BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 10674710)

  • 1. Molecular genetics of hepatic methionine adenosyltransferase deficiency.
    Chou JY
    Pharmacol Ther; 2000 Jan; 85(1):1-9. PubMed ID: 10674710
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency.
    Chamberlin ME; Ubagai T; Mudd SH; Wilson WG; Leonard JV; Chou JY
    J Clin Invest; 1996 Aug; 98(4):1021-7. PubMed ID: 8770875
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations.
    Chamberlin ME; Ubagai T; Mudd SH; Thomas J; Pao VY; Nguyen TK; Levy HL; Greene C; Freehauf C; Chou JY
    Am J Hum Genet; 2000 Feb; 66(2):347-55. PubMed ID: 10677294
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.
    Chamberlin ME; Ubagai T; Mudd SH; Levy HL; Chou JY
    Am J Hum Genet; 1997 Mar; 60(3):540-6. PubMed ID: 9042912
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Methionine adenosyltransferase I/III deficiency: neurological manifestations and relevance of S-adenosylmethionine.
    Furujo M; Kinoshita M; Nagao M; Kubo T
    Mol Genet Metab; 2012 Nov; 107(3):253-6. PubMed ID: 22951388
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of mutations associated with methionine adenosyltransferase I/III deficiency among individuals identified during newborn screening in Japan.
    Nagao M; Tanaka T; Furujo M
    Mol Genet Metab; 2013 Dec; 110(4):460-4. PubMed ID: 24231718
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency.
    Ubagai T; Lei KJ; Huang S; Mudd SH; Levy HL; Chou JY
    J Clin Invest; 1995 Oct; 96(4):1943-7. PubMed ID: 7560086
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity.
    Pérez Mato I; Sanchez del Pino MM; Chamberlin ME; Mudd SH; Mato JM; Corrales FJ
    J Biol Chem; 2001 Apr; 276(17):13803-9. PubMed ID: 11278456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation.
    Kim SZ; Santamaria E; Jeong TE; Levy HL; Mato JM; Corrales FJ; Mudd SH
    J Inherit Metab Dis; 2002 Dec; 25(8):661-71. PubMed ID: 12705496
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III.
    Hazelwood S; Bernardini I; Shotelersuk V; Tangerman A; Guo J; Mudd H; Gahl WA
    Am J Med Genet; 1998 Feb; 75(4):395-400. PubMed ID: 9482646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report.
    Furujo M; Kinoshita M; Nagao M; Kubo T
    Mol Genet Metab; 2012 Mar; 105(3):516-8. PubMed ID: 22178350
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isolated hypermethioninemia: measurements of S-adenosylmethionine and choline.
    Mudd SH; Jenden DJ; Capdevila A; Roch M; Levy HL; Wagner C
    Metabolism; 2000 Dec; 49(12):1542-7. PubMed ID: 11145114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of methionine adenosyltransferase and S-adenosylmethionine in alcohol-associated liver cancer.
    Lu SC; Mato JM
    Alcohol; 2005 Apr; 35(3):227-34. PubMed ID: 16054984
    [TBL] [Abstract][Full Text] [Related]  

  • 14. S-adenosylmethionine synthesis: molecular mechanisms and clinical implications.
    Mato JM; Alvarez L; Ortiz P; Pajares MA
    Pharmacol Ther; 1997; 73(3):265-80. PubMed ID: 9175157
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impaired liver regeneration in mice lacking methionine adenosyltransferase 1A.
    Chen L; Zeng Y; Yang H; Lee TD; French SW; Corrales FJ; García-Trevijano ER; Avila MA; Mato JM; Lu SC
    FASEB J; 2004 May; 18(7):914-6. PubMed ID: 15033934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypermethioninemias of genetic and non-genetic origin: A review.
    Mudd SH
    Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):3-32. PubMed ID: 21308989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract.
    Kido J; Sawada T; Momosaki K; Suzuki Y; Uetani H; Kitajima M; Mitsubuchi H; Nakamura K; Matsumoto S
    Brain Dev; 2019 Apr; 41(4):382-388. PubMed ID: 30389272
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction.
    Hirabayashi K; Shiohara M; Yamada K; Sueki A; Ide Y; Takeuchi K; Hagimoto R; Kinoshita T; Yabuhara A; Mudd SH; Koike K
    Gene; 2013 Nov; 530(1):104-8. PubMed ID: 23973726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.
    Chien YH; Abdenur JE; Baronio F; Bannick AA; Corrales F; Couce M; Donner MG; Ficicioglu C; Freehauf C; Frithiof D; Gotway G; Hirabayashi K; Hofstede F; Hoganson G; Hwu WL; James P; Kim S; Korman SH; Lachmann R; Levy H; Lindner M; Lykopoulou L; Mayatepek E; Muntau A; Okano Y; Raymond K; Rubio-Gozalbo E; Scholl-Bürgi S; Schulze A; Singh R; Stabler S; Stuy M; Thomas J; Wagner C; Wilson WG; Wortmann S; Yamamoto S; Pao M; Blom HJ
    Orphanet J Rare Dis; 2015 Aug; 10():99. PubMed ID: 26289392
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening.
    Couce ML; Bóveda MD; García-Jimémez C; Balmaseda E; Vives I; Castiñeiras DE; Fernández-Marmiesse A; Fraga JM; Mudd SH; Corrales FJ
    Mol Genet Metab; 2013 Nov; 110(3):218-21. PubMed ID: 23993429
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.