A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
about
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesUsing regulatory and epistatic networks to extend the findings of a genome scan: identifying the gene drivers of pigmentation in merino sheepA Sox10 expression screen identifies an amino acid essential for Erbb3 function.Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseA suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.MMTV-Wnt1 and -DeltaN89beta-catenin induce canonical signaling in distinct progenitors and differentially activate Hedgehog signaling within mammary tumorsNetworks and pathways in pigmentation, health, and disease.The exon junction complex component Magoh controls brain size by regulating neural stem cell division.BRG1 interacts with SOX10 to establish the melanocyte lineage and to promote differentiationAllele-specific genetic interactions between Mitf and Kit affect melanocyte development.ENU Mutagenesis in the Mouse.Sox proteins in melanocyte development and melanoma.Modifier genes and the plasticity of genetic networks in mice.Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering.Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in miceThe EJC component Magoh regulates proliferation and expansion of neural crest-derived melanocytes.SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesisGenetic modifiers of neurological diseaseAnimal models of exfoliation syndrome, now and futureGenetic Modifier Screens in Mice.Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci.Advances in the molecular genetics of non-syndromic polydactyly.Generation of a Magoh conditional allele in mice.Gli3 is a negative regulator of Tas1r3-expressing taste cells.Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects.Whole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse
P2860
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P2860
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
description
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2008
@ast
im Juli 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/07/15)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/07/15)
@nl
наукова стаття, опублікована в липні 2008
@uk
مقالة علمية (نشرت في 15-7-2008)
@ar
name
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@ast
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@en
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@nl
type
label
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@ast
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@en
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@nl
prefLabel
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@ast
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@en
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@nl
P2093
P2860
P50
P356
P1476
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
@en
P2093
Arturo Incao
Cecelia Rivas
Debra L Silver
Eugene C Elliott
Ivana Matera
P2860
P304
P356
10.1093/HMG/DDN110
P577
2008-04-07T00:00:00Z