Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis (Q34737294)

4 August 2017

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title

Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis (English)

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4 August 2017

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J Antonie Maassen

1

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4 August 2017

publication date

1 May 2002

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American Journal of Medical Genetics Part A

4 August 2017

published in

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4 August 2017

volume

115

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4 August 2017

issue

1

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4 August 2017

page(s)

66-70

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Importance of maternal history of non-insulin dependent diabetic patients

4 August 2017

cites work

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https://api.crossref.org/works/10.1002%2FAJMG.10346

New windows on the mechanism of action of K(ATP) channel openers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Maternally inherited diabetes and deafness: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Evidence for mitochondrial DNA recombination in a human population of island Melanesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Ethidium bromide-induced inhibition of mitochondrial gene transcription suppresses glucose-stimulated insulin release in the mouse pancreatic beta-cell line betaHC9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Clinical and laboratory characteristics in the families with diabetes and a mitochondrial tRNA(LEU(UUR)) gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Pharmacology of nucleoside and nucleotide reverse transcriptase inhibitor-induced mitochondrial toxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Insulin resistance in mitochondrial gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Maternally inherited diabetes and deafness: a new diabetes subtype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Molecular and clinical aspects of mitochondrial diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Glucokinase as pancreatic beta cell glucose sensor and diabetes gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line, MIN6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

Mitochondrial diseases in man and mouse

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10346

Beta-cell mitochondria in the regulation of insulin secretion: a new culprit in type II diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10346

21 January 2018

Identifiers

DOI

10.1002/AJMG.10346

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4 August 2017

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