Directory
Jordi Tamarit Sumalla

Jordi Tamarit Sumalla

Degree: PhD

973 702 475
jordi.tamarit(ELIMINAR)@udl.cat

ResearcherID: http://www.researcherid.com/rid/C-6316-2008

Publications

  • Reverter-Branchat, Gemma; Cabiscol, Elisa; Tamarit, Jordi; Sorolla, M. Alba; de la Torre, M. Angeles; Ros, Joaquim

    Chronological and replicative life-span extension in Saccharomyces cerevisiae by increased dosage of alcohol dehydrogenase 1.

    MICROBIOLOGY-SGM 153 3667-3676. .

    [doi:10.1099/mic.0.2007/009340-0]

  • Garcera, Ana; Barreto, Lina; Piedrafita, Lidia; Tamarit, Jordi; Herrero, Enrique

    Saccharomyces cerevisiae cells have three Omega class glutathione S-transferases acting as 1-Cys thiol transferases.

    BIOCHEMICAL JOURNAL 398 187-196. .

    [doi:10.1042/BJ20060034]

  • Herrero, Enrique; Ros, Joaquim; Tamarit, Jordi; Belli, Gemma

    Glutaredoxins in fungi.

    Photosynthesis Research 89 127-140. .

    [doi:10.1007/s11120-006-9079-3]

  • Irazusta, V; Cabiscol, E; Reverter-Branchat, G; Ros, J; Tamarit, J

    Manganese is the link between frataxin and iron-sulfur deficiency in the yeast model of Friedreich ataxia.

    Journal Of Biological Chemistry 281 12227-12232. .

    [doi:10.1074/jbc.M511649200]

  • Tamarit, J; Irazusta, V; Moreno-Cermeno, A; Ros, J

    Colorimetric assay for the quantitation of iron in yeast.

    ANAL BIOCHEM 351 149-151. .

    [doi:10.1016/j.ab.2005.12.001]

  • Reverter-Branchat, G; Cabiscol, E; Tamarit, J; Ros, J

    Oxidative damage to specific proteins in replicative and chronological-aged Saccharomyces cerevisiae: common targets and prevention by calorie restriction.

    Journal Of Biological Chemistry 279 31983-31989. .

    [doi:10.1074/jbc.M404849200]

  • Echave, P; Tamarit, J; Cabiscol, E; Ros, J

    Novel antioxidant role of alcohol dehydrogenase E from Escherichia coli.

    Journal Of Biological Chemistry 278 30193-30198. .

    [doi:10.1074/jbc.M304351200]

  • Tamarit, J; Belli, G; Cabiscol, E; Herrero, E; Ros, J

    Biochemical characterization of yeast mitochondrial Grx5 monothiol glutaredoxin.

    Journal Of Biological Chemistry 278 25745-25751. .

    [doi:10.1074/jbc.M303477200]

  • Reverter, G; Cabiscol, E; Tamarit, J; Ros, J

    Chronological aging and protein oxidative damage.

    YEAST 20 187-187. .

  • Tamarit, J; Belli, G; Cabiscol, E; Herrero, E; Ros, J

    Mitochondrial monothiol glutaredoxin Grx5: mechanism of action.

    YEAST 20 45-45. .

  • Cabiscol, E; Belli, G; Tamarit, J; Echave, P; Herrero, E; Ros, J

    Mitochondrial Hsp60, resistance to oxidative stress, and the labile iron pool are closely connected in Saccharomyces cerevisiae.

    Journal Of Biological Chemistry 277 44531-44538. .

    [doi:10.1074/jbc.M206525200]

  • Belli, G; Polaina, J; Tamarit, J; de la Torre, MA; Rodriguez-Manzaneque, MT; Ros, J; Herrero, E

    Structure-function analysis of yeast Grx5 monothiol glutaredoxin defines essential amino acids for the function of the protein.

    Journal Of Biological Chemistry 277 37590-37596. .

    [doi:10.1074/jbc.M201688200]

Projects

  • FI-SDUR
  • Alteraciones moleculares en el modelo murino FXNI151F de Ataxia de Friedreich y análisis de nuevas estrategias terapéuticas
  • Uncovering the function of a conserved site in eukaryotic frataxins.
  • Mecanismos de disfuncion mitocondrial y nuevas estrategias terapéuticas en modelos celulares y animales de Ataxia de Friedreich
  • Nuevo fármaco dirigido a la Ataxia de Friedreich
  • Targeting mitochondria in Friedreich Ataxia: molecular mechanisms and therapeutic approaches
  • MODELOS CELULARES DE ATAXIA DE FRIEDREICH: BASES MOLECULARES DE LA PATOLOGIA E IDENTIFICACION DE BIOMARCADORES Y COMPUESTOS CON POTENCIAL TERAPEUTICO
  • Modelos celulares de ataxia de Friedreich: bases moleculares de la patología e identificación de biomarcadores y compuestos con potencial terapéutico
  • PATHOPHYSIOLOGY AND THERAPEUTICS OF FRIENDREICH ATAXIA: MARKERS OR OXIDATIVE STRESS FROM YEAST TO CARDIOMYOCYTES
  • Papel funcional del estrés oxidativo y nitrosativo en grandes sistemas biológicos.
  • Estrés oxidativo, envejecimiento celular, homeostasis del hierro y patologías relacionadas en S. cerevisae como modelo celular