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昆明动物研究所 [6]
厦门大学 [4]
海洋研究所 [4]
复旦大学上海医学院 [4]
南华大学 [2]
北京大学 [2]
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期刊论文 [52]
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浏览/检索结果:
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Defective EMC1 drives abnormal retinal angiogenesis via Wnt/b-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy
期刊论文
GENES & DISEASES, 2023, 卷号: 10, 期号: 6, 页码: 2572
作者:
Li, Shujin
;
Yang, Mu
;
Zhao, Rulian
;
Peng, Li
;
Liu, Wenjing
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2023/12/01
Rearrangement and domestication as drivers of Rosaceae mitogenome plasticity
期刊论文
BMC BIOLOGY, 2022, 卷号: 20, 期号: 1
作者:
Sun, Manyi
;
Zhang, Mingyue
;
Chen, Xuening
;
Liu, Yueyuan
;
Liu, Binbin
收藏
  |  
浏览/下载:0/0
  |  
提交时间:2024/03/07
Mitogenome
Rosaceae
Rearrangement rate
Domestication
Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene
期刊论文
VIRUS EVOLUTION, 2020, 卷号: 6, 期号: 2, 页码: 10
作者:
Wang, Huinan
;
Zhang, Libo
;
Shang, Yuanbin
;
Tan, Rongrong
;
Ji, Mingxiang
收藏
  |  
浏览/下载:293/0
  |  
提交时间:2021/05/24
porcine epidemic diarrhea virus
evolution
recombination
pathogenicity
spike gene
Novel homozygous ataxia-telangiectasia (A-T) mutated gene mutation identified in a Chinese pedigree with A-T
期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 20, 期号: 2
作者:
Hu, Huifang
;
Chen, Weicheng
;
Liu, Sida
;
Chen, Gang
;
Zhu, Shaicheng
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2019/12/05
ataxia-telangiectasia syndrome
whole-exome sequencing
ataxia-telangiectasia mutated gene
deletion variant
Genetic polymorphism analysis of mitochondrial DNA from Chinese Xinjiang Kazak ethnic group by a novel mitochondrial DNA genotyping panel
期刊论文
MOLECULAR BIOLOGY REPORTS, 2019, 卷号: 46, 期号: 1, 页码: 17-25
作者:
Xie, T
;
Hu, L
;
Guo, YX
;
Li, YC
;
Chen, F
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2019/09/10
The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine
期刊论文
MOLECULAR GENETICS AND METABOLISM REPORTS, 2018, 卷号: 17, 页码: 46-52
作者:
Li, Hong
;
Zhao, Lihua
;
Singh, Rani
;
Ham, J. Nina
;
Fadoju, Doris O.
收藏
  |  
浏览/下载:85/0
  |  
提交时间:2019/01/08
Glucagon receptor
Newborn screening
GCGR mutation
Hyperaminoacidemia
Mahvash disease
Pancreatic alpha cell hyperplasia (ACH)
Pancreatic neuroendocrine tumor (PNET)
Correcting genomic deletion calls with complex boundaries from next generation sequencing data
会议论文
作者:
Zhao, Zhongmeng
;
Tian, Zewen
;
Geng, Yu
;
He, Siyu
;
Zhang, Xuanping
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2019/11/19
next generation sequencing data analysis
tumor clonity
structural variant detection
genomic deletion with complex boundaries
Cancer genomics
PASA: Identifying More Credible Structural Variants of Hedou12
期刊论文
INTELLIGENT COMPUTING THEORIES AND APPLICATION, PT I, 2018, 卷号: 10954, 页码: 553-558
作者:
Jia, Huiqiang
;
Wei, Haichao
;
Zhu, Daming
;
Wang, Ruizhi
;
Feng, Haodi
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/11
Algorithm
Deletion
Insertion
Inversion
Structural variant
Clinical Implications of the BIM Deletion Polymorphism in Advanced Lung Adenocarcinoma Treated With Gefitinib
期刊论文
CLINICAL LUNG CANCER, 2018, 卷号: 19, 期号: 4, 页码: E431-E438
作者:
Yuan, Jupeng
;
Li, Bo
;
Zhang, Nasha
;
Zhu, Hui
;
Zhou, Liqing
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Apoptosis
Drug resistance
EGFR-TKI
Genetic variant
Survival
Brain-specific deletion of histone variant H2A.z results in cortical neurogenesis defects and neurodevelopmental disorder
期刊论文
NUCLEIC ACIDS RESEARCH, 2018, 卷号: 46, 期号: 5, 页码: 2290-2307
作者:
Tianjin Shen
;
Ji F(季芬)
;
Yuanyuan Wang
;
Xuepei Lei
;
Dongming Zhang
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/10/14
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