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The Biochemical Journal|November 24, 2004
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) geneBelén Bornstein, José Antonio Mas, Clarice Patrono, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 23, 2013
Cardiac dysfunction in mitochondrial disease. Clinical and molecular featuresPedro Villar, Begoña Bretón, Pablo García-Pavía, et al.
Mitochondrion|October 12, 2011
Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathiesJuan J Arredondo, M Esther Gallardo, Pablo García-Pavía, et al.
European Heart Journal|August 9, 2011
Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patientsM Esther Gallardo, Pablo García-Pavía, Raquel Chamorro, et al.
Annals of the Rheumatic Diseases|December 7, 2016
Mitochondrial DNA haplogroups influence the risk of incident knee osteoarthritis in OAI and CHECK cohorts. A meta-analysis and functional studyMercedes Fernández-Moreno, Angel Soto-Hermida, María E Vázquez-Mosquera, et al.
Experimental Dermatology|January 22, 2005
Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyriaSusana Navarro, Pilar Del Hoyo, Yolanda Campos, et al.
International Journal of Molecular Sciences|November 26, 2022
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC TechnologyMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo, et al.
The Biochemical Journal|December 10, 2002
Reactive oxygen species mediate the down-regulation of mitochondrial transcripts and proteins by tumour necrosis factor-alpha in L929 cellsJosé A Sánchez-Alcázar, Erasmus Schneider, Inmaculada Hernández-Muñoz, et al.
Mitochondrion|March 16, 2010
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archHenry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
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