Association of Mitochondrial Genetic Variation with Carotid Atherosclerosis

Mitochondrial Mutations are Associated with Atherosclerotic Lesions in the Human Aorta

(2012) Igor A. Sobenin et al.   Clinical & Developmental Immunology

Monogenic Mitochondrial Disorders

(2012) Werner J.H. Koopman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease

(2012) Igor A. Sobenin et al.   PLoS One

Immune and Inflammatory Mechanisms of Atherosclerosis

(2009) Elena Galkina et al.   Annual Review of Immunology

Cross-sectional analysis of baseline data to identify the major determinants of carotid intima–media thickness in a European population: the IMPROVE study

(2009) Damiano Baldassarre et al.   EUROPEAN HEART JOURNAL

Mutations in ND Subunits of Complex I Are an Important Genetic Cause of Childhood Mitochondrial Encephalopathies

(2009) Byung Chan Lim et al.   JOURNAL OF CHILD NEUROLOGY

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

(2008) Hannah R. Elliott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The G13513A Mutation in the ND5 Gene of Mitochondrial DNA as a Common Cause of MELAS or Leigh Syndrome

(2008) Sara Shanske et al.   ARCHIVES OF NEUROLOGY

Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genome

(2008) M. Sazonova et al.   ATHEROSCLEROSIS

Identification of novel mutations in five patients with mitochondrial encephalomyopathy

(2008) Lucia Valente et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS