Cloning and characterization of a novel alternatively spliced transcript of the human CHD7 putative helicase.
about
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.Chromatin remodeling by the CHD7 protein is impaired by mutations that cause human developmental disorders.Identification of CHD7S as a novel splicing variant of CHD7 with functions similar and antagonistic to those of the full-length CHD7L.Enhanced Proteolytic Processing of Recombinant Human Coagulation Factor VIII B-Domain Variants by Recombinant Furins.Differentiation potential of Pluripotent Stem Cells correlates to the level of CHD7.
P2860
Cloning and characterization of a novel alternatively spliced transcript of the human CHD7 putative helicase.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին 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
Cloning and characterization o ...... human CHD7 putative helicase.
@ast
Cloning and characterization o ...... human CHD7 putative helicase.
@en
type
label
Cloning and characterization o ...... human CHD7 putative helicase.
@ast
Cloning and characterization o ...... human CHD7 putative helicase.
@en
prefLabel
Cloning and characterization o ...... human CHD7 putative helicase.
@ast
Cloning and characterization o ...... human CHD7 putative helicase.
@en
P2093
P2860
P356
P1433
P1476
Cloning and characterization o ...... e human CHD7 putative helicase
@en
P2093
Christian Colin
Flávia S Tobaruella
Marcos A Demasi
P2860
P2888
P356
10.1186/1756-0500-3-252
P577
2010-10-06T00:00:00Z
P5875
P6179
1026487350