γ-谷氨酰循环与氨基酸转运。5-氧脯氨酸尿症（谷胱甘肽合成酶缺乏症）患者红细胞中游离氨基酸、γ-谷氨酰半胱氨酸和谷胱甘肽的研究。 - Suppr

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超能文献

The gamma-glutamyl cycle and amino acid transport. Studies of free amino acids, gamma-glutamyl-cysteine and glutathione in erythrocytes from patients with 5-oxoprolinuria (glutathione synthetase deficiency).

作者信息

Hagenfeldt L, Larsson A, Andersson R

出版信息

N Engl J Med. 1978 Sep 14;299(11):587-90. doi: 10.1056/NEJM197809142991107.

DOI:10.1056/NEJM197809142991107

PMID:28482

Abstract

摘要

相似文献

The gamma-glutamyl cycle and amino acid transport. Studies of free amino acids, gamma-glutamyl-cysteine and glutathione in erythrocytes from patients with 5-oxoprolinuria (glutathione synthetase deficiency).γ-谷氨酰循环与氨基酸转运。5-氧脯氨酸尿症（谷胱甘肽合成酶缺乏症）患者红细胞中游离氨基酸、γ-谷氨酰半胱氨酸和谷胱甘肽的研究。

N Engl J Med. 1978 Sep 14;299(11):587-90. doi: 10.1056/NEJM197809142991107.

Ophthalmological, psychometric and therapeutic investigation in two sisters with hereditary glutathione synthetase deficiency (5-oxoprolinuria).对两名患有遗传性谷胱甘肽合成酶缺乏症（5-氧脯氨酸尿症）的姐妹进行的眼科、心理测量学和治疗学调查。

Neuropediatrics. 1985 Aug;16(3):131-6. doi: 10.1055/s-2008-1052557.

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.

5-oxoprolinuria: biochemical observations and case report.5-氧脯氨酸尿症：生化观察与病例报告。

J Pediatr. 1977 Aug;91(2):237-41. doi: 10.1016/s0022-3476(77)80819-6.

Biochemical heterogeneity in glutathione synthetase deficiency.谷胱甘肽合成酶缺乏症中的生化异质性。

J Clin Invest. 1978 Jun;61(6):1417-20. doi: 10.1172/JCI109060.

On the mechanism of 5-oxoproline overproduction in 5-oxoprolinuria.关于5-氧脯氨酸尿症中5-氧脯氨酸过度产生的机制。

Clin Chim Acta. 1976 Mar 15;67(3):245-53. doi: 10.1016/0009-8981(76)90332-6.

Editorial: Glutathione deficiency, pyroglutamic acidemia and amino acid transport.社论：谷胱甘肽缺乏、焦谷氨酸血症与氨基酸转运

N Engl J Med. 1976 Aug 19;295(8):441-3. doi: 10.1056/NEJM197608192950809.

[Glutathion-synthetase deficiency with 5-oxoprolinuria. Two new cases and a review of the literature (author's transl)].[谷胱甘肽合成酶缺乏症伴5-氧脯氨酸尿症。两例新病例及文献复习（作者译）]

Nouv Presse Med. 1978 May 6;7(18):1531-5.

Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).谷胱甘肽合成酶缺乏症，一种涉及5-氧脯氨酸尿症（焦谷氨酸尿症）患者γ-谷氨酰循环的先天性代谢缺陷。

Proc Natl Acad Sci U S A. 1974 Jun;71(6):2505-9. doi: 10.1073/pnas.71.6.2505.

5-oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers--a new inborn error of the gamma-glutamyl cycle.两兄弟因遗传性5-氧脯氨酸酶缺乏导致5-氧脯氨酸尿症——γ-谷氨酰循环中的一种新的先天性代谢缺陷。

Acta Paediatr Scand. 1981;70(3):301-8. doi: 10.1111/j.1651-2227.1981.tb16556.x.

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Mechanisms of postprandial protein accretion in human skeletal muscle. Insight from leucine and phenylalanine forearm kinetics.人类骨骼肌餐后蛋白质积累的机制。亮氨酸和苯丙氨酸前臂动力学的见解。

J Clin Invest. 1996 Sep 15;98(6):1361-72. doi: 10.1172/JCI118923.

Transient glutamic acidaemia.短暂性谷氨酸血症

Eur J Pediatr. 1996 Apr;155(4):308-10. doi: 10.1007/BF02002718.

Biomolecular information analysis in neurotransmitter systems.神经递质系统中的生物分子信息分析

Acta Biotheor. 1984;33(1):3-33. doi: 10.1007/BF00045844.

Isolation and purification of multiple forms of gamma-glutamyl transpeptidase from rat brain.从大鼠脑中分离和纯化多种形式的γ-谷氨酰转肽酶

Neurochem Res. 1980 Feb;5(2):159-70. doi: 10.1007/BF00964329.

Comparative column chromatographic estimations of phenylalanine in plasma, whole blood, native and paper-dried capillary blood of healthy children and adults, and patients with hyperphenylalaninaemia.健康儿童、成人以及高苯丙氨酸血症患者的血浆、全血、新鲜和滤纸干燥毛细血管血中苯丙氨酸的柱色谱比较测定。

J Inherit Metab Dis. 1985;8(3):119-22. doi: 10.1007/BF01819295.

A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria.一个受高鸟氨酸血症、高氨血症和同型瓜氨酸尿症综合征影响的新家族。

J Inherit Metab Dis. 1987;10(1):73-81. doi: 10.1007/BF01799492.

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