Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.

Suppr

超能文献

作者信息

Buist N R, Strandholm J J, Bellinger J F, Kennaway N G

出版信息

Metabolism. 1972 Dec;21(12):1113-23. doi: 10.1016/0026-0495(72)90106-0.

DOI:10.1016/0026-0495(72)90106-0

PMID:4674498

Abstract

摘要

相似文献

Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.

Metabolism. 1972 Dec;21(12):1113-23. doi: 10.1016/0026-0495(72)90106-0.

Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.亚氨基二肽尿症：胶原蛋白循环中的一种基因缺陷；一种测定红细胞中脯氨酰二肽酶的方法。

Can Med Assoc J. 1975 Oct 18;113(8):759, 762-3.

Prolidase deficiency with iminodipeptiduria: biochemical investigations and first results of attempted therapy.伴有亚氨基二肽尿症的脯氨酰寡肽酶缺乏症：生化研究及尝试性治疗的初步结果

J Inherit Metab Dis. 1981;4(2):77-8. doi: 10.1007/BF02263599.

Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.

Physiol Chem Phys. 1978;10(3):279-83.

Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms.伴有亚氨基二肽尿症的脯氨肽酶缺乏症。一例有临床症状和无临床症状的家族病例。

Clin Chim Acta. 1979 May 2;93(3):401-7. doi: 10.1016/0009-8981(79)90291-2.

Prolidase deficiency: a patient without hydroxyproline-containing iminodipeptides in urine.脯氨酰二肽酶缺乏症：一名尿液中无含羟脯氨酸亚氨基二肽的患者。

J Inherit Metab Dis. 1988;11(2):161-5. doi: 10.1007/BF01799866.

Defective hydroxyproline metabolism in type II hyperprolinemia.II型高脯氨酸血症中羟脯氨酸代谢缺陷

Biochem Med. 1974 Aug;10(4):329-36. doi: 10.1016/0006-2944(74)90036-2.

Liquid chromatography-mass spectrometry for the qualitative analyses of iminodipeptides in the urine of patients with prolidase deficiency.

J Chromatogr. 1990 May 18;527(2):279-88. doi: 10.1016/s0378-4347(00)82112-x.

Swine kidney prolidase: assay, isolation procedure, and molecular properties.

Physiol Chem Phys. 1972;4(1):75-87.

[Prolidase deficiency].[脯氨酰肽酶缺乏症]

Ryoikibetsu Shokogun Shirizu. 1998(18 Pt 1):160-2.

引用本文的文献

PROLIDASE: A Review from Discovery to its Role in Health and Disease.脯氨酰肽酶：从发现到其在健康与疾病中作用的综述

Front Mol Biosci. 2021 Aug 31;8:723003. doi: 10.3389/fmolb.2021.723003. eCollection 2021.

Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases.脯氨酸肽酶缺乏症自然病史的定量分析：17 个家系的描述及已发表病例的系统回顾

Genet Med. 2021 Sep;23(9):1604-1615. doi: 10.1038/s41436-021-01200-2. Epub 2021 May 26.

Spurious Elevation of Multiple Urine Amino Acids by Ion-Exchange Chromatography in Patients with Prolidase Deficiency.脯氨酰肽酶缺乏症患者中离子交换色谱法导致多种尿液氨基酸假性升高

JIMD Rep. 2017;31:45-49. doi: 10.1007/8904_2016_552. Epub 2016 Apr 12.

Screening method for prolidase deficiency.脯氨酰肽酶缺乏症的筛查方法。

Hum Genet. 1981;56(3):349-51. doi: 10.1007/BF00274691.

Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiency.来自一名氨肽酶缺乏症患者的皮肤成纤维细胞合成的胶原蛋白中脯氨酸的正常羟基化。

J Inherit Metab Dis. 1982;5(2):111-3. doi: 10.1007/BF01800003.

J Inherit Metab Dis. 1981;4(2):77-8. doi: 10.1007/BF02263599.

In-vitro responses to ascorbate and manganese in fibroblasts from a patient with prolidase deficiency and iminodipeptiduria: cell growth, prolidase activity and collagen metabolism.一名患有脯氨酰二肽酶缺乏症和亚氨基二肽尿症患者的成纤维细胞对抗坏血酸和锰的体外反应：细胞生长、脯氨酰二肽酶活性及胶原蛋白代谢

J Inherit Metab Dis. 1983;6(1):27-31. doi: 10.1007/BF02391189.

An autopsy case of prolidase deficiency.一例脯氨酰肽酶缺乏症尸检病例。

Virchows Arch A Pathol Anat Histopathol. 1985;406(1):125-31. doi: 10.1007/BF00710562.

Peptiduria presumably caused by aminopeptidase-P deficiency. A new inborn error of metabolism.

J Inherit Metab Dis. 1988;11 Suppl 2:240-2. doi: 10.1007/BF01804246.

Can Med Assoc J. 1975 Oct 18;113(8):759, 762-3.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验