Identification of mitochondrial dysfunction in Hutchinson–Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture-Reference-Cited by-同舟云学术

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Identification of mitochondrial dysfunction in Hutchinson–Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture

Published:2013-10 Issue: Volume:91 Page:466-477
ISSN:1874-3919
Container-title:Journal of Proteomics
language:en
Short-container-title:Journal of Proteomics

Author:

Rivera-Torres José,Acín-Perez Rebeca,Cabezas-Sánchez Pablo,Osorio Fernando G.,Gonzalez-Gómez Cristina,Megias Diego,Cámara Carmen,López-Otín Carlos,Enríquez José Antonio,Luque-García José L.,Andrés Vicente

Funder

Spanish Ministry of Economy and Competiveness (MINECO)

Instituto de Salud Carlos III (ISCIII)

Progeria Research Foundation

Comunidad de Madrid

FPU scholarship from the Spanish Ministry of Education

MINECO and Pro-CNIC Foundation

Obra Social Cajastur

Publisher

Elsevier BV

Subject

Biochemistry,Biophysics

Reference56 articles.

1. Role of A-type lamins in signaling, transcription, and chromatin organization;Andres;J Cell Biol,2009

2. The nuclear envelope in genome organization, expression and stability;Mekhail;Nat Rev Mol Cell Biol,2010

3. Nuclear lamins;Dechat;Cold Spring Harb Perspect Biol,2010

4. Hutchinson–Gilford progeria syndrome, cardiovascular disease and oxidative stress;Trigueros-Motos;Front Biosci (Schol Ed),2011

5. Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice;Pendas;Nat Genet,2002

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