(Q33961407)

30 July 2017

title

Mouse models of human phenylketonuria (English)

1 reference

30 July 2017

1 reference

A Shedlovsky

1

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30 July 2017

J D McDonald

series ordinal

2

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30 July 2017

D Symula

series ordinal

3

1 reference

30 July 2017

W F Dove

series ordinal

4

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30 July 2017

language of work or name

English

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publication date

1 August 1993

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30 July 2017

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30 July 2017

volume

134

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30 July 2017

issue

4

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30 July 2017

page(s)

1205-1210

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

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Treatment of phenylketonuria with a diet low in phenylalanine.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Maternal phenylketonuria--results of dietary therapy.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Effects of untreated maternal phenylketonuria and hyperphenylalaninemia on the fetus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Production of antibodies to rat liver phenylalanine hydroxylase. Cross-reactivity with other pterin-dependent hydroxylases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

5 July 2018

Maternal phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Inhibition of in vivo and in vitro transcription by monoclonal antibodies prepared against wheat germ RNA polymerase II that react with the heptapeptide repeat of eukaryotic RNA polymerase II.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Phenylketonuria: screening, treatment and maternal PKU.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Cystic fibrosis. More from the modellers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Phenylketonuria due to a deficiency of dihydropteridine reductase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1205587

Molecular biology of phenylketonuria

29 October 2018

1 reference

12 December 2020

Mutagenic effects of repeated small radiation doses to mouse spermatogonia I. Specific-locus mutation rates

1 reference

12 December 2020

Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen

1 reference

12 December 2020

Experimental hyperphenylalaninemia: effect on central nervous system myelin subfractions

1 reference

12 December 2020

Use of alpha-methylphenylalanine for studies of brain development in experimental phenylketonuria

1 reference

12 December 2020

X-ray-induced mutations in mice

1 reference

12 December 2020

ski can cause selective growth of skeletal muscle in transgenic mice

1 reference

12 December 2020

Identifiers

PMC publication ID

1205587

1 reference

30 July 2017

1 reference