Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture
Publication date:
2013
Publisher version:
Citación:
Journal of Proteomics, 91, p. 466-477 (2013); doi:10.1016/j.jprot.2013.08.008
Descripción física:
p. 466-477
ISSN:
Identificador local:
20131055
Patrocinado por:
Work in the author's laboratories is supported by grants from the Spanish Ministry of Economy and Competiveness(MINECO)(SAF2010-16044; SAF2011-23089, SAF2009-08007, CSD2007-00020, CTQ2010-18644), Instituto de Salud Carlos III(ISCIII) (RD06/0014/0021, RD12/0042/0028), the Progeria Research Foundation (Innovator Award PRF 2012-42), and Comunidad de Madrid (S2011/BMD-2402). P.C.-S. was financially supported by an FPU scholarship from the Spanish Ministry of Education. The Centro Nacional de Investigaciones Cardiovasculares (CNIC) is supported by MINECO and Pro-CNIC Foundation, and the Instituto Universitario de Oncología by Obra Social Cajastur
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