C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals. - Wikidata - wikimedia - TriplyDB

C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals.

C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals.

http://www.wikidata.org/entity/Q28000151

about

Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation A primer on the mouse basal body Human basal body basics Tau-tubulin kinase SAS-1 is a C2 domain protein critical for centriole integrity in C. elegans OFD1 and flotillins are integral components of a ciliary signaling protein complex organized by polycystins in renal epithelia and odontoblasts KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome New frontiers: discovering cilia-independent functions of cilia proteins Proteomic mapping of cytosol-facing outer mitochondrial and ER membranes in living human cells by proximity biotinylation From the cytoplasm into the cilium: bon voyage.Cep164 triggers ciliogenesis by recruiting Tau tubulin kinase 2 to the mother centriole.Ciliopathies: the trafficking connection.The cellular and molecular etiology of the craniofacial defects in the avian ciliopathic mutant talpid2.Using the avian mutant talpid2 as a disease model for understanding the oral-facial phenotypes of oral-facial-digital syndrome The essential roles of transition fibers in the context of cilia.Non-Overlapping Distributions and Functions of the VDAC Family in Ciliogenesis.Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function Utilizing the chicken as an animal model for human craniofacial ciliopathies.The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery.The hydrolethalus syndrome protein HYLS-1 regulates formation of the ciliary gate PCM1 Depletion Inhibits Glioblastoma Cell Ciliogenesis and Increases Cell Death and Sensitivity to Temozolomide.Open Sesame: How Transition Fibers and the Transition Zone Control Ciliary Composition.Centriole splitting caused by loss of the centrosomal linker protein C-NAP1 reduces centriolar satellite density and impedes centrosome amplification.Centrin 2 is required for mouse olfactory ciliary trafficking and development of ependymal cilia planar polarity.The centrosome duplication cycle in health and disease.TTBK2: a tau protein kinase beyond tau phosphorylation.Centrosome positioning in non-dividing cells.Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.Ciliopathies: Genetics in Pediatric Medicine.Binding to Cep164, but not EB1, is essential for centriolar localization of TTBK2 and its function in ciliogenesis.Primary Cilia and Mammalian Hedgehog Signaling.The serologically defined colon cancer antigen-3 (SDCCAG3) is involved in the regulation of ciliogenesis.Photoreceptor outer segment as a sink for membrane proteins: hypothesis and implications in retinal ciliopathies.Genes and molecular pathways underpinning ciliopathies.OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome.Mutations in C2CD3 cause oral-facial-digital syndrome through deregulation of centriole length.Anchoring of the basal body to the plasma membrane Building the right centriole for each cell type.Protein localization screening in vivo reveals novel regulators of multiciliated cell development and function.

P2860

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P2860

C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals.

http://www.wikidata.org/entity/Q28000151

description

2014 nî lūn-bûn

@nan

2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@ast

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@en

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@nl

type

label

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@ast

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@en

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@nl

altLabel

C2cd3 is critical for centriol ...... ary vesicle docking in mammals

@en

prefLabel

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@ast

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

@en

C2cd3 is critical for centriol ...... ry vesicle docking in mammals.

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PNAS.1318737111

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

C2cd3 is critical for centriol ...... ary vesicle docking in mammals

@en

P2093

Aimin Liu

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

Gang Ning

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

Huiqing Zeng

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

Jeremy F Reiter

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

P2860

Discovering regulators of centriole biogenesis through siRNA-based functional genomics in human cells

Primary ciliogenesis requires the distal appendage component Cep123.

Ofd1, a human disease gene, regulates the length and distal structure of centrioles

The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis

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

Centriole distal appendages promote membrane docking, leading to cilia initiation

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Molecular characterization of the 50-kD subunit of dynactin reveals function for the complex in chromosome alignment and spindle organization during mitosis

CCDC41 is required for ciliary vesicle docking to the mother centriole

The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia

P304

2164-2169

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scholarly article

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2112195

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10.1073/PNAS.1318737111

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6

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111

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24469809

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3926046

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