Associated Papers
The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis.
Donato L et al.
Heliyon, 2024
Variants in the Control Region of Mitochondrial Genome Associated with type 2 Diabetes in a Cohort of Mexican Mestizos.
Santander-Lucio H et al.
Archives of Medical Research, 2023
The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome.
Bibi S et al.
Frontiers in Endocrinology, 2023
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
Calabrese C et al.
Plos Genetics, 2022
Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults.
Ebner S et al.
Plos One, 2015
Mitochondrial DNA polymorphisms are associated with the longevity in the Guangxi Bama population of China.
Yang X et al.
Molecular Biology Reports, 2012
A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
Chen FL et al.
Mutation Research, 2006
IKBL promoter polymorphism is strongly associated with resistance to type 1 diabetes in Japanese.
Yamashita T et al.
Tissue Antigens, 2004
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