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科研机构
复旦大学上海医学院 [62]
内容类型
期刊论文 [55]
会议论文 [6]
图书章节 [1]
发表日期
2017 [62]
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共62条,第1-10条
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发表日期:2017
专题:复旦大学上海医学院
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Developmental validation of a custom panel including 273 SNPs for forensic application using Ion Torrent PGM
期刊论文
FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2017, 卷号: 27
作者:
Zhang, Suhua
;
Bian, Yingnan
;
Chen, Anqi
;
Zheng, Hancheng
;
Gao, Yuzhen
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2019/12/05
Forensic Genetics
Personal Genome Machine (PGM)
Massively Parallel Sequencing (MPS)
SNP
Profiling of plasma circulating miRNA in coronary heart disease patients detected by next-generation small RNA sequencing
期刊论文
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 卷号: 10, 期号: 5
作者:
Zhou, Zhiming
;
Chen, Jun
;
Wu, Taishun
;
Liu, Qingcheng
;
Song, Huiwen
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
miRNA
plasma
profiling
coronary heart disease
Genome-Wide Screen of DNA Methylation Changes Reveals GABBR2 as a Novel Potential Target for EGFR 19 Deletion Adenocarcinoma with Erlotinib
会议论文
作者:
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/05
epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI)
lung adenocarcinoma
methyl-sensitive cut counting sequencing (MSCC)
methylation
Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry
期刊论文
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2017, 卷号: 65, 期号: 5
作者:
Gong, Jing-Yu
;
Setchell, Kenneth D. R.
;
Zhao, Jing
;
Zhang, Wujuan
;
Wolfe, Brian
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
bile acid synthesis defect
bile alcohol
CYP27A1
mass spectrometry
next-generation sequencing
Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly
期刊论文
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 卷号: 18, 期号: 4
作者:
You, Guoling
;
Zu, Bailing
;
Wang, Bo
;
Wang, Zhigang
;
Xu, Yunlan
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
congenital contractural arachnodactyly
exome sequencing
fibrillin-2 (FBN2) gene
Variable-number tandem repeat markers for Mycobacterium intracellulare genotyping: comparison to the 16S rRNA gene sequencing
期刊论文
JOURNAL OF INFECTION IN DEVELOPING COUNTRIES, 2017, 卷号: 11, 期号: 2
作者:
Chen, Kaisen
;
Zhang, Yangyi
;
Peng, Yiping
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
nontuberculous mycobacterial
Mycobacterium intracellulare
16S rDNA sequencing
single-nucleotide polymorphism
variable-number tandem repeat genotype
Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype
期刊论文
HUMAN MUTATION, 2017, 卷号: 38, 期号: 12
作者:
Chen, Li
;
Jensik, Philip J.
;
Alaimo, Joseph T.
;
Walkiewicz, Magdalena
;
Berger, Seth
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
clinical exome sequencing (CES)
deformed epidermal autoregulatory factor-1 (DEAF1)
associated neurodevelopmental disorder (DAND)
intellectual disability (ID)
nuclear localization signal (NLS)
SAND
Identification of the key genes implicated in the transformation of OLP to OSCC using RNA-sequencing
期刊论文
ONCOLOGY REPORTS, 2017, 卷号: 37, 期号: 4
作者:
Yang, Qiaozhen
;
Guo, Bin
;
Sun, Hongying
;
Zhang, Jie
;
Liu, Shangfeng
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/05
oral lichen planus
oral squamous cell carcinoma
malignant transformation
RNA-sequencing
weighted gene co-expression network analysis
Next-generation sequencing revealed divergence in deletions of the preS region in the HBV genome between different HBV-related liver diseases
期刊论文
JOURNAL OF GENERAL VIROLOGY, 2017, 卷号: 98, 期号: 11
作者:
Jia, Jian'an
;
Liang, Xiaotao
;
Chen, Shipeng
;
Wang, Hui
;
Li, Huiming
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
Hepatitis B virus
variation
PreS
next generation sequencing
support vector machine
Hepatocellular carcinoma
Targeted bisulfite sequencing identified a panel of DNA methylation-based biomarkers for esophageal squamous cell carcinoma (ESCC)
期刊论文
CLINICAL EPIGENETICS, 2017, 卷号: 9
作者:
Pu, Weilin
;
Wang, Chenji
;
Chen, Sidi
;
Zhao, Dunmei
;
Zhou, Yinghui
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/05
Esophageal squamous cell carcinoma
DNA methylation
Biomarker
Diagnosis
Targeted bisulfite sequencing
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