(Q37542460)

20 August 2017

Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome (English)

1 reference

20 August 2017

1 reference

A S Lidsky

1

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20 August 2017

M L Law

2

1 reference

20 August 2017

H G Morse

3

1 reference

20 August 2017

F T Kao

4

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20 August 2017

M Rabin

5

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20 August 2017

F H Ruddle

6

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20 August 2017

S L Woo

7

1 reference

20 August 2017

language of work or name

English

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publication date

1 September 1985

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

20 August 2017

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20 August 2017

82

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20 August 2017

6221-6225

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20 August 2017

18

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Isolation of a human repetitive sequence and its application to regional chromosome mapping

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

The PKU locus in man is on chromosome 12.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

A polymorphic DNA marker genetically linked to Huntington's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Genetics of somatic mammalian cells: genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

In vitro activation of rat liver phenylalanine hydroxylase by phosphorylation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Phenylketonuria: epitome of human biochemical genetics (first of two parts).

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

PKU locus: Genetic linkage with human amylase (Amy) loci and assignment to linkage group I

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Mechanism of inactivation of phenylalanine hydroxylase by p-chlorophenylalanine in hepatome cells in culture. Two possible models

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Studies on linkage between phenylketonuria and the blood groups

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

The isolation and properties of phenylalanine hydroxylase from rat liver

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Linkage analysis using heterozygote detection in phenylketonuria

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridization.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

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

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391024

Purification and Some Physical Properties of Phenylalanine Hydroxylase from Rat Liver

1 September 2018

1 reference

12 December 2020

Prenatal diagnosis of classical phenylketonuria by gene mapping

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12 December 2020

Some characteristics of partially purified human liver phenylalanine hydroxylase

1 reference

12 December 2020

A linkage study of phenylketonuria

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12 December 2020

Modification of the multiple forms of rat hepatic phenylalanine hydroxylase by in vitro phosphorylation

1 reference

12 December 2020

Induced segregation of human syntenic genes by 5-bromodeozyuridine + near-visible light

1 reference

12 December 2020

Regional assignment of human genes TPI1, GAPDH, LDHB, SHMT, and PEPB on chromosome 12

1 reference

12 December 2020

Prenatal diagnosis of classic phenylketonuria by DNA analysis

1 reference

12 December 2020

Data for the study of linkage in man; phenylketonuria and the ABO and MN loci

1 reference

12 December 2020

Phenylketonuria: epitome of human biochemical genetics (second of two parts)

1 reference

12 December 2020

Regional mapping of the gene coding for enolase-2 on human chromosome 12

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

12 December 2020

Isozymes of phenylalanine hydroxylase

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.82.18.6221

1 reference

20 August 2017

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1 reference

20 August 2017

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