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 *

63 related articles for article (PubMed ID: 412246)

  • 1. Metabolic studies on normal and pyruvate dehydrogenase deficient cultured human fibroblasts.
    Borud O; Stroomme JH
    Scand J Clin Lab Invest; 1977 Sep; 37(5):419-23. PubMed ID: 412246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Magnetic resonance spectroscopic investigation of mitochondrial fuel metabolism and energetics in cultured human fibroblasts: effects of pyruvate dehydrogenase complex deficiency and dichloroacetate.
    Simpson NE; Han Z; Berendzen KM; Sweeney CA; Oca-Cossio JA; Constantinidis I; Stacpoole PW
    Mol Genet Metab; 2006; 89(1-2):97-105. PubMed ID: 16765624
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase.
    Strömme JH; Borud O; Moe PJ
    Pediatr Res; 1976 Jan; 10(1):62-6. PubMed ID: 813176
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.
    Haworth JC; Perry TL; Blass JP; Hansen S; Urquhart N
    Pediatrics; 1976 Oct; 58(4):564-72. PubMed ID: 184426
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inherited lactic acidosis: correction of the defect in cultured fibroblasts.
    Goodyer PR; Lancaster GA
    Pediatr Res; 1984 Nov; 18(11):1144-8. PubMed ID: 6440113
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparative analysis of glucose and glutamine metabolism in transformed mammalian cell lines, insect and primary liver cells.
    Neermann J; Wagner R
    J Cell Physiol; 1996 Jan; 166(1):152-69. PubMed ID: 8557765
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis.
    Robinson BH; Taylor J; Sherwood WG
    Pediatr Res; 1980 Aug; 14(8):956-62. PubMed ID: 6775276
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lactate oxidation for the detection of mitochondrial dysfunction in human skin fibroblasts.
    Ofenstein JP; Kiechle FL; Dandurand DM; Belknap WM; Moore KH; Holmes RD
    Anal Biochem; 1993 May; 210(2):332-6. PubMed ID: 8512068
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A case of congenital lactic acidosis caused by deficiency of pyruvate dehydrogenase].
    Salti R; Galluzzi F; Liguri GF; Marianelli L; Zammarchi E; La Cauza C
    Minerva Pediatr; 1979 Nov; 31(21):1539-46. PubMed ID: 118331
    [No Abstract]   [Full Text] [Related]  

  • 10. An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis.
    Blass JP; Schulman JD; Young DS; Hom E
    J Clin Invest; 1972 Jul; 51(7):1845-51. PubMed ID: 5032527
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deficiency of the pyruvate dehydrogenase complex and of mitochondrial fatty acid oxidation.
    Bindoff LA; Birch-Machin MA; Jackson S; Singh Kler R; Bartlett K; Turnbull DM
    Rev Neurol (Paris); 1991; 147(6-7):526-31. PubMed ID: 1962058
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Utilization of pyruvate and pyruvate precursors by normal and carcinogen-altered rat tracheal epithelial cells in culture.
    Wasilenko WJ; Marchok AC
    J Cell Physiol; 1986 Jan; 126(1):69-76. PubMed ID: 3944199
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Krebs cycle, pentose phosphate pathway, and glycolysis in the uninvolved gastric mucosa of peptic ulcer and gastric cancer patients.
    Orwell RL; Piper DW
    Gastroenterology; 1977 Dec; 73(6):1320-5. PubMed ID: 913974
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Pyruvate dehydrogenase deficiency in a child with persistent lactic acidosis].
    Dworzak E; Grunicke H; Berger H; Jarosch E; Haas H; Höpfel I
    J Clin Chem Clin Biochem; 1985 Jun; 23(6):323-9. PubMed ID: 3926941
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.
    Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Willems JL; Janssen AJ; Slooff JL; Geelen JA; de Jager JP
    Neuropediatrics; 1982 May; 13(2):108-11. PubMed ID: 6813759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Aerobic glycolysis of bone and cartilage: the possible involvement of fatty acid oxidation.
    Dunham J; Dodds RA; Nahir AM; Frost GT; Catterall A; Bitensky L; Chayen J
    Cell Biochem Funct; 1983 Oct; 1(3):168-72. PubMed ID: 6678623
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Differential diagnosis of the symptom of lactic acidosis in childhood].
    Koepp P
    Monatsschr Kinderheilkd; 1984 May; 132(5):264-7. PubMed ID: 6087128
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel functional assay for simultaneous determination of total fatty acid beta-oxidation flux and acylcarnitine profiling in human skin fibroblasts using (2)H(31)-palmitate by isotope ratio mass spectrometry and electrospray tandem mass spectrometry.
    Law LK; Tang NL; Hui J; Ho CS; Ruiter J; Fok TF; Wanders RJ; Lam CW
    Clin Chim Acta; 2007 Jul; 382(1-2):25-30. PubMed ID: 17442290
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A defect in branched-chain amino acid metabolism in a patient with congenital lactic acidosis due to dihydrolipoyl dehydrogenase deficiency.
    Taylor J; Robinson BH; Sherwood WG
    Pediatr Res; 1978 Jan; 12(1):60-2. PubMed ID: 643378
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Glucose metabolism and template synthesis in the mitotic cycle of human diploid fibroblasts].
    Alekseev SB; Ebralidze LK; Stepanova LG; Boĭkov PIa
    Biokhimiia; 1986 Jan; 51(1):140-5. PubMed ID: 2420373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.