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浏览/检索结果: 共3条，第1-3条 帮助 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 Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. 期刊论文 Neuromuscular disorders : NMD, 2019, 卷号: 29, 期号: 4 作者:  Tian Wo-Tu;  Luan Xing-Hua;  Zhou Hai-Yan;  Zhang Chao;  Huang Xiao-Jun 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06 Congenital disorder of glycosylation  Glycogen storage disease  PGM1  Whole exome sequencing   DFT investigation on the reaction mechanism catalyzed by alpha-phosphomannomutase1 in protonated/deprotonated states 期刊论文 journal of molecular modeling, 2011, 卷号: 17, 期号: 3, 页码: 577-585 作者:  Chu, Hui-Ying;  Zheng, Qing-Chuan;  Li, Xue;  Zhao, Yong-Shan;  Zhang, Ji-Long 收藏  |  浏览/下载：13/0  |  提交时间：2015/11/12 alpha-Phosphomannomutase1  Density functional theory  Molecular dynamics  Reaction pathway   Stability and splitting produces revealed by matrix-assisted laser desorption ionization-time of flight-mass Spectrometry in human serum transferrin 期刊论文 2007 Zhuo Hui-Qin; Jin Hong-Wei; Huang He-Qing; 黄河清; Huang Hui-Ying; 黄慧英; Cai ZongWei（Hong Kong Baptist University） 收藏  |  浏览/下载：3/0  |  提交时间：2011/08/22 human serum transferrin  matrix-assisted laser desorption ionization-time of fligth-mass spectrometry  enzymolysis out-gel  reversed phase high performance liquid chromatography  protein marker