Literature DB >> 13084666

The hydroxylation of phenylalanine and antipyrine in phenylpyruvic oligophrenia.

S UDENFRIEND, S P BESSMAN.   

Abstract

Entities:  

Keywords:  ANALGESICS/metabolism; MENTAL DEFICIENCY; PHENYLALANINE/metabolism

Mesh:

Substances:

Year:  1953        PMID: 13084666

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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  13 in total

1.  Synthesis of tyrosine and phenylalanine by Lactobacillus arabinosus.

Authors:  R L ORY; C M LYMAN
Journal:  J Bacteriol       Date:  1955-05       Impact factor: 3.490

2.  [On the biochemistry of essential pentosuria, congenital galactosemia and phenylketonuria].

Authors:  S HOLLMANN
Journal:  Klin Wochenschr       Date:  1959-07-15

3.  Diminished phenylketonuria in phenylpyruvic oligophrenia after administration of L-glutamine, L-glutamate or L-asparagine.

Authors:  A MEISTER; S UDENFRIEND; S P BESSMAN
Journal:  J Clin Invest       Date:  1956-06       Impact factor: 14.808

4.  Genetic implications of certain physiological processes affecting the metabolism of L-phenylalanine in man.

Authors:  R E TASHIAN; S M GARTLER
Journal:  Am J Hum Genet       Date:  1957-09       Impact factor: 11.025

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

Authors:  D W ALLEN; W A SCHROEDER
Journal:  J Clin Invest       Date:  1957-09       Impact factor: 14.808

6.  Phenylketonuria with normal intelligence and Gowers' muscular dystrophy.

Authors:  S COATES; A P NORMAN; L I WOOLF
Journal:  Arch Dis Child       Date:  1957-08       Impact factor: 3.791

7.  The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.

Authors:  W E KNOX; E C MESSINGER
Journal:  Am J Hum Genet       Date:  1958-03       Impact factor: 11.025

8.  Treatment of phenylketonuria with a diet low in phenylalanine.

Authors:  L I WOOLF; R GRIFFITHS; A MONCRIEFF
Journal:  Br Med J       Date:  1955-01-08

Review 9.  [Problems of quantitative diagnosis of hereditary metabolic diseases].

Authors:  F Linneweh
Journal:  Klin Wochenschr       Date:  1965-10-15

10.  Identification of a missense phenylketonuria mutation at codon 408 in Chinese.

Authors:  C H Lin; K J Hsiao; T F Tsai; H K Chao; T S Su
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

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