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Blood–testis barrier and Sertoli cell function: lessons from SCCx43KO 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/(sici)1097-010x(19980801)281:5<472::aid-jez12>3.0.co;2-bopenalex-snapshot

Evolution of the mammalian Y chromosome and sex-determining genes

inferredcites →https://doi.org/10.1002/1526-968x(200101)29:1<1::aid-gene1000>3.0.co;2-0openalex-snapshot

Endothelium-specific replacement of the connexin43 coding region by a lacZ reporter gene

inferredcites →https://doi.org/10.1002/ar.1091850403openalex-snapshot

The postnatal development of the junctional complexes of the mouse Sertoli cells as revealed by freeze‐fracture

inferredcites →https://doi.org/10.1002/gene.10100openalex-snapshot

Sertoli and granulosa cell‐specific Cre recombinase activity in transgenic mice

inferredcites →https://doi.org/10.1002/glia.20429openalex-snapshot

Functional connexin “hemichannels”: A critical appraisal

inferredcites →https://doi.org/10.1002/j.1939-4640.1995.tb00552.xopenalex-snapshot

The Distribution of Connexin 43 is Associated With the Germ Cell Differentiation and With the Modulation of the Sertoli Cell Junctional Barrier in Continual (Guinea Pig) and Seasonal Breeders' (Mink) Testes

inferredcites →https://doi.org/10.1002/jcp.10473openalex-snapshot

Functional characterization of Cx43 based gap junctions during spermatogenesis

inferredcites →https://doi.org/10.1002/jemt.1070200104openalex-snapshot

The blood‐testis barrier and sertoli cell junctions: Structural considerations

inferredcites →https://doi.org/10.1002/jemt.20741openalex-snapshot

Effects of di(2‐ethylhexyl) phthalate on gap and tight junction protein expression in the testis of prepubertal rats

inferredcites →https://doi.org/10.1002/mrd.21200openalex-snapshot

Molecular dynamics of the blood–testis barrier components during murine spermatogenesis

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/10.1006/meth.1999.0938openalex-snapshot

General or Cell Type-Specific Deletion and Replacement of Connexin-Coding DNA in the Mouse

inferredcites →https://doi.org/10.1007/3-540-33713-x_58openalex-snapshot

Physiology of Spermatogenesis

inferredcites →https://doi.org/10.1007/978-0-387-09597-4_13openalex-snapshot

Cross-Talk between Tight and Anchoring Junctions—Lesson from the Testis

inferredcites →https://doi.org/10.1007/978-1-4614-4711-5_13openalex-snapshot

Gap Junctions and Blood-Tissue Barriers

inferredcites →https://doi.org/10.1007/978-3-540-92963-5_1openalex-snapshot

Aufgaben und Ziele der Andrologie

inferredcites →https://doi.org/10.1007/bf00224733openalex-snapshot

Pattern of compartmentation in human seminiferous tubules showing dislocation of spermatogonia

inferredcites →https://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

inferredcites →https://doi.org/10.1007/s004180050004openalex-snapshot

Sox9 protein in rat Sertoli cells is age and stage dependent

inferredcites →https://doi.org/10.1007/s004180050409openalex-snapshot

Expression of connexin 43 in human testis

inferredcites →https://doi.org/10.1007/s00441-015-2126-7openalex-snapshot

A Sertoli cell-specific connexin43 knockout leads to altered interstitial connexin expression and increased Leydig cell numbers

inferredcites →https://doi.org/10.1007/s10495-006-6981-2openalex-snapshot

Blockage of testicular connexins induced apoptosis in rat seminiferous epithelium

inferredcites →https://doi.org/10.1007/s11248-012-9668-1openalex-snapshot

Effects of a murine germ cell-specific knockout of Connexin 43 on Connexin expression in testis and fertility

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.bbamem.2005.01.008openalex-snapshot

Epithelial transport and barrier function in occludin-deficient mice

inferredcites →https://doi.org/10.1016/j.bbamem.2008.10.023openalex-snapshot

Reciprocal influence of connexins and apical junction proteins on their expressions and functions

inferredcites →https://doi.org/10.1016/j.biocel.2009.05.016openalex-snapshot

Disruption of the blood-testis barrier integrity by bisphenol A in vitro: Is this a suitable model for studying blood-testis barrier dynamics?

inferredcites →https://doi.org/10.1016/j.biochi.2004.05.003openalex-snapshot

A proposed role for ZO-1 in targeting connexin 43 gap junctions to the endocytic pathway

inferredcites →https://doi.org/10.1016/j.cardiores.2003.11.013openalex-snapshot

Gap junctions and the connexin protein family

inferredcites →https://doi.org/10.1016/j.ceb.2004.07.014openalex-snapshot

Connexins: functions without junctions

inferredcites →https://doi.org/10.1016/j.diff.2011.03.001openalex-snapshot

Altered differentiation and clustering of Sertoli cells in transgenic mice showing a Sertoli cell specific knockout of the connexin 43 gene

inferredcites →https://doi.org/10.1016/j.febslet.2011.01.028openalex-snapshot

Predicted expansion of the claudin multigene family

inferredcites →https://doi.org/10.1016/j.fertnstert.2013.04.034openalex-snapshot

Claudin-11 and connexin-43 display altered spatial patterns of organization in men with primary seminiferous tubule failure compared with controls

inferredcites →https://doi.org/10.1016/j.proghi.2011.05.001openalex-snapshot

The blood-testis barrier: the junctional permeability, the proteins and the lipids

inferredcites →https://doi.org/10.1016/j.repbio.2012.10.007openalex-snapshot

Expression of the androgen receptor in the testis of mice with a Sertoli cell specific knock-out of the connexin 43 gene (SCCx43KO−/−)

inferredcites →https://doi.org/10.1016/j.reprotox.2004.01.002openalex-snapshot

Sertoli cell junctional proteins as early targets for different classes of reproductive toxicants

inferredcites →https://doi.org/10.1016/j.reprotox.2006.02.004openalex-snapshot

Effect of di-(2-ethylhexyl) phthalate on N-cadherin and catenin protein expression in rat testis

inferredcites →https://doi.org/10.1016/j.taap.2013.01.016openalex-snapshot

Hexavalent chromium at low concentration alters Sertoli cell barrier and connexin 43 gap junction but not claudin-11 and N-cadherin in the rat seminiferous tubule culture model

inferredcites →https://doi.org/10.1016/j.theriogenology.2011.09.007openalex-snapshot

Expression of anti-Müllerian hormone, cyclin-dependent kinase inhibitor (CDKN1B), androgen receptor, and connexin 43 in equine testes during puberty

inferredcites →https://doi.org/10.1016/j.theriogenology.2015.05.009openalex-snapshot

Characterization of the equine blood–testis barrier during tubular development in normal and cryptorchid stallions

inferredcites →https://doi.org/10.1016/j.tibs.2009.03.005openalex-snapshot

Coordinating cellular events during spermatogenesis: a biochemical model

inferredcites →https://doi.org/10.1016/j.tox.2009.09.012openalex-snapshot

Neonatal exposure of male rats to Bisphenol A impairs fertility and expression of sertoli cell junctional proteins in the testis

inferredcites →https://doi.org/10.1016/j.ydbio.2010.07.014openalex-snapshot

Major involvement of connexin 43 in seminiferous epithelial junction dynamics and male fertility

inferredcites →https://doi.org/10.1016/s0074-7696(08)60766-4openalex-snapshot

The Sertoli-Germ Cell Communication Network in Mammals

inferredcites →https://doi.org/10.1016/s0092-8674(00)81282-9openalex-snapshot

The Gap Junction Communication Channel

inferredcites →https://doi.org/10.1016/s0092-8674(00)81553-6openalex-snapshot

CNS Myelin and Sertoli Cell Tight Junction Strands Are Absent in Osp/Claudin-11 Null Mice

inferredcites →https://doi.org/10.1016/s0960-9822(00)00690-4openalex-snapshot

Unique and shared functions of different connexins in mice

inferredcites →https://doi.org/10.1017/cbo9780511781001.006openalex-snapshot

Contraception and Birth Control

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/10.1073/pnas.0506084102openalex-snapshot

Androgens regulate the permeability of the blood–testis barrier

inferredcites →https://doi.org/10.1073/pnas.0901700106openalex-snapshot

Connexin 43 and plakophilin-2 as a protein complex that regulates blood–testis barrier dynamics

inferredcites →https://doi.org/10.1073/pnas.1007047107openalex-snapshot

Connexin 43 is critical to maintain the homeostasis of the blood–testis barrier via its effects on tight junction reassembly

inferredcites →https://doi.org/10.1074/jbc.273.33.21040openalex-snapshot

Testin Secreted by Sertoli Cells Is Associated with the Cell Surface, and Its Expression Correlates with the Disruption of Sertoli-Germ Cell Junctions but Not the Inter-Sertoli Tight Junction

inferredcites →https://doi.org/10.1083/jcb.102.2.457openalex-snapshot

A functional assay for proteins involved in establishing an epithelial occluding barrier: identification of a uvomorulin-like polypeptide.

inferredcites →https://doi.org/10.1083/jcb.113.4.881openalex-snapshot

Endocytosis of junctional cadherins in bovine kidney epithelial (MDBK) cells cultured in low Ca2+ ion medium.

inferredcites →https://doi.org/10.1083/jcb.141.7.1539openalex-snapshot

Claudin-1 and -2: Novel Integral Membrane Proteins Localizing at Tight Junctions with No Sequence Similarity to Occludin

inferredcites →https://doi.org/10.1083/jcb.145.3.579openalex-snapshot

Claudin-11/OSP-based Tight Junctions of Myelin Sheaths in Brain and Sertoli Cells in Testis

inferredcites →https://doi.org/10.1091/mbc.11.12.4131openalex-snapshot

Complex Phenotype of Mice Lacking Occludin, a Component of Tight Junction Strands

inferredcites →https://doi.org/10.1091/mbc.e08-12-1236openalex-snapshot

Zona Occludens-2 Is Critical for Blood–Testis Barrier Integrity and Male Fertility

inferredcites →https://doi.org/10.1093/annonc/mdq177openalex-snapshot

Testicular non-seminoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

inferredcites →https://doi.org/10.1093/biolreprod/3.3.308openalex-snapshot

The Blood-Testis Barrier in the Rat and the Physiological Compartmentation of the Seminiferous Epithelium1

inferredcites →https://doi.org/10.1093/carcin/22.9.1537openalex-snapshot

Disruption of gap junctional intercellular communication by lindane is associated with aberrant localization of connexin43 and zonula occludens-1 in 42GPA9 Sertoli cells

inferredcites →https://doi.org/10.1095/biolreprod.102.010504openalex-snapshot

Neonatal Hypothyroidism Alters the Localization of Gap Junctional Protein Connexin 43 in the Testis and Messenger RNA Levels in the Epididymis of the Rat1

inferredcites →https://doi.org/10.1095/biolreprod.103.026880openalex-snapshot

The Murine Testicular Transcriptome: Characterizing Gene Expression in the Testis During the Progression of Spermatogenesis1

inferredcites →https://doi.org/10.1095/biolreprod.106.059212openalex-snapshot

Proliferation of Adult Sertoli Cells Following Conditional Knockout of the Gap Junctional Protein GJA1 (Connexin 43) in Mice1

inferredcites →https://doi.org/10.1095/biolreprod.108.068627openalex-snapshot

Seminiferous Tubule Degeneration and Infertility in Mice with Sustained Activation of WNT/CTNNB1 Signaling in Sertoli Cells1

inferredcites →https://doi.org/10.1095/biolreprod.109.077040openalex-snapshot

Claudin 5 Expression in Mouse Seminiferous Epithelium Is Dependent upon the Transcription Factor Ets Variant 5 and Contributes to Blood-Testis Barrier Function1

inferredcites →https://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

inferredcites →https://doi.org/10.1095/biolreprod.109.079335openalex-snapshot

Constitutive WNT/Beta-Catenin Signaling in Murine Sertoli Cells Disrupts Their Differentiation and Ability to Support Spermatogenesis1

inferredcites →https://doi.org/10.1095/biolreprod.112.100255openalex-snapshot

Acute Slices of Mice Testis Seminiferous Tubules Unveil Spontaneous and Synchronous Ca2+ Oscillations in Germ Cell Clusters1

inferredcites →https://doi.org/10.1095/biolreprod.112.104851openalex-snapshot

A Novel Subcellular Machine Contributes to Basal Junction Remodeling in the Seminiferous Epithelium1

inferredcites →https://doi.org/10.1095/biolreprod.113.107847openalex-snapshot

Mice Stage-Specific Claudin 3 Expression Regulates Progression of Meiosis in Early Stage Spermatocytes1

inferredcites →https://doi.org/10.1095/biolreprod.113.110197openalex-snapshot

Nondividing, Postpubertal Rat Sertoli Cells Resumed Proliferation after Transplantation1

inferredcites →https://doi.org/10.1095/biolreprod.114.126334openalex-snapshot

Specific Deletion of Cdh2 in Sertoli Cells Leads to Altered Meiotic Progression and Subfertility of Mice1

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/biolreprod60.5.1263openalex-snapshot

Defects in the Germ Line and Gonads of Mice Lacking Connexin431

inferredcites →https://doi.org/10.1095/biolreprod67.3.945openalex-snapshot

Gap Junctions with Varied Permeability Properties Establish Cell-Type Specific Communication Pathways in the Rat Seminiferous Epithelium1

inferredcites →https://doi.org/10.1098/rstb.2009.0114openalex-snapshot

Physiological and physiopathological aspects of connexins and communicating gap junctions in spermatogenesis

inferredcites →https://doi.org/10.1098/rstb.2010.0025openalex-snapshot

Claudin and occludin expression and function in the seminiferous epithelium

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/10.1124/pr.110.002790openalex-snapshot

The Blood-Testis Barrier and Its Implications for Male Contraception

inferredcites →https://doi.org/10.1126/science.1219969openalex-snapshot

Germ Cell Migration Across Sertoli Cell Tight Junctions

inferredcites →https://doi.org/10.1126/science.7892609openalex-snapshot

Cardiac Malformation in Neonatal Mice Lacking Connexin43

inferredcites →https://doi.org/10.1128/mcb.18.11.6653openalex-snapshot

Direct Interaction of SRY-Related Protein SOX9 and Steroidogenic Factor 1 Regulates Transcription of the Human Anti-Müllerian Hormone Gene

inferredcites →https://doi.org/10.1152/ajpregu.00152.2015openalex-snapshot

Complementary expression and phosphorylation of Cx46 and Cx50 during development and following gene deletion in mouse and in normal and orchitic mink testes

inferredcites →https://doi.org/10.1152/ajprenal.1998.274.1.f1openalex-snapshot

Molecular structure and assembly of the tight junction

inferredcites →https://doi.org/10.1152/physrev.00019.2012openalex-snapshot

Claudins and the Modulation of Tight Junction Permeability

inferredcites →https://doi.org/10.1186/1471-213x-7-26openalex-snapshot

Replacement of connexin43 by connexin26 in transgenic mice leads to dysfunctional reproductive organs and slowed ventricular conduction in the heart

inferredcites →https://doi.org/10.1210/en.140.8.3815openalex-snapshot

Cellular Immunolocalization of Occludin during Embryonic and Postnatal Development of the Mouse Testis and Epididymis

inferredcites →https://doi.org/10.1210/en.141.8.3012openalex-snapshot

Developmental and Hormonal Regulation of the Expression of Oligodendrocyte-Specific Protein/Claudin 11 in Mouse Testis

inferredcites →https://doi.org/10.1210/en.2004-0834openalex-snapshot

Androgens and Postmeiotic Germ Cells Regulate Claudin-11 Expression in Rat Sertoli Cells

inferredcites →https://doi.org/10.1210/endo.141.8.7625openalex-snapshot

Developmental and Hormonal Regulation of the Expression of Oligodendrocyte-Specific Protein/Claudin 11 in Mouse Testis1

inferredcites →https://doi.org/10.1210/er.2003-0022openalex-snapshot

Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis

inferredcites →https://doi.org/10.1210/me.2011-0057openalex-snapshot

Adenomatous Polyposis Coli (APC) Is Essential for Maintaining the Integrity of the Seminiferous Epithelium

inferredcites →https://doi.org/10.1242/dev.122.9.2813openalex-snapshot

A male-specific role for SOX9 in vertebrate sex determination

inferredcites →https://doi.org/10.1242/dmm.008649openalex-snapshot

Sertoli-cell-specific knockout of connexin 43 leads to multiple alterations in testicular gene expression in prepubertal mice

inferredcites →https://doi.org/10.1242/jcs.1993.supplement_17.18openalex-snapshot

The making of a tight junction

inferredcites →https://doi.org/10.1371/journal.pmed.1001356openalex-snapshot

National, Regional, and Global Trends in Infertility Prevalence Since 1990: A Systematic Analysis of 277 Health Surveys

inferredcites →https://doi.org/10.14670/hh-26.1343openalex-snapshot

Connexin 43: its regulatory role in testicular junction dynamics and spermatogenesis.

inferredcites →https://doi.org/10.14670/hh-29.935openalex-snapshot

Loss of connexin43 (Cx43) in Sertoli cells leads to spatio-temporal alterations in occludin expression.

inferredcites →https://doi.org/10.1530/rep-09-0384openalex-snapshot

Immunoprotective Sertoli cells: making allogeneic and xenogeneic transplantation feasible

inferredcites →https://doi.org/10.1530/rep-15-0366openalex-snapshot

Blood–testis barrier and Sertoli cell function: lessons from SCCx43KO mice

inferredcites →https://doi.org/10.1530/rep.0.1250769openalex-snapshot

Proliferation and functional maturation of Sertoli cells, and their relevance to disorders of testis function in adulthood

inferredcites →https://doi.org/10.1530/rep.1.01234openalex-snapshot

Leydig cell function in mice lacking connexin43

inferredcites →https://doi.org/10.1593/neo.05847openalex-snapshot

Transition from Preinvasive Carcinoma In Situ to Seminoma Is Accompanied by a Reduction of Connexin 43 Expression in Sertoli Cells and Germ Cells

inferredcites →https://doi.org/10.2337/diab.46.2.317openalex-snapshot

Cotransplantation of Allogeneic Islets With Allogeneic Testicular Cell Aggregates Allows Long-Term Graft Survival Without Systemic Immunosuppression

inferredcites →https://doi.org/10.2353/ajpath.2007.061171openalex-snapshot

A Sertoli Cell-Specific Knockout of Connexin43 Prevents Initiation of Spermatogenesis

inferredcites →https://doi.org/10.2741/2168openalex-snapshot

Junction interaction in the seminiferous epithelium: regulatory roles of connexin-based gap junction

inferredcites →https://doi.org/10.3109/01913129609016317openalex-snapshot

The Human Blood-Testis Barrier in Impaired Spermatogenesis

inferredcites →https://doi.org/10.3727/000000002783985567openalex-snapshot

Identification of a Specific Sertoli Cell Marker, Sox9, for Use in Transplantation

inferredcites →https://doi.org/10.4103/1008-682x.125401openalex-snapshot

Blood-testis barrier and spermatogenesis: lessons from genetically-modified mice

inferredcites →https://doi.org/10.4161/spmg.1.3.17998openalex-snapshot

A study to assess the assembly of a functional blood-testis barrier in developing rat testes

inferredcites →https://doi.org/10.4161/spmg.1.4.18392openalex-snapshot

Testicular connexin 43, a precocious molecular target for the effect of environmental toxicants on male fertility

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Extended exposure to tetrabromobisphenol A-bis(2,3-dibromopropyl ether) leads to subfertility in male mice at the late reproductive age

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Establishment and functional characterization of a murine primary Sertoli cell line deficient of connexin43

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Polystyrene microplastics induce blood–testis barrier disruption regulated by the MAPK-Nrf2 signaling pathway in rats

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MyD88 Signaling in Sertoli Cells Mediates LPS-Induced Orchitis in Mice

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Role of calcium oscillations in sperm physiology

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Prenatal exposure to acetaminophen at different doses, courses and time causes testicular dysplasia in offspring mice and its mechanism

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Responses of the proteome in testis of mice exposed chronically to environmentally relevant concentrations of Microcystin-LR.

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Icariin attenuate microcystin-LR-induced gap junction injury in Sertoli cells through suppression of Akt pathways

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Deoxynivalenol induced spermatogenesis disorder by blood-testis barrier disruption associated with testosterone deficiency and inflammation in mice

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Effect of Bisphenol S on testicular tissue after low-dose lactation exposure

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Cross-talk between Vimentin and autophagy regulates blood-testis barrier disruption induced by cadmium

inferred← citeshttps://doi.org/10.1016/j.etap.2020.103412openalex-snapshot

Nigral and ventral tegmental area lesioning induces testicular and sperm morphological abnormalities in a rotenone model of Parkinson’s disease

inferred← citeshttps://doi.org/10.1016/j.fct.2023.113649openalex-snapshot

Perfluorooctanoic acid induces tight junction injury of Sertoli cells by blocking autophagic flux

inferred← citeshttps://doi.org/10.1016/j.fct.2025.115468openalex-snapshot

Effects of different stages, dosages and courses of prenatal dexamethasone exposure on testicular development in mice

inferred← citeshttps://doi.org/10.1016/j.gene.2021.145531openalex-snapshot

The role of different compounds on the integrity of blood-testis barrier: A concise review based on in vitro and in vivo studies

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.135264openalex-snapshot

Vangl2 regulates intercellular junctions by remodeling actin-based cytoskeleton through the Rock signaling pathway during spermatogenesis in Eriocheir sinensis

inferred← citeshttps://doi.org/10.1016/j.jare.2022.09.001openalex-snapshot

Connexin-43 is a promising target for lycopene preventing phthalate-induced spermatogenic disorders

inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.123799openalex-snapshot

Exposure to titanium dioxide nanoparticles disrupts the BTB by interfering with the assembly of stress granules in germ cells

inferred← citeshttps://doi.org/10.1016/j.jsbmb.2017.07.019openalex-snapshot

Sodium-dependent organic anion transporter ( Slc10a6−/− ) knockout mice show normal spermatogenesis and reproduction, but elevated serum levels for cholesterol sulfate

inferred← citeshttps://doi.org/10.1016/j.repbio.2023.100846openalex-snapshot

PFOS exposure destroys the integrity of the blood-testis barrier (BTB) through PI3K/AKT/mTOR-mediated autophagy

inferred← citeshttps://doi.org/10.1016/j.reprotox.2018.06.014openalex-snapshot

The effects of flutamide on cell-cell junctions in the testis, epididymis, and prostate

inferred← citeshttps://doi.org/10.1016/j.reprotox.2020.06.014openalex-snapshot

Gestational and pubertal exposure to low dose of di-(2-ethylhexyl) phthalate impairs sperm quality in adult mice

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.175606openalex-snapshot

Chronic dietary exposure to glyphosate-induced connexin 43 autophagic degradation contributes to blood-testis barrier disruption in roosters

inferred← citeshttps://doi.org/10.1016/j.toxlet.2016.12.004openalex-snapshot

Urban fine particulate matter exposure causes male reproductive injury through destroying blood-testis barrier (BTB) integrity

inferred← citeshttps://doi.org/10.1016/j.toxlet.2018.07.019openalex-snapshot

Melamine causes testicular toxicity by destroying blood-testis barrier in piglets

inferred← citeshttps://doi.org/10.1016/s2095-3119(19)62564-5openalex-snapshot

miR-10b promotes porcine immature Sertoli cell proliferation by targeting the DAZAP1 gene

inferred← citeshttps://doi.org/10.1017/s0967199417000326openalex-snapshot

Morphofunctional evaluation of the testis, duration of spermatogenesis and spermatogenic efficiency in the Japanese fancy mouse (Mus musculus molossinus)

inferred← citeshttps://doi.org/10.1038/s12276-024-01258-3openalex-snapshot

Development of a novel testis-on-a-chip that demonstrates reciprocal crosstalk between Sertoli and Leydig cells in testicular tissue

inferred← citeshttps://doi.org/10.1038/s41420-025-02749-6openalex-snapshot

Atorvastatin improves spermatogenesis in murine and in vitro human chronic orchitis models through restoring blood-testis barriers

inferred← citeshttps://doi.org/10.1038/s41467-022-34990-3openalex-snapshot

Targeting APLN/APJ restores blood-testis barrier and improves spermatogenesis in murine and human diabetic models

inferred← citeshttps://doi.org/10.1038/s41598-019-51772-yopenalex-snapshot

Fractionated irradiation of right thorax induces abscopal damage on testes leading to decline in 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/10.1038/srep29667openalex-snapshot

Rescue of perfluorooctanesulfonate (PFOS)-mediated Sertoli cell injury by overexpression of gap junction protein connexin 43

inferred← citeshttps://doi.org/10.1071/rd16091openalex-snapshot

Role of the Na+/K+-ATPase ion pump in male reproduction and embryo development

inferred← citeshttps://doi.org/10.1071/rd19088openalex-snapshot

Wilms’ tumour 1 (WT1) negatively regulates the expression of connexin 43 via a non-canonical Wnt signalling pathway in cultured bovine Sertoli cells

inferred← citeshttps://doi.org/10.1071/rd20215openalex-snapshot

Wild-type p53-induced phosphatase 1 (WIP1) regulates the proliferation of swine Sertoli cells through P53

inferred← citeshttps://doi.org/10.1080/10495398.2020.1788044openalex-snapshot

Vitamin E promotes ovine Sertoli cell proliferation by regulation of genes associated with cell division and the cell cycle

inferred← citeshttps://doi.org/10.1080/10934529.2026.2699582openalex-snapshot

In vivo assessment of naringenin-mediated amelioration of lead-induced testicular injury in rats: regulation of Nrf2/Keap1 and PINK1/Parkin pathways

inferred← citeshttps://doi.org/10.1080/21505594.2024.2384564openalex-snapshot

Porcine reproductive and respiratory syndrome virus infects the reproductive system of male piglets and impairs development of the blood–testis barrier

inferred← citeshttps://doi.org/10.1089/scd.2019.0166openalex-snapshot

Androgen Indirectly Regulates Gap Junction Component Connexin 43 Through Wilms Tumor-1 in Sertoli Cells

inferred← citeshttps://doi.org/10.1093/biolre/iox093openalex-snapshot

Deletion of Spata2 by CRISPR/Cas9n causes increased inhibin alpha expression and attenuated fertility in male mice†

inferred← citeshttps://doi.org/10.1093/humrep/dew009openalex-snapshot

Gonadotropin suppression in men leads to a reduction in claudin-11 at the Sertoli cell tight junction

inferred← citeshttps://doi.org/10.1093/molehr/gay012openalex-snapshot

In vitro formation of the blood–testis barrier during long-term organotypic culture of human prepubertal tissue: comparison with a large cohort of pre/peripubertal boys

inferred← citeshttps://doi.org/10.1093/toxsci/kfad016openalex-snapshot

Epigenetic programming of TBX2/CX43 mediates lower sperm quality in male offspring induced by prenatal dexamethasone exposure

inferred← citeshttps://doi.org/10.1093/toxsci/kfx276openalex-snapshot

Identification of a Critical Window for Ganciclovir-Induced Disruption of Testicular Development in Rats

inferred← citeshttps://doi.org/10.1095/biolreprod.115.138016openalex-snapshot

mTOR Regulates Gap Junction Alpha-1 Protein Trafficking in Sertoli Cells and Is Required for the Maintenance of Spermatogenesis in Mice

inferred← citeshttps://doi.org/10.1101/430900openalex-snapshot

Induction of Sertoli Cells from Human Fibroblasts by NR5A1 and GATA4

inferred← citeshttps://doi.org/10.1109/tnb.2025.3566910openalex-snapshot

Size-Dependent Effects of Phyllanthus niruri Nanoemulsions on Blood-Testis Barrier Integrity and Cellular Responses in TM4 Sertoli Cells

inferred← citeshttps://doi.org/10.1111/and.13914openalex-snapshot

Review of COVID‐19 and male genital tract

inferred← citeshttps://doi.org/10.1111/andr.12788openalex-snapshot

Disorganization of claudin‐11 and dysfunction of the blood‐testis barrier during puberty in a cryptorchid rat model

inferred← citeshttps://doi.org/10.1111/andr.12846openalex-snapshot

Selective lysine‐specific demethylase 1 inhibitor, NCL1, could cause testicular toxicity via the regulation of apoptosis

inferred← citeshttps://doi.org/10.1111/andr.12954openalex-snapshot

Sperm immunization and rat spermatogenesis: Dysfunctional blood‐testis barrier and perturbed Sertoli cell cytoskeleton

inferred← citeshttps://doi.org/10.1111/rda.13177openalex-snapshot

miR‐26a suppresses autophagy in swine Sertoli cells by targeting ULK 2

inferred← citeshttps://doi.org/10.1111/rda.13254openalex-snapshot

miR‐26a inhibits proliferation and promotes apoptosis in porcine immature Sertoli cells by targeting thePAK2gene

inferred← citeshttps://doi.org/10.1111/rda.13626openalex-snapshot

miR‐362 knock‐down promotes proliferation and inhibits apoptosis in porcine immature Sertoli cells by targeting the RMI1 gene

inferred← citeshttps://doi.org/10.1186/s12951-022-01291-2openalex-snapshot

Effects of iron oxide nanoparticles as T2-MRI contrast agents on reproductive system in male mice

inferred← citeshttps://doi.org/10.1186/s13062-023-00381-xopenalex-snapshot

LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.1186/s13578-022-00773-yopenalex-snapshot

PA1 participates in the maintenance of blood–testis barrier integrity via cooperation with JUN in the Sertoli cells of mice

inferred← citeshttps://doi.org/10.1186/s40104-022-00687-2openalex-snapshot

Sertoli cell and spermatogonial development in pigs

inferred← citeshttps://doi.org/10.13181/mji.oa.214635openalex-snapshot

Effect of hyperglycemia on fertility in streptozotocin-induced diabetic male Wistar rats: focus on glucose transporters and oxidative stress

inferred← citeshttps://doi.org/10.1371/journal.pone.0198100openalex-snapshot

Loss of connexin43 in murine Sertoli cells and its effect on blood-testis barrier formation and dynamics

inferred← citeshttps://doi.org/10.1371/journal.pone.0321292openalex-snapshot

The impact of Connexin 43 deficiency on the cell shape and cytoskeleton of murine Sertoli cells: A house with ramshackle walls?

inferred← citeshttps://doi.org/10.14670/hh-18-457openalex-snapshot

The PI3K/AKT signaling pathway: How does it regulate development of Sertoli cells and spermatogenic cells?

inferred← citeshttps://doi.org/10.14670/hh-18-775openalex-snapshot

Optimizing the preparation of paraffin sections from stallion testes.

inferred← citeshttps://doi.org/10.17816/maj492313openalex-snapshot

Gap junction protein connexin-43 and its distribution in different tissues

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1153179/v1openalex-snapshot

PA1 Participates in the Maintenance of Blood-Testis Barrier Integrity via Cooperation with JUN in the Sertoli Cells of Mice.

inferred← citeshttps://doi.org/10.2147/ijgm.s241099openalex-snapshot

Some of the Factors Involved in Male Infertility: A Prospective Review

inferred← citeshttps://doi.org/10.21608/javs.2020.118002openalex-snapshot

Immunohistochemistry And Hormonal Investigation For Spermatogenesis Restoration In Degenerated Testes Of Rats After Bone Marrow Stem Cells Transplantation

inferred← citeshttps://doi.org/10.2174/1874104501711010001openalex-snapshot

Monitoring the Level of 14C-Labelled Selegiline Following Oral Administration

inferred← citeshttps://doi.org/10.24275/uami.ww72bb926openalex-snapshot

Efecto del modelo de isquemia-reperfusión en mucosa gástrica sobre la organización tisular de los túbulos seminíferos en ratas macho de la cepa Wistar

inferred← citeshttps://doi.org/10.29252/sjimu.28.5.1openalex-snapshot

Experimental Investigation of Ki67, POU5F1, and ZBTB16 Expression in the Pig and Mouse Testicular Cells using Immunocytochemistry and RT-PCR

inferred← citeshttps://doi.org/10.29296/24999490-2023-05-02openalex-snapshot

CONNEXINS: ROLE IN INTERCELLULAR INTERACTIONS IN NORMAL AND IN PATHOLOGY OF THE RESPIRATORY SYSTEM

inferred← citeshttps://doi.org/10.32707/ercivet.1332031openalex-snapshot

Memeli Testisinde Kan-Testis Bariyeri’nin Bileşenleri ve Üreme ile İlişkileri

inferred← citeshttps://doi.org/10.3389/fcell.2020.00626openalex-snapshot

Functions of Endothelial Cilia in the Regulation of Vascular Barriers

inferred← citeshttps://doi.org/10.3389/fcell.2020.593005openalex-snapshot

Roles of AMP-Activated Protein Kinase (AMPK) in Mammalian Reproduction

inferred← citeshttps://doi.org/10.3389/fcell.2025.1693878openalex-snapshot

Sertoli cells as a hub in testicular development and male reproductive

inferred← citeshttps://doi.org/10.3389/fendo.2022.886085openalex-snapshot

LPS-Induced Systemic Inflammation Caused mPOA-FSH/LH Disturbance and Impaired Testicular Function

inferred← citeshttps://doi.org/10.3389/fendo.2022.897062openalex-snapshot

Sertoli Cell-Germ Cell Interactions Within the Niche: Paracrine and Juxtacrine Molecular Communications

inferred← citeshttps://doi.org/10.3389/fendo.2026.1819705openalex-snapshot

Exploring cadmium exposure as a contributor to male infertility: insights from the relationship between environmental pollutants and the male reproductive system

inferred← citeshttps://doi.org/10.3389/fimmu.2020.583135openalex-snapshot

Pathomechanisms of Autoimmune Based Testicular Inflammation

inferred← citeshttps://doi.org/10.3389/fonc.2020.574977openalex-snapshot

Serum RNA Profiling in the 10-Years Period Prior to Diagnosis of Testicular Germ Cell Tumor

inferred← citeshttps://doi.org/10.3389/fphar.2016.00537openalex-snapshot

Polydeoxyribonucleotide, an Adenosine-A2A Receptor Agonist, Preserves Blood Testis Barrier from Cadmium-Induced Injury

inferred← citeshttps://doi.org/10.3390/ani14020183openalex-snapshot

Caveolin 1 Regulates the Tight Junctions between Sertoli Cells and Promotes the Integrity of Blood–Testis Barrier in Yak via the FAK/ERK Signaling Pathway

inferred← citeshttps://doi.org/10.3390/antiox12010152openalex-snapshot

Lactoferrin Restores the Deoxynivalenol-Impaired Spermatogenesis and Blood–Testis Barrier Integrity via Improving the Antioxidant Capacity and Modifying the Cell Adhesion and Inflammatory Response

inferred← citeshttps://doi.org/10.3390/biology11121791openalex-snapshot

Ldha-Dependent Metabolic Programs in Sertoli Cells Regulate Spermiogenesis in Mouse Testis

inferred← citeshttps://doi.org/10.3390/biomedicines12112599openalex-snapshot

Connexins and Aging-Associated Respiratory Disorders: The Role in Intercellular Communications

inferred← citeshttps://doi.org/10.3390/biomedicines14020423openalex-snapshot

Inflammation-Driven Remodeling of the Blood–Testis Barrier: Roles of Junctional Complexes, Actin Dynamics, and Kinase Signaling

inferred← citeshttps://doi.org/10.3390/ijms20225717openalex-snapshot

Blood Testis Barrier and Somatic Cells Impairment in a Series of 35 Adult Klinefelter Syndrome Patients

inferred← citeshttps://doi.org/10.3390/ijms22157924openalex-snapshot

Connexin43 in Germ Cells Seems to Be Dispensable for Murine Spermatogenesis

inferred← citeshttps://doi.org/10.3390/jcm10194520openalex-snapshot

The Impact of SARS-CoV-2 Infection on Fertility and Female and Male Reproductive Systems

inferred← citeshttps://doi.org/10.3390/life10120363openalex-snapshot

The Role of Connexin 43 in Lung Disease

inferred← citeshttps://doi.org/10.34172/cjmb.2025.3802openalex-snapshot

Impact of Mesenchymal Stem Cells and Quercetin on Protection of Testis Against Cyclophosphamide-Related Damage

inferred← citeshttps://doi.org/10.3892/mmr.2018.9025openalex-snapshot

TLR4/PKCα/occludin signaling pathway may be related to blood‑brain barrier damage

inferred← citeshttps://doi.org/10.4103/aja20248openalex-snapshot

Pharmacological actions of the bioactive compounds of Epimedium on the male reproductive system: current status and future perspective

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520027openalex-snapshot

Additional file 1 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520030openalex-snapshot

Additional file 2 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520033openalex-snapshot

Additional file 3 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520036openalex-snapshot

Additional file 4 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520039openalex-snapshot

Additional file 5 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520042openalex-snapshot

Additional file 6 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.6084/m9.figshare.23520045openalex-snapshot

Additional file 7 of LncRNA5251 inhibits spermatogenesis via modification of cell-cell junctions

inferred← citeshttps://doi.org/10.64898/2026.01.17.699063openalex-snapshot

Chemotherapy-induced transfer of apoptotic machinery in extracellular vesicles between somatic and germ cells of the testis: mechanistic insights into onco-fertility preservation in pre-pubertal boys

inferred← citeshttps://doi.org/10.7554/elife.48767openalex-snapshot

Induction of Sertoli-like cells from human fibroblasts by NR5A1 and GATA4

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