The Role of RPGR and Its Interacting Proteins in Ciliopathies - Wikidata - wikimedia - TriplyDB

The Role of RPGR and Its Interacting Proteins in Ciliopathies

The Role of RPGR and Its Interacting Proteins in Ciliopathies

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Specialized Cilia in Mammalian Sensory Systems Retinal transcriptome sequencing sheds light on the adaptation to nocturnal and diurnal lifestyles in raptors A method for isolation of cone photoreceptors from adult zebrafish retinae Molecular studies of phenotype variation in canine RPGR-XLPRA1.Rpgrip1 is required for rod outer segment development and ciliary protein trafficking in zebrafish.Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice.RPGR protein complex regulates proteasome activity and mediates store-operated calcium entry.

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

http://www.wikidata.org/entity/Q28081883

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2015 nî lūn-bûn

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2015 թուականին հրատարակուած գիտական յօդուած

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2015 թվականին հրատարակված գիտական հոդված

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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name

The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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type

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

@en

The Role of RPGR and Its Interacting Proteins in Ciliopathies

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Journal of Ophthalmology

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The Role of RPGR and Its Interacting Proteins in Ciliopathies

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Rakesh Kotapati Raghupathy

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Sarita Rani Patnaik

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Xun Zhang

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Retinitis pigmentosa

The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase

Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin

RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin

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

Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina

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

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

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414781

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scholarly article

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2653670

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10.1155/2015/414781

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2015

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David Mansfield

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2015-01-01T00:00:00Z

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26124960

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4466403

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