(Q35238993)

7 August 2017

title

Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene (English)

1 reference

7 August 2017

Chamberlin ME

1

1 reference

7 August 2017

Ubagai T

2

1 reference

7 August 2017

Mudd SH

3

1 reference

7 August 2017

Levy HL

4

1 reference

7 August 2017

Chou JY

5

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 March 1997

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

60

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7 August 2017

issue

3

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7 August 2017

page(s)

540-546

1 reference

Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Crystal structure of S-adenosylmethionine synthetase

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Cloning and expression of murine S-adenosylmethionine synthetase

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Methionine adenosyltransferase: structure and function

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Isolated persistent hypermethioninemia.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Cassette mutagenesis: an efficient method for generation of multiple mutations at defined sites

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Complete purification and immunochemical analysis of S-adenosylmethionine synthetase from bovine brain

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Molecular cloning and nucleotide sequence of cDNA encoding the rat kidney S-adenosylmethionine synthetase

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Persistent hypermethioninaemia with dominant inheritance.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Molecular cloning and developmental expression of a human kidney S-adenosylmethionine synthetase.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

S-Adenosylmethionine; a new intermediate formed enzymatically from L-methionine and adenosinetriphosphate.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Structure and function of S-adenosylmethionine synthetase: crystal structures of S-adenosylmethionine synthetase with ADP, BrADP, and PPi at 28 angstroms resolution

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Chromosomal localization and catalytic properties of the recombinant alpha subunit of human lymphocyte methionine adenosyltransferase

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712529

Hypermethioninemia associated with methionine adenosyltransferase deficiency: Clinical, morphologic, and biochemical observations on four patients

26 September 2018

1 reference

12 December 2020

Purification and comparison of two forms of S-adenosyl-L-methionine synthetase from rat liver

1 reference

12 December 2020

Abnormal methionine adenosyltransferase in hypermethioninemia

1 reference

12 December 2020

S-Adenosylmethionine synthetase from human lymphocytes. Purification and characterization

1 reference

12 December 2020

Identifiers

PMC publication ID

1712529

1 reference

7 August 2017

1 reference