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科研机构
山东大学 [239]
内容类型
期刊论文 [218]
会议论文 [21]
发表日期
2019 [38]
2018 [39]
2017 [27]
2016 [19]
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2014 [13]
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浏览/检索结果:
共239条,第1-10条
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专题:山东大学
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The immune response-related mutational signatures and driver genes in non-small-cell lung cancer
期刊论文
CANCER SCIENCE, 2019, 卷号: 110, 期号: 8, 页码: 2348-2356
作者:
Chen, Hao
;
Chong, Wei
;
Teng, Changcai
;
Yao, Yueliang
;
Wang, Xin
收藏
  |  
浏览/下载:19/0
  |  
提交时间:2019/12/11
APOBEC signature
immune checkpoint blockade
neoantigen burden
non-small-cell lung cancer
tumor mutation burden
Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification
期刊论文
HUMAN MUTATION, 2019, 卷号: 40, 期号: 4, 页码: 392-403
作者:
Guo, Xin-Xin
;
Zou, Xiao-Huan
;
Wang, Chong
;
Yao, Xiang-Ping
;
Su, Hui-Zhen
收藏
  |  
浏览/下载:136/0
  |  
提交时间:2019/12/11
primary familial brain calcification
PFBC
mutation spectrum
XPR1
functional assay
The diagnostic accuracy of circulating free DNA for the detection of KRAS mutation status in colorectal cancer: A meta-analysis
期刊论文
CANCER MEDICINE, 2019, 卷号: 8, 期号: 3, 页码: 1218-1231
作者:
Xie, Wenli
;
Xie, Li
;
Song, Xianrang
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/11
cfDNA
colorectal cancer
diagnostic
KRAS mutation
meta-analysis
Genotype-phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21-hydroxylase deficiency
期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 6
作者:
Xu, Chao
;
Jia, Wenyu
;
Cheng, Xiangdeng
;
Ying, Hui
;
Chen, Jing
收藏
  |  
浏览/下载:29/0
  |  
提交时间:2019/12/11
congenital adrenal hyperplasia (CAH)
CYP21A2
genotype-phenotype
associations
mutation
steroid 21-hydroxylase deficiency (21OHD)
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta
期刊论文
HUMAN MUTATION, 2019, 卷号: 40, 期号: 5, 页码: 588-600
作者:
Li, Lulu
;
Mao, Bin
;
Li, Shan
;
Xiao, Jifang
;
Wang, Han
收藏
  |  
浏览/下载:141/0
  |  
提交时间:2019/12/11
Chinese cohort
genomic rearrangements
genotype-phenotype correlations
mutation spectrum
osteogenesis imperfecta
Mutational spectrum and associations with clinical features in patients with acute myeloid leukaemia based on next-generation sequencing
期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 19, 期号: 5, 页码: 4147-4158
作者:
Li, Ying
;
Lv, Xiao
;
Ge, Xueling
;
Yuan, Dai
;
Ding, Mei
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2019/12/11
acute myeloid leukaemia
gene mutation
clinical feature
prognosis
overall survival
DNA methytransferase 3
CCAAT enhancer binding protein
SUVmax and metabolic tumor volume: surrogate image biomarkers of KRAS mutation status in colorectal cancer
期刊论文
ONCOTARGETS AND THERAPY, 2019, 卷号: 12, 页码: 2115-2121
作者:
Lv, Ying
;
Wang, Xin
;
Liang, Lerong
;
Wang, Lei
;
Lu, Jie
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2019/12/11
colorectal cancer
F-18-FDG PET/CT
SUVmax
SUVmean
MTV
KRAS mutation
The Role of HOX Transcription Factors in Cancer Predisposition and Progression
期刊论文
CANCERS, 2019, 卷号: 11, 期号: 4
作者:
Li, Bo
;
Huang, Qilai
;
Wei, Gong-Hong
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/11
HOX
cancer susceptibility
risk SNP
coding mutation
regulatory SNP
mechanism
Challenges and potential of PD-1/PD-L1 checkpoint blockade immunotherapy for glioblastoma 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis
期刊论文
Journal of Experimental and Clinical Cancer Research, 2019, 卷号: 38, 期号: 1
作者:
Wang X.
;
Guo G.
;
Guan H.
;
Yu Y.
;
Lu J.
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Glioblastoma multiforme
Nivolumab
Temozolomide
Tumour infiltrating lymphocytes
Tumour mutation load
Challenges and potential of PD-1/PD-L1 checkpoint blockade immunotherapy for glioblastoma
期刊论文
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2019, 卷号: 38
作者:
Wang, Xin
;
Guo, Gaochao
;
Guan, Hui
;
Yu, Yang
;
Lu, Jie
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2019/12/11
Glioblastoma multiforme
Nivolumab
Tumour infiltrating lymphocytes
Tumour mutation load
Temozolomide
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