Ftm is a novel basal body protein of cilia involved in Shh signalling
about
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeA meckelin-filamin A interaction mediates ciliogenesisTMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zoneMutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamicsFunctional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteinsLoss 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 formationOFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilinDisruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromeThe Hedgehog gene family of the cnidarian, Nematostella vectensis, and implications for understanding metazoan Hedgehog pathway evolutionThe cilia-regulated proteasome and its role in the development of ciliopathies and cancerIns and outs of GPCR signaling in primary ciliaThe role of primary cilia in the development and disease of the retinaThe base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalizationCilia in vertebrate development and diseasePrimary cilia in the developing and mature brainMouse models of ciliopathies: the state of the art.The nonmotile ciliopathies.A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.The Role of RPGR and Its Interacting Proteins in CiliopathiesDisruption of a ciliary B9 protein complex causes Meckel syndromeTHM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in ciliaMouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathwayA mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signalingBroad-minded links cell cycle-related kinase to cilia assembly and hedgehog signal transductionDishevelled stabilization by the ciliopathy protein Rpgrip1l is essential for planar cell polarityArl13b regulates ciliogenesis and the dynamic localization of Shh signaling proteinsAhi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle traffickingGeneration of mice with functional inactivation of talpid3, a gene first identified in chickenThe primary cilium: a signalling centre during vertebrate developmentThe vertebrate primary cilium in development, homeostasis, and diseaseJoubert syndrome: insights into brain development, cilium biology, and complex disease.Regulation of Fto/Ftm gene expression in mice and humans.The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate.Role of primary cilia in brain development and cancerPrimary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool.The genetics of obesity: FTO leads the way.CSPP is a ciliary protein interacting with Nephrocystin 8 and required for cilia formation.Hypomorphism for RPGRIP1L, a ciliary gene vicinal to the FTO locus, causes increased adiposity in mice.Ciliopathies: the trafficking connection.
P2860
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P2860
Ftm is a novel basal body protein of cilia involved in Shh signalling
description
2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2007
@ast
im Juli 2007 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2007/07/01)
@sk
vědecký článek publikovaný v roce 2007
@cs
wetenschappelijk artikel (gepubliceerd op 2007/07/01)
@nl
наукова стаття, опублікована в липні 2007
@uk
مقالة علمية (نشرت في يوليو 2007)
@ar
name
Ftm is a novel basal body protein of cilia involved in Shh signalling
@ast
Ftm is a novel basal body protein of cilia involved in Shh signalling
@en
Ftm is a novel basal body protein of cilia involved in Shh signalling
@nl
type
label
Ftm is a novel basal body protein of cilia involved in Shh signalling
@ast
Ftm is a novel basal body protein of cilia involved in Shh signalling
@en
Ftm is a novel basal body protein of cilia involved in Shh signalling
@nl
prefLabel
Ftm is a novel basal body protein of cilia involved in Shh signalling
@ast
Ftm is a novel basal body protein of cilia involved in Shh signalling
@en
Ftm is a novel basal body protein of cilia involved in Shh signalling
@nl
P2093
P3181
P356
P1433
P1476
Ftm is a novel basal body protein of cilia involved in Shh signalling
@en
P2093
Baolin Wang
Jeanette Vierkotten
Renate Dildrop
Thomas Peters
Ulrich Rüther
P304
P3181
P356
10.1242/DEV.003715
P407
P577
2007-07-01T00:00:00Z