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浏览/检索结果: 共6条，第1-6条 帮助 限定条件 发表日期：2019    内容类型：期刊论文     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Genetic variant in the promoter region of microRNA-137 reduces the warfarin maintenance dose in patients with atrial fibrillation 期刊论文 MOLECULAR MEDICINE REPORTS, 2019, 卷号: 19, 期号: 6 作者:  Wu, Donghui;  Tian, Zhen;  Yang, Yushuang;  Liu, Dongna;  Feng, Zhaohui 收藏  |  浏览/下载：38/0  |  提交时间：2019/12/05 genetic variant  VKORC1  promoter region  microRNA-137  warfarin maintenance dose  atrial fibrillation   Genetic polymorphisms in complement receptor 1 gene and its association with HBV-related liver disease: A case-control study 期刊论文 Gene, 2019, 卷号: Vol.688, 页码: 107-118 作者:  Jingrong Luo;  Siyuan Chen;  Jin Wang 收藏  |  浏览/下载：14/0  |  提交时间：2019/12/13 Complement  receptor  1  HBV-related  liver  disease  Genetic  variant  Single  nucleotide  polymorphism   Association of SMUG1 SNPs in Intron Region and Linkage Disequilibrium with Occurrence of Cervical Carcinoma and HPV Infection in Chinese Population. 期刊论文 Journal of Cancer, 2019, 卷号: Vol.10 No.1, 页码: 238-248 作者:  Feng Ye;  Hanzhi Wang;  Jia Liu;  Qi Cheng;  Xiaojing Chen 收藏  |  浏览/下载：9/0  |  提交时间：2019/12/13 CIN  III  SMUG1  cervical  squamous  cell  carcinoma  genetic  variant  intron  linkage  disequilibrium   Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China 期刊论文 2019, 卷号: 105, 期号: 4, 页码: 803-812 作者:  Dai Pu;  Huang Li-Hui;  Wang Guo-Jian;  Gao Xue;  Qu Chun-Yan 收藏  |  浏览/下载：37/0  |  提交时间：2020/01/03 aminoglycoside antibiotics  deafness genes  genetic deafness  habilitation  late-onset hearing loss  microarray  newborn genetic screening  newborn hearing screening  ototoxicity  pathogenic variant   Insights into genetics, human biology and disease gleaned from family based genomic studies 期刊论文 2019, 卷号: 21, 期号: 4, 页码: 798-812 作者:  Posey, Jennifer E.;  O'Donnell-Luria, Anne H.;  Chong, Jessica X.;  Harel, Tamar;  Jhangiani, Shalini N. 收藏  |  浏览/下载：28/0  |  提交时间：2020/01/03 rare variant phenotypes  Mendelian conditions  Centers for Mendelian Genomics (CMG)  genetic models for disease  disease traits   Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family 期刊论文 2019, 卷号: 46, 期号: 5, 页码: 413-417 作者:  Huang, Ye;  Cai, Chuan;  Ren, Li;  Cui, Caijuan;  Zhang, Xue 收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03 HR  fatty acid-binding protein 12  genetic variant  Marie Unna hereditary hypotrichosis  multiple familial trichoepithelioma