Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10.
about
Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active X.Histone lysine demethylases in mammalian embryonic development.Cellular heterogeneity in the ureteric progenitor niche and distinct profiles of branching morphogenesis in organ development.Epigenetic restriction of extraembryonic lineages mirrors the somatic transition to cancer.A demethylation deficient isoform of the lysine demethylase KDM2A interacts with pericentromeric heterochromatin in an HP1a-dependent manner.
P2860
Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Abnormal X chromosome inactiva ...... tion after ablation of FBXL10.
@en
type
label
Abnormal X chromosome inactiva ...... tion after ablation of FBXL10.
@en
prefLabel
Abnormal X chromosome inactiva ...... tion after ablation of FBXL10.
@en
P2860
P1476
Abnormal X chromosome inactiva ...... ation after ablation of FBXL10
@en
P2093
John R Edwards
Timothy H Bestor
P2860
P2888
P356
10.1186/S13072-016-0069-1
P577
2016-05-31T00:00:00Z
P6179
1035241610