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Proliferative activity of gonocytes, Sertoli cells and interstitial cells during testicular development in mice

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aja.1001070304openalex-snapshot
Studies on the fine structure of the mammalian testis. II. The human interstitial tissue
inferredcites →https://doi.org/10.1002/aja.1001080106openalex-snapshot
Microscopic anatomy of the sex cords and seminiferous tubules in growing and adult male albino rats
inferredcites →https://doi.org/10.1002/aja.1001300407openalex-snapshot
Differentiation of the Leydig cell of the mouse testis during the fetal period — an ultrastructural study
inferredcites →https://doi.org/10.1002/ar.1091430405openalex-snapshot
Development of enzyme activity in the Leydig cells of the mouse testis
inferredcites →https://doi.org/10.1002/ar.1091470208openalex-snapshot
The postnatal development and differentiation of the boundary tissue of the seminiferous tubule of the rat
inferredcites →https://doi.org/10.1002/ar.1092030408openalex-snapshot
Proliferation of sertoli cells in fetal and postnatal rats: A quantitative autoradiographic study
inferredcites →https://doi.org/10.1007/bf00225571openalex-snapshot
Selective destruction and regeneration of rat Leydig cells in vivo
inferredcites →https://doi.org/10.1007/bf00251049openalex-snapshot
Macrophages in the interstitial tissue of the rat testis
inferredcites →https://doi.org/10.1007/bf00300588openalex-snapshot
Proliferation of spermatogonia and Sertoli cells in maturing mice
inferredcites →https://doi.org/10.1007/bf00330725openalex-snapshot
The fine structure of the testicular interstitial cells in men of normal androgenic status
inferredcites →https://doi.org/10.1071/zo9620178openalex-snapshot
Changes in the cells of the Sex Cords and Seminiferous Tubules during the development of the Testis of the rat and mouse.
inferredcites →https://doi.org/10.1073/pnas.81.13.4174openalex-snapshot
The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: macrophages of endocrine organs.
inferredcites →https://doi.org/10.1093/biolreprod/4.1.84openalex-snapshot
Replication Pattern of Sertoli Cells in Maturing Rat Testis in Vivo and in Organ Culture1
inferredcites →https://doi.org/10.1111/j.1365-2605.1981.tb00732.xopenalex-snapshot
A comparison between the morphology and cell kinetics of gonocytes and adult type undifferentiated spermatogonia in the mouse
inferredcites →https://doi.org/10.1111/j.1365-2605.1987.tb00352.xopenalex-snapshot
Morphometric analysis of the components of the neonatal and the adult rat testis interstitium
inferredcites →https://doi.org/10.1159/000141460openalex-snapshot
THE DEVELOPMENT OF THE INTERSTITIAL CELLS IN THE TESTIS OF THE ALBINO RAT
inferredcites →https://doi.org/10.1210/endo-124-2-762openalex-snapshot
Kinetic Studies on the Development of the Adult Population of Leydig Cells in Testes of the Pubertal Rat*
inferredcites →https://doi.org/10.1242/dev.103.3.535openalex-snapshot
The fate of fetal Leydig cells during the development of the fetal and postnatal rat testis
inferredcites →https://doi.org/10.1530/jrf.0.0460279openalex-snapshot
Effect of HCG on the interstitial cells and androgen production in the immature rat testis
inferredcites →https://doi.org/10.1677/joe.0.1220689openalex-snapshot
Proliferation and differentiation of possible Leydig cell precursors after destruction of the existing Leydig cells with ethane dimethyl sulphonate: the role of LH/human chorionic gonadotrophin

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.4180032openalex-extracted
Postnatal Ontogeny of Neuromedin S and its Receptors Nmur1 and Nmur2 Expression in Mouse Testis
inferred← citeshttps://doi.org/10.1002/(sici)1097-0185(199607)245:3<509::aid-ar7>3.0.co;2-mopenalex-snapshot
Immunohistochemical localization of androgen receptor in mouse testicular germ cells during fetal and postnatal development
inferred← citeshttps://doi.org/10.1002/(sici)1097-0185(20000201)258:2<210::aid-ar10>3.0.co;2-xopenalex-snapshot
Reproliferation and relocation of mouse male germ cells (gonocytes) during prespermatogenesis
inferred← citeshttps://doi.org/10.1002/(sici)1521-186x(200001)21:1<19::aid-bem4>3.0.co;2-1openalex-snapshot
Development of mouse testis and epididymis following intrauterine exposure to a static magnetic field
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200300163openalex-snapshot
Male Reproductive System: Testis Development and Spermatogenesis
inferred← citeshttps://doi.org/10.1002/ar.1100openalex-snapshot
Expression of Connexin43 in mouse Leydig, Sertoli, and germinal cells at different stages of postnatal development
inferred← citeshttps://doi.org/10.1002/ar.1164openalex-snapshot
Developmental regulation of connexin 43 expression in fetal mouse testicular cells
inferred← citeshttps://doi.org/10.1002/ar.a.10040openalex-snapshot
Connexin43 is expressed in mouse fetal ovary
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.10015openalex-snapshot
Development and maturation of the male reproductive system
inferred← citeshttps://doi.org/10.1002/bdrc.20142openalex-snapshot
Gonocytes, the forgotten cells of the germ cell lineage
inferred← citeshttps://doi.org/10.1002/bit.26822openalex-snapshot
Neonatal testis growth recreated in vitro by two‐dimensional organ spreading
inferred← citeshttps://doi.org/10.1002/dvdy.10399openalex-snapshot
Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis
inferred← citeshttps://doi.org/10.1002/j.1939-4640.1993.tb03261.xopenalex-snapshot
Neonatal Goitrogen Treatment Increases Adult Testis Size and Sperm Production in the Mouse
inferred← citeshttps://doi.org/10.1002/j.1939-4640.2000.tb02114.xopenalex-snapshot
Genetic and Cellular Analysis of Male Germ Cell Development
inferred← citeshttps://doi.org/10.1002/j.1939-4640.2000.tb03408.xopenalex-snapshot
All You Wanted to Know About Spermatogonia but Were Afraid to Ask
inferred← citeshttps://doi.org/10.1002/jcp.20829openalex-snapshot
The role of p63 in germ cell apoptosis in the developing testis
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.20715openalex-snapshot
Mice lacking cyclin‐dependent kinase inhibitor p19Ink4d show strain‐specific effects on male reproduction
inferred← citeshttps://doi.org/10.1002/mrd.20716openalex-snapshot
p19Ink4d and p18Ink4c cyclin‐dependent kinase inhibitors in the male reproductive axis
inferred← citeshttps://doi.org/10.1002/mrd.20796openalex-snapshot
Ontogeny of leptin and its receptor expression in mouse testis during the postnatal period
inferred← citeshttps://doi.org/10.1002/mrd.22214openalex-snapshot
A current view of the epigenome in mouse primordial germ cells
inferred← citeshttps://doi.org/10.1002/mrd.22832openalex-snapshot
Preservation of chromosomal integrity in murine spermatozoa derived from gonocytes and spermatogonial stem cells surviving prenatal and postnatal exposure to γ‐rays in mice
inferred← citeshttps://doi.org/10.1002/mrd.23739openalex-snapshot
Fetal Leydig cells: What we know and what we don't
inferred← citeshttps://doi.org/10.1002/rmb2.12283openalex-snapshot
Mammalian germ cell migration during development, growth, and homeostasis
inferred← citeshttps://doi.org/10.1002/rmb2.12502openalex-snapshot
Overview of single‐cell RNA sequencing analysis and its application to spermatogenesis research
inferred← citeshttps://doi.org/10.1006/bbrc.1997.6256openalex-snapshot
FGF-8 Is Expressed during Specific Phases of Rodent Oocyte and Spermatogonium Development
inferred← citeshttps://doi.org/10.1006/dbio.1998.9156openalex-snapshot
Regulation of Meiosis during Mammalian Spermatogenesis: The A-Type Cyclins and Their Associated Cyclin-Dependent Kinases Are Differentially Expressed in the Germ-Cell Lineage
inferred← citeshttps://doi.org/10.1006/dbio.2000.9625openalex-snapshot
Regulation of Germ Cell and Sertoli Cell Development by Activin, Follistatin, and FSH
inferred← citeshttps://doi.org/10.1006/dbio.2001.0445openalex-snapshot
BCLW Mediates Survival of Postmitotic Sertoli Cells by Regulating BAX Activity
inferred← citeshttps://doi.org/10.1006/excr.1998.4215openalex-snapshot
Mesonephric Stromal Cells Differentiate into Leydig Cells in the Mouse Fetal Testis
inferred← citeshttps://doi.org/10.1007/978-1-4612-2106-7_4openalex-snapshot
MIS Actions in the Developing Testis
inferred← citeshttps://doi.org/10.1007/978-1-4612-2106-7_6openalex-snapshot
Regulation of Growth and Survival in the Mammalian Germline
inferred← citeshttps://doi.org/10.1007/978-1-4899-0089-0_23openalex-snapshot
The Effect of Parathion on Mouse Testicular and Epididymal Development Cultured in Chicken Allantochorion
inferred← citeshttps://doi.org/10.1007/978-1-4939-7505-1_3openalex-snapshot
Setting the Stage: The First Round of Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-7505-1_7openalex-snapshot
Gonadotropin and Steroid Hormone Control of Spermatogonial Differentiation
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/10.1007/978-1-59259-102-2_7openalex-snapshot
The Role of the C-Kit/Kit Ligand Axis in Mammalian Gametogenesis
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_11openalex-snapshot
Development of Leydig Cell Steroidogenesis
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_14openalex-snapshot
The Role of Estrogen Sulfotransferase in Leydig Cells
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_2openalex-snapshot
Structural and Histological Analysis of Leydig Cell Steroidogenic Function
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_24openalex-snapshot
Androgen Receptor in Leydig Cell Function and Development
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_4openalex-snapshot
Regulation of Leydig Cells During Pubertal Development
inferred← citeshttps://doi.org/10.1007/978-1-59745-453-7_6openalex-snapshot
Dynamics of Leydig Cell Regeneration After EDS
inferred← citeshttps://doi.org/10.1007/978-1-62703-098-4_13openalex-snapshot
Germ Line Stem Cells: A Promising Alternative Source for Stem-Cell-Based Therapies in Regenerative Medicine
inferred← citeshttps://doi.org/10.1007/978-3-319-27610-6_4openalex-snapshot
Spermatogonial Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-29456-8_6-1openalex-snapshot
Male Sexual Differentiation
inferred← citeshttps://doi.org/10.1007/978-3-319-44441-3_6openalex-snapshot
Male Sexual Differentiation
inferred← citeshttps://doi.org/10.1007/978-3-642-00513-8_7openalex-snapshot
Development of the Neuroendocrine Leydig Cells
inferred← citeshttps://doi.org/10.1007/978-3-662-22189-1_3openalex-snapshot
Proliferation and Differentiation of Testicular Interstitial Cells: Aspects of Leydig Cell Development in the (Pre)Pubertal and Adult Testis
inferred← citeshttps://doi.org/10.1007/978-94-007-5690-8_9openalex-snapshot
Spermatogonial Stem Cells
inferred← citeshttps://doi.org/10.1007/978-94-009-1537-4_14openalex-snapshot
Chromosome behaviour in earliest meiotic prophase
inferred← citeshttps://doi.org/10.1007/bf00195762openalex-snapshot
Proliferative activity of the developing seminiferous epithelium during prespermatogenesis in the golden hamster testis measured by bromodeoxyuridine labeling
inferred← citeshttps://doi.org/10.1007/bf00352259openalex-snapshot
A reassessment of Y chromosomal behaviour in germ cells and Sertoli cells of the mouse as revealed by in situ hybridisation
inferred← citeshttps://doi.org/10.1007/bf03041153openalex-snapshot
Développementin vitro de la lignée germinale foetale mâle chez le rat, la souris et l’homme
inferred← citeshttps://doi.org/10.1007/s00018-022-04134-3openalex-snapshot
Mitochondrial regulation during male germ cell development
inferred← citeshttps://doi.org/10.1007/s00412-016-0590-9openalex-snapshot
DNA repair kinetics in SCID mice Sertoli cells and DNA-PKcs-deficient mouse embryonic fibroblasts
inferred← citeshttps://doi.org/10.1007/s00418-012-0955-yopenalex-snapshot
Gonocyte development in rats: proliferation, distribution and death revisited
inferred← citeshttps://doi.org/10.1007/s00441-006-0167-7openalex-snapshot
Organotypic culture, a powerful model for studying rat and mouse fetal testis development
inferred← citeshttps://doi.org/10.1007/s00441-023-03852-9openalex-snapshot
Adropin, a novel hepatokine: localization and expression during postnatal development and its impact on testicular functions of pre-pubertal mice
inferred← citeshttps://doi.org/10.1007/s11356-023-26849-xopenalex-snapshot
Testicular toxicity in mice exposed to terephthalic acid in utero and during lactation
inferred← citeshttps://doi.org/10.1016/0165-0378(93)90016-bopenalex-snapshot
Regulation of the macrophage population in postnatal rat testis
inferred← citeshttps://doi.org/10.1016/0303-7207(94)90033-7openalex-snapshot
hCG-induced changes in LH/CG receptor mRNA transcript levels in the testis of adult hypophysectomized, ethane dimethyl sulphonate-treated rats
inferred← citeshttps://doi.org/10.1016/0960-0760(95)00022-ropenalex-snapshot
Differentiation of adult Leydig cells
inferred← citeshttps://doi.org/10.1016/b978-0-08-046884-6.01136-2openalex-snapshot
Testicular Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-08-091764-1.50006-4openalex-snapshot
Cell Biology of Testicular Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00019-3openalex-snapshot
The Immunophysiology of Male Reproduction
inferred← citeshttps://doi.org/10.1016/b978-0-12-416022-4.00009-3openalex-snapshot
Spermatogonial Stem Cell Functions in Physiological and Pathological Conditions
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00003-xopenalex-snapshot
Early postnatal interactions between Sertoli and germ cells
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/b978-0-12-417047-6.00009-0openalex-snapshot
Retinoic acid metabolism, signaling, and function in the adult testis
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/b978-0-12-801238-3.11110-9openalex-snapshot
Male Germ Cell Differentiation
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64363-5openalex-snapshot
Male Sex Determination—Phenotypic
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.99197-9openalex-snapshot
Testicular Cancer in Relation to Testicular Dysgenesis Syndrome
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.12010-8openalex-snapshot
Testicular Cancer in Relation to Testicular Dysgenesis Syndrome
inferred← citeshttps://doi.org/10.1016/b978-0-443-13825-6.00413-1openalex-snapshot
Male Germ Cell Differentiation
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/b978-0-443-21477-6.00549-6openalex-snapshot
Male Sex Determination – Phenotypic
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00554-xopenalex-snapshot
The First Wave of Mammalian Spermatogenesis
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/b978-012515400-0/50030-0openalex-snapshot
Immunophysiology of the Male Reproductive Tract
inferred← citeshttps://doi.org/10.1016/b978-012563455-7/50010-6openalex-snapshot
Regulation of proliferation and differentiation of stem cells in the male germ line
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50012-xopenalex-snapshot
In Vivo FSH Actions
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50021-0openalex-snapshot
Sertoli Cell Toxicants
inferred← citeshttps://doi.org/10.1016/b978-012647751-1/50023-4openalex-snapshot
Gonocyte Development and Differentiation
inferred← citeshttps://doi.org/10.1016/bs.asn.2020.05.002openalex-snapshot
The aging spermatogonial stem cell niche
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.06.002openalex-snapshot
Cancer and meiotic gene expression: Two sides of the same coin?
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2014.09.010openalex-snapshot
Transcriptional coactivator undifferentiated embryonic cell transcription factor 1 expressed in spermatogonial stem cells: A putative marker of boar spermatogonia
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2024.107470openalex-snapshot
Maternal nutrition and fetal imprinting of the male progeny
inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.02.008openalex-snapshot
Molecular control of rodent spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.biochi.2006.09.022openalex-snapshot
A new method for toxicity assays on human and mouse fetal testis
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.01.021openalex-snapshot
The Dnmt3L ADD Domain Controls Cytosine Methylation Establishment during Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.01.043openalex-snapshot
Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.12.023openalex-snapshot
Non-Canonical and Sexually Dimorphic X Dosage Compensation States in the Mouse and Human Germline
inferred← citeshttps://doi.org/10.1016/j.diff.2023.09.002openalex-snapshot
Effects of a Sertoli cell-specific knockout of Connexin43 on maturation and proliferation of postnatal Sertoli cells
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2010.04.062openalex-snapshot
Cryopreservation of prepubertal mouse testicular tissue by vitrification
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.09.073openalex-snapshot
Ontogeny of QRFP and its receptor expression in mouse testis during post-natal development
inferred← citeshttps://doi.org/10.1016/j.isci.2026.116452openalex-snapshot
Tandem single-cell epigenetic and transcriptomic analysis reveals spatiotemporally distinct genomic features among testis cell lineages
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102072openalex-snapshot
Transcription factor GATA2 may potentiate follicle-stimulating hormone production in mice via induction of the BMP antagonist gremlin in gonadotrope cells
inferred← citeshttps://doi.org/10.1016/j.jprot.2015.02.015openalex-snapshot
Unraveling the proteomic profile of mice testis during the initiation of meiosis
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2013.01.007openalex-snapshot
Fetal origin of endocrine dysfunction in the adult: The phthalate model
inferred← citeshttps://doi.org/10.1016/j.mce.2012.02.018openalex-snapshot
Activins and inhibins in mammalian testis development: New models, new insights
inferred← citeshttps://doi.org/10.1016/j.mce.2012.09.003openalex-snapshot
Testosterone deficiency accompanied by testicular and epididymal abnormalities in TMF−/− mice
inferred← citeshttps://doi.org/10.1016/j.mce.2023.111949openalex-snapshot
Developmental origins of mammalian spermatogonial stem cells: New perspectives on epigenetic regulation and sex chromosome function
inferred← citeshttps://doi.org/10.1016/j.plipres.2018.08.002openalex-snapshot
Properties, metabolism and roles of sulfogalactosylglycerolipid in male reproduction
inferred← citeshttps://doi.org/10.1016/j.reprotox.2022.05.014openalex-snapshot
Toxicity of cerium oxide nanoparticles on neonatal testicular development in mouse organ culture
inferred← citeshttps://doi.org/10.1016/j.scr.2018.01.031openalex-snapshot
Advanced immunostaining approaches to study early male germ cell development
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2004.09.014openalex-snapshot
Spermatogenesis and sperm transit through the epididymis in mammals with emphasis on pigs
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2014.08.003openalex-snapshot
Thyroid hormone inhibits the proliferation of piglet Sertoli cell via PI3K signaling pathway
inferred← citeshttps://doi.org/10.1016/j.toxrep.2020.12.023openalex-snapshot
Chemotherapy induced damage to spermatogonial stem cells in prepubertal mouse in vitro impairs long-term spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.04.046openalex-snapshot
Cell type-autonomous and non-autonomous requirements for Dmrt1 in postnatal testis differentiation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.12.018openalex-snapshot
Krüppel-like factor 4 is involved in functional differentiation of testicular Sertoli cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.03.007openalex-snapshot
TGFβ signaling in male germ cells regulates gonocyte quiescence and fertility in mice
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.07.031openalex-snapshot
Geminin is required for mitotic proliferation of spermatogonia
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.10.009openalex-snapshot
Distinct requirements for Sin3a in perinatal male gonocytes and differentiating spermatogonia
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.01.023openalex-snapshot
The highly conserved LAMMER/CLK2 protein kinases prevent germ cell overproliferation in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.04.010openalex-snapshot
Constitutive WNT/CTNNB1 activation triggers spermatogonial stem cell proliferation and germ cell depletion
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.04.015openalex-snapshot
Wnt4 as a signal coordinates DNA methylation and acetylation to determine germ line fate
inferred← citeshttps://doi.org/10.1016/j.ygcen.2014.03.030openalex-snapshot
Reconstruction of a seminiferous tubule-like structure in a 3 dimensional culture system of re-aggregated mouse neonatal testicular cells within a collagen matrix
inferred← citeshttps://doi.org/10.1016/j.ygcen.2016.05.006openalex-snapshot
Localization and expression of Orexin A and its receptor in mouse testis during different stages of postnatal development
inferred← citeshttps://doi.org/10.1016/j.ygcen.2020.113593openalex-snapshot
Hypothyroidism induced by postnatal PTU (6-n-propyl-2-thiouracil) treatment decreases Sertoli cell number and spermatogenic efficiency in sexually mature pigs
inferred← citeshttps://doi.org/10.1016/s0012-1606(03)00400-7openalex-snapshot
Haploinsufficiency of Bcl-x leads to male-specific defects in fetal germ cells: differential regulation of germ cell apoptosis between the sexes
inferred← citeshttps://doi.org/10.1016/s0014-4827(03)00339-2openalex-snapshot
Alternative patterns of transcription and translation of the ribosomal protein L32 mRNA in somatic and spermatogenic cells in mice
inferred← citeshttps://doi.org/10.1016/s0014-5793(97)00352-9openalex-snapshot
The cytosolic aldehyde dehydrogenase gene (Aldh1) is developmentally expressed in Leydig cells
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62087-2openalex-snapshot
Testicular Macrophages
inferred← citeshttps://doi.org/10.1016/s0303-7207(01)00461-0openalex-snapshot
Origin, differentiation and regulation of fetal and adult Leydig cells
inferred← citeshttps://doi.org/10.1016/s0890-6238(01)00201-5openalex-snapshot
Fetal testosterone insufficiency and abnormal proliferation of Leydig cells and gonocytes in rats exposed to di(n-butyl) phthalate
inferred← citeshttps://doi.org/10.1016/s0925-4773(02)00127-2openalex-snapshot
Developmental and cell type-specific expression of the zinc finger transcription factor Krüppel-like factor 4 (Klf4) in postnatal mouse testis
inferred← citeshttps://doi.org/10.1016/s0925-4773(98)00002-1openalex-snapshot
Differential expression of the Oct-4 transcription factor during mouse germ cell differentiation
inferred← citeshttps://doi.org/10.1016/s1090-0233(03)00029-7openalex-snapshot
A quantitative study of seminiferous tubular cells in the developing Murrah buffalo testis
inferred← citeshttps://doi.org/10.1017/cbo9781139540742.004openalex-snapshot
Male gamete
inferred← citeshttps://doi.org/10.1017/cbo9781139540742.006openalex-snapshot
Adult stem-cell population in the human testis
inferred← citeshttps://doi.org/10.1023/a:1014377926163openalex-snapshot
The Role of Genotype in the Formation of Leydig Cell Hormone Function during Postnatal Ontogeny in Diallele Crosses of Laboratory Mice
inferred← citeshttps://doi.org/10.1023/a:1016845715609openalex-snapshot
Effect of Genotype on Formation of Hormonal Function of Leydig Cells during Mouse Postnatal Development
inferred← citeshttps://doi.org/10.1038/cddis.2014.232openalex-snapshot
Retinoblastoma protein (RB) interacts with E2F3 to control terminal differentiation of Sertoli cells
inferred← citeshttps://doi.org/10.1038/cr.1997.6openalex-snapshot
Identification and expression of epidermal growth factor gene in mouse testis
inferred← citeshttps://doi.org/10.1038/ng0398-251openalex-snapshot
Testicular degeneration in Bclw-deficient mice
inferred← citeshttps://doi.org/10.1038/nsmb.1876openalex-snapshot
Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus
inferred← citeshttps://doi.org/10.1038/s41419-022-04837-2openalex-snapshot
UHRF1 establishes crosstalk between somatic and germ cells in male reproduction
inferred← citeshttps://doi.org/10.1038/s41598-017-02018-2openalex-snapshot
Effect Of Microgravity On Aromatase Expression In Sertoli Cells
inferred← citeshttps://doi.org/10.1038/s41598-022-16919-4openalex-snapshot
Connexin43 represents an important regulator for Sertoli cell morphology, Sertoli cell nuclear ultrastructure, and Sertoli cell maturation
inferred← citeshttps://doi.org/10.1038/s41598-023-39323-yopenalex-snapshot
Culture-space control is effective in promoting haploid cell formation and spermiogenesis in vitro in neonatal mice
inferred← citeshttps://doi.org/10.1038/s41598-024-74895-3openalex-snapshot
Neonatal exposure to high d-galactose affects germ cell development in neonatal testes organ culture
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601447openalex-snapshot
Prepubertal testis development relies on retinoic acid but not rexinoid receptors in Sertoli cells
inferred← citeshttps://doi.org/10.1038/srep43459openalex-snapshot
ESR1 inhibits hCG-induced steroidogenesis and proliferation of progenitor Leydig cells in mice
inferred← citeshttps://doi.org/10.1046/j.1365-2605.1998.00141.xopenalex-snapshot
Immunohistochemical detection of testicular macrophages during the period of postnatal maturation in the mouse
inferred← citeshttps://doi.org/10.1046/j.1365-2605.1999.00191.xopenalex-snapshot
Apoptosis and mitosis in gonocytes of the rat testis during foetal and neonatal development
inferred← citeshttps://doi.org/10.1046/j.1365-2826.1998.00200.xopenalex-snapshot
Developmental Expression and Regulation of Aromatase– and 5α‐Reductase Type 1 mRNA in the Male and Female Mouse Hypothalamus
inferred← citeshttps://doi.org/10.1046/j.1432-1327.1999.00245.xopenalex-snapshot
Expression of 3β‐hydroxysteroid dehydrogenase type I and type VI isoforms in the mouse testis during development
inferred← citeshttps://doi.org/10.1055/a-2216-0269openalex-snapshot
Quantitative Characterization of Ectopic Adrenal Gene Expression in Fetal Testes in 21-Hydroxylase Deficient Mice
inferred← citeshttps://doi.org/10.1055/s-2005-865655openalex-snapshot
Meiosis: Inducing Variation by Reduction
inferred← citeshttps://doi.org/10.1071/rd03046openalex-snapshot
Review: Male germ line stem cells: from cell biology to cell therapy?
inferred← citeshttps://doi.org/10.1071/rd07062openalex-snapshot
Leptin inhibits basal but not gonadotrophin-stimulated testosterone production in the immature mouse and sheep testis
inferred← citeshttps://doi.org/10.1071/rd07134openalex-snapshot
Postnatal Sertoli and Leydig cell proliferation and the establishment of puberty and sexual maturity in Chinchilla lanigera (Rodentia, Chinchillidae)
inferred← citeshttps://doi.org/10.1071/rd12411openalex-snapshot
Germ cell survival and differentiation after xenotransplantation of testis tissue from three endangered species: Iberian lynx (Lynx pardinus), Cuvier’s gazelle (Gazella cuvieri) and Mohor gazelle (G. dama mhorr)
inferred← citeshttps://doi.org/10.1071/rd15239openalex-snapshot
Suppression of Sertoli cell tumour development during the first wave of spermatogenesis in inhibin a-deficient mice
inferred← citeshttps://doi.org/10.1071/rd17102openalex-snapshot
Peri-conception and first trimester diet modifies reproductive development in bulls
inferred← citeshttps://doi.org/10.1073/pnas.0611421104openalex-snapshot
Male fetal germ cells are targets for androgens that physiologically inhibit their proliferation
inferred← citeshttps://doi.org/10.1073/pnas.0807297105openalex-snapshot
Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice
inferred← citeshttps://doi.org/10.1073/pnas.1710837114openalex-snapshot
Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis
inferred← citeshttps://doi.org/10.1074/jbc.272.27.17023openalex-snapshot
Seminiferous Tubule Basement Membrane
inferred← citeshttps://doi.org/10.1080/09553000210134818openalex-snapshot
Study of the gonocyte cell cycle in irradiated TP53 knockout mouse foetuses and newborns
inferred← citeshttps://doi.org/10.1080/09553000600960019openalex-snapshot
p63 expression pattern in foetal and neonatal gonocytes after irradiation and role in the resulting apoptosis by using p63 knockout mice
inferred← citeshttps://doi.org/10.1083/jcb.134.5.1109openalex-snapshot
Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing.
inferred← citeshttps://doi.org/10.1089/cell.2013.0083openalex-snapshot
Reprogramming Sertoli Cells into Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1089/scd.2015.0196openalex-snapshot
Differentiation of Fetal Male Germline and Gonadal Progenitor Cells Is Disrupted in Organ Cultures Containing Knockout Serum Replacement
inferred← citeshttps://doi.org/10.1093/biolre/ioac118openalex-snapshot
Sertoli cell PUMILIO proteins modulate mouse testis size through translational control of cell cycle regulators
inferred← citeshttps://doi.org/10.1093/biolre/ioad077openalex-snapshot
Rhox8 homeobox gene ablation leads to rete testis abnormality and male subfertility in mice
inferred← citeshttps://doi.org/10.1093/biolre/ioaf011openalex-snapshot
Utilization of the QuPath open-source software platform for analysis of mammalian spermatogenesis
inferred← citeshttps://doi.org/10.1093/biolre/iox022openalex-snapshot
Cell-autonomous requirement for mammalian target of rapamycin (Mtor) in spermatogonial proliferation and differentiation in the mouse†
inferred← citeshttps://doi.org/10.1093/biolre/ioy075openalex-snapshot
Mutations causing specific arrests in the development of mouse primordial germ cells and gonocytes
inferred← citeshttps://doi.org/10.1093/humrep/16.5.988openalex-snapshot
Altered prostate growth and daily sperm production in male mice exposed prenatally to subclinical doses of 17α-ethinyl oestradiol
inferred← citeshttps://doi.org/10.1093/humupd/dmu034openalex-snapshot
From gametogenesis and stem cells to cancer: common metabolic themes
inferred← citeshttps://doi.org/10.1093/molehr/gaad004openalex-snapshot
Multiomics approach to profiling Sertoli cell maturation during development of the spermatogonial stem cell niche
inferred← citeshttps://doi.org/10.1093/molehr/gax012openalex-snapshot
Comparison of global gene expression profiles of microdissected human foetal Leydig cells with their normal and hyperplastic adult equivalents
inferred← citeshttps://doi.org/10.1093/molehr/gay023openalex-snapshot
A novel mouse model of testicular granulosa cell tumors
inferred← citeshttps://doi.org/10.1093/nar/gkag699openalex-snapshot
Cap 2′-O-methyltransferase CMTR2 regulates male meiosis independent of its methyltransferase activity
inferred← citeshttps://doi.org/10.1093/nar/gkz992openalex-snapshot
FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis
inferred← citeshttps://doi.org/10.1093/toxsci/kfp153openalex-snapshot
Phthalates Impair Germ Cell Number in the Mouse Fetal Testis by an Androgen- and Estrogen-Independent Mechanism
inferred← citeshttps://doi.org/10.1095/biolreprod.102.005132openalex-snapshot
Determinants of Retroviral-Mediated Gene Delivery to Mouse Spermatogonia1
inferred← citeshttps://doi.org/10.1095/biolreprod.102.008169openalex-snapshot
Relationship of the Hormone-Sensitive Lipase-Mediated Modulation of Cholesterol Metabolism in Individual Compartments of the Testis to Serum Pituitary Hormone and Testosterone Concentrations in a Seasonal Breeder, the Mink (Mustela vison)1
inferred← citeshttps://doi.org/10.1095/biolreprod.103.018895openalex-snapshot
Effects of Mono-(2-Ethylhexyl) Phthalate on Fetal and Neonatal Rat Testis Organ Cultures1
inferred← citeshttps://doi.org/10.1095/biolreprod.103.022590openalex-snapshot
Development of Leydig Cells in the Insulin-Like Growth Factor-I (IGF-I) Knockout Mouse: Effects of IGF-I Replacement and Gonadotropic Stimulation1
inferred← citeshttps://doi.org/10.1095/biolreprod.103.026880openalex-snapshot
The Murine Testicular Transcriptome: Characterizing Gene Expression in the Testis During the Progression of Spermatogenesis1
inferred← citeshttps://doi.org/10.1095/biolreprod.104.028381openalex-snapshot
Immunohistochemical Profiling of Germ Cells Within the Human Fetal Testis: Identification of Three Subpopulations
inferred← citeshttps://doi.org/10.1095/biolreprod.104.031278openalex-snapshot
Effects of Acid Sphingomyelinase Deficiency on Male Germ Cell Development and Programmed Cell Death1
inferred← citeshttps://doi.org/10.1095/biolreprod.104.035238openalex-snapshot
Infertility in 5,10-Methylenetetrahydrofolate Reductase (MTHFR)-Deficient Male Mice Is Partially Alleviated by Lifetime Dietary Betaine Supplementation1
inferred← citeshttps://doi.org/10.1095/biolreprod.105.044404openalex-snapshot
Prepubertal Expansion of Dark and Pale Type A Spermatogonia in the Rhesus Monkey (Macaca mulatta) Results from Proliferation During Infantile and Juvenile Development in a Relatively Gonadotropin Independent Manner1
inferred← citeshttps://doi.org/10.1095/biolreprod.105.047225openalex-snapshot
Vascular Endothelial Growth Factor and Kinase Domain Region Receptor Are Involved in Both Seminiferous Cord Formation and Vascular Development During Testis Morphogenesis in the Rat1
inferred← citeshttps://doi.org/10.1095/biolreprod.108.071662openalex-snapshot
Proliferative Activity In Vitro and DNA Repair Indicate that Adult Mouse and Human Sertoli Cells Are Not Terminally Differentiated, Quiescent Cells1
inferred← citeshttps://doi.org/10.1095/biolreprod.109.078907openalex-snapshot
Claudin 11 Deficiency in Mice Results in Loss of the Sertoli Cell Epithelial Phenotype in the Testis1
inferred← citeshttps://doi.org/10.1095/biolreprod.109.081729openalex-snapshot
Interdependence of Platelet-Derived Growth Factor and Estrogen-Signaling Pathways in Inducing Neonatal Rat Testicular Gonocytes Proliferation1
inferred← citeshttps://doi.org/10.1095/biolreprod.111.094938openalex-snapshot
Rhox13 Is Translated in Premeiotic Germ Cells in Male and Female Mice and Is Regulated by NANOS2 in the Male1
inferred← citeshttps://doi.org/10.1095/biolreprod.113.108639openalex-snapshot
Computer Simulation of the Rodent Spermatogonial Stem Cell Niche1
inferred← citeshttps://doi.org/10.1095/biolreprod.113.109819openalex-snapshot
Translational Activation of Developmental Messenger RNAs During Neonatal Mouse Testis Development1
inferred← citeshttps://doi.org/10.1095/biolreprod.113.113159openalex-snapshot
Retinoblastoma Protein (RB1) Controls Fate Determination in Stem Cells and Progenitors of the Mouse Male Germline1
inferred← citeshttps://doi.org/10.1095/biolreprod.113.114645openalex-snapshot
Retinoic Acid Induces Multiple Hallmarks of the Prospermatogonia-to-Spermatogonia Transition in the Neonatal Mouse1
inferred← citeshttps://doi.org/10.1095/biolreprod.115.135145openalex-snapshot
The Role of Retinoic Acid (RA) in Spermatogonial Differentiation1
inferred← citeshttps://doi.org/10.1095/biolreprod.116.140947openalex-snapshot
mTORC1 Activation Promotes Spermatogonial Differentiation and Causes Subfertility in Mice
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