Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1. - Wikidata - awgldk - TriplyDB

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

http://www.wikidata.org/entity/Q34050900

about

Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome Copy number loss upstream of RAI1 uncovers gene expression regulatory region that may impact Potocki-Lupski syndrome diagnosis.RAI1 gene mutations: mechanisms of Smith-Magenis syndrome.

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P2860

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

http://www.wikidata.org/entity/Q34050900

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@ast

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@en

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@nl

type

label

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@ast

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@en

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@nl

prefLabel

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@ast

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@en

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@nl

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JOURNAL.PONE.0105077

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P1476

Dietary regimens modify early onset of obesity in mice haploinsufficient for Rai1.

@en

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Joseph T Alaimo

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

Natalie C Hahn

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

Sarah H Elsea

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

Sureni V Mullegama

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P2860

Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

Genetic background modulates the phenotype of a mouse model of DYT1 dystonia

A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men

Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum

Smith-Magenis syndrome

Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome

Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike

Knockout mice: simple solutions to the problems of genetic background and flanking genes.

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e105077

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scholarly article

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10.1371/JOURNAL.PONE.0105077

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8

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haploinsufficiency

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