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A comparison of the phenylalanine content of the hemoglobin of normal and phenylketonuric individuals: determination by ion exchange chromatography.

作者信息

ALLEN D W, SCHROEDER W A

出版信息

J Clin Invest. 1957 Sep;36(9):1343-9. doi: 10.1172/JCI103533.

DOI:10.1172/JCI103533
PMID:13463099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1072732/
Abstract
摘要

相似文献

1
A comparison of the phenylalanine content of the hemoglobin of normal and phenylketonuric individuals: determination by ion exchange chromatography.正常个体与苯丙酮尿症患者血红蛋白中苯丙氨酸含量的比较：通过离子交换色谱法测定
J Clin Invest. 1957 Sep;36(9):1343-9. doi: 10.1172/JCI103533.
2
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J Chromatogr A. 2009 Jul 24;1216(30):5709-14. doi: 10.1016/j.chroma.2009.06.004. Epub 2009 Jun 7.
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Depletion of phenylalanine in the blood of phenylketonuric patients using a PAL-enzyme reactor. An in vitro study.
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Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer.使用日立L - 8800分析仪通过离子交换色谱法测定干血标本中的苯丙氨酸和酪氨酸。
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[Amino acids in the intestinal fluid in a subject with high blood phenylalanine. Comparative study with a control group].[高血苯丙氨酸受试者肠液中的氨基酸。与对照组的比较研究]
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A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum.一种基于微孔板的酶法，用于同时测定血清中的苯丙氨酸和酪氨酸。
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引用本文的文献

1
Hair amino acids: normal values and results in metabolic errors.毛发氨基酸：正常值及代谢紊乱的结果
Arch Dis Child. 1970 Oct;45(243):678-81. doi: 10.1136/adc.45.243.678.

本文引用的文献

1
[Pathological physiology of the dementia caused by phenylpyruvic acid].[苯丙酮酸所致痴呆的病理生理学]
Nervenarzt. 1952 May;23(5):175-80.
2
Chromatography of amino acids on sulfonated polystyrene resins.氨基酸在磺化聚苯乙烯树脂上的色谱分析。
J Biol Chem. 1951 Oct;192(2):663-81.
3
Amino acid composition of hemoglobins of normal Negroes and sickle-cell anemics.正常黑人与镰状细胞贫血患者血红蛋白的氨基酸组成。
J Biol Chem. 1950 Nov;187(1):221-40.
4
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.苯丙酮尿症研究。I. 苯丙酮尿症患者苯丙氨酸摄入受限
J Clin Invest. 1955 Apr;34(4):565-80. doi: 10.1172/JCI103105.
5
Phenylketonuria.苯丙酮尿症
AMA J Dis Child. 1957 Apr;93(4):405-19. doi: 10.1001/archpedi.1957.02060040407009.
6
[Analysis of the amino-acid structure of somatic proteins in phenylpyruvic oligophrenia].[苯丙酮尿性智力发育不全中体细胞蛋白质的氨基酸结构分析]
Monatsschr Psychiatr Neurol. 1955 Oct;130(4):299-303.
7
Amino-acid composition of human crystallized myoglobin and haemoglobin.人结晶肌红蛋白和血红蛋白的氨基酸组成。
Biochim Biophys Acta. 1955 Jul;17(3):377-81. doi: 10.1016/0006-3002(55)90386-3.
8
The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child.苯丙氨酸摄入对一名苯丙酮尿症患儿的生化指标及行为的影响。
Acta Paediatr (Stockh). 1954 Jan;43(1):64-77. doi: 10.1111/j.1651-2227.1954.tb04000.x.
9
The hydroxylation of phenylalanine and antipyrine in phenylpyruvic oligophrenia.苯丙酮尿症中苯丙氨酸和安替比林的羟基化作用
J Biol Chem. 1953 Aug;203(2):961-6.
10
Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.苯丙酮酸性智力发育不全——苯丙氨酸氧化系统缺乏症
Proc Soc Exp Biol Med. 1953 Mar;82(3):514-5.