A mutation in the mouse Chd2 chromatin remodeling enzyme results in a complex renal phenotype.
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De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeThe role of epigenetics in the pathology of diabetic complicationsNew susceptibility loci associated with kidney disease in type 1 diabetes.Architects of the genome: CHD dysfunction in cancer, developmental disorders and neurological syndromesGenetics and genomics of autism spectrum disorder: embracing complexity.Epigenetics of diabetic complications.Catalog of mRNA expression patterns for DNA methylating and demethylating genes in developing mouse lower urinary tractTranscription-coupled recruitment of human CHD1 and CHD2 influences chromatin accessibility and histone H3 and H3.3 occupancy at active chromatin regionsGestational age-related patterns of AMOT methylation are revealed in preterm infant endothelial progenitors.Chromatin Remodeling Proteins in Epilepsy: Lessons From CHD2-Associated Epilepsy.
P2860
Q24600816-E594ED3B-F100-490F-881C-32E0C3524EA1Q24609124-6B8E821E-4E6F-4CF3-B9BB-E5BC1E535F7DQ29417066-53830B62-A788-4FD4-925C-6D4E3A3210F8Q34520690-D5C3570C-339F-480E-9421-68CB60A30BC6Q36363394-A36C0B7E-4C38-4C27-B6E3-7C9536950BEEQ37200532-8415F85B-EEC8-46CC-A67D-EFB161A57521Q37302747-B4E8A501-086D-4BAD-9E1F-36100AC2E3F8Q41814157-76B2E52E-77F0-47B7-9CE4-DA9DC22899C5Q42696297-18418DA2-C7DF-4503-B757-C482B3E8F546Q55353815-17752BE1-085A-467B-A89B-54664B32E185
P2860
A mutation in the mouse Chd2 chromatin remodeling enzyme results in a complex renal phenotype.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@ast
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@en
type
label
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@ast
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@en
prefLabel
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@ast
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@en
P2093
P2860
P356
P1476
A mutation in the mouse Chd2 c ...... in a complex renal phenotype.
@en
P2093
Anthony N Imbalzano
Concetta G A Marfella
David S Garlick
Lawrence B Holzman
Namrata Krishnan
Nils Henninger
Scott E LeBlanc
P2860
P304
P356
10.1159/000190788
P577
2008-01-01T00:00:00Z