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Proliferation and functional maturation of Sertoli cells, and their relevance to disorders of testis function in adulthood
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-2795(200006)56:2<124::aid-mrd2>3.0.co;2-jopenalex-snapshot
GATA-1 is a potential repressor of anti-M�llerian hormone expression during the establishment of puberty in the mouse
inferredcites →https://doi.org/10.1002/ar.1092420108openalex-snapshot
Neonatal hypothyroidism causes delayed sertoli cell maturation in rats treated with propylthiouracil: Evidence that the sertoli cell controls testis growth
inferredcites →https://doi.org/10.1002/j.1939-4640.1995.tb00550.xopenalex-snapshot
NCAM Mediates Adhesion Between Gonocytes and Sertoli Cells in Cocultures from Testes of Neonatal Rats
inferredcites →https://doi.org/10.1002/jez.1096openalex-snapshot
Structural and regulatory macromolecules in sex differentiation of gonads
inferredcites →https://doi.org/10.1002/path.1140openalex-snapshot
Altered expression of connexins 26 and 43 in Sertoli cells in seminiferous tubules infiltrated with carcinoma‐in‐situ or seminoma
inferredcites →https://doi.org/10.1002/path.1372openalex-snapshot
Histological evidence of testicular dysgenesis in contralateral biopsies from 218 patients with testicular germ cell cancer
inferredcites →https://doi.org/10.1006/taap.2000.8972openalex-snapshot
A Single Dose of Di-(2-ethylhexyl) Phthalate in Neonatal Rats Alters Gonocytes, Reduces Sertoli Cell Proliferation, and Decreases Cyclin D2 Expression
inferredcites →https://doi.org/10.1007/bf00199510openalex-snapshot
Expression of vimentin, cytokeratin, and desmin in Sertoli cells of human fetal, cryptorchid, and tumour-adjacent testicular tissue
inferredcites →https://doi.org/10.1016/b978-0-08-091764-1.50012-xopenalex-snapshot
Paracrine Mechanisms in Testicular Control
inferredcites →https://doi.org/10.1016/j.mce.2004.10.007openalex-snapshot
Molecular and Cellular Endocrinology
inferredcites →https://doi.org/10.1016/s0015-0282(02)03060-1openalex-snapshot
Sertoli cell maturation in men with azoospermia of different etiologies
inferredcites →https://doi.org/10.1016/s0022-5347(01)62439-xopenalex-snapshot
ALTERATION OF SERTOLI CELL DIFFERENTIATION IN THE PRESENCE OF CARCINOMA IN SITU IN HUMAN TESTES
inferredcites →https://doi.org/10.1016/s0041-008x(88)80012-7openalex-snapshot
Testicular toxicity and reduced sertoli cell numbers in neonatal rats by di(2-ethylhexyl) phthalate and the recovery of fertility as adults
inferredcites →https://doi.org/10.1016/s0046-8177(82)80132-9openalex-snapshot
Hyperplasia and the immature appearance of sertoli cells in primary testicular disorders
inferredcites →https://doi.org/10.1016/s0070-2153(00)50006-4openalex-snapshot
Gonocyte-Sertoli cell interactions during development of the neonatal rodent testis
inferredcites →https://doi.org/10.1016/s0303-7207(01)00467-1openalex-snapshot
Anti-Müllerian hormone and its receptors
inferredcites →https://doi.org/10.1016/s0378-4274(01)00298-3openalex-snapshot
Hormones and testis development and the possible adverse effects of environmental chemicals
inferredcites →https://doi.org/10.1046/j.1365-2605.1999.00172.xopenalex-snapshot
Sources of oestrogen in the testis and reproductive tract of the male
inferredcites →https://doi.org/10.1046/j.1365-2605.2000.00248.xopenalex-snapshot
Regulatory influence of germ cells on Sertoli cell function in the pre‐pubertal rat after acute irradiation of the testis
inferredcites →https://doi.org/10.1093/humrep/15.7.1537openalex-snapshot
Maturation phenotype of Sertoli cells in testicular biopsies of azoospermic men
inferredcites →https://doi.org/10.1093/humrep/16.5.972openalex-snapshot
Testicular dysgenesis syndrome: an increasingly common developmental disorder with environmental aspects: Opinion
inferredcites →https://doi.org/10.1093/humrep/17.5.1367openalex-snapshot
Testicular changes during infantile 'quiescence' in the marmoset and their gonadotrophin dependence: a model for investigating susceptibility of the prepubertal human testis to cancer therapy?
inferredcites →https://doi.org/10.1093/humrep/17.8.2062openalex-snapshot
Absence of anti-Mullerian hormone (AMH) and M2A immunoreactivities in Sertoli cell-only syndrome and maturation arrest with and without AZF microdeletions
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/humupd/7.3.236openalex-snapshot
Neonatal exposure to potent and environmental oestrogens and abnormalities of the male reproductive system in the rat: evidence for importance of the androgen-oestrogen balance and assessment of the relevance to man
inferredcites →https://doi.org/10.1095/biolreprod31.4.785openalex-snapshot
Quantification of the Human Sertoli Cell Population: Its Distribution, Relation to Germ Cell Numbers, and Age-Related Decline 1
inferredcites →https://doi.org/10.1095/biolreprod53.6.1345openalex-snapshot
Evidence for Germ Cell Control of Sertoli Cell Function in Three Models of Germ Cell Depletion in Adult Rat
inferredcites →https://doi.org/10.1095/biolreprod54.1.36openalex-snapshot
Neonatal exposure of rats to recombinant follicle stimulating hormone increases adult Sertoli and spermatogenic cell numbers
inferredcites →https://doi.org/10.1095/biolreprod62.3.664openalex-snapshot
Developmental Expression of Thyroid Hormone Receptors in the Rat Testis1
inferredcites →https://doi.org/10.1095/biolreprod63.1.82openalex-snapshot
Pulsatile Stimulation with Recombinant Single Chain Human Luteinizing Hormone Elicits Precocious Sertoli Cell Proliferation in the Juvenile Male Rhesus Monkey (Macaca mulatta)1
inferredcites →https://doi.org/10.1095/biolreprod63.6.1629openalex-snapshot
Cell Proliferation and Hormonal Changes During Postnatal Development of the Testis in the Pig1
inferredcites →https://doi.org/10.1095/biolreprod64.2.689openalex-snapshot
Specific Staining of Sertoli Cell Nuclei and Evaluation of Sertoli Cell Number and Proliferative Activity in Meishan and White Composite Boars During the Neonatal Period1
inferredcites →https://doi.org/10.1096/fj.01-0992comopenalex-snapshot
Estrogen regulates development of the somatic cell phenotype in the eutherian ovary
inferredcites →https://doi.org/10.1111/j.1365-2605.1987.tb00358.xopenalex-snapshot
Proliferation of Sertoli cells during development of the human testis assessed by stereological methods
inferredcites →https://doi.org/10.1111/j.1365-2605.1989.tb01285.xopenalex-snapshot
Determination of Sertoli cell numbers in the developing rat testis by stereological methods
inferredcites →https://doi.org/10.1111/j.1365-2605.1989.tb01324.xopenalex-snapshot
A novel maturation marker for human Sertoli cells
inferredcites →https://doi.org/10.1111/j.1365-2605.1990.tb01054.xopenalex-snapshot
Quantitative and ultrastructural alterations in the lamina propria and Sertoli cells in human cryptorchid testes
inferredcites →https://doi.org/10.1111/j.1365-2605.1993.tb01155.xopenalex-snapshot
Relative roles of testosterone and the germ cell complement in determining stageldependent changes in protein secretion by isolated rat seminiferous tubules
inferredcites →https://doi.org/10.1111/j.1365-2605.1993.tb01364.xopenalex-snapshot
Effect of age on seminiferous tubule protein secretion and the adverse effects of testicular toxicants in the rat
inferredcites →https://doi.org/10.1111/j.1365-2605.1996.tb00448.xopenalex-snapshot
Immunohistochemical detection of immature Sertoli cell markers in testicular tissue of infertile adult men: a preliminary study
inferredcites →https://doi.org/10.1111/j.1432-0436.1990.tb00431.xopenalex-snapshot
Expression of cytokeratins 8 and 18 in human Sertoli cells of immature and atrophic seminiferous tubules*
inferredcites →https://doi.org/10.1111/j.1464-410x.1989.tb05325.xopenalex-snapshot
Testicular Size in Infertile Men: Relationship to Semen Characteristics and Hormonal Blood Levels
inferredcites →https://doi.org/10.1126/science.286.5448.2328openalex-snapshot
Postnatal Sex Reversal of the Ovaries in Mice Lacking Estrogen Receptors α and β
inferredcites →https://doi.org/10.1159/000474300openalex-snapshot
Ultrasonic Testicular Texture and Size in 444 Men from the General Population: Correlation to Semen Quality
inferredcites →https://doi.org/10.1210/edrv-16-4-443openalex-snapshot
Thyroid Hormone and Male Gonadal Function*
inferredcites →https://doi.org/10.1210/edrv.18.2.0298openalex-snapshot
Anatomical and Functional Aspects of Testicular Descent and Cryptorchidism
inferredcites →https://doi.org/10.1210/en.132.6.2607openalex-snapshot
Adult testicular enlargement induced by neonatal hypothyroidism is accompanied by increased Sertoli and germ cell numbers
inferredcites →https://doi.org/10.1210/en.133.2.755openalex-snapshot
High neonatal triiodothyronine levels reduce the period of Sertoli cell proliferation and accelerate tubular lumen formation in the rat testis, and increase serum inhibin levels
inferredcites →https://doi.org/10.1210/en.139.1.156openalex-snapshot
Macroorchidism in FMR1 Knockout Mice Is Caused by Increased Sertoli Cell Proliferation during Testicular Development
inferredcites →https://doi.org/10.1210/en.139.11.4489openalex-snapshot
Thyroid Hormone and Follicle-Stimulating Hormone Regulate Mullerian-Inhibiting Substance Messenger Ribonucleic Acid Expression in Cultured Neonatal Rat Sertoli Cells
inferredcites →https://doi.org/10.1210/en.140.11.5364openalex-snapshot
Permanent Effects of Neonatal Estrogen Exposure in Rats on Reproductive Hormone Levels, Sertoli Cell Number, and the Efficiency of Spermatogenesis in Adulthood
inferredcites →https://doi.org/10.1210/en.140.4.1834openalex-snapshot
Regulatory Role of p27kip1 in the Mouse and Human Testis
inferredcites →https://doi.org/10.1210/en.141.5.1633openalex-snapshot
Thyroid Hormone Down-Regulates Neural Cell Adhesion Molecule Expression and Affects Attachment of Gonocytes in Sertoli Cell-Gonocyte Cocultures
inferredcites →https://doi.org/10.1210/endo.140.11.7108openalex-snapshot
Permanent Effects of Neonatal Estrogen Exposure in Rats on Reproductive Hormone Levels, Sertoli Cell Number, and the Efficiency of Spermatogenesis in Adulthood1
inferredcites →https://doi.org/10.1210/endo.141.5.7468openalex-snapshot
Thyroid Hormone Down-Regulates Neural Cell Adhesion Molecule Expression and Affects Attachment of Gonocytes in Sertoli Cell-Gonocyte Cocultures1
inferredcites →https://doi.org/10.1210/jc.82.12.4059openalex-snapshot
Inhibin B as a Serum Marker of Spermatogenesis: Correlation to Differences in Sperm Concentration and Follicle-Stimulating Hormone Levels. A Study of 349 Danish Men
inferredcites →https://doi.org/10.1210/jc.83.2.675openalex-snapshot
Longitudinal Reproductive Hormone Profiles in Infants: Peak of Inhibin B Levels in Infant Boys Exceeds Levels in Adult Men
inferredcites →https://doi.org/10.1210/jc.85.9.3453openalex-snapshot
Ontogenetic Pattern of Thyroid Hormone Receptor Expression in the Human Testis
inferredcites →https://doi.org/10.1210/jcem-73-3-596openalex-snapshot
Localized Irradiation of Testes with Carcinomain Situ: Effects on Leydig Cell Function and Eradication of Malignant Germ Cells in 20 Patients*
inferredcites →https://doi.org/10.1210/jcem.82.12.4456openalex-snapshot
Inhibin B as a Serum Marker of Spermatogenesis: Correlation to Differences in Sperm Concentration and Follicle-Stimulating Hormone Levels. A Study of 349 Danish Men1
inferredcites →https://doi.org/10.1210/jcem.82.6.4021openalex-snapshot
Inhibin-B in the Male Rhesus Monkey: Impact of Neonatal Gonadotropin-Releasing Hormone Antagonist Treatment and Sexual Development1
inferredcites →https://doi.org/10.1210/jcem.83.2.4603openalex-snapshot
Longitudinal Reproductive Hormone Profiles in Infants: Peak of Inhibin B Levels in Infant Boys Exceeds Levels in Adult Men1
inferredcites →https://doi.org/10.1210/jcem.84.1.5410openalex-snapshot
Androgen Receptor Distribution in Adult Human Testis1
inferredcites →https://doi.org/10.1210/jcem.84.10.6047openalex-snapshot
Expression of Anti-Müllerian Hormone during Normal and Pathological Gonadal Development: Association with Differentiation of Sertoli and Granulosa Cells1
inferredcites →https://doi.org/10.1210/jcem.84.8.5972openalex-snapshot
Antimüllerian Hormone in Patients with Hypogonadotropic Hypogonadism
inferredcites →https://doi.org/10.1210/jcem.86.1.7109openalex-snapshot
Androgen Receptor Expression in Sertoli Cells as a Function of Seminiferous Tubule Maturation in the Human Cryptorchid Testis1
inferredcites →https://doi.org/10.1210/me.15.6.985openalex-snapshot
Inhibin and p27 Interact to Regulate Gonadal Tumorigenesis
inferredcites →https://doi.org/10.1289/ehp.00108979openalex-snapshot
Levels of Seven Urinary Phthalate Metabolites in a Human Reference Population
inferredcites →https://doi.org/10.1292/jvms.63.5openalex-snapshot
Effects of Exposure of Lactating Female Rats to Polychlorinated Biphenyls(PCBs) on Testis Weight, Sperm Production and Sertoli Cell Numbers in the Adult Male Offspring.
inferredcites →https://doi.org/10.1530/eje.0.1320236openalex-snapshot
Follow-up study on the effects of thyroid hormone administration on androgen metabolism of peripubertal rat Sertoli cells
inferredcites →https://doi.org/10.1530/jrf.0.1040207openalex-snapshot
Increased numbers of Sertoli and germ cells in adult rat testes induced by synergistic action of transient neonatal hypothyroidism and neonatal hemicastration
inferredcites →https://doi.org/10.1677/joe.0.1400431openalex-snapshot
Inhibition of aromatase activity in rat Sertoli cells by thyroid hormone
inferredcites →https://doi.org/10.1677/joe.0.1450355openalex-snapshot
Tri-iodothyronine directly affects rat Sertoli cell proliferation and differentiation
inferredcites →https://doi.org/10.1677/joe.0.1560043openalex-snapshot
Thyroid hormone effects on androgen receptor messenger RNA expression in rat Sertoli and peritubular cells
inferredcites →https://doi.org/10.1677/joe.0.1620393openalex-snapshot
Inhibin B is a more sensitive marker of spermatogenetic damage than FSH in the irradiated non-human primate model
inferredcites →https://doi.org/10.5858/1999-123-0225-aisopenalex-snapshot
Androgen Insensitivity Syndrome
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1001/jamapediatrics.2013.95openalex-snapshot
Association of Breastfeeding With Higher Serum Inhibin B Level at Adolescence
inferred← citeshttps://doi.org/10.1002/adhm.202402606openalex-snapshot
3D Bioprinted Coaxial Testis Model Using Human Induced Pluripotent Stem Cells:A Step Toward Bicompartmental Cytoarchitecture and Functionalization
inferred← citeshttps://doi.org/10.1002/ar.70370openalex-snapshot
Hormonal control and signaling of the testis of the bat Molossus molossus during the processes of testicular maturation, regression, and recrudescence
inferred← citeshttps://doi.org/10.1002/bdr2.1133openalex-snapshot
Comparative Aspects of Pre‐ and Postnatal Development of the Male Reproductive System
inferred← citeshttps://doi.org/10.1002/bdrb.10045openalex-snapshot
Role of thyroid hormones in human and laboratory animal reproductive health
inferred← citeshttps://doi.org/10.1002/bdrb.20057openalex-snapshot
Review on testicular development, structure, function, and regulation in common marmoset
inferred← citeshttps://doi.org/10.1002/bdrb.20213openalex-snapshot
Influence of persistent thyroxine reduction on spermatogenesis in rats neonatally exposed to 2,2′,4,4′,5,5′‐hexa‐chlorobiphenyl
inferred← citeshttps://doi.org/10.1002/bdrb.20307openalex-snapshot
Impaired reproduction in adult male, but not female, rats following juvenile treatment with the aromatase inhibitor, exemestane
inferred← citeshttps://doi.org/10.1002/dvdy.22468openalex-snapshot
GPR56 is essential for testis development and male fertility in mice
inferred← citeshttps://doi.org/10.1002/dvdy.299openalex-snapshot
The Sertoli cell expressed gene secernin‐1 (Scrn1) is dispensable for male fertility in the mouse
inferred← citeshttps://doi.org/10.1002/dvg.70031openalex-snapshot
ATRX : From Chromatin Remodeling to Disease
inferred← citeshttps://doi.org/10.1002/ece3.2193openalex-snapshot
Cytological study on Sertoli cells and their interactions with germ cells during annual reproductive cycle in turtle
inferred← citeshttps://doi.org/10.1002/jbt.21908openalex-snapshot
BEX4 upregulation alters Sertoli cell growth properties and protein expression profiles: An explanation for cadmium‐induced testicular Sertoli cell injury
inferred← citeshttps://doi.org/10.1002/jbt.23416openalex-snapshot
Bisphenols as promoters of the dysregulation of cellular junction proteins of the blood‐testis barrier in experimental animals: A systematic review of the literature
inferred← citeshttps://doi.org/10.1002/jcb.25554openalex-snapshot
Glycogen Synthase in Sertoli Cells: More Than Glycogenesis?
inferred← citeshttps://doi.org/10.1002/jcb.26698openalex-snapshot
Sertoli cell specific decline in NOR‐1 leads to germ cell apoptosis and reduced fertility
inferred← citeshttps://doi.org/10.1002/jcb.27350openalex-snapshot
Effect of resveratrol on Sertoli cell proliferation
inferred← citeshttps://doi.org/10.1002/jcp.20910openalex-snapshot
The radiation‐induced block in spermatogonial differentiation is due to damage to the somatic environment, not the germ cells
inferred← citeshttps://doi.org/10.1002/jcp.20952openalex-snapshot
Fas ligand expression in TM4 sertoli cells is enhanced by estradiol “in situ” production
inferred← citeshttps://doi.org/10.1002/jcp.21545openalex-snapshot
Molecular identification and functional characterization of the vitamin C transporters expressed by Sertoli cells
inferred← citeshttps://doi.org/10.1002/jemt.20684openalex-snapshot
Dose‐dependent effects on cell proliferation, seminiferous tubules, and male germ cells in the fetal rat testis following exposure to di(n‐butyl) phthalate
inferred← citeshttps://doi.org/10.1002/jemt.20754openalex-snapshot
Ontogeny of the androgen receptor expression in the fetal and postnatal testis: Its relevance on Sertoli cell maturation and the onset of adult spermatogenesis
inferred← citeshttps://doi.org/10.1002/med.21325openalex-snapshot
The Warburg Effect Revisited—Lesson from the Sertoli Cell
inferred← citeshttps://doi.org/10.1002/mrd.20654openalex-snapshot
Donor cell differentiation, reprogramming, and cloning efficiency: Elusive or illusive correlation?
inferred← citeshttps://doi.org/10.1002/mrd.20715openalex-snapshot
Mice lacking cyclin‐dependent kinase inhibitor p19Ink4d show strain‐specific effects on male reproduction
inferred← citeshttps://doi.org/10.1002/mrd.20889openalex-snapshot
Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome
inferred← citeshttps://doi.org/10.1002/mrd.21291openalex-snapshot
Nxf3 is expressed in Sertoli cells, but is dispensable for spermatogenesis
inferred← citeshttps://doi.org/10.1002/mrd.22437openalex-snapshot
Direct and indirect consequences on gene expression of a thyroid hormone receptor alpha 1 mutation restricted to Sertoli cells
inferred← citeshttps://doi.org/10.1002/mrd.22527openalex-snapshot
Expression profile of doublesex/male abnormal‐3‐related transcription factor‐1 during gonadal sex change in the protogynous wrasse, Halichoeres trimaculatus
inferred← citeshttps://doi.org/10.1002/mrd.23124openalex-snapshot
Identification of microRNAs for regulating adenosine monophosphate‐activated protein kinase expression in immature boar Sertoli cells in vitro
inferred← citeshttps://doi.org/10.1002/mrd.23246openalex-snapshot
Pubertal orchestration of hormones and testis in primates
inferred← citeshttps://doi.org/10.1002/mrd.23302openalex-snapshot
CYP26B1 declines postnatally in Sertoli cells independently of androgen action in the mouse testis
inferred← citeshttps://doi.org/10.1002/mrd.23402openalex-snapshot
Characterization of rodent Sertoli cell primary cultures
inferred← citeshttps://doi.org/10.1002/stem.2065openalex-snapshot
A Niche for GFRα1-Positive Spermatogonia in the Terminal Segments of the Seminiferous Tubules in Hamster Testes
inferred← citeshttps://doi.org/10.1002/tox.22175openalex-snapshot
Exploration of intrinsic and extrinsic apoptotic pathways in zearalenone-treated rat sertoli cells
inferred← citeshttps://doi.org/10.1007/16833_2022_7openalex-snapshot
Immunobiology of Testicular Cancer
inferred← citeshttps://doi.org/10.1007/3-540-33713-x_58openalex-snapshot
Physiology of Spermatogenesis
inferred← citeshttps://doi.org/10.1007/3-540-33713-x_79openalex-snapshot
Evaluation of Testicular Biopsy Samples from the Clinical Perspective
inferred← citeshttps://doi.org/10.1007/978-0-387-09597-4openalex-snapshot
Molecular Mechanisms in Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-0-387-09597-4_1openalex-snapshot
Spermatogenesis and Cycle of the Seminiferous Epithelium
inferred← citeshttps://doi.org/10.1007/978-1-4419-1783-6_20openalex-snapshot
Impact of Radiotherapy and Chemotherapy on the Testis
inferred← citeshttps://doi.org/10.1007/978-1-4419-8456-2_11openalex-snapshot
Environmental Insults on Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4471-2763-5_10openalex-snapshot
Cryptorchidism (Undescended Testis)
inferred← citeshttps://doi.org/10.1007/978-1-4614-5620-9_4openalex-snapshot
Impact of Radiotherapy and Chemotherapy on the Testis
inferred← citeshttps://doi.org/10.1007/978-1-4939-7698-0_15openalex-snapshot
Testicular Cell Selective Ablation Using Diphtheria Toxin Receptor Transgenic Mice
inferred← citeshttps://doi.org/10.1007/978-1-4939-7698-0_4openalex-snapshot
Rabbit Sertoli Cells: Immunohistochemical Profile from Neonatal to Adult Age
inferred← citeshttps://doi.org/10.1007/978-1-4939-7698-0_5openalex-snapshot
Identification of Proliferative and Apoptotic Sertoli Cells Using Fluorescence and Confocal Microscopy
inferred← citeshttps://doi.org/10.1007/978-1-61779-191-8_15openalex-snapshot
Phenotyping the Claudin 11 Deficiency in Testis: From Histology to Immunohistochemistry
inferred← citeshttps://doi.org/10.1007/978-2-287-72080-2_18openalex-snapshot
Compréhension de l’anatomie et des fonctions normales
inferred← citeshttps://doi.org/10.1007/978-3-030-32300-4_24openalex-snapshot
Novel Approaches in the Management of Klinefelter Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-030-47767-7_34openalex-snapshot
Impact of Cancer Treatment on Testicular Function
inferred← citeshttps://doi.org/10.1007/978-3-031-31574-9_11openalex-snapshot
Biopsy and Histology of the Testis
inferred← citeshttps://doi.org/10.1007/978-3-031-58214-1_34openalex-snapshot
Fertility Preservation in Prepubertal and Adolescent Males Facing Gonadotoxic Therapies: Recent Developments and New Insights
inferred← citeshttps://doi.org/10.1007/978-3-031-82990-1_14openalex-snapshot
The Biology and Regulation of Spermatogonial Stem Cells in the Niche
inferred← citeshttps://doi.org/10.1007/978-3-031-82990-1_9openalex-snapshot
scRNA-Seq-Based Transcriptome Profiling and Relevant Bioinformatics Approaches to Uncover Novel Insights in Studying Human Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-3-031-96376-6_10openalex-snapshot
Leydig Cell Interaction with Macrophages, Peritubular Cells, and Sertoli Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-11578-8_21openalex-snapshot
Male Reproductive Toxicology
inferred← citeshttps://doi.org/10.1007/978-3-319-29456-8_9-1openalex-snapshot
Functional Anatomy and Histology of the Testis
inferred← citeshttps://doi.org/10.1007/978-3-319-31973-5_14openalex-snapshot
Methods for the Study of Gonadal Development
inferred← citeshttps://doi.org/10.1007/978-3-319-31973-5_9openalex-snapshot
Biology of the Sertoli Cell in the Fetal, Pubertal, and Adult Mammalian Testis
inferred← citeshttps://doi.org/10.1007/978-3-319-32122-6_8openalex-snapshot
The Environmental Factors and Epigenetics of Gametogenesis in Puberty
inferred← citeshttps://doi.org/10.1007/978-3-319-40007-5_43-1openalex-snapshot
Maternal Undernutrition and Developmental Programming: Implications for Offspring Reproductive Potential
inferred← citeshttps://doi.org/10.1007/978-3-319-44441-3_9openalex-snapshot
Functional Anatomy and Histology of the Testis
inferred← citeshttps://doi.org/10.1007/978-3-319-49364-0_16openalex-snapshot
Value of Testicular Biopsy in Nonobstructive Azoospermia
inferred← citeshttps://doi.org/10.1007/978-3-319-53298-1_3openalex-snapshot
Human Spermatogenesis and Its Regulation
inferred← citeshttps://doi.org/10.1007/978-3-319-53298-1_5openalex-snapshot
Congenital Hypogonadotropic Hypogonadism in Males: Clinical Features and Pathophysiology
inferred← citeshttps://doi.org/10.1007/978-3-319-55387-0_43openalex-snapshot
Maternal Undernutrition and Developmental Programming: Implications for Offspring Reproductive Potential
inferred← citeshttps://doi.org/10.1007/978-3-540-29676-8_1611openalex-snapshot
Sertoli Cell Only Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-540-78355-8_11openalex-snapshot
Testicular Biopsy and Histology
inferred← citeshttps://doi.org/10.1007/978-3-540-92963-5_11openalex-snapshot
Biopsie und Histologie der Hoden
inferred← citeshttps://doi.org/10.1007/978-3-642-22775-2_11openalex-snapshot
Origin of Testicular Dysgenesis Syndrome Disorders in the Masculinization Programming Window: Relevance to Final Testis Size (=Sperm Production)
inferred← citeshttps://doi.org/10.1007/978-3-662-61901-8_11openalex-snapshot
Biopsie und Histologie des Hodens
inferred← citeshttps://doi.org/10.1007/978-3-662-61904-9_11-1openalex-snapshot
Biopsie und Histologie des Hodens
inferred← citeshttps://doi.org/10.1007/978-4-431-56550-5_17openalex-snapshot
Drebrin and Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-88-470-1487-9_18openalex-snapshot
Comprensione dell’anatomia e delle funzioni normali
inferred← citeshttps://doi.org/10.1007/978-981-97-0896-3_3openalex-snapshot
Reaping the Benefits of Gene Modulations in Animals in the Era of Genomics
inferred← citeshttps://doi.org/10.1007/bf03061576openalex-snapshot
Gonadotrofinen als indirecte maat voor testisfunctie bij jonge mannen na behandeling voor kanker op de kinderleeftijd
inferred← citeshttps://doi.org/10.1007/bf03194250openalex-snapshot
Density-dependent regulatory mechanisms of the generative potency in the males of a bank voleMyodes glareolus
inferred← citeshttps://doi.org/10.1007/s00018-012-1079-1openalex-snapshot
Hormonal control of Sertoli cell metabolism regulates spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00018-012-1121-3openalex-snapshot
Connexin 43 a check-point component of cell proliferation implicated in a wide range of human testis diseases
inferred← citeshttps://doi.org/10.1007/s00018-021-03757-2openalex-snapshot
Targeted disruption of galectin 3 in mice delays the first wave of spermatogenesis and increases germ cell apoptosis
inferred← citeshttps://doi.org/10.1007/s00018-022-04174-9openalex-snapshot
Follicle-stimulating hormone-mediated decline in miR-92a-3p expression in pubertal mice Sertoli cells is crucial for germ cell differentiation and fertility
inferred← citeshttps://doi.org/10.1007/s00204-011-0736-8openalex-snapshot
Sertoli cells proliferate in adult rats with prenatal exposure to 3,3′,4,4′,5-pentachlorobiphenyl
inferred← citeshttps://doi.org/10.1007/s00204-022-03259-5openalex-snapshot
Effects of postnatal exposure to tetrabromobisphenol A on testis development in mice and early key events
inferred← citeshttps://doi.org/10.1007/s00204-024-03767-6openalex-snapshot
Mechanistic screening of reproductive toxicity in a novel 3D testicular co-culture model shows significant impairments following exposure to low-dibutyl phthalate concentrations
inferred← citeshttps://doi.org/10.1007/s00232-010-9294-xopenalex-snapshot
Tubular Fluid Secretion in the Seminiferous Epithelium: Ion Transporters and Aquaporins in Sertoli Cells
inferred← citeshttps://doi.org/10.1007/s00292-004-0693-6openalex-snapshot
Immunhistochemische Darstellung von Lymphgef��en mit D2?40 in der diagnostischen Pathologie
inferred← citeshttps://doi.org/10.1007/s00292-019-00711-9openalex-snapshot
Die Multitasking-Sertoli-Zelle
inferred← citeshttps://doi.org/10.1007/s00418-006-0155-8openalex-snapshot
The expression of neurotrophins and their receptors in the prenatal and adult human testis: evidence for functions in Leydig cells
inferred← citeshttps://doi.org/10.1007/s00418-009-0576-2openalex-snapshot
Claudin-11 is over-expressed and dislocated from the blood–testis barrier in Sertoli cells associated with testicular intraepithelial neoplasia in men
inferred← citeshttps://doi.org/10.1007/s00418-011-0871-6openalex-snapshot
Evaluation of CAG repeat length of androgen receptor expressing cells in human testes showing different pictures of spermatogenic impairment
inferred← citeshttps://doi.org/10.1007/s00424-013-1287-zopenalex-snapshot
PI3K-dependent actions of insulin and IGF-I on seminiferous tubules from immature rats
inferred← citeshttps://doi.org/10.1007/s00428-008-0677-7openalex-snapshot
Investigating differentiation mechanisms of the constituent cells of sex cord-stromal tumours of the ovary
inferred← citeshttps://doi.org/10.1007/s00429-004-0385-2openalex-snapshot
Histological organization of roe deer testis throughout the seasonal cycle: variable and constant components of tubular and interstitial compartment
inferred← citeshttps://doi.org/10.1007/s00429-005-0075-8openalex-snapshot
Mitotic activity of Sertoli cells in adult human testis: an immunohistochemical study to characterize Sertoli cells in testicular cords from patients showing testicular dysgenesis syndrome
inferred← citeshttps://doi.org/10.1007/s00439-020-02159-xopenalex-snapshot
A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse
inferred← citeshttps://doi.org/10.1007/s00441-011-1288-1openalex-snapshot
Coordination of spermatogenic processes in the testis: lessons from cystic spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00441-015-2164-1openalex-snapshot
Developmental expression patterns of chemokines CXCL11, CXCL12 and their receptor CXCR7 in testes of common marmoset and human
inferred← citeshttps://doi.org/10.1007/s00441-017-2667-zopenalex-snapshot
MicroRNAs in Sertoli cells: implications for spermatogenesis and fertility
inferred← citeshttps://doi.org/10.1007/s00441-017-2698-5openalex-snapshot
Defective Wnt3 expression by testicular Sertoli cells compromise male fertility
inferred← citeshttps://doi.org/10.1007/s10059-009-0024-0openalex-snapshot
Ankrd7, a Novel Gene Specifically Expressed in Sertoli Cells and Its Potential Roles in Sertoli Cell Maturation
inferred← citeshttps://doi.org/10.1007/s10522-026-10392-6openalex-snapshot
Sertoli cell aging: damage accumulation and epigenetic alterations affecting male fertility
inferred← citeshttps://doi.org/10.1007/s10735-017-9714-7openalex-snapshot
Effects of androgen receptor mutation on testicular histopathology of patient having complete androgen insensitivity
inferred← citeshttps://doi.org/10.1007/s10815-014-0369-yopenalex-snapshot
Association of single nucleotide polymorphisms in the USF1, GTF2A1L and OR2W3 genes with non-obstructive azoospermia in the Chinese population
inferred← citeshttps://doi.org/10.1007/s11033-014-3666-8openalex-snapshot
Molecular characterization, expression profiles of the ovine FSHR gene and its association with litter size
inferred← citeshttps://doi.org/10.1007/s11033-026-11566-8openalex-snapshot
Protective effect of alpha-tocopherol succinate on Al₂O₃-NPs induced damage in NMRI mice Sertoli cells: the role of inhibin B and Connexin 43
inferred← citeshttps://doi.org/10.1007/s11248-005-7216-yopenalex-snapshot
Gonadal Effects of a Mouse Denys-Drash Syndrome Mutation
inferred← citeshttps://doi.org/10.1007/s11250-019-01842-0openalex-snapshot
Improved early postnatal nutrition and its effect on histomorphological parameters in the testes of Sanjabi ram lambs
inferred← citeshttps://doi.org/10.1007/s11356-020-10115-5openalex-snapshot
Hypomethylation of LINE-1 retrotransposons is associated with cadmium-induced testicular injury
inferred← citeshttps://doi.org/10.1007/s11356-023-25767-2openalex-snapshot
Changes in testicular histomorphometry and ultrastructure of Leydig cells in adult male Japanese quail exposed to di (n-butyl) phthalate (DBP) during the prepubertal period
inferred← citeshttps://doi.org/10.1007/s11604-026-02073-8openalex-snapshot
Physiological testicular 18F-FDG uptake in boys: age-related patterns and association with body mass index
inferred← citeshttps://doi.org/10.1007/s11626-013-9648-7openalex-snapshot
Long-term culture and analysis of cashmere goat Sertoli cells
inferred← citeshttps://doi.org/10.1007/s11626-015-9994-8openalex-snapshot
Characterization of swine testicular cell line as immature porcine Sertoli cell line
inferred← citeshttps://doi.org/10.1007/s11845-014-1167-3openalex-snapshot
Increases in interleukin-6 and interferon-gamma levels is progressive in immature rats with varicocele
inferred← citeshttps://doi.org/10.1007/s12020-026-04732-2openalex-snapshot
Incomplete male puberty: a new nosographic entity
inferred← citeshttps://doi.org/10.1007/s12079-016-0367-1openalex-snapshot
1,25(OH)2 vitamin D3 signalling on immature rat Sertoli cells: gamma-glutamyl transpeptidase and glucose metabolism
inferred← citeshttps://doi.org/10.1007/s12522-014-0193-1openalex-snapshot
Hormonal therapy for non‐obstructive azoospermia: basic and clinical perspectives
inferred← citeshttps://doi.org/10.1007/s12595-021-00417-yopenalex-snapshot
Hexavalent Chromium and Male Reproduction: An Update
inferred← citeshttps://doi.org/10.1007/s12610-010-0096-xopenalex-snapshot
Anomalies postnatales du développement de la spermatogenèse associées aux troubles de la migration testiculaire
inferred← citeshttps://doi.org/10.1007/s13258-017-0560-5openalex-snapshot
RNA binding protein QKI contributes to WT1 mRNA and suppresses apoptosis in ST cells
inferred← citeshttps://doi.org/10.1007/s40071-014-0068-4openalex-snapshot
Histological observation of doublesex-mab 3-related transcription factor 1 (DMRT1) localization in the adult testis of three-spot wrasse
inferred← citeshttps://doi.org/10.1007/s42000-023-00472-4openalex-snapshot
High cholesterol diet–induced testicular dysfunction in rats
inferred← citeshttps://doi.org/10.1007/s43032-020-00156-zopenalex-snapshot
TBC1D20 Is Essential for Mouse Blood–Testis Barrier Integrity Through Maintaining the Epithelial Phenotype and Modulating the Maturation of Sertoli Cells
inferred← citeshttps://doi.org/10.1007/s43032-023-01401-xopenalex-snapshot
Etiology of Male Infertility: an Update
inferred← citeshttps://doi.org/10.1016/b978-0-08-046884-6.01106-4openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-08-100601-6.02137-2openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-12-382032-7.10067-0openalex-snapshot
Endocrine disruptors
inferred← citeshttps://doi.org/10.1016/b978-0-12-382032-7.10069-4openalex-snapshot
Developmental and reproductive disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-385926-6.00019-3openalex-snapshot
Reproductive toxicity and endocrine disruption
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00014-4openalex-snapshot
Testicular Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00032-6openalex-snapshot
Puberty in Non-human Primates and Man
inferred← citeshttps://doi.org/10.1016/b978-0-12-416021-7.00003-1openalex-snapshot
Mammalian Sex Determination and Gonad Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00001-6openalex-snapshot
Sertoli cell anatomy and cytoskeleton
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00005-3openalex-snapshot
DMRT1 and the road to masculinity
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00011-9openalex-snapshot
MicroRNAs and Sertoli cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00012-0openalex-snapshot
Biochemistry of Sertoli cell/germ cell junctions, germ cell transport, and spermiation in the seminiferous epithelium
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00014-4openalex-snapshot
Adult Sertoli cell differentiation status in humans
inferred← citeshttps://doi.org/10.1016/b978-0-12-417144-2.00026-3openalex-snapshot
Juvenile Animal Studies and Experience
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02137-1openalex-snapshot
The Sertoli Cell as a Target for Toxicants ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64362-3openalex-snapshot
Cell–Cell Interactions—Molecular
inferred← citeshttps://doi.org/10.1016/b978-0-12-802682-3.00008-2openalex-snapshot
Male Reproductive System
inferred← citeshttps://doi.org/10.1016/b978-0-12-809965-0.00044-6openalex-snapshot
Vitamin D, Reproductive Biology, and Dysfunction in Men
inferred← citeshttps://doi.org/10.1016/b978-0-12-811410-0.00017-9openalex-snapshot
Reproductive Toxicity and Endocrine Disruption
inferred← citeshttps://doi.org/10.1016/b978-0-12-812501-4.00015-8openalex-snapshot
Thyroid Dysfunction and Testicular Redox Status
inferred← citeshttps://doi.org/10.1016/b978-0-12-821045-1.00009-2openalex-snapshot
Male Reproductive System
inferred← citeshttps://doi.org/10.1016/b978-0-323-01970-5.50014-2openalex-snapshot
Non-neoplastic diseases of the testis
inferred← citeshttps://doi.org/10.1016/b978-0-323-29738-7.00025-3openalex-snapshot
Physiology and Disorders of Puberty
inferred← citeshttps://doi.org/10.1016/b978-0-323-47912-7.00012-3openalex-snapshot
Hypothalamo-Pituitary Unit, Testis, and Male Accessory Organs
inferred← citeshttps://doi.org/10.1016/b978-0-323-54941-7.00012-8openalex-snapshot
Nonneoplastic Diseases of the Testis
inferred← citeshttps://doi.org/10.1016/b978-0-323-91386-7.00039-8openalex-snapshot
Vitamin D, reproductive endocrinology, and male reproductive organ function in health and disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-91704-9.00020-3openalex-snapshot
The Warburg-like effect in male reproductive events
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00208-4openalex-snapshot
Anatomy and Physiology of the Male Reproductive System and Potential Targets of Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00241-2openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-443-06684-9.50086-xopenalex-snapshot
Development of the urogenital system
inferred← citeshttps://doi.org/10.1016/b978-0-443-06811-9.10015-6openalex-snapshot
Development of the Urogenital System
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00323-0openalex-snapshot
The Blood-Testis Barrier: An Overview of the Physical, Physiological, and Immunological Functions
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00545-9openalex-snapshot
Cell–Cell Interactions—Molecular
inferred← citeshttps://doi.org/10.1016/b978-0-443-29007-7.00077-7openalex-snapshot
Reproductive toxicity and endocrine disruption
inferred← citeshttps://doi.org/10.1016/b978-012370467-2/50111-5openalex-snapshot
Reproductive toxicity and endocrine disruption
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50023-3openalex-snapshot
Cytology of the Testis and Intrinsic Control Mechanisms
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50026-9openalex-snapshot
Endocrine Regulation of Spermatogenesis
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50045-2openalex-snapshot
Puberty in Nonhuman Primates and Humans
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50005-2openalex-snapshot
Embryonic Sertoli Cell Differentiation
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50013-1openalex-snapshot
Sertoli Cell Endocrinology and Signal Transduction
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50014-3openalex-snapshot
Thyroid Hormone Regulation of Sertoli Cell Development
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50015-5openalex-snapshot
The Transforming Growth Factor β Superfamily in Sertoli Cell Biology
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50018-0openalex-snapshot
The Role of the Sertoli Cell in Spermatogonial Stem Cell Fate
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50021-0openalex-snapshot
Sertoli Cell Toxicants
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50022-2openalex-snapshot
Conditions Affecting Sertoli Cells
inferred← citeshttps://doi.org/10.1016/b978-1-4160-2911-3.50026-1openalex-snapshot
10.1016/b978-1-4160-2911-3.50026-1
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4907-4.00012-7openalex-snapshot
The Hypothalamo-Pituitary Unit, Testes, and Male Accessory Organs
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6911-9.00132-8openalex-snapshot
Abnormalities of the Testis and Scrotum and Their Surgical Management
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2758-2.00013-5openalex-snapshot
The Hypothalamo-Pituitary Unit, Testis, and Male Accessory Organs
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4327-8.00012-7openalex-snapshot
Nonneoplastic diseases of the testis
inferred← citeshttps://doi.org/10.1016/b978-141604090-3.50021-1openalex-snapshot
The Testes: Disorders of Sexual Differentiation and Puberty in the Male
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2016.08.003openalex-snapshot
Clinical Applications of Gonadotropins in the Male
inferred← citeshttps://doi.org/10.1016/j.aanat.2016.01.003openalex-snapshot
Changes in rat testis morphology and androgen receptor expression around the age of puberty
inferred← citeshttps://doi.org/10.1016/j.acthis.2007.10.009openalex-snapshot
Sertoli cell proliferation in the fetal and neonatal rat testis: A continuous phenomenon?
inferred← citeshttps://doi.org/10.1016/j.ajpath.2018.07.013openalex-snapshot
Testosterone and Follicle Stimulating Hormone–Dependent Glyoxalase 1 Up-Regulation Sustains the Viability of Porcine Sertoli Cells through the Control of Hydroimidazolone– and Argpyrimidine-Mediated NF-κB Pathway
inferred← citeshttps://doi.org/10.1016/j.ando.2014.03.001openalex-snapshot
Mini-puberty and true puberty: Differences in testicular function
inferred← citeshttps://doi.org/10.1016/j.androl.2016.10.010openalex-snapshot
Effects of cypermethrin on cytokeratin 8/18 and androgen receptor expression in the adult mouse Sertoli cell
inferred← citeshttps://doi.org/10.1016/j.androl.2019.11.001openalex-snapshot
The mouse testis tissue culture could resume spermatogenesis as same as in vivo condition after human spermatogonial stem cells transplantation
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.10.025openalex-snapshot
Ontogeny of androgen and estrogen receptor expression in porcine testis: Effect of reducing testicular estrogen synthesis
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2007.11.029openalex-snapshot
Role of Sertoli cell number and function on regulation of spermatogenesis
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