(Q35248235)

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Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.

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Europe PubMed Central

PubMed publication ID

7 August 2017

Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7. (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

gyrate atrophy of the choroid

1 reference

based on heuristic

inferred from title

author name string

J J O'Donnell

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

K Vannas-Sulonen

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

T B Shows

3

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Europe PubMed Central

PubMed publication ID

7 August 2017

D R Cox

4

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Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

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publication date

1 December 1988

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Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

7 August 2017

43

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Europe PubMed Central

PubMed publication ID

7 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

922-928

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Assignment of the gene for beta 2-microglobulin (B2m) to mouse chromosome 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Starch gel electrophoretic phenotypes of mouse×human somatic cell hybrids and mouse isozyme polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Raised plasma-ornithine and gyrate atrophy of the choroid and retina.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Molecular cloning of human ornithine aminotransferase mRNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

27 July 2018

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

26 September 2018

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715611

26 September 2018

Gyrate atrophy of choroid and retina: deficient activity of ornithine ketoacid aminotransferase in cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient L-ornithine: 2-oxoacid aminotransferase activity in cultured fibroblasts from a patient with gyrate atrophy of the retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the beta-glucuronidase structural gene to the pter leads to q22 region of chromosome 7 in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperornithinemia and gyrate atrophy of the choroid and retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The natural history of gyrate atrophy of the choroid and retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interleukin 2 (IL2) is assigned to human chromosome 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative gene mapping of human chromosome 21 and mouse chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3195589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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