Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
about
Common defects of mitochondria and iron in neurodegeneration and diabetes (MIND): a paradigm worth exploringA mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicineInvolvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.Mitochondrial metabolism and diabetesDecrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus.Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expressionHyperinsulinism in infancy: from basic science to clinical disease.1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and agingSomatic alterations in mitochondrial DNA produce changes in cell growth and metabolism supporting a tumorigenic phenotype.Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELASMitochondrial-associated metabolic disorders: foundations, pathologies and recent progress.Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity.Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing.Maternally inherited diabetes and deafness: a new diabetes subtype.Length variation in the mouse mitochondrial tRNA(Arg) DHU loop size promotes oxidative phosphorylation functional differences.Insulin secretion and insulin sensitivity are normal in non-diabetic subjects from maternal inheritance diabetes and deafness families.Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study.Mitochondrial Etiology of Neuropsychiatric Disorders.Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.Assessment of the distribution of mitochondrial ribosomal RNA in melas and in thrombotic cerebral infarcts by in situ hybridization.The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.[Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation].
P2860
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P2860
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
description
1994 nî lūn-bûn
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1994年の論文
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1994年学术文章
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1994年学术文章
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1994年学术文章
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1994年学术文章
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1994年学术文章
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name
Maternally inherited diabetes ...... tion in the mitochondrial tRNA
@nl
Maternally inherited diabetes ...... chondrial tRNA(Leu(UUR)) gene.
@en
type
label
Maternally inherited diabetes ...... tion in the mitochondrial tRNA
@nl
Maternally inherited diabetes ...... chondrial tRNA(Leu(UUR)) gene.
@en
prefLabel
Maternally inherited diabetes ...... tion in the mitochondrial tRNA
@nl
Maternally inherited diabetes ...... chondrial tRNA(Leu(UUR)) gene.
@en
P2093
P356
P1433
P1476
Maternally inherited diabetes ...... chondrial tRNA(Leu(UUR)) gene.
@en
P2093
P304
P356
10.2337/DIAB.43.6.746
P407
P577
1994-06-01T00:00:00Z