Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.
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 intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assemblyCandidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathyBBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesLoss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasiaThe Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formationLoss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transportPolaris, a protein involved in left-right axis patterning, localizes to basal bodies and ciliaMutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in miceCilia/Ift protein and motor -related bone diseases and mouse modelsPathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapyA Cilia Independent Role of Ift88/Polaris during Cell MigrationThe exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypesThe intraflagellar transport machinery of Chlamydomonas reinhardtii.Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier?Architecture and function of IFT complex proteins in ciliogenesisIFT20 links kinesin II with a mammalian intraflagellar transport complex that is conserved in motile flagella and sensory ciliaMutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationThe primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiationADP-ribosylation factor-like 3 is involved in kidney and photoreceptor developmentPhenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotypeNek8 regulates the expression and localization of polycystin-1 and polycystin-2Primary cilia dynamics instruct tissue patterning and repair of corneal endotheliumPrimary cilia regulate Shh activity in the control of molar tooth numberDifferential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesionKnockdown of the intraflagellar transport protein IFT46 stimulates selective gene expression in mouse chondrocytes and affects early development in zebrafishCystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney diseaseChlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagellaIFT80 is essential for chondrocyte differentiation by regulating Hedgehog and Wnt signaling pathwaysEndothelial cilia are fluid shear sensors that regulate calcium signaling and nitric oxide production through polycystin-1A mutation in the mouse ttc26 gene leads to impaired hedgehog signalingThe intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenanceDicer regulates the development of nephrogenic and ureteric compartments in the mammalian kidney.Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella.XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans.Cftr controls lumen expansion and function of Kupffer's vesicle in zebrafish.Situs inversus and ciliary abnormalities: 20 years later, what is the connection?The role for HNF-1beta-targeted collectrin in maintenance of primary cilia and cell polarity in collecting duct cells.The hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules.
P2860
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P2860
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.
description
1994 nî lūn-bûn
@nan
1994 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
name
Candidate gene associated with ...... cystic kidney disease in mice.
@ast
Candidate gene associated with ...... cystic kidney disease in mice.
@en
Candidate gene associated with ...... cystic kidney disease in mice.
@nl
type
label
Candidate gene associated with ...... cystic kidney disease in mice.
@ast
Candidate gene associated with ...... cystic kidney disease in mice.
@en
Candidate gene associated with ...... cystic kidney disease in mice.
@nl
prefLabel
Candidate gene associated with ...... cystic kidney disease in mice.
@ast
Candidate gene associated with ...... cystic kidney disease in mice.
@en
Candidate gene associated with ...... cystic kidney disease in mice.
@nl
P2093
P356
P1433
P1476
Candidate gene associated with ...... ycystic kidney disease in mice
@en
P2093
J E Wilkinson
J J Schrick
M J Lee-Tischler
N L Cacheiro
V L Godfrey
W E Sweeney
P304
P356
10.1126/SCIENCE.8191288
P407
P577
1994-05-01T00:00:00Z