BPS, and BPF on Oxidative Stress and Antioxidant Enzyme Expression in Bovine Oocytes and Spermatozoa
inferred← citeshttps://doi.org/10.3390/molecules26216515openalex-snapshot
Application of Molecularly Imprinted Polymers in the Analysis of Waters and Wastewaters
inferred← citeshttps://doi.org/10.3390/nu12020532openalex-snapshot
Bisphenol S in Food Causes Hormonal and Obesogenic Effects Comparable to or Worse than Bisphenol A: A Literature Review
inferred← citeshttps://doi.org/10.52763/pjsir.phys.sci.64.2.2021.173.190openalex-snapshot
Bisphenol A and its Analogues: Human Exposure and Biological Effects-A Review
inferred← citeshttps://doi.org/10.5772/intechopen.78538openalex-snapshot
Endocrine Disruptors and Reproductive Health in Males
inferred← citeshttps://doi.org/10.5772/intechopen.88142openalex-snapshot
Endocrine Disruptors: Very Low Doses with Genuinely High Impacts on Male Reproduction
inferred← citeshttps://doi.org/10.70675/37d7b33dz8861z484fz925fzecba953877eeopenalex-snapshot
Développement d'une approche intégrative pour évaluer l'exposition interne foetale au Bisphénol S
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