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Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
title
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase
(English)
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
main subject
Phenylalanine hydroxylase
1 reference
stated in
GOA release 2020-03-11
author name string
J. D. McDonald
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
V. C. Bode
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
W. F. Dove
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
A. Shedlovsky
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 March 1990
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
volume
87
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
page(s)
1965–1967
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stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
issue
5
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stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
cites work
A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
19 March 2017
Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
19 March 2017
A general method for isolation of high molecular weight DNA from eukaryotes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
7 April 2017
THE STRUCTURE OF THE PHENYLALANINE-HYDROXYLATION COFACTOR
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
The phenylalanine hydroxylating system from mammalian liver
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Mendelian hyperphenylalaninemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Genetic analysis of the mouse using interspecific crosses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Mapping to molecular resolution in the T to H-2 region of the mouse genome with a nested set of meiotic recombinants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
29 September 2017
Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retroviruses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
2 June 2018
Phenylalanine hydroxylase from rat liver
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53605
retrieved
2 June 2018
Liver phenylalanine hydroxylase assay
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rat liver phenylalanine hydroxylase. Activation by sulfhydryl modification
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylase
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Biochemical defect of the hph-1 mouse mutant is a deficiency in GTP-cyclohydrolase activity
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hyperphenylalaninemia in the hph-1 mouse mutant
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Localization of mouse phenylalanine hydroxylase locus on chromosome 10
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The enzymatic conversion of phenylalanine to tyrosine
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Phenylalanine hydroxylation cofactor in phenylketonuria
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Phenylalanine hydroxylase activity in dilute and nondilute strains of mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Phenylalanine Hydroxylase Activity in Liver Biopsies from Hyperphenylalaninemia Heterozygotes: Deviation from Proportionality with Gene Dosage
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetics and biochemistry of the phenylketonuria-present state
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2308957
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.87.5.1965
0 references
ADS bibcode
1990PNAS...87.1965M
0 references
PMCID
53605
0 references
PubMed ID
2308957
1 reference
stated in
PubMed
PubMed ID
2308957
retrieved
24 January 2017
ResearchGate publication ID
20847043
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