Analysis of mitochondrial DNA sequence variants in patients with polycystic ovary syndrome

Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation

(2010) Minglian Zhang et al.   MOLECULAR GENETICS AND METABOLISM

A 9-bp Deletion Homoplasmy in Women with Polycystic Ovary Syndrome Revealed by Mitochondrial Genome-Mutation Screen

(2009) Guangchao Zhuo et al.   BIOCHEMICAL GENETICS

Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population

(2009) Hai-Yan Zhu et al.   CLINICA CHIMICA ACTA

Mitochondrial Complex I Impairment in Leukocytes from Polycystic Ovary Syndrome Patients with Insulin Resistance

(2009) Victor M. Victor et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

(2009) Jianxin Lu et al.   MITOCHONDRION

Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation

(2008) Yanli Ji et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Polycystic ovary syndrome is associated with severe platelet and endothelial dysfunction in both obese and lean subjects

(2008) Sharmalar Rajendran et al.   ATHEROSCLEROSIS

The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report

(2008) Ricardo Azziz et al.   FERTILITY AND STERILITY

Exaggerated status of “novel” and “pathogenic” mtDNA sequence variants due to inadequate database searches

(2008) Hans-Jürgen Bandelt et al.   HUMAN MUTATION

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

(2008) Wanshi Cai et al.   Journal of Genetics and Genomics

Pioglitazone Enhances Mitochondrial Biogenesis and Ribosomal Protein Biosynthesis in Skeletal Muscle in Polycystic Ovary Syndrome

(2008) Vibe Skov et al.   PLoS One