BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 15024124)

  • 1. S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism.
    Baric I; Fumic K; Glenn B; Cuk M; Schulze A; Finkelstein JD; James SJ; Mejaski-Bosnjak V; Pazanin L; Pogribny IP; Rados M; Sarnavka V; Scukanec-Spoljar M; Allen RH; Stabler S; Uzelac L; Vugrek O; Wagner C; Zeisel S; Mudd SH
    Proc Natl Acad Sci U S A; 2004 Mar; 101(12):4234-9. PubMed ID: 15024124
    [TBL] [Abstract][Full Text] [Related]  

  • 2. S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy.
    Barić I; Cuk M; Fumić K; Vugrek O; Allen RH; Glenn B; Maradin M; Pazanin L; Pogribny I; Rados M; Sarnavka V; Schulze A; Stabler S; Wagner C; Zeisel SH; Mudd SH
    J Inherit Metab Dis; 2005; 28(6):885-902. PubMed ID: 16435181
    [TBL] [Abstract][Full Text] [Related]  

  • 3. S-adenosylhomocysteine hydrolase deficiency in a 26-year-old man.
    Buist NR; Glenn B; Vugrek O; Wagner C; Stabler S; Allen RH; Pogribny I; Schulze A; Zeisel SH; Barić I; Mudd SH
    J Inherit Metab Dis; 2006 Aug; 29(4):538-45. PubMed ID: 16736098
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function.
    Bjursell MK; Blom HJ; Cayuela JA; Engvall ML; Lesko N; Balasubramaniam S; Brandberg G; Halldin M; Falkenberg M; Jakobs C; Smith D; Struys E; von Döbeln U; Gustafsson CM; Lundeberg J; Wedell A
    Am J Hum Genet; 2011 Oct; 89(4):507-15. PubMed ID: 21963049
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.
    Honzík T; Magner M; Krijt J; Sokolová J; Vugrek O; Belužić R; Barić I; Hansíkova H; Elleder M; Veselá K; Bauerová L; Ondrušková N; Ješina P; Zeman J; Kožich V
    Mol Genet Metab; 2012 Nov; 107(3):611-3. PubMed ID: 22959829
    [TBL] [Abstract][Full Text] [Related]  

  • 7. S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes.
    Grubbs R; Vugrek O; Deisch J; Wagner C; Stabler S; Allen R; Barić I; Rados M; Mudd SH
    J Inherit Metab Dis; 2010 Dec; 33(6):705-13. PubMed ID: 20852937
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
    Augoustides-Savvopoulou P; Luka Z; Karyda S; Stabler SP; Allen RH; Patsiaoura K; Wagner C; Mudd SH
    J Inherit Metab Dis; 2003; 26(8):745-59. PubMed ID: 14739680
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Elucidation of the mechanism by which homocysteine potentiates the anti-vaccinia virus effects of the S-adenosylhomocysteine hydrolase inhibitor 9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine.
    Hasobe M; McKee JG; Ishii H; Cools M; Borchardt RT; De Clercq E
    Mol Pharmacol; 1989 Sep; 36(3):490-6. PubMed ID: 2779528
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effects of 4'-modified analogs of aristeromycin on the metabolism of S-adenosyl-L-homocysteine in murine L929 cells.
    Ault-Riché DB; Lee Y; Yuan CS; Hasobe M; Wolfe MS; Borcherding DR; Borchardt RT
    Mol Pharmacol; 1993 Jun; 43(6):989-97. PubMed ID: 8316227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiency.
    Stender S; Chakrabarti RS; Xing C; Gotway G; Cohen JC; Hobbs HH
    Mol Genet Metab; 2015 Dec; 116(4):269-74. PubMed ID: 26527160
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inactivation of S-adenosylhomocysteine hydrolase by 9-beta-D-arabinofuranosyladenine in intact cells.
    Helland S; Ueland PM
    Cancer Res; 1982 Mar; 42(3):1130-6. PubMed ID: 7059972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase in various tissues of mice given injections of 9-beta-D-arabinofuranosyladenine.
    Helland S; Ueland PM
    Cancer Res; 1983 Apr; 43(4):1847-50. PubMed ID: 6831422
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of 9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine and -3-deazaadenine on the metabolism of S-adenosylhomocysteine in mouse L929 cells.
    Hasobe M; Mckee JG; Borcherding DR; Keller BT; Borchardt RT
    Mol Pharmacol; 1988 Jun; 33(6):713-20. PubMed ID: 2454388
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiency.
    Strauss KA; Ferreira C; Bottiglieri T; Zhao X; Arning E; Zhang S; Zeisel SH; Escolar ML; Presnick N; Puffenberger EG; Vugrek O; Kovacevic L; Wagner C; Mazariegos GV; Mudd SH; Soltys K
    Mol Genet Metab; 2015; 116(1-2):44-52. PubMed ID: 26095522
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Plasma biomarker identification in S-adenosylhomocysteine hydrolase deficiency.
    Sedic M; Kraljevic Pavelic S; Cindric M; Vissers JP; Peronja M; Josic D; Cuk M; Fumic K; Pavelic K; Baric I
    Electrophoresis; 2011 Aug; 32(15):1970-5. PubMed ID: 21732553
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disposition of homocysteine in rat hepatocytes and in nontransformed and malignant mouse embryo fibroblasts following exposure to inhibitors of S-adenosylhomocysteine catabolism.
    Svardal AM; Djurhuus R; Refsum H; Ueland PM
    Cancer Res; 1986 Oct; 46(10):5095-100. PubMed ID: 3756867
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The effect of aliphatic adenine analogues on S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase in intact rat hepatocytes.
    Schanche JS; Schanche T; Ueland PM; Holý A; Votruba I
    Mol Pharmacol; 1984 Nov; 26(3):553-8. PubMed ID: 6493210
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial hypermethioninemia partially responsive to dietary restriction.
    Labrune P; Perignon JL; Rault M; Brunet C; Lutun H; Charpentier C; Saudubray JM; Odievre M
    J Pediatr; 1990 Aug; 117(2 Pt 1):220-6. PubMed ID: 2380820
    [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 10.