The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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wetenschappelijk artikel

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наукова стаття, опублікована в березні 2013

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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The Bardet–Biedl and orofacial digital type 1 ciliopathies

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P1476

The Bardet–Biedl and orofacial digital type 1 ciliopathies

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P2093

Brunella Franco

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Nicholas Katsanis

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P2860

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

The Ciliopathies: An Emerging Class of Human Genetic Disorders

TCTN3 mutations cause Mohr-Majewski syndrome

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

BBS-induced ciliary defect enhances adipogenesis, causing paradoxical higher-insulin sensitivity, glucose usage, and decreased inflammatory response

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

Wnt-4 activates the canonical beta-catenin-mediated Wnt pathway and binds Frizzled-6 CRD: functional implications of Wnt/beta-catenin activity in kidney epithelial cells

BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes

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

P304

90-112

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P31

scholarly article

P356

10.2217/EBO.13.92

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P577

2013-03-01T00:00:00Z

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