DNMT1 mutations found in HSANIE patients affect interaction with UHRF1 and neuronal differentiation.
about
Association of DNMT3b gene variants with sporadic Parkinson's disease in a Chinese Han population.Structural and mechanistic insights into UHRF1-mediated DNMT1 activation in the maintenance DNA methylation.DNA Methyltransferases, DNA Methylation, and Age-Associated Cognitive Function.Critical Role of the UBL Domain in Stimulating the E3 Ubiquitin Ligase Activity of UHRF1 toward Chromatin
P2860
DNMT1 mutations found in HSANIE patients affect interaction with UHRF1 and neuronal differentiation.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@en
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@nl
type
label
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@en
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@nl
prefLabel
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@en
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@nl
P2093
P2860
P356
P1476
DNMT1 mutations found in HSANI ...... and neuronal differentiation.
@en
P2093
Daniela Meilinger
Heinrich Leonhardt
Katrin Schneider
Martha Smets
Patricia Wolf
Stephanie Link
Veronica Solis
Weihua Qin
P2860
P304
P356
10.1093/HMG/DDX057
P50
P577
2017-03-03T00:00:00Z