Dra. Alicia Cabezas Martín
Licenciada en Farmacia. Doctora en Bioquímica y Biología Molecular y Genética
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acabezas@unex.es
Afiliaciones:
UEx - Profesor Titular de Universidad
BBB023 - Configuración de Sistemas Moleculares y Celulares
Miembro desde 2025.
CV resumido
Licenciada en Farmacia, Univ. Sevilla 1995.
Becaria pre-doctoral M.E.C. (F.P.I) Facultad de Medicina. Univ. De Extremadura Ene 1997- Dic 2000
Becaria (beca puente) UEx Facultad de Medicina. Univ. De Extremadura Ene 2001- Mar2001
Doctora en Medicina y Cirugía, Facultad de Medicina, Dpto. Bioquímica, UEx Marzo 2001.
Becaria Postdoctoral U.E. Institute for Cancer Research. RadiumHospital. Oslo Abril 2001-Feb 2004
Prof. Titular Interina, UEx, Dpto. Bioquímica y Biología Molecular y Genética, Fac. Medicina. 2004-2010
Prof. Titular de Universidad, UEx, Dpto. Bioquímica y Biología Molecular y Genética, Fac. Medicina. 2010
Publicaciones destacadas
Cabezas A, Costas MJ, Canales J, Pinto RM, Rodrigues JR, Ribeiro JM, Cameselle JC. Enzyme Characterization of Pro-virulent SntA, a Cell Wall-Anchored Protein of Streptococcus suis, With Phosphodiesterase Activity on cyclic-di-AMP at a Level Suited to Limit the Innate Immune System. Frontiers in Microbiology 13, 2022.
Cabezas A, Ribeiro JM, Rodrigues JR, López-Villamizar I, Fernández A, Canales J, Pinto RM, Costas MJ, Cameselle JC. Molecular Bases of Catalysis and ADP-Ribose Preference of Human Mn2+-Dependent ADP-Ribose/CDP-Alcohol Diphosphatase and Conversion by Mutagenesis to a Preferential Cyclic ADP-Ribose Phosphohydrolase. PLOS ONE 10(2):e0118680, 2015.
Cabezas A, Bache KG, Brech A, Stenmark H. Alix regulates cortical actin and the spatial distribution of endosomes. Journal of Cell Science 118(12):2625-2635, 2005.
Hoepfner S, Severin F, Cabezas A, Habermann B, Runge A, Gillooly D, Stenmark H, Zerial M. Modulation of Receptor Recycling and Degradation by the Endosomal Kinesin KIF16B. Cell 121(3):437-450, 2005.
Cameselle, JC. Purification, characterization, and substrate and inhibitor structure-activity studies of rat liver FAD-AMP lyase (cyclizing): Preference for FAD and specificity for splitting ribonucleoside diphosphate-X into ribonucleotide and a five-atom cyclic phosphodiester of X, either a monocyclic compound or a cic-bicyclic phosphodiester-pyranose fusion. Biochemistry 40(45):13710-13722, 2001.
