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Proliferation of spermatogonia and Sertoli cells in maturing 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.1001000205openalex-snapshot
Quantitative study of the cell population of the seminiferous tubules in immature rats
inferredcites →https://doi.org/10.1002/aja.1001220205openalex-snapshot
Re‐examination of spermatogonial renewal in the rat by means of seminiferous tubules mounted “in toto”
inferredcites →https://doi.org/10.1002/aja.1001530107openalex-snapshot
Spermatogonial intercellular bridges in whole‐mounted seminiferous tubules from normal and irradiated rodent testes
inferredcites →https://doi.org/10.1002/ar.1091690305openalex-snapshot
Spermatogonial stem‐cell renewal in the mouse
inferredcites →https://doi.org/10.1002/ar.1091690306openalex-snapshot
The spermatogonial stem cell population in adult rats. I. Their morphology, proliferation and maturation
inferredcites →https://doi.org/10.1002/ar.1091920406openalex-snapshot
Morphological and quantitative analysis of spermatogonia in mouse testes using whole mounted seminiferous tubules. I. The normal testes
inferredcites →https://doi.org/10.1002/ar.1092030109openalex-snapshot
Morphology, proliferation, and differentiation of undifferentiated spermatogonia in the chinese hamster and the ram
inferredcites →https://doi.org/10.1051/rnd:19620104openalex-snapshot
DÉVELOPPEMENT DU TESTICULE CHEZ L'AGNEAU. ÉTABLISSEMENT DE LA SPERMATOGENÈSE
inferredcites →https://doi.org/10.1051/rnd:19630302openalex-snapshot
DÉVELOPPEMENT TESTICULAIRE ET ÉTABLISSEMENT DE LA SPERMATOGENÈSE CHEZ LE TAUREAU
inferredcites →https://doi.org/10.1080/09553008314551561openalex-snapshot
Stem Cells–Their Identification and Characterization
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.1365-2184.1973.tb01617.xopenalex-snapshot
SPERMATOGONIAL STEM CELL RENEWAL IN THE MOUSE: I. NORMAL SITUATION
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.1365-2605.1982.tb00257.xopenalex-snapshot
Spermatogenesis in the immature mouse proceeds faster than in the adult
inferredcites →https://doi.org/10.1111/j.1365-2605.1983.tb00321.xopenalex-snapshot
Testicular development in Macaca irus after birth
inferredcites →https://doi.org/10.1210/endo-100-1-122openalex-snapshot
Developmental Changes in Serum Luteinizing Hormone, Follicle Stimulating Hormone and Androgen Levels in Males of Two Inbred Mouse Strains1
inferredcites →https://doi.org/10.1530/jrf.0.0140427openalex-snapshot
DEVELOPMENT OF THE RECTUM-TESTIS TEMPERATURE DIFFERENCE IN THE POST-NATAL RAT
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(199602)244:2<155::aid-ar3>3.0.co;2-0openalex-snapshot
Differential expression of placental (P)-cadherin in sertoli cells and peritubular myoid cells during postnatal development of the mouse testis
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)1098-2795(199602)43:2<236::aid-mrd13>3.0.co;2-1openalex-snapshot
Boar proacrosin expressed in spermatids of transgenic mice does not reach the acrosome and disrupts spermatogenesis
inferred← citeshttps://doi.org/10.1002/9781118628003.ch22openalex-snapshot
Retinoic Acid Receptor Signaling in Post‐Natal Male Germ Cell Differentiation
inferred← citeshttps://doi.org/10.1002/aja.1002040407openalex-snapshot
Cdk family genes are expressed not only in dividing but also in terminally differentiated mouse germ cells, suggesting their possible function during both cell division and differentiation
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/dvg.1020160209openalex-snapshot
Distinct patterns of expression of the D‐type cycling during testicular development in the mouse
inferred← citeshttps://doi.org/10.1002/dvg.20453openalex-snapshot
Epithelial‐mesenchymal crosstalk in Wolffian duct and fetal testis cord development
inferred← citeshttps://doi.org/10.1002/iub.1115openalex-snapshot
Smads and cell fate: Distinct roles in specification, development, and tumorigenesis in the testis
inferred← citeshttps://doi.org/10.1002/j.1939-4640.1992.tb00323.xopenalex-snapshot
Oligotriche and Quaking Gene Mutations Phenotypic Effects on Mouse Spermatogenesis and Testicular Steroidogenesis
inferred← citeshttps://doi.org/10.1006/dbio.1998.9004openalex-snapshot
The MouseTsxGene Is Expressed in Sertoli Cells of the Adult Testis and Transiently in Premeiotic Germ Cells during Puberty
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/10.1007/978-3-031-96376-6_10openalex-snapshot
Leydig Cell Interaction with Macrophages, Peritubular Cells, and Sertoli Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-35049-8_4openalex-snapshot
Factors Affecting Boar Reproduction, Testis Function, and Sperm Quality
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/10.1016/b978-0-08-091764-1.50006-4openalex-snapshot
Cell Biology of Testicular Development
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/b978-0-443-21477-6.00554-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/b978-012647751-1/50021-0openalex-snapshot
Sertoli Cell Toxicants
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.bbagrm.2014.05.019openalex-snapshot
Role of retinoic acid receptor (RAR) signaling in post-natal male germ cell differentiation
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.03.077openalex-snapshot
Distinct Roles for Rac1 in Sertoli Cell Function during Testicular Development and Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109885openalex-snapshot
Cdc42 activity in Sertoli cells is essential for maintenance of spermatogenesis
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.domaniend.2014.02.006openalex-snapshot
Nursing supports neonatal porcine testicular development
inferred← citeshttps://doi.org/10.1016/j.mod.2011.12.003openalex-snapshot
Retinoic acid metabolism links the periodical differentiation of germ cells with the cycle of Sertoli cells in mouse seminiferous epithelium
inferred← citeshttps://doi.org/10.1016/j.peptides.2022.170899openalex-snapshot
Postnatal ontogeny of Neuromedin S and its receptors NMUR1 and NMUR2 expression in mouse testis
inferred← citeshttps://doi.org/10.1016/j.repbio.2013.04.001openalex-snapshot
Relationships of serum thyroid hormones and follicle-stimulating hormone concentrations to Sertoli cell differentiation during the first wave of spermatogenesis in euthyroid ram lambs
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.136139openalex-snapshot
Exposure of DBP in gestation induces inflammation of testicular Sertoli cells in progeny by activating NLRP3 inflammasomes
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.2005.03.016openalex-snapshot
Testicular development in Brahman bulls
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.08.004openalex-snapshot
Mammalian target of rapamycin complex 1 (mTORC1) Is required for mouse spermatogonial differentiation in vivo
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/s0303-7207(97)00214-1openalex-snapshot
A mouse Sertoli cell line expressing anti-Müllerian hormone and its type II receptor
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/10.1034/j.1600-0463.2003.1110121.xopenalex-snapshot
Genetic engineering to study testicular tumorigenesis
inferred← citeshttps://doi.org/10.1038/78161openalex-snapshot
Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions
inferred← citeshttps://doi.org/10.1038/ncomms3889openalex-snapshot
Low paternal dietary folate alters the mouse sperm epigenome and is associated with negative pregnancy outcomes
inferred← citeshttps://doi.org/10.1038/ng0297-201openalex-snapshot
Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility
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/10.1046/j.1365-2605.1998.00136.xopenalex-snapshot
Higher thyroid hormone levels in neonatal life result in reduced testis volume in postpubertal bulls
inferred← citeshttps://doi.org/10.1071/rd14368openalex-snapshot
Nutrition affects Sertoli cell function but not Sertoli cell numbers in sexually mature male sheep
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/10.1073/pnas.1710837114openalex-snapshot
Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis
inferred← citeshttps://doi.org/10.1080/15287398909531329openalex-snapshot
Effect of 1,3‐dinitrobenzene on prepubertal, pubertal, and adult mouse spermatogenesis
inferred← citeshttps://doi.org/10.1093/biolre/ioac148openalex-snapshot
Synchronizing spermatogenesis in the mouse
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/ioag032openalex-snapshot
Undifferentiated spermatogonia modulate their behavior via the expression of basement membrane protein laminin
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/ioy198openalex-snapshot
The mTORC1 component RPTOR is required for maintenance of the foundational spermatogonial stem cell pool in mice†
inferred← citeshttps://doi.org/10.1093/genetics/158.1.333openalex-snapshot
Genetic Architecture of Testis and Seminal Vesicle Weights in Mice
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/10.1095/biolreprod.102.003368openalex-snapshot
Identification and Characterization of Testis- and Epididymis-Specific Genes: Cystatin SC and Cystatin TE-11
inferred← citeshttps://doi.org/10.1095/biolreprod.102.011619openalex-snapshot
A 3-Kilobase Region Derived from the Rat Cathepsin L Gene Directs In Vivo Expression of a Reporter Gene in Sertoli Cells in a Manner Comparable to That of the Endogenous Gene1
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.115.135145openalex-snapshot
The Role of Retinoic Acid (RA) in Spermatogonial Differentiation1
inferred← citeshttps://doi.org/10.1095/biolreprod47.1.29openalex-snapshot
Genes Regulating Testis Size1
inferred← citeshttps://doi.org/10.1095/biolreprod48.4.786openalex-snapshot
Immunoreactive Arginine Vasopressin in the Testis: Immunocytochemical Localization and Testicular Content in Normal and in Experimental Cryptorchid Mouse1
inferred← citeshttps://doi.org/10.1095/biolreprod54.6.1192openalex-snapshot
Puberty Occurring Either Spontaneously or Induced Precociously in Rhesus Monkey (Macaca Mulatta) is Associated with a Marked Proliferation of Sertoli Cells1
inferred← citeshttps://doi.org/10.1095/biolreprod62.3.789openalex-snapshot
Expression of Deoxyribonucleic Acid Repair Enzymes During Spermatogenesis in Mice1
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1095/biolreprod65.3.829openalex-snapshot
Failure of Spermatogenesis in Mice Lacking Connexin431
inferred← citeshttps://doi.org/10.1096/fj.202202152rropenalex-snapshot
SRSF2 in Sertoli cells is essential for testicular development and spermatogenesis in mice
inferred← citeshttps://doi.org/10.1097/01.ehx.0000460765.30106.daopenalex-snapshot
Prepubertal to postpubertal development of testes in Wistar rats
inferred← citeshttps://doi.org/10.1111/and.12035openalex-snapshot
Icariin stimulates the proliferation of rat S ertoli cells in an ERK 1/2‐dependent manner in vitro
inferred← citeshttps://doi.org/10.1111/andr.13397openalex-snapshot
Comparing the adult and pre‐pubertal testis: Metabolic transitions and the change in the spermatogonial stem cell metabolic microenvironment
inferred← citeshttps://doi.org/10.1111/cpr.13760openalex-snapshot
Inactivation of JNK signalling results in polarity loss and cell senescence of Sertoli cell
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2005.00441.xopenalex-snapshot
Postzygotic isolation between the two European subspecies of the house mouse: estimates from fertility patterns in wild and laboratory-bred hybrids
inferred← citeshttps://doi.org/10.1111/j.1439-0531.1988.tb00979.xopenalex-snapshot
Nutzbarkeit der Ganz‐ und Halbpräparate der aus Hodenbiopsiematerialien isolierten Samenkanälchen am Modell des Ziegenbocks
inferred← citeshttps://doi.org/10.1111/j.1439-0531.1994.tb00593.xopenalex-snapshot
Examination of Spermatogonial Multiplication in the Bull using Whole‐mount Seminiferous Tubules
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2005.00493.xopenalex-snapshot
Atypical development of Sertoli cells and impairment of spermatogenesis in the hypogonadal (hpg) mouse
inferred← citeshttps://doi.org/10.1111/j.1600-0463.2001.tb05777.xopenalex-snapshot
Altered prostate growth and daily sperm production in male mice exposed prenatally to subclinical doses of 17α‐ethinyl oestradiol
inferred← citeshttps://doi.org/10.1111/j.1600-0897.2012.01137.xopenalex-snapshot
Sertoli Cell Quiescence – New Insights
inferred← citeshttps://doi.org/10.1155/2022/4755514openalex-snapshot
Models and Molecular Markers of Spermatogonial Stem Cells in Vertebrates: To Find Models in Nonmammals
inferred← citeshttps://doi.org/10.1159/000069295openalex-snapshot
Postnatal Testicular Development, Cellular Organization and Paracrine Regulation
inferred← citeshttps://doi.org/10.1177/0192623317709091openalex-snapshot
In Utero Exposure to Di( n -butyl)phthalate Induces Morphological and Biochemical Changes in Rats Postpuberty
inferred← citeshttps://doi.org/10.1186/s12964-015-0101-2openalex-snapshot
Long-term culture and significant expansion of human Sertoli cells whilst maintaining stable global phenotype and AKT and SMAD1/5 activation
inferred← citeshttps://doi.org/10.1210/en.137.11.4796openalex-snapshot
Targeted disruption of the estrogen receptor gene in male mice causes alteration of spermatogenesis and infertility
inferred← citeshttps://doi.org/10.1210/en.2014-1555openalex-snapshot
Murine Inhibin α-Subunit Haploinsufficiency Causes Transient Abnormalities in Prepubertal Testis Development Followed by Adult Testicular Decline
inferred← citeshttps://doi.org/10.1210/endo.141.7.7545openalex-snapshot
Localization of 17β-Hydroxysteroid Dehydrogenase/17-Ketosteroid Reductase Isoform Expression in the Developing Mouse Testis—Androstenedione Is the Major Androgen Secreted by Fetal/Neonatal Leydig Cells*
inferred← citeshttps://doi.org/10.1210/endocr/bqab269openalex-snapshot
Human INHBB Gene Variant (c.1079T>C:p.Met360Thr) Alters Testis Germ Cell Content, but Does Not Impact Fertility in Mice
inferred← citeshttps://doi.org/10.1210/endocr/bqz020openalex-snapshot
Primary Sertoli Cell Cultures From Adult Mice Have Different Properties Compared With Those Derived From 20-Day-Old Animals
inferred← citeshttps://doi.org/10.1210/me.2002-0186openalex-snapshot
Follicle-Stimulating Hormone Increases Testicular Anti-Mullerian Hormone (AMH) Production through Sertoli Cell Proliferation and a Nonclassical Cyclic Adenosine 5′-Monophosphate-Mediated Activation of the AMH Gene
inferred← citeshttps://doi.org/10.1242/dev.094045openalex-snapshot
An epigenetic switch is crucial for spermatogonia to exit the undifferentiated state toward a Kit-positive identity
inferred← citeshttps://doi.org/10.1242/dev.173088openalex-snapshot
Differential RA responsiveness directs formation of functionally distinct spermatogonial populations at the initiation of spermatogenesis in the mouse
inferred← citeshttps://doi.org/10.1242/dev.200713openalex-snapshot
Modeling mammalian spermatogonial differentiation and meiotic initiationin vitro
inferred← citeshttps://doi.org/10.1242/jcs.01226openalex-snapshot
KIN17 encodes an RNA-binding protein and is expressed during mouse spermatogenesis
inferred← citeshttps://doi.org/10.1292/jvms.61.465openalex-snapshot
Changes in Lectin Binding Patterns of Mouse Male Germ Cells (Gonocytes) during Prespermatogenesis.
inferred← citeshttps://doi.org/10.1369/jhc.2008.952440openalex-snapshot
Expression, Localization, and Binding Activity of the Ezrin/Radixin/Moesin Proteins in the Mouse Testis
inferred← citeshttps://doi.org/10.15252/embr.201846566openalex-snapshot
A microRNA cluster in the Fragile‐X region expressed during spermatogenesis targets FMR1
inferred← citeshttps://doi.org/10.1530/jrf.0.0930233openalex-snapshot
Proliferative activity of gonocytes, Sertoli cells and interstitial cells during testicular development in mice
inferred← citeshttps://doi.org/10.1530/rep-17-0061openalex-snapshot
Cellular and molecular responses of adult testis to changes in nutrition: novel insights from the sheep model
inferred← citeshttps://doi.org/10.1677/joe-07-0258openalex-snapshot
Inactivation of the IGF-I receptor gene in primary Sertoli cells highlights the autocrine effects of IGF-I
inferred← citeshttps://doi.org/10.1677/joe.0.1780395openalex-snapshot
Stereological evaluation of Sertoli cell ontogeny during fetal and neonatal life in two diverse breeds of swine
inferred← citeshttps://doi.org/10.2307/3578829openalex-snapshot
Radiosensitivity of Testicular Cells in the Prepubertal Mouse
inferred← citeshttps://doi.org/10.3390/ani12030271openalex-snapshot
Sertoli, Leydig, and Spermatogonial Cells’ Specific Gene and Protein Expressions as Dog Testes Evolve from Immature into Mature States
inferred← citeshttps://doi.org/10.3390/cells11030352openalex-snapshot
Action and Interaction between Retinoic Acid Signaling and Blood–Testis Barrier Function in the Spermatogenesis Cycle
inferred← citeshttps://doi.org/10.53846/goediss-4168openalex-snapshot
The p53 homolog p73 takes hold of the male germ line – a novel function of TAp73 in protecting sperm cell adhesion, migration and maturation within the seminiferous epithelium of the testis
inferred← citeshttps://doi.org/10.7554/elife.15635openalex-snapshot
Sox9 and Sox8 protect the adult testis from male-to-female genetic reprogramming and complete degeneration
inferred← citeshttps://doi.org/10.7554/elife.56523openalex-snapshot
DAZL mediates a broad translational program regulating expansion and differentiation of spermatogonial progenitors
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