about
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceBug22p, a conserved centrosomal/ciliary protein also present in higher plants, is required for an effective ciliary stroke in Paramecium.Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesiaRecurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesStructure and function of mammalian ciliaGenetic factors contributing to human primary ciliary dyskinesia and male infertilityA primer on the mouse basal bodyMammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypesEfhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in miceAlix-mediated assembly of the actomyosin-tight junction polarity complex preserves epithelial polarity and epithelial barrierThe PDZ Protein Na+/H+ Exchanger Regulatory Factor-1 (NHERF1) Regulates Planar Cell Polarity and Motile Cilia OrganizationKinesin-2 and kinesin-9 have atypical functions during ciliogenesis in the male gametophyte of Marsilea vestitaInvestigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndromeBasal foot MTOC organizes pillar MTs required for coordination of beating cilia.Ectopic expression of human BBS4 can rescue Bardet-Biedl syndrome phenotypes in Bbs4 null miceSCO-ping out the mechanisms underlying the etiology of hydrocephalusPcdp1 is a central apparatus protein that binds Ca(2+)-calmodulin and regulates ciliary motilityCongenital hydrocephalus in genetically engineered miceTubulin polyglutamylation is essential for airway ciliary function through the regulation of beating asymmetryAbnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse modelSperm-associated antigen-17 gene is essential for motile cilia function and neonatal survivalDisruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalusTubulin glycylases and glutamylases have distinct functions in stabilization and motility of ependymal ciliaFunctional deficiencies and a reduced response to calcium in the flagellum of mouse sperm lacking SPAG16LConvergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene.Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway.An outer arm Dynein conformational switch is required for metachronal synchrony of motile cilia in planariaRegulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50.Analyses of functional domains within the PF6 protein of the central apparatus reveal a role for PF6 sub-complex members in regulating flagellar beat frequencyLysophosphatidic acid signaling may initiate fetal hydrocephalus.Total internal reflection fluorescence (TIRF) microscopy of Chlamydomonas flagellaConserved structural motifs in the central pair complex of eukaryotic flagella.FAP206 is a microtubule-docking adapter for ciliary radial spoke 2 and dynein cA novel mouse model reveals that polycystin-1 deficiency in ependyma and choroid plexus results in dysfunctional cilia and hydrocephalus.Kinesin 9 family members perform separate functions in the trypanosome flagellum.Role of red blood cell lysis and iron in hydrocephalus after intraventricular hemorrhage.A bioactive peptide amidating enzyme is required for ciliogenesisEvidences showing wide presence of small genomic aberrations in chronic lymphocytic leukemiaSensing the mechanical state of the axoneme and integration of Ca2+ signaling by outer arm dynein.
P2860
Q21134928-4975ACAC-B07D-465D-A315-D84D4243FAAFQ24297955-E3D598C7-3E58-4954-92B1-FCAAE2037106Q24635321-52E0D325-3882-43B3-9667-B4D3933B48EFQ24647145-02B8FA68-C247-4BC0-AB64-4CCDC1614EDEQ24654284-AAEBF08C-5D2A-4AC2-8511-06BA20734B87Q26748534-E5CF5A0C-24AF-48D5-A08B-ED279BE69CCBQ26750292-BC032593-4EA6-47B1-8522-E1904BDC1164Q26770927-21E0CA5C-1FDD-49AC-ABC1-99D77471560CQ27301367-9EE0C175-B543-4629-AEA5-673BC8F1B18DQ27306183-1D1DAB27-9A86-4E53-B9E2-049EFD154D30Q27313202-886980FC-021D-4AA5-AD60-9EE57690E70CQ27314709-D84C7F6E-9140-4BBF-8288-1E304812A167Q27318622-5FE28A3E-B1C7-46DC-A4D7-8D709004BDD7Q27319191-D4D90B0F-10E1-4A86-B424-30F38A86F304Q27324611-B3C18B97-0AD1-46C7-B8E4-6CB3E24B2F74Q27334338-53965360-48FA-4F1E-99B7-B34AAFF096FEQ28241174-EA6CD3AE-FA17-43CA-B7A1-F5BF2278E729Q28504586-22C4B186-A0D4-4992-BCCD-9A68E5C8EFB6Q28506486-E8FE968B-F3F0-4FFF-BD04-85E7FB1B99BBQ28507689-5C8AC8E0-6A42-4D89-8450-EA6CA21EB20FQ28511697-03079079-DD67-40D6-9C21-776BFA29FF01Q28512056-1D696D44-04B3-4F34-A542-9F69B994F700Q28585348-940E38AC-F9AE-414A-84ED-95D846765C01Q28587615-D180FD6B-07D2-486B-80C2-14EDB1A51E74Q28593298-03622060-546A-4134-8557-4F5F1F481C2CQ30485917-864C2190-5025-4B75-85E3-7D8C8BC39608Q30488046-C7F65602-50C5-4A78-AB9A-617E49CC0C99Q30497172-AF7EFB91-568C-4E97-85D0-748DF221FE0DQ30499289-1BE4C7AC-1D84-48B4-8FFC-18D708C4B98BQ30511826-64AFF88E-66D7-41DF-A399-CFBF5069A865Q30539772-26A67F2A-3536-46BB-B17E-1D81760D23A4Q30540740-C2F102E0-5A51-4DCB-9840-A32449BA2911Q30570932-4CD0BF9C-5D87-4EE5-8081-7A3C643A3C3CQ30620300-60FE224A-88F4-4EAF-A4F5-347083276F0DQ33506091-DBE90EE4-2B65-438C-B189-2EA5849A7063Q33590937-608086D3-F3F8-4E9C-9D65-30DC544EC146Q33729291-EEBF33C4-2B3C-402C-9332-CD5CAEA85858Q33769785-521E50E9-A478-44D2-80D7-FAAA2B3E2E0EQ33776198-F65BF57A-D1B9-4F4A-A19D-77A714485E6BQ33809670-5D97EA5E-95BC-41F3-8043-C031CF052123
P2860
description
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2008
@ast
im Februar 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/02/11)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/02/11)
@nl
наукова стаття, опублікована в лютому 2008
@uk
مقالة علمية (نشرت في 11-2-2008)
@ar
name
Mutations in Hydin impair ciliary motility in mice
@ast
Mutations in Hydin impair ciliary motility in mice
@en
Mutations in Hydin impair ciliary motility in mice
@nl
type
label
Mutations in Hydin impair ciliary motility in mice
@ast
Mutations in Hydin impair ciliary motility in mice
@en
Mutations in Hydin impair ciliary motility in mice
@nl
prefLabel
Mutations in Hydin impair ciliary motility in mice
@ast
Mutations in Hydin impair ciliary motility in mice
@en
Mutations in Hydin impair ciliary motility in mice
@nl
P2093
P2860
P3181
P356
P1476
Mutations in Hydin impair ciliary motility in mice
@en
P2093
George B. Witman
Karl-Ferdinand Lechtreck
Michael J. Sanderson
Michael L. Robinson
Philippe Delmotte
P2860
P304
P3181
P356
10.1083/JCB.200710162
P407
P577
2008-02-11T00:00:00Z