Approaches to the treatment of inborn errors of sulphur amino acid and peptide metabolism.
作者信息
Schulman J D
出版信息
Prog Clin Biol Res. 1979;34:201-15.
PMID:531052
Abstract
摘要
相似文献
1
Approaches to the treatment of inborn errors of sulphur amino acid and peptide metabolism.
Prog Clin Biol Res. 1979;34:201-15.
2
Genetic disorders of glutathione and sulfur amino-acid metabolism. New biochemical insights and therapeutic approaches.
Ann Intern Med. 1980 Aug;93(2):330-46. doi: 10.7326/0003-4819-93-2-330.
3
High-dose vitamin E therapy in glutathione synthetase deficiency.谷胱甘肽合成酶缺乏症的高剂量维生素E治疗
J Inherit Metab Dis. 1994;17(6):749-50. doi: 10.1007/BF00712019.
4
Effect of ascorbate or N-acetylcysteine treatment in a patient with hereditary glutathione synthetase deficiency.
J Pediatr. 1994 Feb;124(2):229-33. doi: 10.1016/s0022-3476(94)70309-4.
5
Vitamin responsive inborn errors of metabolism.
J Assoc Physicians India. 1979 Aug;27(8):769-71.
6
Homocystinuria--response to pyridoxine therapy.
J Assoc Physicians India. 1979 Aug;27(8):713-7.
7
Effect of pyridoxine treatment of a homocystinuric patient on the urinary excretion of some sulfur-containing amino acids.吡哆醇治疗一名同型胱氨酸尿症患者对某些含硫氨基酸尿排泄的影响。
Acta Med Okayama. 1974 Aug;28(4):243-6.
8
Sulphur amino-acid degradation in subjects with hereditary glutathione synthetase deficiency (5-oxoprolinuria).
Eur J Clin Invest. 1985 Dec;15(6):371-4. doi: 10.1111/j.1365-2362.1985.tb00287.x.
9
Thioredoxin and glutathione in cultured fibroblasts from human cases with 5-oxoprolinuria and cystinosis.
FEBS Lett. 1978 Mar 1;87(1):61-4. doi: 10.1016/0014-5793(78)80133-1.
10
In vivo alteration of a mutant human protein using the free thiol cysteamine.使用游离硫醇半胱胺对突变型人类蛋白质进行体内改造。
Am J Med Genet. 1985 Feb;20(2):409-17. doi: 10.1002/ajmg.1320200226.
引用本文的文献
1
Role of thiols in degradation of proteins by cathepsins.硫醇在组织蛋白酶降解蛋白质中的作用。
Biochem J. 1982 May 15;204(2):471-7. doi: 10.1042/bj2040471.
Zotero 插件