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Sertoli cells – Immunological sentinels of spermatogenesis
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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.1001450406openalex-snapshot
Light cells within the limiting membrane of rat seminiferous tubules
inferredcites →https://doi.org/10.1002/aja.1001750109openalex-snapshot
Cyclic formation and decay of the blood‐testis barrier in the mink (Mustela vison), a seasonal breeder
inferredcites →https://doi.org/10.1002/ar.1091080208openalex-snapshot
In vivo affinity of diaminoacridines for nuclei
inferredcites →https://doi.org/10.1002/ar.1091490104openalex-snapshot
Observations on the early events of cadmium necrosis of the testis
inferredcites →https://doi.org/10.1002/ar.1091750402openalex-snapshot
The fine structure of the monkey (Macaca) sertoli cell and its role in maintaining the blood‐testis barrier
inferredcites →https://doi.org/10.1006/scdb.1998.0203openalex-snapshot
The central role of Sertoli cells in spermatogenesis
inferredcites →https://doi.org/10.1007/978-0-387-09597-4_1openalex-snapshot
Spermatogenesis and Cycle of the Seminiferous Epithelium
inferredcites →https://doi.org/10.1007/978-0-387-09597-4_12openalex-snapshot
Blood-Testis Barrier, Junctional and Transport Proteins and Spermatogenesis
inferredcites →https://doi.org/10.1007/bf00305816openalex-snapshot
Dye permeability and alkaline phosphatase activity of testicular capillaries in the postnatal rat
inferredcites →https://doi.org/10.1007/s001250051331openalex-snapshot
Testicular Sertoli cells exert both protective and destructive effects on syngeneic islet grafts in non-obese diabetic mice
inferredcites →https://doi.org/10.1016/0005-2787(65)90019-5openalex-snapshot
Concentration of [14C]actinomycin D in various tissues following intravenous injection
inferredcites →https://doi.org/10.1016/0012-1606(77)90178-6openalex-snapshot
Appearance of cell surface auto- and isoantigens during spermatogenesis in the rabbit
inferredcites →https://doi.org/10.1016/0012-1606(78)90080-5openalex-snapshot
Specific surface antigens on rat pachytene spermatocytes and successive classes of germinal cells
inferredcites →https://doi.org/10.1016/0162-3109(92)90004-vopenalex-snapshot
Species-specific effect of proteins secreted by cultured pre-pubertal rat Sertoli cells on natural killer cell activity
inferredcites →https://doi.org/10.1016/0165-0378(88)90033-2openalex-snapshot
Suppression of lymphocyte proliferation by proteins secreted by cultured Sertoli cells
inferredcites →https://doi.org/10.1016/0165-0378(88)90064-2openalex-snapshot
Testicular immunosuppressive protein
inferredcites →https://doi.org/10.1016/0165-0378(90)90020-7openalex-snapshot
The testis and tissue transplantation: historical aspects
inferredcites →https://doi.org/10.1016/0165-0378(92)90010-2openalex-snapshot
Immunosuppressive activity in the rat seminiferous tubules
inferredcites →https://doi.org/10.1016/j.it.2004.04.009openalex-snapshot
Cornerstone of peripheral tolerance: naturally occurring CD4+CD25+ regulatory T cells
inferredcites →https://doi.org/10.1016/j.jri.2013.01.001openalex-snapshot
Phenotypic and functional heterogeneity of the testicular macrophage population: a new regulatory model
inferredcites →https://doi.org/10.1016/j.mce.2010.03.022openalex-snapshot
Immunological, paracrine and endocrine aspects of testicular immune privilege
inferredcites →https://doi.org/10.1016/s0006-291x(05)81596-7openalex-snapshot
Immunosuppressive molecules produced by sertoli cells cultured in vitro: Biological effects on lymphocytes
inferredcites →https://doi.org/10.1016/s0070-2153(05)71008-5openalex-snapshot
The Blood‐Testis Barrier: Its Biology, Regulation, and Physiological Role in Spermatogenesis
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/s0303-7207(99)00016-7openalex-snapshot
Clusterin in the male reproductive system: localization and possible function
inferredcites →https://doi.org/10.1038/embor.2009.211openalex-snapshot
Molecular aspects of male fertility
inferredcites →https://doi.org/10.1038/nri2536openalex-snapshot
Turning 'sweet' on immunity: galectin–glycan interactions in immune tolerance and inflammation
inferredcites →https://doi.org/10.1046/j.1365-2567.1999.00861.xopenalex-snapshot
Molecular cloning, expression and characterization of the rat analogue of human membrane cofactor protein (MCP/CD46)
inferredcites →https://doi.org/10.1046/j.1365-2605.1999.00186.xopenalex-snapshot
Major differences between the testis and epididymis in the induction of granulomas in response to extravasated germ cells. I. A light microscopical study in mice
inferredcites →https://doi.org/10.1073/pnas.1017615108openalex-snapshot
Regulatory T cells control tolerogenic versus autoimmune response to sperm in vasectomy
inferredcites →https://doi.org/10.1073/pnas.90.23.11069openalex-snapshot
Barrier properties of testis microvessels.
inferredcites →https://doi.org/10.1084/jem.20090134openalex-snapshot
Therapy of experimental type 1 diabetes by isolated Sertoli cell xenografts alone
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/molehr/7.12.1133openalex-snapshot
Perforin-independent expression of granzyme B and proteinase inhibitor 9 in human testis and placenta suggests a role for granzyme B-mediated proteolysis in reproduction
inferredcites →https://doi.org/10.1093/molehr/gam067openalex-snapshot
Expression of co-stimulatory molecules, chemokine receptors and proinflammatory cytokines in dendritic cells from normal and chronically inflamed rat testis
inferredcites →https://doi.org/10.1095/biolreprod.103.018788openalex-snapshot
Fertility and Germline Transmission of Donor Haplotype Following Germ Cell Transplantation in Immunocompetent Goats
inferredcites →https://doi.org/10.1095/biolreprod.107.063578openalex-snapshot
Mouse Sertoli Cells Display Phenotypical and Functional Traits of Antigen-Presenting Cells in Response to Interferon Gamma
inferredcites →https://doi.org/10.1095/biolreprod.109.076299openalex-snapshot
Histological and Stereological Evaluation of Zebrafish (Danio rerio) Spermatogenesis with an Emphasis on Spermatogonial Generations1
inferredcites →https://doi.org/10.1095/biolreprod.109.078279openalex-snapshot
Irradiation Enhances the Efficiency of Testicular Germ Cell Transplantation in Sheep
inferredcites →https://doi.org/10.1095/biolreprod.110.087452openalex-snapshot
The Blood-Testis and Blood-Epididymis Barriers Are More than Just Their Tight Junctions1
inferredcites →https://doi.org/10.1095/biolreprod.110.089425openalex-snapshot
Immunoprotective Properties of Primary Sertoli Cells in Mice: Potential Functional Pathways that Confer Immune Privilege1
inferredcites →https://doi.org/10.1095/biolreprod.110.090621openalex-snapshot
Sertoli Cell-Specific Deletion of the Androgen Receptor Compromises Testicular Immune Privilege in Mice1
inferredcites →https://doi.org/10.1095/biolreprod59.1.84openalex-snapshot
Developmental Schedule of the Postnatal Rat Testis Determined by Flow Cytometry1
inferredcites →https://doi.org/10.1095/biolreprod60.6.1304openalex-snapshot
Expression and Action of Transforming Growth Factor Beta (TGFβ1, TGFβ2, and TGFβ3) during Embryonic Rat Testis Development1
inferredcites →https://doi.org/10.1095/biolreprod66.1.21openalex-snapshot
Germ Cell Transplantation in Pigs1
inferredcites →https://doi.org/10.1096/fj.05-4144comopenalex-snapshot
Targeted and reversible disruption of the blood‐testis barrier by an ΔFSH mutant‐occludin peptide conjugate
inferredcites →https://doi.org/10.1097/00007890-199111000-00018openalex-snapshot
PRODUCTION OF A FACTOR, OR FACTORS, SUPPRESSING IL-2 PRODUCTION AND T CELL PROLIFERATION BY SERTOLI CELL-ENRICHED PREPARATIONS
inferredcites →https://doi.org/10.1101/cshperspect.a006957openalex-snapshot
T-Cell Tolerance: Central and Peripheral
inferredcites →https://doi.org/10.1111/j.0105-2896.2006.00404.xopenalex-snapshot
The role of physiological self‐antigen in the acquisition and maintenance of regulatory T‐cell function
inferredcites →https://doi.org/10.1111/j.1365-2249.2009.03877.xopenalex-snapshot
Immune regulation by non-lymphoid cells in transplantation
inferredcites →https://doi.org/10.1111/j.1365-2605.1992.tb01108.xopenalex-snapshot
Blood‐testis barriers revisited A homage to Lennart Nicander
inferredcites →https://doi.org/10.1111/j.1600-065x.1981.tb00344.xopenalex-snapshot
Autoimmunity to Spermatozoa and the Testis
inferredcites →https://doi.org/10.1111/j.1600-065x.2011.01015.xopenalex-snapshot
Dendritic cell control of tolerogenic responses
inferredcites →https://doi.org/10.1113/jphysiol.1964.sp007370openalex-snapshot
Flow and protein content of testicular lymph in conscious rams
inferredcites →https://doi.org/10.1113/jphysiol.1969.sp008682openalex-snapshot
A blood‐testis barrier restricting passage from blood into rete testis fluid but not into lymph
inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141040openalex-snapshot
Tolerogenic Dendritic Cells
inferredcites →https://doi.org/10.1152/physrev.00025.2011openalex-snapshot
The Germline Stem Cell Niche Unit in Mammalian Testes
inferredcites →https://doi.org/10.1177/13.5.376openalex-snapshot
EXTRAVASCULAR AND INTRATUBULAR DIFFUSION OF LABELED SERUM PROTEINS IN THE RAT TESTIS
inferredcites →https://doi.org/10.1182/blood-2006-03-006403openalex-snapshot
Tolerogenic dendritic cells: cytokine modulation comes of age
inferredcites →https://doi.org/10.1371/journal.pone.0016456openalex-snapshot
Spinal Cord Injury Causes Sustained Disruption of the Blood-Testis Barrier in the Rat
inferredcites →https://doi.org/10.14670/hh-14.779openalex-snapshot
Sertoli cell expression of galectin-1 and -3 and accessible binding sites in normal human testis and Sertoli cell only-syndrome.
inferredcites →https://doi.org/10.1530/jrf.0.0170403openalex-snapshot
PROTEIN AND IMMUNOGLOBULIN CONTENT OF RETE TESTIS FLUID OF RAMS
inferredcites →https://doi.org/10.1530/jrf.0.0270463openalex-snapshot
A DIFFERENCE IN THE IMMUNOGLOBULIN CONTENT OF SEMINIFEROUS TUBULE FLUID AND RETE TESTIS FLUID OF THE RAT
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.0.1230389openalex-snapshot
Expression of a blood-brain barrier-specific antigen in the reproductive tract of the male rat
inferredcites →https://doi.org/10.1530/rep.1.01125openalex-snapshot
Successful transplantation of bovine testicular cells to heterologous recipients
inferredcites →https://doi.org/10.1681/asn.2009060592openalex-snapshot
IL-10/TGF-β–Modified Macrophages Induce Regulatory T Cells and Protect against Adriamycin Nephrosis
inferredcites →https://doi.org/10.2337/diabetes.49.11.1810openalex-snapshot
Testicular sertoli cells protect islet beta-cells from autoimmune destruction in NOD mice by a transforming growth factor-beta1-dependent mechanism.
inferredcites →https://doi.org/10.3346/jkms.2007.22.2.277openalex-snapshot
Role of Complement Regulatory Proteins in the Survival of Murine Allo-transplanted Sertoli Cells
inferredcites →https://doi.org/10.3727/000000007783472417openalex-snapshot
Comparison of Successful and Unsuccessful Islet/Sertoli Cell Cotransplant Grafts in Streptozotocin-Induced Diabetic Mice
inferredcites →https://doi.org/10.3727/096368908785096033openalex-snapshot
Sertoli Cell Line Lacks the Immunoprotective Properties Associated with Primary Sertoli Cells
inferredcites →https://doi.org/10.3727/096368910x536563openalex-snapshot
Characterization and Functionality of Proliferative Human Sertoli Cells
inferredcites →https://doi.org/10.4049/jimmunol.126.1.100openalex-snapshot
The role of an X-linked gene in the regulation of secondary humoral response kinetics to sperm-specific LDH-C4 antigens.
inferredcites →https://doi.org/10.4049/jimmunol.141.4.1161openalex-snapshot
Autoantigenic germ cells exist outside the blood testis barrier.
inferredcites →https://doi.org/10.4049/jimmunol.166.5.3218openalex-snapshot
The Granzyme B Inhibitor, Protease Inhibitor 9, Is Mainly Expressed by Dendritic Cells and at Immune-Privileged Sites
inferredcites →https://doi.org/10.4049/jimmunol.177.8.5051openalex-snapshot
Identification of a Novel Human Granzyme B Inhibitor Secreted by Cultured Sertoli Cells
inferredcites →https://doi.org/10.4161/spmg.23870openalex-snapshot
Dual role of immune cells in the testis
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.4586300openalex-extracted
Regulation of Blood-Testis Barrier Tight Junction Protein Expression in Tm4 Cells by Bitter Taste Receptor Tas2r143-Induced Nf-Κb Signaling Pathway
inferred← citeshttps://doi.org/10.1002/adbi.202101184openalex-snapshot
Small‐Molecule‐Driven Direct Reprogramming of Fibroblasts into Functional Sertoli‐Like Cells as a Model for Male Reproductive Toxicology
inferred← citeshttps://doi.org/10.1002/jcb.28643openalex-snapshot
The N‐terminal His‐tag affects the triglyceride lipase activity of hormone‐sensitive lipase in testis
inferred← citeshttps://doi.org/10.1002/jmv.28145openalex-snapshot
Is monkeypox a new, emerging sexually transmitted disease? A rapid review of the literature
inferred← citeshttps://doi.org/10.1002/mnfr.201800843openalex-snapshot
Luteolin Ameliorates Testis Injury and Blood–Testis Barrier Disruption through the Nrf2 Signaling Pathway and by Upregulating Cx43
inferred← citeshttps://doi.org/10.1002/mrd.23332openalex-snapshot
Differential gene regulation in selected lines for high and low sperm production in male guppies
inferred← citeshttps://doi.org/10.1002/tox.23096openalex-snapshot
Puerarin prevents cadmium‐induced disorder of testicular lactic acid metabolism in rats by activating 5′ AMP ‐activated protein kinase ( AMPK )/sirtuin 1 ( SIRT1 ) signaling pathway
inferred← citeshttps://doi.org/10.1007/16833_2022_7openalex-snapshot
Immunobiology of Testicular Cancer
inferred← citeshttps://doi.org/10.1007/978-1-0716-4698-4_8openalex-snapshot
Isolation of Pig or Rodent Sertoli Cells for Use in Transplantation
inferred← citeshttps://doi.org/10.1007/978-1-4939-7698-0_17openalex-snapshot
Monitoring the Integrity of the Blood-Testis Barrier (BTB): An In Vivo Assay
inferred← citeshttps://doi.org/10.1007/978-3-030-32300-4_45openalex-snapshot
New Developments for the Enhancement of Male Reproductive Health Using Antioxidant Therapy: A Critical Review of the Literature
inferred← citeshttps://doi.org/10.1007/978-3-030-77779-1_13openalex-snapshot
Regulation of Human Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-3-030-77779-1_2openalex-snapshot
The Good, the Bad and the Ugly of Testicular Immune Regulation: A Delicate Balance Between Immune Function and Immune Privilege
inferred← citeshttps://doi.org/10.1007/978-3-031-31574-9_28openalex-snapshot
Immunologically Induced Infertility
inferred← citeshttps://doi.org/10.1007/978-3-031-96376-6_10openalex-snapshot
Leydig Cell Interaction with Macrophages, Peritubular Cells, and Sertoli Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-40788-3_5openalex-snapshot
The Immune Privilege of the Testis
inferred← citeshttps://doi.org/10.1007/978-3-662-61901-8_28openalex-snapshot
Immunologisch bedingte Infertilität
inferred← citeshttps://doi.org/10.1007/978-3-662-61904-9_28-1openalex-snapshot
Immunologisch bedingte Infertilität
inferred← citeshttps://doi.org/10.1007/s00018-022-04521-wopenalex-snapshot
Sertoli cell survival and barrier function are regulated by miR-181c/d-Pafah1b1 axis during mammalian spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00281-024-01032-7openalex-snapshot
Galectin-1 and galectin-3 in male reproduction - impact in health and disease
inferred← citeshttps://doi.org/10.1007/s00281-026-01073-0openalex-snapshot
Advances in understanding the dual roles of testicular immune responses: From immune privilege to inflammation
inferred← citeshttps://doi.org/10.1007/s00441-019-03143-2openalex-snapshot
Therapeutic prospects of hydroxytyrosol on experimentally induced diabetic testicular damage: potential interplay with AMPK expression
inferred← citeshttps://doi.org/10.1007/s00580-026-03834-7openalex-snapshot
Roles of Toll-like receptor 4 in the normal testis and during testicular ischemia-reperfusion injury: a sanitiser or a killer?
inferred← citeshttps://doi.org/10.1007/s11033-022-07316-1openalex-snapshot
Extracellular vesicles derived from human Sertoli cells: characterizations, proteomic analysis, and miRNA profiling
inferred← citeshttps://doi.org/10.1007/s12015-021-10197-9openalex-snapshot
Sertoli Cells Possess Immunomodulatory Properties and the Ability of Mitochondrial Transfer Similar to Mesenchymal Stromal Cells
inferred← citeshttps://doi.org/10.1007/s12020-018-1670-9openalex-snapshot
Evaluation of testicular function in prepubertal children
inferred← citeshttps://doi.org/10.1007/s12031-020-01522-xopenalex-snapshot
Effect of Sertoli Cell Transplantation on Reducing Neuroinflammation-Induced Necroptosis and Improving Motor Coordination in the Rat Model of Cerebellar Ataxia Induced by 3-Acetylpyridine
inferred← citeshttps://doi.org/10.1007/s12250-020-00343-xopenalex-snapshot
Rearrangement of Actin Cytoskeleton by Zika Virus Infection Facilitates Blood–Testis Barrier Hyperpermeability
inferred← citeshttps://doi.org/10.1007/s43032-021-00721-0openalex-snapshot
Somatic-Immune Cells Crosstalk In-The-Making of Testicular Immune Privilege
inferred← citeshttps://doi.org/10.1016/b978-0-08-100601-6.02137-2openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-12-417047-6.00012-0openalex-snapshot
Biochemistry of Sertoli cell/germ cell junctions, germ cell transport, and spermiation in the seminiferous epithelium
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02134-6openalex-snapshot
Anatomy and Physiology of the Male Reproductive System and Potential Targets of Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02137-1openalex-snapshot
The Sertoli Cell as a Target for Toxicants ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64572-5openalex-snapshot
Blood-Testis Barrier
inferred← citeshttps://doi.org/10.1016/b978-0-12-814833-4.00058-7openalex-snapshot
Progress toward islet transplantation tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-85389-7.00022-3openalex-snapshot
Testicular immune tolerance and viral infections
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00208-4openalex-snapshot
Anatomy and Physiology of the Male Reproductive System and Potential Targets of Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00241-2openalex-snapshot
The Sertoli Cell as a Target for Toxicants
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00323-0openalex-snapshot
The Blood-Testis Barrier: An Overview of the Physical, Physiological, and Immunological Functions
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.10.005openalex-snapshot
The action of retinoic acid on spermatogonia in the testis
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2026.04.004openalex-snapshot
Role of macrophages in testis function
inferred← citeshttps://doi.org/10.1016/j.aca.2023.341054openalex-snapshot
Time-resolved ICP-MS analysis of mineral element contents and distribution patterns in spermatogenic cells of different types
inferred← citeshttps://doi.org/10.1016/j.addr.2019.01.013openalex-snapshot
Nanotechnology in cell replacement therapies for type 1 diabetes
inferred← citeshttps://doi.org/10.1016/j.ajpath.2018.07.013openalex-snapshot
Testosterone and Follicle Stimulating Hormone–Dependent Glyoxalase 1 Up-Regulation Sustains the Viability of Porcine Sertoli Cells through the Control of Hydroimidazolone– and Argpyrimidine-Mediated NF-κB Pathway
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2026.108144openalex-snapshot
HSP72 alleviates heat stress-induced oxidative damage in boar Sertoli cells through modulating the AGE-RAGE/NOX4/NF-κB axis
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2025.743468openalex-snapshot
Integrated brain and testis transcriptomic analyses reveal the benefits of sandy environmental enrichment in Senegalese sole male (Solea senegalensis) reproduction
inferred← citeshttps://doi.org/10.1016/j.bbamem.2017.04.020openalex-snapshot
Signaling pathways regulating blood–tissue barriers — Lesson from the testis
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110773openalex-snapshot
Retinoic acid signaling in development and differentiation commitment and its regulatory topology
inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102104openalex-snapshot
Sperm-specific proteins: new implications for diagnostic development and cancer immunotherapy
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.chemosphere.2016.10.023openalex-snapshot
Fluoride reduced the immune privileged function of mouse Sertoli cells via the regulation of Fas/FasL system
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.01.007openalex-snapshot
Adverse effects of bisphenol A on Sertoli cell blood-testis barrier in rare minnow Gobiocypris rarus
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111476openalex-snapshot
Bisphenol A exposure increases epididymal susceptibility to infection in mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.115930openalex-snapshot
Cadmium exposure induces pyroptosis of TM4 cells through oxidative stress damage and inflammasome activation
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116636openalex-snapshot
Bta-miR-149–3p suppresses inflammatory response in bovine Sertoli cells exposed to microcystin-leucine arginine (MC-LR) through TLR4/NF-kB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117071openalex-snapshot
Establishment of tumor microenvironment following bisphenol A exposure in the testis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117556openalex-snapshot
BP-3 exposure at environmentally relevant concentrations induced male developmental reproductive toxicity via ER/CCL27/ROS pathway in mice
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110165openalex-snapshot
Perinatal exposure to polystyrene microplastics induces multigenerational impairment of male reproduction via disrupted steroidogenesis and proteostasis
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128622openalex-snapshot
Developmental effects of intrauterine and lactational exposure to nanoplastics and phthalates on rat testis
inferred← citeshttps://doi.org/10.1016/j.envres.2016.06.033openalex-snapshot
In vitro functional screening as a means to identify new plasticizers devoid of reproductive toxicity
inferred← citeshttps://doi.org/10.1016/j.euros.2023.06.004openalex-snapshot
Proteomic Analysis of Testicular Interstitial Fluid in Men with Azoospermia
inferred← citeshttps://doi.org/10.1016/j.fct.2021.111972openalex-snapshot
Aflatoxin B1 disrupts blood-testis barrier integrity by reducing junction protein and promoting apoptosis in mice testes
inferred← citeshttps://doi.org/10.1016/j.fct.2023.113784openalex-snapshot
Hydrogen sulfide protects Sertoli cells against toxicant Acrolein-induced cell injury
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2026.03.018openalex-snapshot
Testicular immune privilege revisited: when protection fails
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104756openalex-snapshot
Interplay between male reproductive system dysfunction and the therapeutic effect of flavonoids
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.09.020openalex-snapshot
Superoxide dismutase 2 haplodeficiency alters spermatogenesis and early development in mice
inferred← citeshttps://doi.org/10.1016/j.fsi.2021.03.002openalex-snapshot
Testicular subcutaneous allografting followed by immunosuppressive treatment promotes maintenance of spermatogonial cells in rainbow trout (Oncorhynchus mykiss)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125842openalex-snapshot
Myosin VI stabilizes intercellular junctions in the testis through the LHR and MAPK signalling pathway during spermatogenesis in Eriocheir sinensis
inferred← citeshttps://doi.org/10.1016/j.immuni.2023.09.004openalex-snapshot
Cancer cell-intrinsic mechanisms driving acquired immune tolerance
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122370openalex-snapshot
Structural characterization of an oligosaccharide from Cistanche deserticola and its protective effect on diabetes-induced spermatogenic dysfunction
inferred← citeshttps://doi.org/10.1016/j.isci.2025.114174openalex-snapshot
Single-cell analysis of testicular bacterial microbiome changes during aging and effect on reproductive capacity in mice
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110221openalex-snapshot
UCHL1 regulates adiponectin receptors in Sertoli cells to maintain testicular homeostatic balance
inferred← citeshttps://doi.org/10.1016/j.jconrel.2019.04.034openalex-snapshot
Immunoisolation of pancreatic islets via thin-layer surface modification
inferred← citeshttps://doi.org/10.1016/j.jep.2025.119899openalex-snapshot
From TCM “Shen-nourishing” and “Yang-strengthening” theory to blood-testis barrier reorganization, GuiLuBuShen attenuates age-related male reproductive dysfunction
inferred← citeshttps://doi.org/10.1016/j.jiec.2017.02.027openalex-snapshot
The anterior chamber of the eye as a site for pancreatic islet transplantation
inferred← citeshttps://doi.org/10.1016/j.jri.2020.103178openalex-snapshot
Natural killer and NKT cells in the male reproductive tract
inferred← citeshttps://doi.org/10.1016/j.jri.2023.103984openalex-snapshot
A review on immunological aspects in male reproduction: An immune cells and cytokines
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119605openalex-snapshot
Myristic acid defends against testicular oxidative stress, inflammation, apoptosis: Restoration of spermatogenesis, steroidogenesis in diabetic rats
inferred← citeshttps://doi.org/10.1016/j.mce.2022.111664openalex-snapshot
Smtnl2 regulates apoptotic germ cell clearance and lactate metabolism in mouse Sertoli cells
inferred← citeshttps://doi.org/10.1016/j.mce.2023.112034openalex-snapshot
Melatonin improves oxidative state and lactate metabolism in rodent Sertoli cells
inferred← citeshttps://doi.org/10.1016/j.phymed.2019.153057openalex-snapshot
Aucubin, a natural iridoid glucoside, attenuates oxidative stress-induced testis injury by inhibiting JNK and CHOP activation via Nrf2 up-regulation
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.semcdb.2016.04.009openalex-snapshot
Spermatogenesis in humans and its affecting factors
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.06.018openalex-snapshot
Regulation of the blood-testis barrier
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.09.037openalex-snapshot
Cell polarity and cytoskeletons—Lesson from the testis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.01.013openalex-snapshot
Regulation of spermatid polarity by the actin- and microtubule (MT)-based cytoskeletons
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.04.007openalex-snapshot
Therapeutic application of Sertoli cells for treatment of various diseases
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.06.016openalex-snapshot
Sertoli cells as key drivers of testis function
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2024.03.003openalex-snapshot
Heme oxygenase 1 (HO1) regulates autophagy and apoptosis via the PI3K/AKT/mTOR signaling pathway of yak Sertoli cells
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2024.07.005openalex-snapshot
Tas2R143 regulates the expression of the Blood-Testis Barrier tight junction protein in TM4 cells through the NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2026.118008openalex-snapshot
Expression patterns and proliferative effect of OTUD6A on Sertoli cells and Leydig cells in cattleyak
inferred← citeshttps://doi.org/10.1016/j.tiv.2020.104882openalex-snapshot
Effects of nicotine on porcine pre-pupertal sertoli cells: An in vitro study
inferred← citeshttps://doi.org/10.1016/j.tria.2020.100073openalex-snapshot
The human testes: Estrogen and ageing outlooks
inferred← citeshttps://doi.org/10.1021/acsami.6c02897openalex-snapshot
Testosterone-Modified Liposomes Loaded with the Zn–Polyphenol Complex for Treatment of Male Infertility
inferred← citeshttps://doi.org/10.1038/nrurol.2016.265openalex-snapshot
A new threat on the horizon — Zika virus and male fertility
inferred← citeshttps://doi.org/10.1038/s41419-019-1782-zopenalex-snapshot
Multiple signaling pathways in Sertoli cells: recent findings in spermatogenesis
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/s41420-025-02875-1openalex-snapshot
Multi-omics analysis the effects of Dhx37 deficiency on testis development and nucleolar homeostasis
inferred← citeshttps://doi.org/10.1038/s41467-023-37199-0openalex-snapshot
Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions
inferred← citeshttps://doi.org/10.1038/s41467-026-76120-3openalex-snapshot
Multi-omic analysis of androgen-deprived human testes reveals Sertoli cell regulation and niche reprogramming
inferred← citeshttps://doi.org/10.1038/s41585-019-0149-7openalex-snapshot
Persistence and clinical relevance of Zika virus in the male genital tract
inferred← citeshttps://doi.org/10.1038/s41598-018-23899-xopenalex-snapshot
Human Sertoli cells support high levels of Zika virus replication and persistence
inferred← citeshttps://doi.org/10.1038/s41598-018-25468-8openalex-snapshot
Multiple aspects of male germ cell development and interactions with Sertoli cells require inositol hexakisphosphate kinase-1
inferred← citeshttps://doi.org/10.1038/s41598-018-27027-7openalex-snapshot
Immunoprofiles of human Sertoli cells infected with Zika virus reveals unique insights into host-pathogen crosstalk
inferred← citeshttps://doi.org/10.1038/s41598-018-28668-4openalex-snapshot
Glucose and glutamine handling in the Sertoli cells of transgenic rats overexpressing regucalcin: plasticity towards lactate production
inferred← citeshttps://doi.org/10.1038/s41598-019-48441-5openalex-snapshot
The effects of di-butyl phthalate exposure from medications on human sperm RNA among men
inferred← citeshttps://doi.org/10.1038/s41598-021-98036-2openalex-snapshot
Wuzi-Yanzong prescription alleviates spermatogenesis disorder induced by heat stress dependent on Akt, NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1038/s42003-026-09636-5openalex-snapshot
PTBP1 supports mouse spermatogenesis by facilitating cytoskeletal organization through the mTORC2–PKCα pathway in Sertoli cells
inferred← citeshttps://doi.org/10.1038/s44298-024-00022-8openalex-snapshot
Characterizing changes in transcriptome and kinome responses in testicular cells during infection by Ebola virus
inferred← citeshttps://doi.org/10.1080/19396368.2026.2741742openalex-snapshot
Busulfan affects the transcript levels of mitochondrial dynamics regulators without cytotoxicity in rat Sertoli cells
inferred← citeshttps://doi.org/10.1089/dna.2017.3839openalex-snapshot
In Vitro Evaluation of Damage by Heavy Metals in Tight and Gap Junctions of Sertoli Cells
inferred← citeshttps://doi.org/10.1089/dna.2017.3937openalex-snapshot
Sertoli Cells Engineered to Express Insulin to Lower Blood Glucose in Diabetic Mice
inferred← citeshttps://doi.org/10.1089/dna.2017.4081openalex-snapshot
Toxic Effect of Cadmium, Lead, and Arsenic on the Sertoli Cell: Mechanisms of Damage Involved
inferred← citeshttps://doi.org/10.1089/neu.2016.4641openalex-snapshot
Changes in Gene Expression and Metabolism in the Testes of the Rat following Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/ten.teb.2020.0326openalex-snapshot
Applying Immunomodulation to Promote Longevity of Immunoisolated Pancreatic Islet Grafts
inferred← citeshttps://doi.org/10.1093/biolre/ioac166openalex-snapshot
ARHGEF15 in Sertoli cells contributes to germ cell development and testicular immune privilege
inferred← citeshttps://doi.org/10.1093/biolre/ioaf162openalex-snapshot
Identification and characterization of a novel CD2-positive cell population in the seminiferous tubule of Fischer CDF344 rats
inferred← citeshttps://doi.org/10.1093/biolre/ioag040openalex-snapshot
Loss of KIAA1210 leads to increased pyroptotic cell death in mouse spermatogenesis
inferred← citeshttps://doi.org/10.1093/eep/dvx012openalex-snapshot
An overview of a Sertoli cell transplantation model to study testis morphogenesis and the role of the Sertoli cells in immune privilege
inferred← citeshttps://doi.org/10.1093/g3journal/jkac267openalex-snapshot
Genomics of sexual cell fate transdifferentiation in the mouse gonad
inferred← citeshttps://doi.org/10.1093/humupd/dmy009openalex-snapshot
Infectious, inflammatory and ‘autoimmune’ male factor infertility: how do rodent models inform clinical practice?
inferred← citeshttps://doi.org/10.1093/molehr/gaab049openalex-snapshot
MicroRNA-125a-5p modulates the proliferation and apoptosis of TM4 Sertoli cells by targeting RAB3D and regulating the PI3K/AKT signaling pathway
inferred← citeshttps://doi.org/10.1093/procel/pwac057openalex-snapshot
A single-nucleus transcriptomic atlas of primate testicular aging reveals exhaustion of the spermatogonial stem cell reservoir and loss of Sertoli cell homeostasis
inferred← citeshttps://doi.org/10.1093/reprod/xaag066openalex-snapshot
The role of heterogeneous nuclear ribonucleoproteins in mammalian spermatogenesis: mechanisms and clinical implications
inferred← citeshttps://doi.org/10.1093/toxres/tfaf097openalex-snapshot
Dose-dependent testis infiltration of peritubular macrophages after MEHP exposure of Peri-pubertal rats and their role in the recovery of spermatogenesis
inferred← citeshttps://doi.org/10.1093/toxsci/kfae043openalex-snapshot
The blood-testis barrier disruption is a prerequisite for toxicant-induced peritubular macrophage increases in the testis of peripubertal rats
inferred← citeshttps://doi.org/10.1093/toxsci/kfaf132openalex-snapshot
In vitro models of the male reproductive system: applications for developmental and reproductive toxicology
inferred← citeshttps://doi.org/10.1095/biolreprod.114.121996openalex-snapshot
Sertoli Cell-Based Gene Therapy?
inferred← citeshttps://doi.org/10.1096/fj.202002484ropenalex-snapshot
Sperm proteins and cancer‐testis antigens are released by the seminiferous tubules in mice and men
inferred← citeshttps://doi.org/10.1098/rsob.200347openalex-snapshot
Viral pathogenesis of SARS-CoV-2 infection and male reproductive health
inferred← citeshttps://doi.org/10.1101/2022.05.05.490754openalex-snapshot
Testicular macrophages are recruited during a narrow time window by fetal Sertoli cells to promote organ-specific developmental functions
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/imbioc.2019.8777768openalex-snapshot
Effects of 220 MHz Radiofrequency Field on Sperm Quality of SD Rat
inferred← citeshttps://doi.org/10.1111/acel.70023openalex-snapshot
Deciphering the Contribution of Circular RNAs to Age‐Related Decline in Sertoli Cell Survivor
inferred← citeshttps://doi.org/10.1111/ahe.12354openalex-snapshot
Distribution of CD 68‐, CD 8‐, MHCI ‐ and MHCII ‐positive cells in the bull and ram testis and epididymis
inferred← citeshttps://doi.org/10.1111/aji.12710openalex-snapshot
The roles of the PD ‐1/ PD ‐L1 pathway at immunologically privileged sites
inferred← citeshttps://doi.org/10.1111/aji.13079openalex-snapshot
Identification of programmed cell death 1 and its ligand in the testicular tissue of mice
inferred← citeshttps://doi.org/10.1111/and.13743openalex-snapshot
The role of infections and leukocytes in male infertility
inferred← citeshttps://doi.org/10.1111/andr.12165openalex-snapshot
The Sertoli cell: one hundred fifty years of beauty and plasticity
inferred← citeshttps://doi.org/10.1111/andr.12484openalex-snapshot
Sertoli cells for cell transplantation: pre‐clinical studies and future perspectives
inferred← citeshttps://doi.org/10.1111/andr.12682openalex-snapshot
Activins, follistatin and immunoregulation in the epididymis
inferred← citeshttps://doi.org/10.1111/andr.12764openalex-snapshot
Protective effect of Berberine on reproductive function and spermatogenesis in diabetic rats via inhibition of ROS/JAK2/NFκB pathway
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.13386openalex-snapshot
What are Sertoli cells? Historical, methodological, and functional aspects
inferred← citeshttps://doi.org/10.1111/andr.70255openalex-snapshot
Diacerein Disrupts Testicular Homeostasis: The Essential Role of Basal Cytokines in Maintaining Sertoli Cell Integrity and the Immune Microenvironment
inferred← citeshttps://doi.org/10.1111/cpr.12599openalex-snapshot
Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy?
inferred← citeshttps://doi.org/10.1111/dom.12556openalex-snapshot
Accessory cells for β‐cell transplantation
inferred← citeshttps://doi.org/10.1111/febs.17366openalex-snapshot
Exploring the interplay between inflammation and male fertility
inferred← citeshttps://doi.org/10.1111/jpi.12806openalex-snapshot
Melatonin modulates Nrf2 activity to protect porcine pre‐pubertal Sertoli cells from the abnormal H2O2 generation and reductive stress effects of cadmium
inferred← citeshttps://doi.org/10.1111/xen.12742openalex-snapshot
Xenogeneic Sertoli cells modulate immune response in an evolutionary distant mouse model through the production of interleukin‐10 and PD‐1 ligands expression
inferred← citeshttps://doi.org/10.1128/mbio.01372-19openalex-snapshot
Axl Promotes Zika Virus Entry and Modulates the Antiviral State of Human Sertoli Cells
inferred← citeshttps://doi.org/10.1134/s0006297923110123openalex-snapshot
Immune Privileges as a Result of Mutual Regulation of Immune and Stem Systems
inferred← citeshttps://doi.org/10.1152/physrev.00021.2019openalex-snapshot
From Ancient to Emerging Infections: The Odyssey of Viruses in the Male Genital Tract
inferred← citeshttps://doi.org/10.1155/2022/5182172openalex-snapshot
Effects of 5.8 GHz Microwaves on Testicular Structure and Function in Rats
inferred← citeshttps://doi.org/10.1155/2023/2966391openalex-snapshot
Androgen Receptor (AR) Depletion Underlies the Reproductive Dysfunctions in Male Rats Exposed to Alcohol and Combination Antiretroviral Therapy (cART)
inferred← citeshttps://doi.org/10.1159/000439039openalex-snapshot
Circannual Testis Changes in Seasonally Breeding Mammals
inferred← citeshttps://doi.org/10.11603/mcch.2410-681x.2022.i2.13088openalex-snapshot
ІМУНОФЕНОТИПІЧНІ ВЛАСТИВОСТІ ЛІМФОЦИТІВ ПЕРИФЕРИЧНОЇ КРОВІ НЕПЛІДНИХ ЧОЛОВІКІВ ІЗ СУПУТНЬОЮ ПАТОЛОГІЄЮ
inferred← citeshttps://doi.org/10.1177/0271678x251317374openalex-snapshot
Advances in clinical translation of stem cell-based therapy in neurological diseases
inferred← citeshttps://doi.org/10.1177/0963689720947102openalex-snapshot
Neonatal Pig Sertoli Cells Survive Xenotransplantation by Creating an Immune Modulatory Environment Involving CD4 and CD8 Regulatory T Cells
inferred← citeshttps://doi.org/10.1186/s12610-022-00157-9openalex-snapshot
The NLRP3 inflammasome: molecular activation and regulation in spermatogenesis and male infertility; a systematic review
inferred← citeshttps://doi.org/10.1186/s12951-019-0474-2openalex-snapshot
SF-1 mediates reproductive toxicity induced by Cerium oxide nanoparticles in male mice
inferred← citeshttps://doi.org/10.1186/s12951-025-03998-4openalex-snapshot
Multimodal electroconductive PLGA-based scaffold orchestrates neuroprotection and regeneration following severe spinal cord injury
inferred← citeshttps://doi.org/10.1186/s13287-024-03897-9openalex-snapshot
Therapeutic potential of Sertoli cells in vivo: alleviation of acute inflammation and improvement of sperm quality
inferred← citeshttps://doi.org/10.1186/s40104-020-00487-6openalex-snapshot
Profiling of miRNAs in porcine Sertoli cells
inferred← citeshttps://doi.org/10.1186/s40104-022-00687-2openalex-snapshot
Sertoli cell and spermatogonial development in pigs
inferred← citeshttps://doi.org/10.1186/s40851-022-00195-1openalex-snapshot
Allogeneic testes transplanted into partially castrated adult medaka (Oryzias latipes) can produce donor-derived offspring by natural mating over a prolonged period
inferred← citeshttps://doi.org/10.1186/s41021-023-00279-0openalex-snapshot
M6A transcriptome-wide map of circRNAs identified in the testis of normal and AZ-treated Xenopus laevis
inferred← citeshttps://doi.org/10.1186/s43043-026-00348-8openalex-snapshot
Micro-TESE in men with non-obstructive azoospermia: a narrative review of sperm retrieval benefit, testicular injury, and endocrine risk
inferred← citeshttps://doi.org/10.1186/s43094-024-00677-3openalex-snapshot
Flavonoids as potential therapeutics in male reproductive disorders
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/10.1242/dev.114967openalex-snapshot
A somatic permeability barrier around the germline is essential forDrosophilaspermatogenesis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010088openalex-snapshot
Lrh1 can help reprogram sexual cell fate and is required for Sertoli cell development and spermatogenesis in the mouse testis
inferred← citeshttps://doi.org/10.1371/journal.pone.0197685openalex-snapshot
Sertoli cell-specific ablation of miR-17-92 cluster significantly alters whole testis transcriptome without apparent phenotypic effects
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.0204851openalex-snapshot
Germ cell desquamation-based testis regression in a seasonal breeder, the Egyptian long-eared hedgehog, Hemiechinus auritus
inferred← citeshttps://doi.org/10.14670/hh-18-734openalex-snapshot
HSP47 expression in the hamster Sertoli cell: An immunohistochemical study.
inferred← citeshttps://doi.org/10.1515/jbcpp-2020-0156openalex-snapshot
Testis and blood-testis barrier in Covid-19 infestation: role of angiotensin-converting enzyme 2 in male infertility
inferred← citeshttps://doi.org/10.1530/ec-24-0630openalex-snapshot
From biological marker to clinical application: the role of anti-Müllerian hormone for delayed puberty and idiopathic non-obstructive azoospermia in males
inferred← citeshttps://doi.org/10.1530/rep-15-0463openalex-snapshot
Regulation of blood–testis barrier by actin binding proteins and protein kinases
inferred← citeshttps://doi.org/10.1530/rep-17-0346openalex-snapshot
Isolation of human testicular cells and co-culture with embryonic stem cells
inferred← citeshttps://doi.org/10.1530/rep-18-0111openalex-snapshot
NLRP3 in somatic non-immune cells of rodent and primate testes
inferred← citeshttps://doi.org/10.1530/rep-18-0457openalex-snapshot
The cytoskeleton in spermatogenesis
inferred← citeshttps://doi.org/10.1530/rep-23-0486openalex-snapshot
Reproductive Ageing: Current insights and a potential role of NAD in the reproductive health of aging fathers and their children
inferred← citeshttps://doi.org/10.17077/etd.mo6vawwgopenalex-snapshot
Characterization of miR-888 expression and regulation in endometrial cancer
inferred← citeshttps://doi.org/10.17352/ijsrhc.000046openalex-snapshot
Potential role of autophagy in the male reproductive system
inferred← citeshttps://doi.org/10.17650/2070-9781-2022-23-3-61-71openalex-snapshot
Sperm agglutination and ejaculate liquefaction time as negative prognostic factor in ICSI
inferred← citeshttps://doi.org/10.18632/oncotarget.12823openalex-snapshot
MKP-1 attenuates LPS-induced blood-testis barrier dysfunction and inflammatory response through p38 and IκBα pathways
inferred← citeshttps://doi.org/10.20473/jbmv.v10i2.31812openalex-snapshot
Protection Effectiveness Of Bit (Beta vulgaris) Fruit Extract In Maintaining Spermatogenesis Ability In White Rats (Rattus novergicus) Induced Carbon Tetracloride (CCl4)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1797646/v1openalex-snapshot
Metadichol® a nano lipid emulsion that expresses all 48 nuclear receptors in stem and somatic cells
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1797646/v2openalex-snapshot
METADICHOL: A natural nano lipid emulsion that expresses all 48 Nuclear receptors in the Stem, somatic, and Cancer cells.
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1797646/v3openalex-snapshot
Metadichol® is a nano lipid emulsion that expresses all 48 nuclear receptors in stem and somatic cells
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1797646/v4openalex-snapshot
Metadichol® is a nano lipid emulsion that expresses all 48 nuclear receptors in stem and somatic cells
inferred← citeshttps://doi.org/10.21203/rs.3.rs-313760/v1openalex-snapshot
Sertoli Cells Possess Immunomodulatory Properties and the Ability of Mitochondrial Transfer Similar to Mesenchymal Stem Cells
inferred← citeshttps://doi.org/10.2174/9789815305302125010005openalex-snapshot
Immune Homeostasis in the Male Reproductive System
inferred← citeshttps://doi.org/10.22029/jlupub-14247openalex-snapshot
Uropathogenic Escherichia coli cause resistance to apoptotic cell death of infected cells by epigenetically suppressing BIM expression
inferred← citeshttps://doi.org/10.2217/imt-2016-0137openalex-snapshot
Possible Damage to Immune-Privileged Sites in Natural Killer Cell Therapy in Cancer Patients: Side Effects of Natural Killer Cell Therapy
inferred← citeshttps://doi.org/10.24108/preprints-3112745openalex-snapshot
Immune privileges as a result of mutual regulation of the immune and stem systems
inferred← citeshttps://doi.org/10.2478/enr-2020-0012openalex-snapshot
Involvement of Asc and Nlrp3 inflammasomes in the testes following spinal cord injury
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