Phenylalanine metabolism 青云英语翻译 请在下面的文本框内输入文字,然后点击开始翻译按钮进行翻译,如果您看不到结果,请重新翻译! 翻译结果1翻译结果2翻译结果3翻译结果4翻译结果5 翻译结果1复制译文编辑译文朗读译文返回顶部 苯丙氨酸代谢 翻译结果2复制译文编辑译文朗读译文返回顶部...
phenylalanine metabolism 苯丙氨酸正常代谢产生酪氨酸。在患有苯酮尿的儿童体内缺少这种代谢的酶,而使积蓄于体内的L-苯丙氨酸被转换为丙酮酸在尿中排出。 苯丙氨酸(英文名:L-Phenylalanine)为无色至白色片状晶体或白色结晶性粉末,是一种营养增补剂,是必需氨基酸之一。在体内大部分经苯丙氨酸羟化酶催化作用氧化成酪...
求翻译:Phenylalanine metabolism是什么意思?待解决 悬赏分:1 - 离问题结束还有 Phenylalanine metabolism问题补充:匿名 2013-05-23 12:21:38 苯丙氨酸代谢 匿名 2013-05-23 12:23:18 氨基苯基丙酸新陈代谢 匿名 2013-05-23 12:24:58 氨基苯基丙酸新陈代谢 匿名 2013-05-23 12:26:38 苯丙氨酸...
Phenylalanine metabolism in uremic and normal man. The metabolism of phenylalanine and tyrosine was evaluated in six normal men, five chronically uremic men, and three men undergoing maintenance hemodialysis. Phenylalanine, tyrosine, and 13 acidic metabolites of those amino acids were measured in plasma...
Discussion: Given that these metabolites are precursors to several other metabolic pathways, the intensities of many metabolites such as dopamine, norepinephrine, and 3-hydroxyanthranilic acid, which connects phenylalanine metabolism to that of tryptophan, have been altered. Consequently,...
Biogenetic Outline (Fig. 6.1). Two out of three aromatic amino acids, L-tyrosine and L-tryptophan, are precursors from the primary metabolism which retain — predominantly via the corresponding biogenic amine — their principal C- and...
Phenylalanine Metabolism in a Dilute-Lethal Strain of Mice M Irving,MB Sideman - 《Journal of Heredity》 被引量: 0发表: 1967年 Activity of the yeast MAP kinase homologue Slt2 is critically required for cell integrity at 37° C Deletion of the SLT2 gene of Saccharomyces cerevisiae, which ...
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency of the enzyme phenylalanine hydroxylase, which metabolizes phenylalanine (phe... EA Sawin,SG Murali,DM Ney - 《Molecular Genetics & Metabolism》 被引量: 32发表: 2014年 Expression of human phenylalanine hydroxylase activi...
Phenylalanine Metabolism and Hyperphenylalaninemia Phenylalanineis the starting point for a series of reactions essential in metabolism. Reflected in this pathway of reactions are several inherited defects:phenylketonuria,albinism,tyrosinemia, andalkaptonuria(Fig. 4-3). Each of the fourmetabolic disordersresu...
PHENYLALANINE METABOLISM IN DILUTE-LETHAL MICE HAROLD MUCH AND MARTHA T. YOST Zoology Department, University of Massachusetts, Amherst, Massachusetts Received June 5, 1963 ILUTE-LETHAL (dl) is a juvenile lethal mutation affecting both pigmen- tation and the nervous system. SEARLE (1952) showed tha...