中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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CAS IR Grid
机构
金属研究所 [3]
物理研究所 [1]
上海药物研究所 [1]
上海应用物理研究所 [1]
上海生物化学与细胞生... [1]
采集方式
OAI收割 [7]
内容类型
期刊论文 [7]
发表日期
2019 [1]
2018 [3]
2009 [1]
2008 [1]
2004 [1]
学科主题
Oncology [1]
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Structural mechanism of the active bicarbonate transporter from cyanobacteria
期刊论文
OAI收割
NATURE PLANTS, 2019, 卷号: 5, 期号: 11, 页码: 1184-+
作者:
Wang, CC
;
Sun, B
;
Zhang, X
;
Huang, XW
;
Zhang, MH
  |  
收藏
  |  
浏览/下载:50/0
  |  
提交时间:2020/10/16
RENAL TUBULAR-ACIDOSIS
STAS DOMAIN
FUNCTIONAL-CHARACTERIZATION
INCREASE PHOTOSYNTHESIS
SULFATE TRANSPORTER
ANION TRANSPORTERS
CRYSTAL-STRUCTURE
MUTATIONS
MEMBRANE
FAMILY
Targeting HER2 Aberrations in Non-Small Cell Lung Cancer with Osimertinib
期刊论文
OAI收割
CLINICAL CANCER RESEARCH, 2018, 卷号: 24, 期号: 11, 页码: 2594-2604
作者:
Liu, Shengwu
;
Hai, Josephine
;
Wang, Xiaoen
;
Quinn, Max M.
;
Gao, Peng
  |  
收藏
  |  
浏览/下载:95/0
  |  
提交时间:2019/04/28
Receptor Tyrosine Kinase
Phase-ii Trial
Bromodomain Inhibition
Combination Therapy
Acquired-resistance
Domain Mutations
Bet Bromodomains
Breast-cancer
Egfr
Mutant
Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
期刊论文
OAI收割
SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953
作者:
Wang Rongrong
;
Yang Shuanghao
;
Xu Ming
;
Huang Jia
;
Liu Hongyan
  |  
收藏
  |  
浏览/下载:33/0
  |  
提交时间:2021/02/02
RED-CELL MEMBRANE
HEMATOLOGICALLY IMPORTANT MUTATIONS
RENAL TUBULAR-ACIDOSIS
HEMOLYTIC-ANEMIA
BETA-SPECTRIN
CYTOPLASMIC DOMAIN
BAND-3 DEFICIENCY
DISORDERS
ANKYRIN
VARIANTS
hereditary spherocytosis
mutation
ANK1
SPTB
SLC4A1
whole-exome sequencing
Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
期刊论文
OAI收割
SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953
作者:
Wang Rongrong
;
Yang Shuanghao
;
Xu Ming
;
Huang Jia
;
Liu Hongyan
  |  
收藏
  |  
浏览/下载:19/0
  |  
提交时间:2021/02/02
RED-CELL MEMBRANE
HEMATOLOGICALLY IMPORTANT MUTATIONS
RENAL TUBULAR-ACIDOSIS
HEMOLYTIC-ANEMIA
BETA-SPECTRIN
CYTOPLASMIC DOMAIN
BAND-3 DEFICIENCY
DISORDERS
ANKYRIN
VARIANTS
hereditary spherocytosis
mutation
ANK1
SPTB
SLC4A1
whole-exome sequencing
Functional implications of C-terminus of TBX5 with high homology to C-terminal domain of yeast DNA-directed RNA polymerase II largest subunit
期刊论文
OAI收割
CHINESE MEDICAL JOURNAL, 2008, 卷号: 121, 期号: 8, 页码: 762-765
作者:
Zhou Zhuren
;
Gong Liguo
;
Geng Wenqing
;
Qiu Guangrong
;
Sun Kailai
  |  
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2021/02/02
HOLT-ORAM-SYNDROME
WW DOMAIN
PHOSPHORYLATION
PREDICTION
MUTATIONS
SERVER
TBX5
Holt-Oram syndrome
computational biology
RNA polymerase II
The zinc finger motif of Escherichia coli RecQ is implicated in both DNA binding and protein folding
期刊论文
OAI收割
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 卷号: 279, 期号: 41, 页码: 42794
Liu, JL
;
Rigolet, P
;
Dou, SX
;
Wang, PY
;
Xi, XG
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2013/09/23
BLOOMS-SYNDROME GENE
SACCHAROMYCES-CEREVISIAE
CRYSTAL-STRUCTURES
FAMILY HELICASES
DOMAIN
MUTATIONS
MECHANISM
RECOMBINATION
REPLICATION
NUCLEOTIDES