Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function-Reference-Cited by-同舟云学术

Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function

Published:2015-05 Issue: Volume:22 Page:96-118
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Iommarini Luisa,Peralta Susana,Torraco Alessandra,Diaz Francisca

Funder

Florida Department of Health

National Institute of Health

United Mitochondrial Disease Foundation

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference255 articles.

1. A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy;Acham-Roschitz;Mol. Genet. Metab.,2009

2. Somatic progenitor cell vulnerability to mitochondrial DNA mutagenesis underlies progeroid phenotypes in Polg mutator mice;Ahlqvist;Cell Metab.,2012

3. Ketogenic diet slows down mitochondrial myopathy progression in mice;Ahola-Erkkilä;Hum. Mol. Genet.,2010

4. Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance;Akman;Hum. Mol. Genet.,2008

5. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy;Alavi;Brain,2007

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