Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase (Q28509842)

GOA release 2020-03-11

author name string

J. D. McDonald

1

1 reference

24 January 2017

V. C. Bode

2

1 reference

24 January 2017

W. F. Dove

3

1 reference

24 January 2017

A. Shedlovsky

Proceedings of the National Academy of Sciences of the United States of America

4

1 reference

24 January 2017

language of work or name

English

0 references

publication date

1 March 1990

1 reference

24 January 2017

1 reference

24 January 2017

87

1 reference

24 January 2017

5

1 reference

24 January 2017

1965–1967

1 reference

24 January 2017

A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

A general method for isolation of high molecular weight DNA from eukaryotes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

THE STRUCTURE OF THE PHENYLALANINE-HYDROXYLATION COFACTOR

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

The phenylalanine hydroxylating system from mammalian liver

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Mendelian hyperphenylalaninemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Genetic analysis of the mouse using interspecific crosses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Mapping to molecular resolution in the T to H-2 region of the mouse genome with a nested set of meiotic recombinants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retroviruses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Phenylalanine hydroxylase from rat liver

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605

Liver phenylalanine hydroxylase assay

2 June 2018

1 reference

12 December 2020

Rat liver phenylalanine hydroxylase. Activation by sulfhydryl modification

1 reference

12 December 2020

Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots

1 reference

12 December 2020

Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylase

1 reference

12 December 2020

Biochemical defect of the hph-1 mouse mutant is a deficiency in GTP-cyclohydrolase activity

1 reference

12 December 2020

Hyperphenylalaninemia in the hph-1 mouse mutant

1 reference

12 December 2020

Localization of mouse phenylalanine hydroxylase locus on chromosome 10

1 reference

12 December 2020

The enzymatic conversion of phenylalanine to tyrosine

1 reference

12 December 2020

Phenylalanine hydroxylation cofactor in phenylketonuria

1 reference

12 December 2020

Phenylalanine hydroxylase activity in dilute and nondilute strains of mice

1 reference

12 December 2020

Phenylalanine Hydroxylase Activity in Liver Biopsies from Hyperphenylalaninemia Heterozygotes: Deviation from Proportionality with Gene Dosage

1 reference

12 December 2020

Genetics and biochemistry of the phenylketonuria-present state

1 reference

12 December 2020