Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Noelia Artime"'
Autor:
Lucia Cabal-Hierro, Lorea J Ugarte-Gil, Noelia Artime, Miguel A. Prado, Bryant G. Darnay, Pedro Casado, J. Iglesias, Pedro S. Lazo, Belén Fernández-García
Publikováno v:
Oncotarget
Tumor Necrosis Factor (TNF) interacts with two receptors known as TNFR1 and TNFR2. TNFR1 activation may result in either cell proliferation or cell death. TNFR2 activates Nuclear Factor-kappaB (NF-kB) and c-Jun N-terminal kinase (JNK) which lead to t
Autor:
Pedro S. Lazo, Patricia Ruperez, Pedro Zuazua-Villar, Alma L. Burlingame, Lucia Cabal-Hierro, Sofía Ramos, Miguel A. Prado, Noelia Artime, Pedro Casado, Eva del Valle
Publikováno v:
Journal of Proteomics. 71:592-600
Microtubule interfering agents (MIAs) are anti-tumor drugs that inhibit microtubule dynamics, while kinesin spindle protein (KSP) inhibitors are substances that block the formation of the bipolar spindle during mitosis. All these compounds cause G2/M
Autor:
Lucia Cabal-Hierro, Noelia Artime, Pedro Zuazua-Villar, Eva del Valle, Carlos Martínez-Campa, Pedro S. Lazo, Pedro Casado, Sofía Ramos, Miguel A. Prado
Publikováno v:
PROTEOMICS. 7:3299-3304
Departamento de Bioquimica y Biologia Molecular, Instituto Universitario de Oncologiadel Principado de Asturias, Universidad de Oviedo, Oviedo, SpainPaclitaxel (Ptx) is an antitumoural drug that inhibits microtubule dynamics, causes G2/M arrestand in
Autor:
Pedro S. Lazo, Lorea Ugarte, Noelia Artime, Miguel A. Prado, Lucia Cabal-Hierro, J. Iglesias, Montserrat Rodríguez
Publikováno v:
Cellular signalling. 26(12)
Tumor Necrosis Factor Receptor 2 (TNFR2) activates transcription factor κB (NF-κB) and c-Jun N-terminal kinase (JNK). Most of the biological activities triggered by TNFR2 depend on the recruitment of TNF Receptor-Associated Factor 2 (TRAF2) to the
Autor:
Juan Antonio López, Enrique Calvo, Pedro S. Lazo, Lucia Cabal-Hierro, Lorea J Ugarte-Gil, Pedro Casado, Miguel A. Prado, Belén Fernández-García, Noelia Artime, Sofía Ramos
Publikováno v:
Journal of proteome research. 9(9)
Microtubule interfering agents (MIAs) are antitumor drugs that inhibit microtubule dynamics, while kinesin spindle protein (KSP) inhibitors are substances that block the formation of the bipolar spindle during mitosis. All these compounds cause the a
Autor:
Belen Fernandez-Garcia, Pedro Casado, Miguel A. Prado, Lorea J. Ugarte-Gil, Noelia Artime, Lucía Cabal-Hierro, Enrique Calvo, Juan Antonio López, Sofía Ramos, Pedro S. Lazo
Publikováno v:
Journal of Proteome Research; Sep2010, Vol. 9 Issue 9, p4649-4660, 12p