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知网期刊论文(23052)
在“
SpringerLink电子期刊
”中,
命中:
5,387
条,耗时:0.0929538 秒
在所有数据库中总计命中:
51,539
条
1.
Prognostic significance of IKZF1
deletion
in adult B cell acute lymphoblastic leukemia: a meta-
analysis
作者:
Wanhua Zhang
;
Pu Kuang
;
He Li
;
Fengjuan Wang
;
Yu Wang
关键词:
Acute lymphoblastic leukemia
;
IKZF1
;
Prognosis
;
Meta
;
analysis
刊名:Annals of Hematology
出版年:2017
2.
Genomic findings in patients with clinical suspicion of 22q11.2
deletion
syndrome
作者:
Magdalena Koczkowska
;
Jolanta Wierzba
;
Robert Śmigiel…
关键词:
22q11.2
deletion
syndrome
;
Array comparative genomic hybridization
;
17q21.31 micro
deletion
syndrome
;
NF1 microduplication syndrome
;
chromosome 6p25.3p25.2
deletion
;
NAALADL2
刊名:Journal of Applied Genetics
出版年:2017
3.
Genome-wide comparative
analysis
of
LEAFY
promoter sequence in angiosperms
作者:
Zhichao Sun
;
Zheng Li
;
Jianqin Huang…
关键词:
LFY genes
;
Promoter
;
Carya cathayensis
;
Sequence
analysis
;
Transient expression
;
Fluorometric
analysis
刊名:Physiology and Molecular Biology of Plants
出版年:2017
4.
Isolation and functional characterization of a novel stress inducible promoter from pigeonpea (
Cajanus cajan
L)
作者:
T. Srinath
;
V. D. Reddy
;
K. V. Rao
关键词:
Abiotic stress
;
Deletion
analysis
;
Genome walking
;
GUS activity
;
Hybrid proline
;
rich
;
protein gene
;
Transgenic Arabidopsis
刊名:Plant Cell, Tissue and Organ Culture (PCTOC)
出版年:2017
5.
A de novo 3p13
deletion
induced by a complex chromosomal rearrangement combined with a pericentric inversion of chromosome, inv(3)(p13q12), and a translocation between chromosome 3 and 8, t(3;8)(q13.1;q24.2), in a child with developmental delay
作者:
Kye Hee Cho
;
Sung Han Shim
;
MinYoung Kim
关键词:
De novo complex chromosomal rearrangement
;
Micro
deletion
;
Global developmental delay
;
Dysmorphism
刊名:Genes & Genomics
出版年:2017
6.
Notable Carrier Risks for Individuals Having Two Copies of
SMN1
in Spinal Muscular Atrophy Families with 2-copy Alleles: Estimation Based on Chinese Meta-
analysis
Data
作者:
Xianda Wei
;
Hu Tan
;
Pu Yang
;
Rui Zhang
;
Bo Tan
;
Yue Zhang…
关键词:
Spinal muscular atrophy
;
Genetic counseling
;
Carrier risks
刊名:Journal of Genetic Counseling
出版年:2017
7.
A novel
deletion
mutation in
IL2RG
gene results in X-linked severe combined immunodeficiency with an atypical phenotype
作者:
Wenjun Mou
;
Jianxin He
;
Xi Chen
;
Hui Zhang
;
Xiaoya Ren
;
Xunyao Wu
;
Xin Ni…
关键词:
Primary immunodeficiency diseases
;
Atypical SCID
;
IL2RG gene
X ;
linked SCID
;
Frameshift
;
Signal peptide
刊名:Immunogenetics
出版年:2017
8.
Global transcriptomic
analysis
of the response of
Corynebacterium glutamicum
to ferulic acid
作者:
Can Chen
;
Junfeng Pan
;
Xiaobing Yang
;
He Xiao
;
Yaoling Zhang…
关键词:
Corynebacterium glutamicum
;
Ferulic acid
;
KatA
;
SigE
;
Lignocellulosic biomass
刊名:Archives of Microbiology
出版年:2017
9.
Identification of Heterozygous Single- and Multi-exon
Deletion
s in
IL7R
by Whole Exome Sequencing
作者:
Karin R. Engelhardt
;
Yaobo Xu
;
Angela Grainger…
关键词:
IL7R
;
copy number variation
;
compound heterozygous
;
SCID
;
whole exome sequencing
刊名:Journal of Clinical Immunology
出版年:2017
10.
An improved parameterized algorithm for the
p
-cluster vertex
deletion
problem
作者:
Bang Ye Wu
;
Li-Hsuan Chen
关键词:
Parameterized algorithm
;
Exact algorithm
;
Cluster graph
;
Graph modification
刊名:Journal of Combinatorial Optimization
出版年:2017
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