Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
about
Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and functionIdentification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesiaA novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cellsPKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cellsLoss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transportCP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary diseaseLoss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesiaLoss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and functionCentrin4p, a novel mammalian centrin specifically expressed in ciliated cellsMicroscale imaging of cilia-driven fluid flowEfhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.Zfp423 Regulates Sonic Hedgehog Signaling via Primary Cilium FunctionAirway epithelial homeostasis and planar cell polarity signaling depend on multiciliated cell differentiationThe exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypesDirect interactions of intraflagellar transport complex B proteins IFT88, IFT52, and IFT46.IFT20 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 determinationCiliary calcium signaling is modulated by kidney injury molecule-1 (Kim1)Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory ciliaCongenital hydrocephalus in genetically engineered miceFailure of epithelial tube maintenance causes hydrocephalus and renal cysts in Dlg5-/- miceLaminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesisRole of epidermal primary cilia in the homeostasis of skin and hair folliclesThe primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiationA role for the primary cilium in Notch signaling and epidermal differentiation during skin developmentOverexpression of RPGR leads to male infertility in mice due to defects in flagellar assemblyGlomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1Ran, a GTP-binding protein involved in nucleocytoplasmic transport and microtubule nucleation, relocates from the manchette to the centrosome region during rat spermiogenesisGMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tailLRGUK-1 is required for basal body and manchette function during spermatogenesis and male fertilityCiliary proteins link basal body polarization to planar cell polarity regulationMutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.Primary cilia regulate Shh activity in the control of molar tooth numberNative polycystin 2 functions as a plasma membrane Ca2+-permeable cation channel in renal epitheliaCystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney diseaseThe mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterningMutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndromeMammalian Clusterin associated protein 1 is an evolutionarily conserved protein required for ciliogenesis.When cilia go bad: cilia defects and ciliopathiesThe vertebrate primary cilium in development, homeostasis, and disease
P2860
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P2860
Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
description
2001 nî lūn-bûn
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2001 թուականի Մարտին հրատարակուած գիտական յօդուած
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2001 թվականի մարտին հրատարակված գիտական հոդված
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2001年の論文
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2001年論文
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2001年論文
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2001年論文
@zh-hk
2001年論文
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2001年論文
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2001年论文
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name
Polaris, a protein involved in ...... izes to basal bodies and cilia
@ast
Polaris, a protein involved in ...... izes to basal bodies and cilia
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Polaris, a protein involved in ...... izes to basal bodies and cilia
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label
Polaris, a protein involved in ...... izes to basal bodies and cilia
@ast
Polaris, a protein involved in ...... izes to basal bodies and cilia
@en
Polaris, a protein involved in ...... izes to basal bodies and cilia
@nl
prefLabel
Polaris, a protein involved in ...... izes to basal bodies and cilia
@ast
Polaris, a protein involved in ...... izes to basal bodies and cilia
@en
Polaris, a protein involved in ...... izes to basal bodies and cilia
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P2093
P2860
P3181
P356
P1476
Polaris, a protein involved in ...... izes to basal bodies and cilia
@en
P2093
C J Haycraft
D F Balkovetz
P D Taulman
P2860
P304
P3181
P356
10.1091/MBC.12.3.589
P407
P577
2001-03-01T00:00:00Z