BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 16322984)

  • 1. Mitochondrial transport in proline catabolism in plants: the existence of two separate translocators in mitochondria isolated from durum wheat seedlings.
    Di Martino C; Pizzuto R; Pallotta ML; De Santis A; Passarella S
    Planta; 2006 May; 223(6):1123-33. PubMed ID: 16322984
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proline transport in rat kidney mitochondria.
    Atlante A; Passarella S; Pierro P; Quagliariello E
    Arch Biochem Biophys; 1994 Feb; 309(1):139-48. PubMed ID: 7906935
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The mechanism of proline/glutamate antiport in rat kidney mitochondria. Energy dependence and glutamate-carrier involvement.
    Atlante A; Passarella S; Pierro P; Di Martino C; Quagliariello E
    Eur J Biochem; 1996 Oct; 241(1):171-7. PubMed ID: 8898903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Possible plant mitochondria involvement in cell adaptation to drought stress. A case study: durum wheat mitochondria.
    Pastore D; Trono D; Laus MN; Di Fonzo N; Flagella Z
    J Exp Bot; 2007; 58(2):195-210. PubMed ID: 17261694
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Plant inner membrane anion channel (PIMAC) function in plant mitochondria.
    Laus MN; Soccio M; Trono D; Cattivelli L; Pastore D
    Plant Cell Physiol; 2008 Jul; 49(7):1039-55. PubMed ID: 18511459
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Kinetic and energetic characterization of solute flux through the reconstituted aspartate/glutamate carrier from beef heart mitochondria after modification with mercurials.
    Herick K; Krämer R
    Biochim Biophys Acta; 1995 Aug; 1238(1):63-71. PubMed ID: 7654752
    [TBL] [Abstract][Full Text] [Related]  

  • 8. L-Proline uptake in Saccharomyces cerevisiae mitochondria can contribute to bioenergetics during nutrient stress as alternative mitochondrial fuel.
    Pallotta ML
    World J Microbiol Biotechnol; 2014 Jan; 30(1):19-31. PubMed ID: 23824663
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The existence of phospholipase A(2) activity in plant mitochondria and its activation by hyperosmotic stress in durum wheat (Triticum durum Desf.).
    Trono D; Soccio M; Laus MN; Pastore D
    Plant Sci; 2013 Feb; 199-200():91-102. PubMed ID: 23265322
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transport and metabolism of L-lactate occur in mitochondria from cerebellar granule cells and are modified in cells undergoing low potassium dependent apoptosis.
    Atlante A; de Bari L; Bobba A; Marra E; Passarella S
    Biochim Biophys Acta; 2007 Nov; 1767(11):1285-99. PubMed ID: 17950241
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reactive oxygen species inhibit the succinate oxidation-supported generation of membrane potential in wheat mitochondria.
    Pastore D; Laus MN; Di Fonzo N; Passarella S
    FEBS Lett; 2002 Apr; 516(1-3):15-9. PubMed ID: 11959094
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Durum wheat dehydrin (DHN-5) confers salinity tolerance to transgenic Arabidopsis plants through the regulation of proline metabolism and ROS scavenging system.
    Saibi W; Feki K; Ben Mahmoud R; Brini F
    Planta; 2015 Nov; 242(5):1187-94. PubMed ID: 26105651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectroscopic study of hydroxyproline transport in rat kidney mitochondria.
    Atlante A; Passarella S; Quagliariello E
    Biochem Biophys Res Commun; 1994 Jul; 202(1):58-64. PubMed ID: 8037764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of the sodium chloride-dependent respiratory kinetics of wheat mitochondria reveals differential effects on phosphorylating and non-phosphorylating electron transport pathways.
    Jacoby RP; Che-Othman MH; Millar AH; Taylor NL
    Plant Cell Environ; 2016 Apr; 39(4):823-33. PubMed ID: 26470009
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proline accumulation is a general response to abiotic stress in the date palm tree (Phoenix dactylifera L.).
    Yaish MW
    Genet Mol Res; 2015 Aug; 14(3):9943-50. PubMed ID: 26345930
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carrier mediated GABA translocation into rat brain mitochondria.
    Passarella S; Atlante A; Barile M; Quagliariello E
    Biochem Biophys Res Commun; 1984 Jun; 121(3):770-8. PubMed ID: 6743319
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-Wide Expression Analysis of Glyoxalase I Genes Under Hyperosmotic Stress and Existence of a Stress-Responsive Mitochondrial Glyoxalase I Activity in Durum Wheat (
    Soccio M; Marangi M; Laus MN
    Front Plant Sci; 2022; 13():934523. PubMed ID: 35832233
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Proline transport by tsetse fly Glossina morsitans flight muscle mitochondria.
    Njagi EN; Olembo NK; Pearson DJ
    Comp Biochem Physiol B; 1992 Jul; 102(3):579-84. PubMed ID: 1499295
    [TBL] [Abstract][Full Text] [Related]  

  • 19. D-Lactate transport and metabolism in rat liver mitochondria.
    de Bari L; Atlante A; Guaragnella N; Principato G; Passarella S
    Biochem J; 2002 Jul; 365(Pt 2):391-403. PubMed ID: 11955284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Potassium channel-oxidative phosphorylation relationship in durum wheat mitochondria from control and hyperosmotic-stressed seedlings.
    Trono D; Soccio M; Laus MN; Pastore D
    Plant Cell Environ; 2011 Dec; 34(12):2093-108. PubMed ID: 21819416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.