Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa. - Wikidata - wikimedia - TriplyDB

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

http://www.wikidata.org/entity/Q33961074

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Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

http://www.wikidata.org/entity/Q33961074

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2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@ast

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@en

type

label

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@ast

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@en

prefLabel

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@ast

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@en

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978-1-4419-1399-9_62

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Advances in Experimental Medicine and Biology

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Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

@en

P2093

Catherine J Spellicy

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

Dong Xu

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

Garrett Cobb

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

Lizbeth Hedstrom

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Lori S Sullivan

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

Sara J Bowne

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

P2860

Inosine 5'-monophosphate dehydrogenase binds nucleic acids in vitro and in vivo

Autosomal dominant retinitis pigmentosa mutations in inosine 5'-monophosphate dehydrogenase type I disrupt nucleic acid binding

Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?

Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis

IMP dehydrogenase type 1 associates with polyribosomes translating rhodopsin mRNA

Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene

Retinal isoforms of inosine 5'-monophosphate dehydrogenase type 1 are poor nucleic acid binding proteins

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.

Two distinct cDNAs for human IMP dehydrogenase

Recombinant human inosine monophosphate dehydrogenase type I and type II proteins. Purification and characterization of inhibitor binding

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541-548

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scholarly article

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10.1007/978-1-4419-1399-9_62

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664

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Stephen P. Daiger

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2010-01-01T00:00:00Z

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20238057

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4113320

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