Regulation of ectoplasmic specialization dynamics in the seminiferous epithelium by focal adhesion-associated proteins in testosterone-suppressed rat testes
about
Testicular cell junction: a novel target for male contraceptionRole of non-receptor protein tyrosine kinases in spermatid transport during spermatogenesisThe Mammalian Blood-Testis Barrier: Its Biology and RegulationThe blood-testis barrier and its implications for male contraceptionNovel Role for p110β PI 3-Kinase in Male Fertility through Regulation of Androgen Receptor Activity in Sertoli CellsLKB1 is an essential regulator of spermatozoa release during spermiation in the mammalian testisHypogonadism Associated with Cyp19a1 (Aromatase) Posttranscriptional Upregulation in Celf1 Knockout Mice.The somatostatin 2A receptor is enriched in migrating neurons during rat and human brain development and stimulates migration and axonal outgrowthUnraveling the molecular targets pertinent to junction restructuring events during spermatogenesis using the Adjudin-induced germ cell depletion model14-3-3 and its binding partners are regulators of protein-protein interactions during spermatogenesisMitogen-activated protein kinases in male reproductive functionEctoplasmic specialization: a friend or a foe of spermatogenesis?Extracellular matrix and its role in spermatogenesisThe regulation of spermatogenesis by androgens.Cross-talk between tight and anchoring junctions-lesson from the testisA local autocrine axis in the testes that regulates spermatogenesis.Androgens and spermatogenesis: lessons from transgenic mouse models.Blood-testis barrier dynamics are regulated by an engagement/disengagement mechanism between tight and adherens junctions via peripheral adaptorsGerm cell transport across the seminiferous epithelium during spermatogenesis.Placental growth factor (PlGF) enhances breast cancer cell motility by mobilising ERK1/2 phosphorylation and cytoskeletal rearrangement.The cell-cell junctions of mammalian testes: I. The adhering junctions of the seminiferous epithelium represent special differentiation structures.Anchoring junctions as drug targets: role in contraceptive development.c-Yes regulates cell adhesion at the blood-testis barrier and the apical ectoplasmic specialization in the seminiferous epithelium of rat testesThe β1-integrin-p-FAK-p130Cas-DOCK180-RhoA-vinculin is a novel regulatory protein complex at the apical ectoplasmic specialization in adult rat testes.Restoration of spermatogenesis and male fertility using an androgen receptor transgene.The myotubularin family of lipid phosphatases in disease and in spermatogenesisImpaired fertility and spermiogenetic disorders with loss of cell adhesion in male mice expressing an interfering Rap1 mutant.Interactions of laminin β3 fragment with β1-integrin receptor: A revisit of the apical ectoplasmic specialization-blood-testis-barrier-hemidesmosome functional axis in the testisRole of FYN kinase in spermatogenesis: defects characteristic of Fyn-null sperm in mice.Actin-based dynamics during spermatogenesis and its significanceRegulation of Sertoli-germ cell adhesion and sperm release by FSH and nonclassical testosterone signaling.Coxsackie and adenovirus receptor (CAR) is a product of Sertoli and germ cells in rat testes which is localized at the Sertoli-Sertoli and Sertoli-germ cell interface.Secreted Frizzled-related protein 1 (sFRP1) regulates spermatid adhesion in the testis via dephosphorylation of focal adhesion kinase and the nectin-3 adhesion protein complex.Mouse Spermatogenesis Requires Classical and Nonclassical Testosterone Signaling.Biology and regulation of ectoplasmic specialization, an atypical adherens junction type, in the testisImpaired function of the blood-testis barrier during aging is preceded by a decline in cell adhesion proteins and GTPases.Non-classical actions of testosterone and spermatogenesis.Gonadotropin suppression in men leads to a reduction in claudin-11 at the Sertoli cell tight junction.Adjudin-mediated Sertoli-germ cell junction disassembly affects Sertoli cell barrier function in vitro and in vivo.Does blood transfusion affect pituitary gonadal axis and sperm parameters in young males with sickle cell disease?
P2860
Q24647811-63D48C34-11C8-4C0A-814C-8E44A64865C6Q27021461-39BC5F33-998D-44C3-8A64-AD4539CF1CA3Q28088573-159A6C71-61AE-4BD0-8E5C-A6B5C068060BQ28395237-ABDCF7DA-0B18-4C77-A6D0-06020F06E537Q28546072-BA0EB689-4683-44E8-BDB3-D153EA971C6DQ28742048-EB530C96-6332-4942-BD7A-BFDA7811F02FQ30360551-62B5BA3E-BDB8-416D-ADF1-6956C1B2C7CCQ33443929-AE246E4F-C657-46B9-BB35-971E4D4B2ABDQ33580682-D863B93F-FCD6-4594-8E8E-D9038BE8AA3AQ33584128-8CAF0C64-2C3E-4E2E-BA71-DB46DB3225FDQ33584135-D9121250-A7C3-4F06-B5DB-0CE33ED83694Q33584186-A055AACE-78D9-42C1-A9CE-D57CFB25B25FQ33674054-99462948-B80F-4FC4-B129-5BFB7DEE7601Q33707093-AC1386E9-90A1-4148-9278-36F02E30664BQ33841456-5531D7C7-B719-4974-8E83-86FFC9126B47Q33841603-7F5404C1-16AC-493E-B2ED-3FB31874D7EBQ33856942-7B5EBA87-16FE-4B56-B503-4C0452D261D1Q33912703-264F473E-CE6C-4561-88C8-2C816AB7AC92Q33918591-4CB51C31-EFF3-4310-ABAA-7D7D430B208AQ34000345-537E960E-5E5C-4F21-BA32-A4844D473ED0Q34106151-D5942C35-D4B2-4126-AED6-A390C45121AAQ34501400-431F64DE-11A9-453D-B330-A5FF8474943FQ34618797-034F99A0-E5A3-47E7-BE44-285CBFD40230Q35172313-1C1AED6E-CC37-40EF-AFFE-72371A4B487BQ35214257-5783DBA8-3D64-4BA9-8BE9-2AD8947E3C59Q35240346-2FB73ACD-8D74-4E2F-BF56-D22E378D5BD2Q35723724-7D1CD94C-B82A-47F5-AFB8-797C6B7630D9Q35733335-495778F5-1049-406D-99A1-01554D4D1AE4Q35855885-C574817A-EE89-43E2-8A8B-FD0CF14575B8Q35868541-C61B4284-6213-440D-B38C-DAAC91187AD4Q36067427-0CDD1DB2-86D3-485A-A703-AE08916CA610Q36171460-CB7A597C-F356-477C-B83C-995325605B8EQ36534407-93E906A0-6800-4DF2-9224-17F5EC96EB03Q36734054-3ED5AC14-AE74-42B5-8EF0-A450B1769627Q37027899-77AE9A5E-F492-4AF2-9486-1CC56C5AD1A5Q37423560-A6383F0B-4316-411A-8095-8F582AE667FAQ37733948-97EFB2BB-AE87-4EFC-B387-03A00EEBC578Q38382035-7B3550E3-A6D8-403E-9E60-162BD51901A7Q41913835-227B3C8A-C531-4565-8FE3-5E61A22B8872Q42451730-EF631B82-D4B5-421B-AE04-48D68D95D0DF
P2860
Regulation of ectoplasmic specialization dynamics in the seminiferous epithelium by focal adhesion-associated proteins in testosterone-suppressed rat testes
description
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im März 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/03/01)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/03/01)
@nl
наукова стаття, опублікована в березні 2005
@uk
مقالة علمية (نشرت في مارس 2005)
@ar
name
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@ast
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@en
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@nl
type
label
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@ast
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@en
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@nl
prefLabel
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@ast
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@en
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@nl
P2093
P356
P1433
P1476
Regulation of ectoplasmic spec ...... osterone-suppressed rat testes
@en
P2093
C. Yan Cheng
Ching-Hang Wong
Dolores D. Mruk
Nikki P. Y. Lee
Weiliang Xia
Will M. Lee
P304
P356
10.1210/EN.2004-1275
P407
P577
2005-03-01T00:00:00Z