Literature DB >> 1191305

Abnormal methionine adenosyltransferase in hypermethioninemia.

J D Finkelstein, W E Kyle, J J Martin.   

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Year:  1975        PMID： 1191305     DOI： 10.1016/0006-291x(75)90527-6

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


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  14 in total

Review 1.  Biochemistry and pharmacology of S-adenosyl-L-methionine and rationale for its use in liver disease.

Authors:  R K Chawla; H L Bonkovsky; J T Galambos
Journal:  Drugs       Date:  1990       Impact factor: 9.546

2.  One-carbon metabolism nutrient status and plasma S-adenosylmethionine concentrations in middle-aged and older Chinese in Singapore.

Authors:  Maki Inoue-Choi; Heather H Nelson; Kim Robien; Erland Arning; Teodoro Bottiglieri; Woon-Puay Koh; Jian-Min Yuan
Journal:  Int J Mol Epidemiol Genet       Date:  2012-05-15

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

Authors:  M E Chamberlin; T Ubagai; S H Mudd; W G Wilson; J V Leonard; J Y Chou
Journal:  J Clin Invest       Date:  1996-08-15       Impact factor: 14.808

4.  Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.

Authors:  M E Chamberlin; T Ubagai; S H Mudd; H L Levy; J Y Chou
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

5.  Intermittent hypermethioninaemia associated with normal hepatic methionine adenosyltransferase activity: report of a case.

Authors:  B M Jhaveri; N R Buist; G E Gaull; H H Tallan
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

6.  Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations.

Authors:  M E Chamberlin; T Ubagai; S H Mudd; J Thomas; V Y Pao; T K Nguyen; H L Levy; C Greene; C Freehauf; J Y Chou
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

7.  Persistent hypermethioninaemia with dominant inheritance.

Authors:  H J Blom; A J Davidson; J D Finkelstein; A S Luder; I Bernardini; J J Martin; A Tangerman; J M Trijbels; S H Mudd; S I Goodman
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

8.  Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.

Authors:  W A Gahl; J D Finkelstein; K D Mullen; I Bernardini; J J Martin; P Backlund; K G Ishak; J H Hoofnagle; S H Mudd
Journal:  Am J Hum Genet       Date:  1987-01       Impact factor: 11.025

9.  Isolated persistent hypermethioninemia.

Authors:  S H Mudd; H L Levy; A Tangerman; C Boujet; N Buist; A Davidson-Mundt; L Hudgins; K Oyanagi; M Nagao; W G Wilson
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

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

Authors:  T Ubagai; K J Lei; S Huang; S H Mudd; H L Levy; J Y Chou
Journal:  J Clin Invest       Date:  1995-10       Impact factor: 14.808
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