Hyperactivated sperm motility driven by CatSper2 is required for fertilization
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Association of Catsper1 or -2 with Ca(v)3.3 leads to suppression of T-type calcium channel activityAs the world grows: contraception in the 21st centuryHuman spermatozoa contain multiple targets for protein S-nitrosylation: an alternative mechanism of the modulation of sperm function by nitric oxide?All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motilityCatsper3 and catsper4 encode two cation channel-like proteins exclusively expressed in the testisContributions of extracellular and intracellular Ca2+ to regulation of sperm motility: Release of intracellular stores can hyperactivate CatSper1 and CatSper2 null sperm.CatSper1 required for evoked Ca2+ entry and control of flagellar function in spermA polycystin-1 controls postcopulatory reproductive selection in miceSLO3 auxiliary subunit LRRC52 controls gating of sperm KSPER currents and is critical for normal fertilityLack of Spem1 causes aberrant cytoplasm removal, sperm deformation, and male infertilityA novel gene required for male fertility and functional CATSPER channel formation in spermatozoa.Phosphorylation of mouse sperm axoneme central apparatus protein SPAG16L by a testis-specific kinase, TSSK2CatSperζ regulates the structural continuity of sperm Ca2+ signaling domains and is required for normal fertilityLoss of polyadenylation protein tauCstF-64 causes spermatogenic defects and male infertility.Egg coat proteins activate calcium entry into mouse sperm via CATSPER channelsSpermatogenetic but not immunological defects in mice lacking the τCstF-64 polyadenylation proteinUnexpected flagellar movement patterns and epithelial binding behavior of mouse sperm in the oviduct.Ciliary contact interactions dominate surface scattering of swimming eukaryotes.Ca2+ signals generated by CatSper and Ca2+ stores regulate different behaviors in human sperm.Episodic rolling and transient attachments create diversity in sperm swimming behavior.Mechanical tuning of mammalian sperm behaviour by hyperactivation, rheology and substrate adhesion: a numerical exploration.Evolutionary genomics reveals lineage-specific gene loss and rapid evolution of a sperm-specific ion channel complex: CatSpers and CatSperbeta.Combining RNA interference mutants and comparative proteomics to identify protein components and dependences in a eukaryotic flagellum.Pharmacological targeting of native CatSper channels reveals a required role in maintenance of sperm hyperactivation.Evolution and spermatogenesis.Calcium influx and male fertility in the context of the sperm proteome: an updateRoles of the oviduct in mammalian fertilization.Inhibiting sperm pyruvate dehydrogenase complex and its E3 subunit, dihydrolipoamide dehydrogenase affects fertilization in Syrian hamsters.Structurally distinct Ca(2+) signaling domains of sperm flagella orchestrate tyrosine phosphorylation and motility.Male infertility caused by spermiogenic defects: lessons from gene knockouts.Protective effect of royal jelly on the sperm parameters and testosterone level and lipid peroxidation in adult mice treated with oxymetholoneCalcium channels in the development, maturation, and function of spermatozoa.Rethinking the relationship between hyperactivation and chemotaxis in mammalian sperm.Stimulation of human spermatozoa with progesterone gradients to simulate approach to the oocyte. Induction of [Ca(2+)](i) oscillations and cyclical transitions in flagellar beating.Identical phenotypes of CatSper1 and CatSper2 null sperm.Panax ginseng induces the expression of CatSper genes and sperm hyperactivationControl of hyperactivation in sperm.Ion channels that control fertility in mammalian spermatozoaClassification of mouse sperm motility patterns using an automated multiclass support vector machines modelTargeted disruption of tyrosylprotein sulfotransferase-2, an enzyme that catalyzes post-translational protein tyrosine O-sulfation, causes male infertility
P2860
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P2860
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
description
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 2003
@ast
im Dezember 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2003/12/09)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/12/09)
@nl
наукова стаття, опублікована в грудні 2003
@uk
name
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@ast
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@en
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@nl
type
label
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@ast
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@en
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@nl
prefLabel
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@ast
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@en
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@nl
P2093
P2860
P3181
P356
P1476
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
@en
P2093
David L. Garbers
Kristen L. Rossi
Lynda K. Doolittle
Robert E. Hammer
Sarah A. Sugden
Timothy A. Quill
P2860
P304
14869–14874
P3181
P356
10.1073/PNAS.2136654100
P407
P577
2003-12-09T00:00:00Z