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科研机构
复旦大学上海医学... [124]
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期刊论文 [114]
会议论文 [10]
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2019 [14]
2018 [13]
2017 [13]
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专题:复旦大学上海医学院
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Chinese Society of Clinical Oncology (CSCO) diagnosis and treatment guidelines for colorectal cancer 2018
期刊论文
CHINESE JOURNAL OF CANCER RESEARCH, 2019, 卷号: 31, 期号: 1
作者:
Zhang, Zhen
;
Zhang, Suzhan
;
Li, Jin
;
Cai, Sanjun
;
Xu, Ruihua
收藏
  |  
浏览/下载:39/0
  |  
提交时间:2019/12/05
Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract
期刊论文
MOLECULAR GENETICS AND GENOMICS, 2019, 卷号: 294, 期号: 2
作者:
Yang, Nan
;
Song, Chengcheng
;
Xu, Hong
;
Zhang, Feng
;
Wang, Hongyan
收藏
  |  
浏览/下载:33/0
  |  
提交时间:2019/12/05
CAKUT
Gene dosage
Noncoding variant
TBX6
Delivery of Glucosylceramidase Beta Gene Using AAV9 Vector Therapy as a Treatment Strategy in Mouse Models of Gaucher Disease
期刊论文
HUMAN GENE THERAPY, 2019, 卷号: 30, 期号: 2
作者:
Jiang, Nan
;
Du, Sichen
;
Ou, Huayuan
;
Cui, Renjie
;
Zhang, Meiqin
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/12/05
Gaucher disease
gene therapy
AAV9
GD mouse model
Mobile Health (mHealth) technology for improved screening, patient involvement and optimising integrated care in atrial fibrillation: The mAFA (mAF-App) II randomised trial
期刊论文
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2019, 卷号: 73, 期号: 7
作者:
Guo, Yutao
;
Lane, Deirdre A.
;
Wang, Liming
;
Chen, Yundai
;
Lip, Gregory Y. H.
收藏
  |  
浏览/下载:63/0
  |  
提交时间:2019/12/05
Predictive factors of early recurrence after R0 resection of hilar cholangiocarcinoma: A single institution experience in China
期刊论文
CANCER MEDICINE, 2019, 卷号: 8, 期号: 4
作者:
Hu, Hai-Jie
;
Jin, Yan-Wen
;
Shrestha, Anuj
;
Ma, Wen-Jie
;
Wang, Jun-Ke
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  |  
浏览/下载:22/0
  |  
提交时间:2019/12/05
early recurrence
hilar cholangiocrcinoma
prognosis
survival
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
期刊论文
GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 7
作者:
Liu, Jiaqi
;
Wu, Nan
;
Yang, Nan
;
Takeda, Kazuki
;
Chen, Weisheng
收藏
  |  
浏览/下载:63/0
  |  
提交时间:2019/12/05
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway
期刊论文
FEBS LETTERS, 2019, 卷号: 593, 期号: 15
作者:
Xia, Wenjun
;
Hu, Jiongjiong
;
Ma, Jing
;
Huang, Jianbo
;
Jing, Tianrui
收藏
  |  
浏览/下载:31/0
  |  
提交时间:2019/12/05
deafness genes
nonsyndromic hearing loss
PI3K-Akt signalling pathway
TOP2B
zebrafish
The size and depth of lesions measured by endoscopic ultrasonography are novel prognostic factors of primary gastric diffuse large B-cell lymphoma
期刊论文
LEUKEMIA & LYMPHOMA, 2019, 卷号: 60, 期号: 4
作者:
Liu, Yi-Zhen
;
Xue, Kai
;
Wang, Bo-Shi
;
Li, Chun-Yan
;
Lv, Fang-Fang
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
Primary gastric diffuse large B-cell lymphoma
endoscopic ultrasound
prognosis
Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis
期刊论文
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2019, 卷号: 23, 期号: 6
作者:
Hao, Lili
;
Li, Shanshan
;
Ma, Duan
;
Chen, Shiyu
;
Zhang, Bowen
收藏
  |  
浏览/下载:16/0
  |  
提交时间:2019/12/05
ANK1
hereditary spherocytosis
in vitro experiment
mutation
NGS
FDG-PET as an independent biomarker for Alzheimer's biological diagnosis: a longitudinal study
期刊论文
ALZHEIMERS RESEARCH & THERAPY, 2019, 卷号: 11
作者:
Ou, Ya-Nan
;
Xu, Wei
;
Li, Jie-Qiong
;
Guo, Yu
;
Cui, Mei
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2019/12/05
F-18-Fluorodeoxyglucose positron emission tomography (FDG-PET)
Alzheimer's disease
ATN profile
Biomarker
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