BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 212270)

  • 1. Mitochondrial transport processes and oxidation of NADH by hypotonically-treated boar spermatozoa.
    Calvin J; Tubbs PK
    Eur J Biochem; 1978 Aug; 89(1):315-20. PubMed ID: 212270
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Calcium transport in bovine sperm mitochondria: effect of substrates and phosphate.
    Breitbart H; Wehbie R; Lardy HA
    Biochim Biophys Acta; 1990 Jul; 1026(1):57-63. PubMed ID: 1696124
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial metabolism of pyruvate in bovine spermatozoa.
    Hutson SM; Van Dop C; Lardy HA
    J Biol Chem; 1977 Feb; 252(4):1309-15. PubMed ID: 838719
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Occurrence of the malate-aspartate shuttle in various tumor types.
    Greenhouse WV; Lehninger AL
    Cancer Res; 1976 Apr; 36(4):1392-6. PubMed ID: 177206
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Malate-aspartate shuttle, cytoplasmic NADH redox potential, and energetics in vascular smooth muscle.
    Barron JT; Gu L; Parrillo JE
    J Mol Cell Cardiol; 1998 Aug; 30(8):1571-9. PubMed ID: 9737943
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Metabolic activity of hypotonically treated mature boar spermatozoa.
    Jones AR
    Reprod Fertil Dev; 1997; 9(6):583-6. PubMed ID: 9551661
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Operation and energy dependence of the reducing-equivalent shuttles during lactate metabolism by isolated hepatocytes.
    Berry MN; Phillips JW; Gregory RB; Grivell AR; Wallace PG
    Biochim Biophys Acta; 1992 Sep; 1136(3):223-30. PubMed ID: 1520699
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isolated durum wheat and potato cell mitochondria oxidize externally added NADH mostly via the malate/oxaloacetate shuttle with a rate that depends on the carrier-mediated transport.
    Pastore D; Di Pede S; Passarella S
    Plant Physiol; 2003 Dec; 133(4):2029-39. PubMed ID: 14671011
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Oxidation of reduced cytosolic nicotinamide adenine dinucleotide by the malate-aspartate shuttle in the K-562 human leukemia cell line.
    López-Alarcón L; Eboli ML
    Cancer Res; 1986 Nov; 46(11):5589-91. PubMed ID: 3756905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The transport of L-cysteinesulfinate in rat liver mitochondria.
    Palmieri F; Stipani I; Iacobazzi V
    Biochim Biophys Acta; 1979 Aug; 555(3):531-46. PubMed ID: 486467
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Importance of the malate-aspartate shuttle for the reoxidation of glycolytically produced NADH and for cell aggregation in porcine blood platelets.
    Tomasiak M
    Acta Biochim Pol; 1987; 34(3):269-84. PubMed ID: 3687299
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The oxidation of glutamine and glutamate in relation to anion transport in enterocyte mitochondria.
    Evered DF; Masola B
    Biochem J; 1984 Mar; 218(2):449-58. PubMed ID: 6143554
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The lactate/pyruvate shuttle in spermatozoa: operation in vitro.
    Gallina FG; Gerez de Burgos NM; Burgos C; Coronel CE; Blanco A
    Arch Biochem Biophys; 1994 Feb; 308(2):515-9. PubMed ID: 8109982
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reactive oxygen species production in cardiac mitochondria after complex I inhibition: Modulation by substrate-dependent regulation of the NADH/NAD(+) ratio.
    Korge P; Calmettes G; Weiss JN
    Free Radic Biol Med; 2016 Jul; 96():22-33. PubMed ID: 27068062
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Studies on the active transfer of reducing equivalents into mitochondria via the malate-aspartate shuttle.
    Bremer J; Davis EJ
    Biochim Biophys Acta; 1975 Mar; 376(3):387-97. PubMed ID: 164904
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Malate-aspartate shuttle and exogenous NADH/cytochrome c electron transport pathway as two independent cytosolic reducing equivalent transfer systems.
    Abbrescia DI; La Piana G; Lofrumento NE
    Arch Biochem Biophys; 2012 Feb; 518(2):157-63. PubMed ID: 22239987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Oxidation of cytosolic NADH by the malate-aspartate shuttle in HuH13 human hepatoma cells.
    Matsuno T
    Int J Biochem; 1992 Feb; 24(2):313-5. PubMed ID: 1310290
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aminooxyacetic acid inhibits the malate-aspartate shuttle in isolated nerve terminals and prevents the mitochondria from utilizing glycolytic substrates.
    Kauppinen RA; Sihra TS; Nicholls DG
    Biochim Biophys Acta; 1987 Sep; 930(2):173-8. PubMed ID: 3620514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evaluation of functioning of mitochondrial electron transport chain with NADH and FAD autofluorescence.
    Danylovych HV
    Ukr Biochem J; 2016; 88(1):31-43. PubMed ID: 29227076
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Absence of NADH channeling in coupled reaction of mitochondrial malate dehydrogenase and complex I in alamethicin-permeabilized rat liver mitochondria.
    Kotlyar AB; Maklashina E; Cecchini G
    Biochem Biophys Res Commun; 2004 Jun; 318(4):987-91. PubMed ID: 15147970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.