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Novel insertion in the TCOF1 gene and partial non-penetrance in a Chinese family with Treacher Collins syndrome 会议论文
定理临床学院(温州市中心医院), 2014浙江省医学会医学遗传学学术年会论文汇编
作者:  Yijian Mao;  Binjiao Zheng;  Yinyin Chen;  Xiangnan Chen;  Minxin Guan
收藏  |  浏览/下载:24/0  |  提交时间:2022/11/28
Mitochondrial Lon Protease and Cancer 期刊论文
Wenzhou Medical University School of Laboratory Medicine Attardi Institute of Mitochondrial Biomedicine, Advances in experimental medicine and biology, 2017, 卷号: 1038, 页码: 173-182
作者:  Lu, Bin
收藏  |  浏览/下载:17/0  |  提交时间:2023/12/14

New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population 中国人群中非综合征耳聋相关 MARVELD2 (DFNB49)基因新单核苷酸多态性位点分析 其他
Attardei线粒体研究院, Journal of Zhejiang University: Science B;, 2019, 卷号: 20, 期号: 2, 页码: 164-169
作者:  Zheng, Jing;  Meng, Wen-fang;  Zhang, Chao-fan;  Liu, Han-qing;  Yao, Juan
收藏  |  浏览/下载:56/0  |  提交时间:2023/12/08
The Mitochondrial tRNA(Phe) 625G>A Mutation in Three Han Chinese Families With Cholecystolithiasis 期刊论文
Wenzhou Medical University First Affiliated Hospital, FRONTIERS IN GENETICS, 2022, 卷号: 13, 页码: 814729
作者:  Hou, Lingling;  Hu, Cuifang;  Ji, Lili;  Wang, Qiongdan;  Liang, Min
收藏  |  浏览/下载:59/0  |  提交时间:2022/07/11

N-glycosylation stabilizes MerTK and promotes hepatocellular carcinoma tumor growth 期刊论文
Wenzhou Medical University School of Laboratory Medicine, REDOX BIOLOGY, 2022, 卷号: 54, 页码: 102366
作者:  Liu, Yongzhang;  Lan, Linhua;  Li, Yujie;  Lu, Jing;  He, Lipeng
收藏  |  浏览/下载:118/0  |  提交时间:2022/09/09

口腔黏膜拭子法可用于无创检测线粒体tRNAThr15927G>A突变 期刊论文
Attardei线粒体研究院, 南方医科大学学报, 2021, 卷号: 41, 期号: 01, 页码: 151-156
作者:  唐志宁;  唐霄雯;  薛凌;  管敏鑫
收藏  |  浏览/下载:85/0  |  提交时间:2022/04/04

New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population 其他
Wenzhou Medical University School of Laboratory Medicine Attardi Institute of Mitochondrial Biomedicine, JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2019, 卷号: 20, 期号: 2, 页码: 164-169
作者:  Zheng, Jing;  Meng, Wen-fang;  Zhang, Chao-fan;  Liu, Han-qing;  Yao, Juan
收藏  |  浏览/下载:42/0  |  提交时间:2022/03/30
Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A > G mutation 其他
Wenzhou Medical University, PROTEIN & CELL, 2015, 卷号: 6, 期号: 11, 页码: 844-848
作者:  Ying, Zhengbiao;  Zheng, Jing;  Cai, Zhaoyang;  Liu, Li;  Dai, Yu
收藏  |  浏览/下载:53/0  |  提交时间:2022/03/30
Mitochondria couple cellular Ca(2+) signal transduction 期刊论文
Wenzhou Medical University School of Laboratory Medicine Attardi Institute of Mitochondrial Biomedicine, Sheng li xue bao : [Acta physiologica Sinica], 2012, 卷号: 64, 期号: 3, 页码: 333-40.
作者:  Ya-Man Song;  Zhong-Qiu Lu;  Min-Xin Guan
收藏  |  浏览/下载:42/0  |  提交时间:2022/04/08
Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models 期刊论文
Wenzhou Medical University School of Laboratory Medicine Attardi Institute of Mitochondrial Biomedicine, Sheng li xue bao : [Acta physiologica Sinica], 2012, 卷号: 64, 期号: 4, 页码: 481-8.
作者:  Ling-Zhi Liang;  Bin-Jiao Zheng;  Jing Zheng;  Fang Fang;  Yue Wu
收藏  |  浏览/下载:38/0  |  提交时间:2022/04/08