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New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome
- Source :
- Endocrinology and metabolism clinics of North America. 35(2)
- Publication Year :
- 2006
-
Abstract
- The 3243A>G mutation in mitochondrial DNA (mtDNA) is a genetic variant that is associated with a high risk of developing diabetes during life. Enhanced aging of pancreatic beta-cells, a reduced capacity of these cells to synthesize large amounts of insulin,and a resetting of the ATP/ADP-regulated K-channel seem to be the pathogenic factors involved.
- Subjects :
- medicine.medical_specialty
Mitochondrial DNA
Endocrinology, Diabetes and Metabolism
medicine.medical_treatment
Deafness
medicine.disease_cause
DNA, Mitochondrial
Pathogenesis
Endocrinology
Internal medicine
Diabetes mellitus
Insulin-Secreting Cells
medicine
Diabetes Mellitus
Humans
Insulin
Point Mutation
Genetics
Mutation
business.industry
Genetic variants
Molecular pathogenesis
medicine.disease
Mitochondria
Glucose
Female
business
Subjects
Details
- ISSN :
- 08898529
- Volume :
- 35
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Endocrinology and metabolism clinics of North America
- Accession number :
- edsair.doi.dedup.....958897b385019fb300fcccddb6772abf