Analysis of the Ush2a gene in medaka fish (Oryzias latipes). - Wikidata - wikimedia - TriplyDB

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

http://www.wikidata.org/entity/Q35005306

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A Synthetic Transcriptional Activator of Genes Associated with the Retina in Human Dermal Fibroblasts.

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Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

http://www.wikidata.org/entity/Q35005306

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2013 nî lūn-bûn

@nan

2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@ast

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@en

type

label

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@ast

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@en

prefLabel

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@ast

Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@en

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JOURNAL.PONE.0074995

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Analysis of the Ush2a gene in medaka fish (Oryzias latipes).

@en

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Ana V Sánchez-Sánchez

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Elena Aller

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Gema García-García

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José L Mullor

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José M Millán

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Laura Cavallé

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Manuel Díaz-Llopis

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Marina Piquer-Gil

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Patricia Udaondo

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P2860

Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

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

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Usherin expression is highly conserved in mouse and human tissues

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II

RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins

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e74995

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scholarly article

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10.1371/JOURNAL.PONE.0074995

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9

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8

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Antonio García-España

Javier U Chicote

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2013-09-23T00:00:00Z

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257302474

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24086419

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Japanese rice fish

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3781144

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