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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：2018     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 association between SHANK2 polymorphisms and susceptibility to autism spectrum disorder 期刊论文 IUBMB LIFE, 2018, 卷号: 70, 期号: 8 作者:  Bai, Ye;  Qiu, Shuang;  Li, Yan;  Li, Yong;  Zhong, Weijing 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05 autism spectrum disorder  SH3 and multiple ankyrin repeat domains protein 2  single nucleotide polymorphisms   The Transient Receptor Potential Ankyrin Type 1 Plays a Critical Role in Cortical Spreading Depression 期刊论文 NEUROSCIENCE, 2018, 卷号: 382, 页码: 23-34 作者:  Jiang, Liwen;  Wang, Yan;  Xu, Yuewei;  Ma, Dongqing;  Wang, Minyan 收藏  |  浏览/下载：3/0  |  提交时间：2019/11/26 migraine  mouse brain slice  cortical spreading depression  calcitonin-gene-related peptide  the transient receptor potential ankyrin type 1   Structural analyses of key features in the KANK1 center dot KIF21A complex yield mechanistic insights into the cross-talk between microtubules and the cell cortex 期刊论文 JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 卷号: 293, 期号: 1, 页码: 215-225 作者:  Weng, Zhuangfeng;  Yao, Deqiang;  Zhu, Jinwei;  Zhang, Rongguang;  Shang, Yuan 收藏  |  浏览/下载：33/0  |  提交时间：2019/04/28 Muscles Type-1 Cfeom1  Spindle Orientation  Congenital Fibrosis  Adhesion Dynamics  Kinesin Kif21a  Kank Proteins  Migration  Ends  Mutations  Actin   Ankyrin repeat domain 1 regulates innate immune responses against herpes simplex virus 1: A potential role in eczema herpeticum 期刊论文 2018, 卷号: 141, 期号: 6, 页码: 2085 作者:  Bin, Lianghua[1,2,3];  Li, Xiaozhao[1];  Richers, Brittany[1];  Streib, Joanne E.[1];  Hu, Jack W.[4] 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/10 Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang Rongrong;  Yang Shuanghao;  Xu Ming;  Huang Jia;  Liu Hongyan 收藏  |  浏览/下载：63/0  |  提交时间：2021/02/02 RED-CELL MEMBRANE  HEMATOLOGICALLY IMPORTANT MUTATIONS  RENAL TUBULAR-ACIDOSIS  HEMOLYTIC-ANEMIA  BETA-SPECTRIN  CYTOPLASMIC DOMAIN  BAND-3 DEFICIENCY  DISORDERS  ANKYRIN  VARIANTS  hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing   Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang Rongrong;  Yang Shuanghao;  Xu Ming;  Huang Jia;  Liu Hongyan 收藏  |  浏览/下载：6/0  |  提交时间：2021/02/02 RED-CELL MEMBRANE  HEMATOLOGICALLY IMPORTANT MUTATIONS  RENAL TUBULAR-ACIDOSIS  HEMOLYTIC-ANEMIA  BETA-SPECTRIN  CYTOPLASMIC DOMAIN  BAND-3 DEFICIENCY  DISORDERS  ANKYRIN  VARIANTS  hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing