The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
about
A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescenceGli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and functionThe dynamic cilium in human diseasesThe intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assemblyPericentrin forms a complex with intraflagellar transport proteins and polycystin-2 and is required for primary cilia assemblyNephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargosA novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cellsLoss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasiaDefects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humansLoss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transportIntraflagellar transport molecules in ciliary and nonciliary cells of the retinaDisruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromePolaris, a protein involved in left-right axis patterning, localizes to basal bodies and ciliaLoss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesiaThe hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formationCilia/Ift protein and motor -related bone diseases and mouse modelsTbx6 regulates left/right patterning in mouse embryos through effects on nodal cilia and perinodal signalingA Cilia Independent Role of Ift88/Polaris during Cell MigrationAcute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypesKif3a guides microtubular dynamics, migration and lumen formation of MDCK cellsCrystal structure of the intraflagellar transport complex 25/27MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesisArchitecture and function of IFT complex proteins in ciliogenesisTrafficking in and to the primary cilium.Cilia and developmental signalingAn Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of ciliaMechanical stimuli induce cleavage and nuclear translocation of the polycystin-1 C terminusHippi is essential for node cilia assembly and Sonic hedgehog signalingThe primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiationADP-ribosylation factor-like 3 is involved in kidney and photoreceptor developmentGlomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tailPrimary cilia regulate Shh activity in the control of molar tooth numberDisruption of IFT complex A causes cystic kidneys without mitotic spindle misorientationAhi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle traffickingAnalysis of mouse embryonic patterning and morphogenesis by forward geneticsThe retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated proteinFuz regulates craniofacial development through tissue specific responses to signaling factorsThe transcription factor RFX3 directs nodal cilium development and left-right asymmetry specificationGeneration of mice with functional inactivation of talpid3, a gene first identified in chicken
P2860
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P2860
The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
description
2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2000
@ast
im Juni 2000 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2000/06/01)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd op 2000/06/01)
@nl
наукова стаття, опублікована в червні 2000
@uk
مقالة علمية (نشرت في يونيو 2000)
@ar
name
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@ast
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@en
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@nl
type
label
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@ast
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@en
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@nl
prefLabel
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@ast
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@en
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@nl
P2093
P3181
P1433
P1476
The Oak Ridge Polycystic Kidne ...... left-right axis determination
@en
P2093
B. K. Yoder
J. R. Dunlap
M. L. Mucenski
N. S. Murcia
R. P. Woychik
W. G. Richards
P304
P3181
P407
P577
2000-06-01T00:00:00Z