CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations.
about
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic DystrophyRecent advances in assays for the fragile X-related disorders.Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome.Targeted Reactivation of Transcription in Fragile X Syndrome Embryonic Stem Cells
P2860
CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@en
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@nl
type
label
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@en
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@nl
prefLabel
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@en
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@nl
P2093
P2860
P1433
P1476
CGG Repeat-Induced FMR1 Silenc ...... g Unmethylated Full Mutations.
@en
P2093
Anke Thiemeyer
Baltazar Gomez-Mancilla
Carole Manneville
Edward J Oakeley
Eline Pecho-Vrieseling
Elisabetta Tabolacci
Francesco Paolo Di Giorgio
Giovanni Neri
Guglielmo Roma
Isabelle Fruh
P2860
P304
P356
10.1016/J.STEMCR.2016.10.004
P577
2016-11-08T00:00:00Z