HYPERPHENYLALANINEMIA IN THE HPH-1 MOUSE MUTANT

被引：43

作者：

MCDONALD, JD

BODE, VC

机构：

来源：

PEDIATRIC RESEARCH | 1988年 / 23卷 / 01期

关键词：

D O I：

10.1203/00006450-198801000-00014

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

收藏

页码：63 / 67

页数：5

相关论文

共 19 条

[1]

BERRY HK, 1975, BIOL NEONATE, V26, P88, DOI 10.1159/000240720

[2]

BODE VC, 1984, GENETICS, V108, P457

[3]

BODE VC, 1987, IN PRESS GENETICS

[4]

COTTON RGH, 1986, J INHERITED METAB DI, V9, P1

[5]

CRISPENS C, 1975, HDB LABORATORY MOUSE, P114

[6] ATYPICAL PHENYLKETONURIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCY - DIAGNOSIS AND TREATMENT WITH TETRAHYDROBIOPTERIN, DIHYDROBIOPTERIN AND SEPIAPTERIN [J].

CURTIUS, HC ;

NIEDERWIESER, A ;

VISCONTINI, M ;

OTTEN, A ;

SCHAUB, J ;

SCHEIBENREITER, S ;

SCHMIDT, H .

CLINICA CHIMICA ACTA, 1979, 93 (02) :251-262

[7] COMPARISON OF ALPHA-METHYLPHENYLALANINE AND PARA-CHLOROPHENYLALANINE AS INDUCERS OF CHRONIC HYPERPHENYLALANINEMIA IN DEVELOPING RATS [J].

DELVALLE, JA ;

DIENEL, G ;

GREENGARD, O .

BIOCHEMICAL JOURNAL, 1978, 170 (03) :449-459

[8] DIFFERENCES IN THE METABOLISM OF THE AROMATIC AMINO-ACID HYDROXYLASE COFACTOR, TETRAHYDROBIOPTERIN, IN MUTANT MICE WITH NEUROLOGICAL AND IMMUNOLOGICAL DEFECTS [J].

DUCH, DS ;

BOWERS, SW ;

WOOLF, JH ;

DAVISSON, MT ;

MALTAIS, LJ ;

NICHOL, CA .

BIOCHEMICAL GENETICS, 1986, 24 (9-10) :657-668

[9]

GUTHRIE R, 1963, PEDIATRICS, V32, P328

[10]

Kaufman S, 1978, Methods Enzymol, V53, P278