Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

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Protective effect of paraoxonase 1 gene variant Gln192Arg in age-related macular degeneration A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity A large scale screen for neural stem cell markers in Xenopus retina.

P2860

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P2860

Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

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http://www.wikidata.org/entity/Q42576060

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2006 nî lūn-bûn

@nan

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

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2006年论文

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2006年论文

@zh-cn

name

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@en

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@nl

type

Item

label

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@en

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@nl

prefLabel

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@en

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@nl

P1476

Mutation screen of the TUB gen ...... nd Leber congenital amaurosis.

@en

P2093

Elias I Traboulsi

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Gayle J T Pauer

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

Quansheng Xi

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

Stephanie A Hagstrom

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

P2860

GFP-tagged expression and immunohistochemical studies to determine the subcellular localization of the tubby gene family members

G-protein signaling through tubby proteins

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

Implication of tubby proteins as transcription factors by structure-based functional analysis

Tyrosine phosphorylation of tub and its association with Src homology 2 domain-containing proteins implicate tub in intracellular signaling by insulin

A candidate gene for the mouse mutation tubby

Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family

Cochlear and retinal degeneration in the tubby mouse

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene

P304

569-573

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scholarly article

P356

10.1016/J.EXER.2006.02.003

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P433

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P478

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2006-04-27T00:00:00Z

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7137117

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16643894

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P921

birth defect

P932

3023989

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Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

about

P2860

P2860

Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P932