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内部出版物
CNKI学位论文(313)
知网期刊论文(234)
在“
Elsevier电子期刊
”中,
命中:
181
条,耗时:小于0.01 秒
在所有数据库中总计命中:
547
条
1.
Prenatal diagnosis of familial transmission of
17q12
microduplication associated with no apparent phenotypic abnormality
作者:
Chih-Ping Chen
a
;
b
;
c
;
d
;
e
;
f
;
cpc_mmh@yahoo.com
;
Chung-Hu Fu
g
;
Yi-Hui Lin
h
;
Schu-Rern Chern
b
;
Peih-Shan Wu
i
;
Yen-Ni Chen
a
;
Shin-Wen Chen
a
;
Wayseen Wang
b
;
j
关键词:
17q12
duplication
;
ACACA
;
HNF1B
;
LHX1
;
prenatal diagnosis
刊名:Taiwanese Journal of Obstetrics and Gynecology
出版年:2016
2.
Functional variants of
17q12
-21 are associated with allergic asthma but not allergic rhinitis
作者:
Anand Kumar Andiappan
;
PhD
a
;
b
;
Yang Yie Sio
;
BSc
b
;
Bernett Lee
;
PhD
a
;
Bani Kaur Suri
;
PhD
b
;
Sri Anusha Matta
;
BTech
b
;
Josephine Lum
;
BSc
a
;
Shihui Foo
;
BSc
a
;
Geraldine Koh
;
BSc
a
;
Jianjun Liu
;
PhD
c
;
Francesca Zolezzi
;
PhD
a
;
Michael Poidinger
;
PhD
a
;
De Yun Wang
;
MD
;
PhD
d
;
entwdy@nus.edu.sg" class="auth_mail" title="E-mail the corresponding author
;
Olaf Rotzschke
;
PhD
a
;
olaf_rotzschke@immunol.a-star.edu.sg" class="auth_mail" title="E-mail the corresponding author
;
Fook Tim Chew
;
PhD
b
;
dbscft@nus.edu.sg" class="auth_mail" title="E-mail the corresponding author
关键词:
ORMDL3
;
17q
21
;
allergic asthma
;
allergic rhinitis
;
Singapore Chinese
;
IgE
;
eosinophil counts
刊名:Journal of Allergy and Clinical Immunology
出版年:2016
3.
Polymorphisms and haplotypes of the chromosome locus
17q12
-
17q
21.1 contribute to adult asthma susceptibility in Slovenian patients
作者:
Mateja Žavbi
;
Peter Koro&scaron
;
ec
;
Matjaž Fležar
;
Sabina &Scaron
;
krgat Kristan
;
Mateja Marc Malovrh
;
Matija Rijavec
;
matija.rijavec@klinika-golnik.si" class="auth_mail" title="E-mail the corresponding author
关键词:
GWAS
;
genome-wide association study
;
SNP
;
single nucleotide polymorphism
;
CSF3
;
colony stimulating factor 3
;
ORMDL3
;
ORM1-like 3 (S. cerevisiae)
;
MED24
;
mediator complex subunit 24
;
GSDMA
;
gasdermin A
;
GSDMB
;
gasdermin B
;
PSMD3
;
proteasome non-ATPase regulatory subunit 3
;
ZBPB2
;
zona pellucida binding protein 2
;
LD
;
linkage disequilibrium
;
FEV1%
;
percentage of predicted forced expiratory volume in 1
s ;
VC%
;
percentage of lung vital capacity
;
PCR
;
polymerase chain reaction
;
ORs
;
odds ratios
刊名:Human Immunology
出版年:2016
4.
Microdélétion
17q12
et hernie diaphragmatique
作者:
Gaë
;
lle Salaü
;
n
a
;
gsalaun@chu-clermontferrand.fr" class="auth_mail" title="E-mail the corresponding author
;
Stephan Kemeny
a
;
Cé
;
line Pebrel-Richard
a
;
Elé
;
onore Eymard-Pierre
a
;
Laetitia Gouas
a
;
Fanny Laffargue
b
;
Hé
;
lè
;
ne Laurichesse
c
;
Philippe Vago
a
;
Carole Goumy
a
关键词:
Microdé
;
lé
;
tion
17q12
;
Hernie diaphragmatique congé
;
nitale
;
CGH array
刊名:Morphologie
出版年:2015
5.
Identification of a new locus at 16
q12
associated with time to asthma onset
作者:
Chloé
;
Sarnowski
;
PhD
a
;
b
;
Pierre-Emmanuel Sugier
;
MSc
a
;
b
;
Raquel Granell
;
PhD
c
;
Debbie Jarvis
;
MD
d
;
e
;
Marie-Hé
;
lè
;
ne Dizier
;
PhD
a
;
b
;
Markus Ege
;
MD
f
;
g
;
Medea Imboden
;
PhD
h
;
i
;
Catherine Laprise
;
PhD
j
;
Elza K. Khusnutdinova
;
PhD
k
;
l
;
Maxim B. Freidin
;
PhD
m
;
William O.C. Cookson
;
MD
;
DPhil
n
;
Miriam Moffatt
;
DPhil
n
;
Mark Lathrop
;
PhD
o
;
Valé
;
rie Siroux
;
PhD
p
;
q
;
r
;
Ludmila M. Ogorodova
;
MD
;
PhD
s
;
Alexandra S. Karunas
;
MD
;
PhD
k
;
l
;
Alan James
;
MD
t
;
Nicole M. Probst-Hensch
;
PhD
h
;
i
;
Erika von Mutius
;
MD
f
;
g
;
Isabelle Pin
;
MD
;
PhD
p
;
q
;
u
;
Manolis Kogevinas
;
MD
;
PhD
v
;
w
;
x
;
y
;
A. John Henderson
;
MD
c
;
Florence Demenais
;
MD
a
;
b
;
Emmanuelle Bouzigon
;
MD
;
PhD
a
;
b
;
emmanuelle.bouzigon@inserm.fr" class="auth_mail" title="E-mail the corresponding author
关键词:
Asthma
;
age of onset
;
genetics
;
genome-wide association study
;
survival analysis
;
conditional analysis
;
CYLD
;
NOD2
刊名:Journal of Allergy and Clinical Immunology
出版年:2016
6.
Treatment-Resistant Schizophrenia in a Patient With
17q12
Duplication
作者:
Maria Rogdaki
a
;
maria.rogdaki@kcl.ac.uk" class="auth_mail" title="E-mail the corresponding author
;
Sameer Jauhar
a
;
Robert McCutcheon
a
;
Oliver Howes
a
;
b
刊名:Biological Psychiatry
出版年:2016
7.
Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states
作者:
Javier Gonzá
;
lez-Peñ
;
as
a
;
Jorge Amigo
a
;
b
;
c
;
Luis Santomé
;
c
;
1
;
Beatriz Sobrino
a
;
b
;
c
;
Julio Brenlla
a
;
d
;
Santiago Agra
a
;
d
;
Eduardo Paz
a
;
d
;
Mario Pá
;
ramo
a
;
d
;
Á
;
ngel Carracedo
a
;
b
;
c
;
Manuel Arrojo
a
;
d
;
Javier Costas
a
;
javier.costas.costas@sergas.es" class="auth_mail" title="E-mail the corresponding author
关键词:
Next-generation sequencing
;
Polycomb
;
CNV
;
Single nucleotide variant
;
Rare variant
;
Chromatin remodeling
刊名:Schizophrenia Research
出版年:2016
8.
Acute promyelocytic leukemia with isochromosome
17q
and cryptic PML-RARA successfully treated with all-trans retinoic acid and arsenic trioxide
作者:
Daniel Shepshelovich
a
;
b
;
Shepshelovich@yahoo.com" class="auth_mail" title="E-mail the corresponding author
;
Nino Oniashvili
c
;
Doris Parnes
d
;
Alina Klein
a
;
Eli Muchtar
b
;
e
;
Josepha Yeshaya
c
;
Adina Aviram
d
;
Esther Rabizadeh
d
;
f
;
Pia Raanani
b
;
e
关键词:
APL
;
isochromosome
17q
;
ATRA
;
ATO
刊名:Cancer Genetics
出版年:2015
9.
Oesophageal atresia with tracheoesophageal fistula and anal atresia in a patient with a de novo microduplication in
17q12
作者:
Robert Smigiel
;
Carlo Marcelis
;
Dariusz Patkowski
;
Nicole de Leeuw
;
Damian Bednarczyk
;
Ewa Barg
;
Katarzyna Mascianica
;
M. Maria Sasiadek
;
Han Brunner
关键词:
Oesophageal atresia with tracheoesophageal fistula
;
Anal atresia
;
VATER association
;
17q12
microduplication
;
SNP array
刊名:European Journal of Medical Genetics
出版年:January, 2014
10.
Detection of recurrent transmission of
17q12
microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family
作者:
Chih-Ping Chen
;
Shuenn-Dyh Chang
;
Tzu-Hao Wang
;
Liang-Kai Wang
;
Jeng-Daw Tsai
;
Yu-Peng Liu
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Jun-Wei Su
;
Yu-Ting Chen
;
Wayseen Wang
关键词:
17q12
microdeletion
;
HNF1B
;
hydronephrosis
;
LHX1
;
multicystic kidney
刊名:Taiwanese Journal of Obstetrics and Gynecology
出版年:December, 2013
1
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4
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