Use of human genetic variation to study membrane transport of amino acids in kidney.
作者信息
Scriver C R
出版信息
Am J Dis Child. 1969 Jan;117(1):4-12. doi: 10.1001/archpedi.1969.02100030006002.
Abstract
摘要
相似文献
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Use of human genetic variation to study membrane transport of amino acids in kidney.利用人类遗传变异研究肾脏中氨基酸的膜转运。
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Human genetics of membrane transport with emphasis on amino acids.
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Iminoaciduria.亚氨基酸尿症
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[Congenital metabolic inborn errors, with the exception of amino acid metabolism].[先天性代谢性遗传病，氨基酸代谢异常除外]
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Intravenous proline tolerance in a patient with hyperprolinaemia type II and his relatives.一名II型高脯氨酸血症患者及其亲属的静脉内脯氨酸耐受性
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Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes.肌氨酸血症和正常表型中肌氨酸的转运与代谢
J Clin Invest. 1971 Nov;50(11):2313-22. doi: 10.1172/JCI106729.
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Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney.上皮结构和细胞内代谢在PRO/re小鼠肾脏脯氨酸摄取和肾小管重吸收中的作用。
Proc Natl Acad Sci U S A. 1975 Apr;72(4):1431-5. doi: 10.1073/pnas.72.4.1431.
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