These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 15739)

  • 1. Detection of errors in methylmalonyl-CoA metabolism by using amniotic fluid.
    Morrow G; Revsin B; Lebowitz J; Britt W; Giles H
    Clin Chem; 1977 May; 23(5):791-5. PubMed ID: 15739
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzyme.
    Baumgartner ER; Bachmann C; Wick H
    Enzyme; 1976; 21(6):553-67. PubMed ID: 12939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemia.
    Ampola MG; Mahoney MJ; Nakamura E; Tanaka K
    N Engl J Med; 1975 Aug; 293(7):313-7. PubMed ID: 239344
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Studies of methylmalonyl-coenzyme A carbonylmutase activity in methylmalonic acidemia. II. In vitro binding kinetics with adenosylcobalamin.
    Morrow G; Lebowitz J
    Biochem Med; 1976 Jun; 15(3):241-5. PubMed ID: 11786
    [No Abstract]   [Full Text] [Related]  

  • 5. Improved prenatal diagnosis of methylmalonic acidemia: mass fragmentography of methylmalonic acid in amniotic fluid and maternal urine.
    Trefz FK; Schmidt H; Tauscher B; Depène E; Baumgartner R; Hammersen G; Kochen W
    Eur J Pediatr; 1981 Nov; 137(3):261-6. PubMed ID: 7318836
    [No Abstract]   [Full Text] [Related]  

  • 6. Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia.
    Narisawa K; Saito T; Hisa S; Suzuki H; Hayasaka K
    Tohoku J Exp Med; 1977 Sep; 123(1):1-8. PubMed ID: 21471
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
    Morel CF; Watkins D; Scott P; Rinaldo P; Rosenblatt DS
    Mol Genet Metab; 2005; 86(1-2):160-71. PubMed ID: 16150626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Studies of methylmalonyl coenzyme A carbonylmutase activity in methylmalonic acidemia. I. Correlation of clinical, hepatic, and fibroblast data.
    Morrow G; Mahoney MJ; Mathews C; Lebowitz J
    Pediatr Res; 1975 Aug; 9(8):641-4. PubMed ID: 239382
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of methylmalonic aciduria.
    Mahoney MJ; Rosenberg LE; Lindblad B; Waldenström J; Zetterström R
    Acta Paediatr Scand; 1975 Jan; 64(1):44-48. PubMed ID: 1114896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts.
    Willard HF; Rosenberg LE
    Biochem Genet; 1979 Feb; 17(1-2):57-75. PubMed ID: 36882
    [TBL] [Abstract][Full Text] [Related]  

  • 11. First trimester diagnosis of methylmalonic aciduria.
    Fowler B; Giles L; Sardharwalla IB; Donnai P; Clayton JK
    Prenat Diagn; 1988 Mar; 8(3):207-13. PubMed ID: 2897685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of methylmalonic aciduria.
    Gompertz D; Goodey PA; Saudubray JM; Charpentier C; Chignolle A; Girard S
    Pediatrics; 1974 Oct; 54(4):511-3. PubMed ID: 4415169
    [No Abstract]   [Full Text] [Related]  

  • 13. [Methylmalonic acidemia. Diagnosis and treatment in various patients].
    Bakker HD; Duran M; van Gennip AH; van Sprang FJ; Wadman SK
    Ned Tijdschr Geneeskd; 1978 May; 122(20):707-12. PubMed ID: 26029
    [No Abstract]   [Full Text] [Related]  

  • 14. Possible interrelationship between vitamins E and b12 in the disturbance in methylmalonate metabolism in vitamin E deficiency.
    Pappu AS; Fatterpaker P; Sreenivasan A
    Biochem J; 1978 Apr; 172(1):115-21. PubMed ID: 656065
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: use in prenatal diagnosis of methylmalonic acidemia and in studies of isovaleric acidemia.
    Nakamura E; Rosenberg LE; Tanaka K
    Clin Chim Acta; 1976 Apr; 68(2):127-40. PubMed ID: 1261058
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells.
    Willard HF; Ambani LM; Hart AC; Mahoney MJ; Rosenberg LE
    Hum Genet; 1976 Dec; 34(3):277-83. PubMed ID: 1002151
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase.
    Drennan CL; Matthews RG; Rosenblatt DS; Ledley FD; Fenton WA; Ludwig ML
    Proc Natl Acad Sci U S A; 1996 May; 93(11):5550-5. PubMed ID: 8643613
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
    Morrow G; Revsin B; Clark R; Lebowitz J; Whelan DT
    Clin Chim Acta; 1978 Apr; 85(1):67-72. PubMed ID: 25730
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homology modeling of human methylmalonyl-CoA mutase: a structural basis for point mutations causing methylmalonic aciduria.
    Thomä NH; Leadlay PF
    Protein Sci; 1996 Sep; 5(9):1922-7. PubMed ID: 8880917
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemia.
    Ledley FD; Jansen R; Nham SU; Fenton WA; Rosenberg LE
    Proc Natl Acad Sci U S A; 1990 Apr; 87(8):3147-50. PubMed ID: 1970180
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.