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SpringerLink电子期刊(4)
Elsevier电子期刊(11)
在“
Elsevier电子期刊
”中,
命中:
11
条,耗时:小于0.01 秒
在所有数据库中总计命中:
15
条
1.
Transcriptional profiling of the epigenetic regulator
Smchd1
作者:
Ruijie Liu
a
;
Kelan Chen
a
;
b
;
Natasha Jansz
a
;
b
;
Marnie E. Blewitt
a
;
b
;
blewitt@wehi.edu.au" class="auth_mail" title="E-mail the corresponding author
;
Matthew E. Ritchie
a
;
b
;
c
;
mritchie@wehi.edu.au" class="auth_mail" title="E-mail the corresponding author
关键词:
RNA-sequencing
;
voom
;
Sample variability
;
Epigenetics
刊名:Genomics Data
出版年:2016
2.
Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with
SMCHD1
mutations
作者:
Kohei Hamanaka
a
;
b
;
Kanako Goto
a
;
Mami Arai
a
;
Koji Nagao
c
;
Chikashi Obuse
c
;
Satoru Noguchi
a
;
d
;
Yukiko K. Hayashi
e
;
Satomi Mitsuhashi
a
;
smitsuhashi@ncnp.go.jp" class="auth_mail" title="E-mail the corresponding author
;
Ichizo Nishino
a
;
d
关键词:
Facioscapulohumeral muscular dystrophy 2
;
Structural maintenance of chromosomes flexible hinge domain containing 1
;
D4Z4
;
DNA methylation
;
Pyrosequence
刊名:Neuromuscular Disorders
出版年:2016
3.
A complex interplay of genetic and epigenetic events leads to abnormal expression of the DUX4 gene in facioscapulohumeral muscular dystrophy
作者:
Laura Virginia Gatica
a
;
1
;
Alberto Luis Rosa
a
;
b
;
c
;
alberto_l_rosa@yahoo.com.ar
关键词:
Facioscapulohumeral muscular dystrophy
;
FSHD1
;
FSHD2
;
DUX4
;
SMCHD1
刊名:Neuromuscular Disorders
出版年:2016
4.
Corrigendum to “Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with
SMCHD1
mutations”: [Neuromuscular Disorders 26/4-5 (2016) 300-308]
作者:
Kohei Hamanaka
a
;
b
;
Kanako Goto
a
;
Mami Arai
a
;
Koji Nagao
c
;
Chikashi Obuse
c
;
Satoru Noguchi
a
;
d
;
Yukiko K. Hayashi
e
;
Satomi Mitsuhashi
a
;
smitsuhashi@ncnp.go.jp" class="auth_mail" title="E-mail the corresponding author
;
Ichizo Nishino
a
;
d
刊名:Neuromuscular Disorders
出版年:2016
5.
A Tale of Two Cities: How Xist and its partners localize to and silence the bicompartmental X
作者:
Stefan F. Pinter
;
spinter@uchc.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
XCI
;
X chromosome inactivation
;
GRO-UP
;
Genome ReOrganization Upon Pluripotency-exit
;
ncRNA
;
non-coding RNA
;
Xi
;
inactive X
;
Xa
;
active X
;
RNAPII
;
RNA polymerase II
;
H2A
;
histone H2A
;
H3
;
histone 3
;
H4
;
histone 4
;
H2AK119ub
;
H2A lysine 119 mono-ubiquitination
;
H3K27me3
;
H3 lysine 27 tri-methylation
;
H4K20me1
;
H4 lysine 20 mono-methylation
;
H3K9me2/3
;
H3 lysine 9 di/tri-methylation
;
H3K4me3
;
H3 lysine 4 tri-methylation
;
H3K36me3
;
H3 lysine 36 tri-methylation
;
H3K27ac
;
H3 lysine 27 acetylation
;
H3
刊名:Seminars in Cell & Developmental Biology
出版年:2016
6.
Exome sequencing identifies a novel
SMCHD1
mutation in facioscapulohumeral muscular dystrophy 2
作者:
Satomi Mitsuhashi
;
Steven E. Boyden
;
Elicia A. Estrella
;
Takako I. Jones
;
Fedik Rahimov
;
Timothy W. Yu
;
Basil T. Darras
;
Anthony A. Amato
;
Rebecca D. Folkerth
;
Peter L. Jones
;
Louis M. Kunkel
;
Peter B. Kang
关键词:
Facioscapulohumeral muscular dystrophy 2
;
SMCHD1
;
DUX4
刊名:Neuromuscular Disorders
出版年:December, 2013
7.
Genetic and epigenetic contributors to FSHD
作者:
Lucia Daxinger
1
;
Stephen J Tapscott
2
;
Silvè
;
re M van der Maarel
1
;
maarel@lumc.nl" class="auth_mail" title="E-mail the corresponding author
刊名:Current Opinion in Genetics & Development
出版年:2015
8.
The FSHD2 Gene
SMCHD1
Is a Modifier of Disease Severity in Families Affected by FSHD1
作者:
Sabrina Sacconi
;
Richard?J.L.F. Lemmers
;
Judit Balog
;
Patrick?J. van?der?Vliet
;
Pauline Lahaut
;
Merlijn?P. van?Nieuwenhuizen
;
Kirsten?R. Straasheijm
;
Rashmie?D. Debipersad
;
Marianne Vos-Versteeg
;
Leonardo Salviati
;
Alberto Casarin
;
Elena Pegoraro
;
Rabi Tawil
;
Egbert Bakker
;
Stephen?J. Tapscott
;
Claude Desnuelle
;
Silv¨¨re?M. van?der?Maarel
刊名:The American Journal of Human Genetics
出版年:2013
9.
Smchd1
-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
作者:
Anne-Valerie Gendrel
;
Anwyn Apedaile
;
Heather Coker
;
Ausma Termanis
;
Ilona Zvetkova
;
Jonathan Godwin
;
Y.?Amy Tang
;
Derek Huntley
;
Giovanni Montana
;
Steven Taylor
;
Eleni Giannoulatou
;
Edith Heard
;
Irina Stancheva
;
Neil Brockdorff
刊名:Developmental Cell
出版年:2012
10.
G.I.1 New advances in facioscapulohumeral dystrophy
作者:
S.M. van der Maarel
刊名:Neuromuscular Disorders
出版年:2013
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