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浏览/检索结果: 共2条，第1-2条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择发表日期升序发表日期降序提交时间升序提交时间降序题名升序题名降序作者升序作者降序 Deleterious mutation V369M in the mouse GCGR gene causes abnormal plasma amino acid levels indicative of a possible liver & ndash;alpha-cell axis 期刊论文 BIOSCIENCE REPORTS, 2021, 卷号: 41, 期号: 6, 页码: 12 作者:  Liu, Qiaofeng;  Lin, Guangyao;  Chen, Yan;  Feng, Wenbo;  Xu, Yingna 收藏  |  浏览/下载：25/0  |  提交时间：2021/11/16 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：84/0  |  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)