Discovery Genetics - The History and Future of Spontaneous Mutation Research. - Wikidata - awgldk - TriplyDB

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

http://www.wikidata.org/entity/Q34432711

about

A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment The relevance of inter- and intrastrain differences in mice and rats and their implications for models of seizures and epilepsy.

P2860

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P2860

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

http://www.wikidata.org/entity/Q34432711

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@ast

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@en

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@nl

type

label

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@ast

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@en

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@nl

prefLabel

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@ast

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@en

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@nl

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9780470942390.MO110200

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Current protocols in mouse biology

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Discovery Genetics - The History and Future of Spontaneous Mutation Research.

@en

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David E Bergstrom

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

Laura G Reinholdt

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

Leah Rae Donahue

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

Muriel T Davisson

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

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Initial sequencing and comparative analysis of the mouse genome

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics

Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse

Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP

P304

103-118

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

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scholarly article

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10.1002/9780470942390.MO110200

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

P478

2

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2012-06-01T00:00:00Z

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25364627

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4215558

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