New frontiers: discovering cilia-independent functions of cilia proteins - Test2 - elhamkhani - TriplyDB

New frontiers: discovering cilia-independent functions of cilia proteins

New frontiers: discovering cilia-independent functions of cilia proteins

http://www.wikidata.org/entity/Q28081713

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Human basal body basics Current topics of functional links between primary cilia and cell cycle Centrosomal clustering contributes to chromosomal instability and cancer.Mechanisms of ciliogenesis suppression in dividing cells Functional Diversity of Ciliary Proteins in Bone Development and Disease.Nuclear roles for cilia-associated proteins.Fixation methods can differentially affect ciliary protein immunolabeling.Interkinetic nuclear migration in the mouse embryonic ureteric epithelium: Possible implication for congenital anomalies of the kidney and urinary tract.Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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New frontiers: discovering cilia-independent functions of cilia proteins

http://www.wikidata.org/entity/Q28081713

description

2015 nî lūn-bûn

@nan

2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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New frontiers: discovering cilia-independent functions of cilia proteins

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Alison Bright

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

Anastassiia Vertii

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Benedicte Delaval

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Stephen Doxsey

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P2860

The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex

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

The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

Ccdc13 is a novel human centriolar satellite protein required for ciliogenesis and genome stability

Cep164, a novel centriole appendage protein required for primary cilium formation

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

ATM substrate Chk2-interacting Zn2+ finger (ASCIZ) Is a bi-functional transcriptional activator and feedback sensor in the regulation of dynein light chain (DYNLL1) expression

Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy

Mutation of POC1B in a severe syndromic retinal ciliopathy

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1275-1287

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scholarly article

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10.15252/EMBR.201540632

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26358956

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