Cilia in cell signaling and human disorders. - Wikidata - wikimedia - TriplyDB

Cilia in cell signaling and human disorders.

Cilia in cell signaling and human disorders.

http://www.wikidata.org/entity/Q37825815

about

Rabin8 Protein Interacts with GTPase Rheb and Inhibits Phosphorylation of Ser235/Ser236 in Small Ribosomal Subunit Protein S6.Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry.Evolution of modular intraflagellar transport from a coatomer-like progenitor.Earliest ultrasound findings and description of splicing mutations in Meckel-Gruber syndrome.Sterol targeting drugs reveal life cycle stage-specific differences in trypanosome lipid rafts What are those cilia doing in the neural tube?Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome.Amyloid-β interrupts canonical Sonic hedgehog signaling by distorting primary cilia structure

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Cilia in cell signaling and human disorders.

http://www.wikidata.org/entity/Q37825815

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 28 August 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Cilia in cell signaling and human disorders.

@en

Cilia in cell signaling and human disorders.

@nl

type

label

Cilia in cell signaling and human disorders.

@en

Cilia in cell signaling and human disorders.

@nl

prefLabel

Cilia in cell signaling and human disorders.

@en

Cilia in cell signaling and human disorders.

@nl

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Cilia in cell signaling and human disorders.

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Jade Li

http://www.w3.org/2001/XMLSchema#string

Neil A Duldulao

http://www.w3.org/2001/XMLSchema#string

Zhaoxia Sun

http://www.w3.org/2001/XMLSchema#string

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Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity

Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

Motile cilia of human airway epithelia are chemosensory

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s13238-010-0098-7

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726-736

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scholarly article

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10.1007/S13238-010-0098-7

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8

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2010-08-28T00:00:00Z

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4875200

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