Coronary heart disease is associated with a mutation in mitochondrial tRNA

Mitochondrial Control of Cellular Life, Stress, and Death

(2012) Lorenzo Galluzzi et al.   CIRCULATION RESEARCH

Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees

(2012) Qiaomeng Qiu et al.   HUMAN MUTATION

Association of Genetic Variation in the Mitochondrial Genome With Blood Pressure and Metabolic Traits

(2012) Chunyu Liu et al.   HYPERTENSION

Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases

(2011) Tsutomu Suzuki et al.   Annual Review of Genetics

Mitochondrial Genetics and Human Systemic Hypertension

(2011) A. J. Marian   CIRCULATION RESEARCH

Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNA Ile Gene in a Large Han Chinese Family

(2011) Shiwen Wang et al.   CIRCULATION RESEARCH

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIle mutation causing hypertrophic cardiomyopathy

(2011) Elena Perli et al.   HUMAN MOLECULAR GENETICS

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour

(2011) J. F. Peden et al.   HUMAN MOLECULAR GENETICS

The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation

(2011) Yaping Qian et al.   MITOCHONDRION

Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population

(2011) Fan Wang et al.   NATURE GENETICS

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

(2011) Heribert Schunkert et al.   NATURE GENETICS

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

(2011) John F Peden et al.   NATURE GENETICS

Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNALeu(UUR) A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Symptoms and Diabetes

(2010) R. Li et al.   MOLECULAR AND CELLULAR BIOLOGY

Failures in Mitochondrial tRNA Met and tRNA Gln Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese Family

(2009) Ronghua Li et al.   HYPERTENSION

Mitochondrial Transfer RNA Met 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree

(2009) Yuqi Liu et al.   HYPERTENSION

Mitochondria and Reactive Oxygen Species

(2009) Francesco Addabbo et al.   HYPERTENSION

Relation Between Modifiable Lifestyle Factors and Lifetime Risk of Heart Failure

(2009) Luc Djoussé   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

(2009) David-Alexandre Trégouët et al.   NATURE GENETICS

Evaluation of chemiluminescence and flow cytometry as tools in assessing production of hydrogen peroxide and superoxide anion in human spermatozoa

(2008) Reda Mahfouz et al.   FERTILITY AND STERILITY

Coronary heart disease in China

(2008) X-H Zhang et al.   HEART

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

(2008) Xinjian Wang et al.   Pharmacogenetics and Genomics