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 *

223 related articles for article (PubMed ID: 12939)

  • 61. Inhibition by methylmalonate of glycine uptake by synaptosomes from rat spinal cord.
    Lopez-Lahoya J; García ML; Benavides J; Ugarte M
    J Neurochem; 1981 Jan; 36(1):325-7. PubMed ID: 6109757
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes.
    Chandler RJ; Tsai MS; Dorko K; Sloan J; Korson M; Freeman R; Strom S; Venditti CP
    BMC Med Genet; 2007 Apr; 8():24. PubMed ID: 17470278
    [TBL] [Abstract][Full Text] [Related]  

  • 63. The natural history of the inherited methylmalonic acidemias.
    Matsui SM; Mahoney MJ; Rosenberg LE
    N Engl J Med; 1983 Apr; 308(15):857-61. PubMed ID: 6132336
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Function of vitamin B12 in methylmalonate metabolism. I. Effect of a cofactor form of B12 on the activity of methylmalonyl-CoA isomerase.
    GURNANI S; MISTRY SP; JOHNSON BC
    Biochim Biophys Acta; 1960 Feb; 38():187-8. PubMed ID: 13830365
    [No Abstract]   [Full Text] [Related]  

  • 65. Isolated methylmalonic acidemia: a case report.
    Es Sadki T; Badiou S; Boubal M; Baleine J; Sieso V; Vallat C; Cristol JP; Vianey-Saban C; Cambonie G
    Ann Biol Clin (Paris); 2016 Aug; 74(4):472-6. PubMed ID: 27492701
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [13C]Valine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate.
    Tanaka K; Armitage IM; Ramsdell HS; Hsia YE; Lipsky SR; Rosenberg LE
    Proc Natl Acad Sci U S A; 1975 Sep; 72(9):3692-6. PubMed ID: 1059159
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.
    Crane AM; Ledley FD
    Am J Hum Genet; 1994 Jul; 55(1):42-50. PubMed ID: 7912889
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Assembly and protection of the radical enzyme, methylmalonyl-CoA mutase, by its chaperone.
    Padovani D; Banerjee R
    Biochemistry; 2006 Aug; 45(30):9300-6. PubMed ID: 16866376
    [TBL] [Abstract][Full Text] [Related]  

  • 69. [Studies on the biological function of the nucleotide base of vitamin B12].
    Eberhard G; Schlayer H; Joseph H; Fridrich E; Utz B; Müller O
    Biol Chem Hoppe Seyler; 1988 Oct; 369(10):1091-8. PubMed ID: 2907405
    [TBL] [Abstract][Full Text] [Related]  

  • 70. A radio-HPLC assay for the measurement of methylmalonyl-CoA mutase.
    Causey AG; Bartlett K
    Clin Chim Acta; 1984 May; 139(2):179-86. PubMed ID: 6145531
    [No Abstract]   [Full Text] [Related]  

  • 71. Genome and RNA sequencing in patients with methylmalonic aciduria of unknown cause.
    Abdrabo LS; Watkins D; Wang SR; Lafond-Lapalme J; Riviere JB; Rosenblatt DS
    Genet Med; 2020 Feb; 22(2):432-436. PubMed ID: 31462756
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Genetic testing is necessary for correct diagnosis and treatment in patients with isolated methylmalonic aciduria: a case report.
    Brennerová K; Škopková M; Ostrožlíková M; Šaligová J; Staník J; Bzdúch V; Gašperíková D
    BMC Pediatr; 2021 Dec; 21(1):578. PubMed ID: 34915869
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Mirror "base-off" conformation of coenzyme B12 in human adenosyltransferase and its downstream target, methylmalonyl-CoA mutase.
    Yamanishi M; Labunska T; Banerjee R
    J Am Chem Soc; 2005 Jan; 127(2):526-7. PubMed ID: 15643868
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Isolation and characterization of DL-methylmalonyl-coenzyme A racemase from rat liver.
    Stabler SP; Marcell PD; Allen RH
    Arch Biochem Biophys; 1985 Aug; 241(1):252-64. PubMed ID: 2862845
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Novel mutation of methylmalonyl-CoA mutase gene causing the mut0 form of methylmalonic acidemia in a Japanese girl.
    Oyama C; Takahashi T; Matsumori M; Shoji Y; Tajima G; Sakura N; Hasegawa Y; Yamaguchi S; Kakinuma H; Takada G
    Pediatr Int; 2007 Apr; 49(2):232-4. PubMed ID: 17445044
    [No Abstract]   [Full Text] [Related]  

  • 76. Congenital absence of insulin cells in a neonate with diabetes mellitus and mutase-deficient methylmalonic acidaemia.
    Blum D; Dorchy H; Mouraux T; Vamos E; Mardens Y; Kumps A; De Prez C; Heimann P; Fowler B; Baumgartner R
    Diabetologia; 1993 Apr; 36(4):352-7. PubMed ID: 8097481
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Studies on the urinary acidic metabolites from three patients with methylmalonic aciduria.
    Kuhara T; Matsumoto I
    Biomed Mass Spectrom; 1980 Oct; 7(10):424-8. PubMed ID: 6111361
    [TBL] [Abstract][Full Text] [Related]  

  • 78. 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]  

  • 79. Novel c.2216T > C (p.I739T) mutation in exon 13 and c.1481T > A (p.L494X) mutation in exon 8 of MUT gene in a female with methylmalonic acidemia.
    Imataka G; Sakamoto O; Yamanouchi H; Yoshihara S; Omura-Hasegawa Y; Tajima G; Arisaka O
    Cell Biochem Biophys; 2013 Sep; 67(1):185-7. PubMed ID: 23479330
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria.
    Bikker H; Bakker HD; Abeling NG; Poll-The BT; Kleijer WJ; Rosenblatt DS; Waterham HR; Wanders RJ; Duran M
    Hum Mutat; 2006 Jul; 27(7):640-3. PubMed ID: 16752391
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.