必应词典为您提供phenylalaninehydroxylase的释义,网络释义: 苯丙胺酸氢化酶;苯丙氨酸羟化酶;
假使苯丙胺酸羟化酵素(phenylalanine hydroxylase)在苯丙胺酸(phenylalanine)的苯环上添加一个氢氧基,苯丙胺酸(phe… www.dls.ym.edu.tw|基于29个网页 3. 苯丙胺酸羟化胺 ...,高苯丙胺酸血症是一个常见的遗传性代谢疾病,起因于苯丙胺酸羟化胺(phenylalanine hydroxylase)的缺乏,至少一半以 … ...
2011. Phenylalanine hydroxylase (PAH) from the lower eukaryote Leishmania major. Mol. Biochem. Parasitol. 175:58-67. doi: 10.1016/j. molbiopara.2010.09.004 PMID: 20887755Lye LF, Kang SO, Nosanchuk JD, Casadevall A, Beverley SM (2011) Phenylalanine hydroxylase (PAH) from the lower eukaryote...
Phenylalanine hydroxylase Phenylalanine hydroxylase (PheOH, alternatively PheH or PAH) () is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine. PheOH is one of three members of the pterin-dependent amino acid hydroxylases, a class of monooxy...
1. 苯丙氨酸羟化酶 苯丙酮尿症是一种常染色体隐形遗传病,多由苯丙氨酸羟化酶(phenylalanine hydroxylase PAH)基因突变引起.未经治疗的患儿可表现严 …d.wanfangdata.com.cn|基于1 个网页 例句 释义: 全部,苯丙氨酸羟化酶 更多例句筛选 1. Phenylketonuria (PKU) is one kinds of autosomal recessive disease caused...
Phenylalanine hydroxylase is a mixed-function oxidase that uses the cofactor tetrahydrobiopterin to split molecular O2, adding one atom to the phenylalanine ring and converting the other to water. From: Elsevier's Integrated Review Biochemistry (Second Edition), 2012 ...
当人体苯丙氨酸羟化酶(phenylalanine hydroxylase,PAH)缺乏或其辅酶四氢生物蝶呤(tetrahydrobiopterin,BH4)缺乏,导致血液苯丙氨酸(Phe)水平增高,如果血苯丙氨酸浓度高于120μmol/L且血苯丙氨酸(Phe)与酪氨酸(Tyr)比值>2.0,则统称为高苯丙氨酸血症(hyperphenylalaninemia,HPA)。
Pentium 4 奔腾4 这款代号原为Willamette的英特尔新一代中央处理器,于2000年下半年推出,使用了家喻户晓的Pentium商标,唯一的改变是将罗马数字改换成阿拉伯数字。Pentium4处理器初期先推出 sodium 4,4 dimethyl 4 silapentanesulfonate 【化】 4,4-二甲基-4-硅代戊磺酸钠 April fish4 月1日愚人节受愚弄者 4 cya...
网络苯丙氨酸羟化酶缺乏症 网络释义 1. 苯丙氨酸羟化酶缺乏症 ...尿症(phenylketonuria,PKU)或称苯丙氨酸羟化酶缺乏症(phenylalanine hydroxylase deficiency)是由于肝脏苯丙氨酸羟 … www.wiki8.com|基于7个网页