Language
English
German
^M
Dutch
Spanish
Title:
Generation of a transgene-free iPSC line and genetically modified line from a facioscapulohumeral muscular dystrophy type 2 (FSHD2) patient with SMCHD1 p.Lys607Ter mutation
Source:
Stem Cell Research [1873-5061] Sasaki Honda, Mitsuru yr:2020
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
"Smchd1 is a maternal effect gene required for genomic imprinting."
ELife.
9.
description
2.
"Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in Humans."
Genetics.
213.2: 685-703.
description
3.
"The variability of SMCHD1 gene in FSHD patients: evidence of new mutations."
Human molecular genetics.
28.23: 3912-.
description
4.
Jansz, N.
"Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters."
Nature structural & molecular biology.
25.9: 766-777.
Select All
Clear All
Save Citations
Select Format
RefWorks
EndNote
ProCite
Reference Manager
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Sasaki Honda, Mitsuru
Kagita, Akihiro
Jonouchi, Tatsuya
Araki, Toshiyuki
Hotta, Akitsu
Sakurai, Hidetoshi
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Sasaki Honda, Mitsuru
Kagita, Akihiro
Jonouchi, Tatsuya
Araki, Toshiyuki
Hotta, Akitsu
Sakurai, Hidetoshi
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.