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Elsevier电子期刊(10)
在“
Elsevier电子期刊
”中,
命中:
10
条,耗时:小于0.01 秒
在所有数据库中总计命中:
10
条
1.
SMC1A
recruits tumor-associated-fibroblasts (TAFs) and promotes colorectal cancer metastasis
作者:
Pengyang Zhou
a
;
1
;
Nan Xiao
a
;
1
;
Jian Wang
a
;
Zhanhuai Wang
a
;
Shuchun Zheng
a
;
Siyang Shan
a
;
Jianping Wang
b
;
Jinlin Du
b
;
Jianwei Wang
a
;
sypzju@zju.edu.cn
关键词:
SMC1A
;
Colorectal liver metastasis
;
Tumor-associated-fibroblasts
;
Tumorigenesis
;
Recruitment
刊名:Cancer Letters
出版年:2017
2.
Novel
SMC1A
frameshift mutations in children with developmental delay and epilepsy
作者:
Jessica H.R. Goldstein
a
;
1
;
Thipwimol Tim-aroon
b
;
1
;
Joseph Shieh
c
;
Michelle Merrill
b
;
Kristin K. Deeb
d
;
Shulin Zhang
d
;
Nancy E. Bass
a
;
Jirair K. Bedoyan
b
;
jirair.bedoyan@uhhospitals.org" class="auth_mail" title="E-mail the corresponding author
关键词:
Cornelia de Lange syndrome
;
SMC1A
;
Status epilepticus
;
Whole exome sequencing
刊名:European Journal of Medical Genetics
出版年:2015
3.
Cohesin mutations in human cancer
作者:
Victoria K. Hill
;
Jung-Sik Kim
;
Todd Waldman
关键词:
Cohesin
;
Cancer
;
STAG2
;
Urothelial carcinoma
;
Ewing sarcoma
;
Myeloid malignancy
刊名:Biochimica et Biophysica Acta (BBA)-Reviews on Cancer
出版年:2016
4.
Mutations of myelodysplastic syndromes (MDS): An update
作者:
Bani Bandana Ganguly
a
;
mgmgeneticlab@yahoo.com" class="auth_mail" title="E-mail the corresponding author
;
center.genetics@gmail.com" class="auth_mail" title="E-mail the corresponding author
;
N.N. Kadam
b
关键词:
Myelodysplastic syndromes
;
Mutations in pathway genes
;
Complex chromosomal aberration
;
Monosomal karyotype
;
EZH2/IDH inhibitors as drug targets
刊名:Mutation Research/Reviews in Mutation Research
出版年:2016
5.
Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotype
作者:
Cristina Gervasini
a
;
cristina.gervasini@unimi.it
;
Ilaria Parenti
a
;
Chiara Picinelli
b
;
Jacopo Azzollini
a
;
Maura Masciadri
b
;
Anna Cereda
c
;
Angelo Selicorni
c
;
Silvia Russo
b
;
Palma Finelli
b
;
d
;
Lidia Larizza
a
;
b
关键词:
CdLS
;
NIPBL deletion
;
Mosaicism
;
MLPA
;
FISH
;
Array-CGH
;
Deletion junction
刊名:European Journal of Medical Genetics
出版年:2013
6.
RAD21 Mutations Cause a Human Cohesinopathy
作者:
Matthew
;
A. Deardorff
1
;
2
;
deardorff@email.chop.edu
;
Jonathan
;
J. Wilde
1
;
Melanie Albrecht
3
;
Emma Dickinson
4
;
Stephanie Tennstedt
5
;
Diana Braunholz
3
;
Maren Mö
;
nnich
4
;
Yuqian Yan
6
;
Weizhen Xu
3
;
7
;
Marí
;
a
;
Concepcion Gil-Rodrí
;
guez
3
;
8
;
Dinah Clark
1
;
Hakon Hakonarson
1
;
2
;
9
;
Sara Halbach
10
;
Laura
;
Daniela Michelis
1
;
Abhinav Rampuria
1
;
Eva Rossier
11
;
Stephanie Spranger
12
;
Lionel Van
;
Maldergem
13
;
Sally
;
Ann Lynch
14
;
Gabriele Gillessen-Kaesbach
3
;
Hermann-Josef Lü
;
decke
15
;
Robert
;
G. Ramsay
6
;
16
;
Michael
;
J. McKay
17
;
18
;
Ian
;
D. Krantz
1
;
2
;
Huiling Xu
6
;
16
;
Julia
;
A. Horsfield
4
;
Frank
;
J. Kaiser
3
;
frank.kaiser@uk-sh.de
刊名:The American Journal of Human Genetics
出版年:2012
7.
Expression of cohesin and condensin genes during zebrafish development supports a non-proliferative role for cohesin
作者:
Maren Mö
;
nnich
;
Stephen Banks
;
Michael Eccles
;
Emma Dickinson
;
Julia Horsfield
关键词:
Sister chromatid cohesion
;
Cohesin
;
Condensin
;
Rad21
;
Scc1
;
Mcd1
;
Pds5
;
Smc1a
;
Smc3
;
Smc2
;
Smc4
;
Zebrafish
;
Cornelia de Lange syndrome
刊名:Gene Expression Patterns
出版年:2009
8.
Consequences of metaphase II oocyte cryopreservation on mRNA content
作者:
S. Chamayou
a
;
s.chamayou@yahoo.fr
;
G. Bonaventura
b
;
C. Alecci
a
;
D. Tibullo
c
;
F. Di Raimondo
c
;
A. Guglielmino
a
;
M.L. Barcellona
b
关键词:
Cryopreservation
;
Human
;
mRNA
;
Oocyte
;
Slow freezing
;
Vitrification
刊名:Cryobiology
出版年:2011
9.
Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL
作者:
Magdalena Ratajska
;
Jolanta Wierzba
;
Davut Pehlivan
;
Zhilian Xia
;
Ellen K. Brundage
;
Sau Wai Cheung
;
Pawel Stankiewicz
;
James R. Lupski
;
Janusz Limon
关键词:
Cornelia de Lange Syndrome
;
NIPBL
;
MLPA
;
aCGH
刊名:European Journal of Medical Genetics
出版年:2010
10.
Mutations in Cohesin Complex Members SMC3 and
SMC1A
Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation
作者:
Matthew A. Deardorff
;
Maninder Kaur
;
Dinah Yaeger
;
Abhinav Rampuria
;
Sergey Korolev
;
Juan Pie
;
Concepcion Gil-Rodrí
;
guez
;
Marí
;
a Arnedo
;
Bart Loeys
;
Antonie D. Kline
;
Meredith Wilson
;
Kaj Lillquist
;
Victoria Siu
;
Feliciano J. Ramos
;
Antonio Musio
;
Laird S. Jackson
;
Dale Dorsett
;
Ian D. Krant
刊名:The American Journal of Human Genetics
出版年:2007
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