Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency.

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第一作者： Lindsay C,Burrage

第一单位： Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

作者： Lindsay C,Burrage ^[1] ; Simran,Madan ^[2] ; Xiaohui,Li ^[1] ; Saima,Ali ^[3] ; Mahmoud,Mohammad ^[1] ; Bridget M,Stroup ^[1] ; Ming-Ming,Jiang ^[4] ; Racel,Cela ^[5] ; Terry,Bertin ^[1] ; Zixue,Jin ^[1] ; Jian,Dai ^[1] ; Danielle,Guffey ^[1] ; Milton,Finegold ^[1] ; Members of the Urea Cycle Disorders Consortium (UCDC) ^[6] ; Sandesh,Nagamani ^[7] ; Charles G,Minard ^[8] ; Juan,Marini ^[1] ; Prakash,Masand ^[2] ; Deborah,Schady ^[7] ; Benjamin L,Shneider ^[4] ; Daniel H,Leung ^[9] ; Deeksha,Bali ^[10] ; Brendan,Lee ^[8]

作者单位： Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA. ^[1] Texas Children's Hospital, Houston, Texas, USA. ^[2] Interdepartmental Program in Translational Biology and Molecular Medicine and. ^[3] USDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA. ^[4] Department of Food Science and Nutrition, National Research Centre, Dokki, Giza, Egypt. ^[5] Department of Pediatrics, Duke Health, Durham, North Carolina, USA. ^[6] Dan L. Duncan Institute for Clinical and Translational Research and. ^[7] Department of Pathology, Baylor College of Medicine, Houston, Texas, USA. ^[8] Pediatric Critical Care Medicine, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA. ^[9] Edward B. Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, Texas, USA. ^[10] Section of Pediatric Gastroenterology, Hepatology, and Nutrition, Baylor College of Medicine, Houston, Texas, USA. ^[11]

关键词 Amino acid metabolism Glucose metabolism Hepatology Metabolism Mouse models

主题词丙氨酸转氨酶(Alanine Transaminase);动物(Animals);精氨基琥珀酸裂合酶(Argininosuccinate Lyase);慢性病(Chronic Disease);疾病模型, 动物(Disease Models, Animal);人类(Humans);肝疾病(Liver Diseases);肝糖原(Liver Glycogen);纵向研究(Longitudinal Studies);小鼠(Mice);尿素循环障碍, 先天性(Urea Cycle Disorders, Inborn)

DOI 10.1172/jci.insight.132342

PMID 31990680

发布时间 2024-03-16

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Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency.

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Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency.

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