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中国医学科学院 北... [46]
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期刊论文 [39]
会议论文 [7]
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2019 [10]
2018 [11]
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专题:中国医学科学院 北京协和医学院
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Prevalence and clinical significance of pathogenic germline BRCA1/2 mutations in Chinese non-small cell lung cancer patients
期刊论文
2019, 卷号: 16, 期号: 3, 页码: 556-564
作者:
Hu Xingsheng
;
Yang Dongyong
;
Li Yalun
;
Li Li
;
Wang Yan
收藏
  |  
浏览/下载:53/0
  |  
提交时间:2020/01/03
BRCA1
BRCA2
Germline BRCA mutations
non-small cell lung cancer
prevalence
Germline and somatic mutations of multi-gene panel in Chinese patients with epithelial ovarian cancer: a prospective cohort study
期刊论文
2019, 卷号: 12, 期号: 1, 页码: 80
作者:
Li Wenhui
;
Shao Di
;
Li Lei
;
Wu Ming
;
Ma Shuiqing
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2020/01/03
Epithelial ovarian cancer
Germline mutation
Homologous recombination deficiency
Next-generation sequencing
Somatic mutation
Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China
期刊论文
2019, 卷号: 39, 期号: 1, 页码: 42
作者:
Chao, Xiaopei
;
Li, Lei
;
Wu, Ming
;
Ma, Shuiqing
;
Tan, Xianjie
收藏
  |  
浏览/下载:30/0
  |  
提交时间:2020/01/03
Endometrial carcinoma
Lynch syndrome
Immunohistochemistry
Microsatellite instability
Germline mutations
DNA mismatch repair genes
Patient-reported outcomes in patients with a germline BRCA mutation and HER2-negative metastatic breast cancer receiving olaparib versus chemotherapy in the OlympiAD trial
期刊论文
2019, 卷号: 120, 页码: 20-30
作者:
Robson Mark
;
Ruddy Kathryn J
;
Im Seock-Ah
;
Senkus Elżbieta
;
Xu Binghe
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2020/01/03
BRCA
Breast cancer
EORTC QLQ-C30
Health-related quality of life
Olaparib
OlympiAD
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome
期刊论文
2019, 卷号: 18, 期号: 2, 页码: 261-265
作者:
Baig, Shahid Mahmood
;
Fatima, Ambrin
;
Tariq, Muhammad
;
Khan, Tahir Naeem
;
Ali, Zafar
收藏
  |  
浏览/下载:31/0
  |  
提交时间:2020/01/03
Constitutional mismatch repair deficiency (CMMRD) syndrome
Hereditary brain tumor
Prenatal diagnosis
Genetic counseling
PMS2
MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations
期刊论文
2019, 卷号: 76, 页码: 70-75
作者:
McReynolds, Lisa J.
;
Yang, Yanqin
;
Wong, Hong Yuen
;
Tang, Jingrong
;
Zhang, Yubo
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2020/01/03
bone marrow failure
myelodysplastic syndrome
cytogenetics
molecular genetics
immunodeficiencies
infectious diseases
Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension
期刊论文
2019, 卷号: 53, 期号: 3
作者:
Wang, Xiao-Jian
;
Lian, Tian-Yu
;
Jiang, Xin
;
Liu, Shao-Fei
;
Li, Su-Qi
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  |  
浏览/下载:12/0
  |  
提交时间:2020/01/03
OlympiAD final overall survival and tolerability results: Olaparib versus chemotherapy treatment of physician's choice in patients with a germline BRCA mutation and HER2-negative metastatic breast cancer
期刊论文
2019, 卷号: 30, 期号: 4, 页码: 558-566
作者:
Robson, M. E.
;
Tung, N.
;
Conte, P.
;
Im, S-A
;
Senkus, E.
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2020/01/03
breast cancer
germline BRCA mutation
overall survival
PARP inhibitor
olaparib
tolerability
Germline mutation landscape of Chinese patients with familial breast/ovarian cancer in a panel of 22 susceptibility genes
期刊论文
2019, 卷号: 8, 期号: 5, 页码: 2074-2084
作者:
Wang, Jiayu
;
Li, Weiwei
;
Shi, Yujian
;
Huang, Yan
;
Sun, Tao
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2020/01/03
BRCA1
BRCA2
familial breast cancer
multigenes
novel mutation
Experiments that led to the first gene-edited babies: the ethical failings and the urgent need for better governance
期刊论文
2019, 卷号: 20, 期号: 1, 页码: 32-38
作者:
Li, Jing-ru
;
Walker, Simon
;
Nie, Jing-bao
;
Zhang, Xin-qing
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2020/01/03
Jian-kui HE
Human germline gene editing
Human immunodeficiency virus (HIV)
Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9
Ethical review
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