(Q36194894)

12 August 2017

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title

Molecular mechanisms of mitochondrial diabetes (MIDD). (English)

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12 August 2017

Leen M 't Hart

3

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author name string

Johannes A Maassen

series ordinal

1

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12 August 2017

George M C Janssen

series ordinal

2

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12 August 2017

language of work or name

English

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publication date

1 January 2005

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12 August 2017

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12 August 2017

volume

37

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12 August 2017

issue

3

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12 August 2017

page(s)

213-221

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Glucokinase as pancreatic beta cell glucose sensor and diabetes gene

12 August 2017

cites work

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https://api.crossref.org/works/10.1080%2F07853890510007188

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/10.1080%2F07853890510007188

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/10.1080%2F07853890510007188

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Diseases of the mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Mitochondrial function in normal and diabetic beta-cells

21 January 2018

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https://api.crossref.org/works/10.1080%2F07853890510007188

Glucose-regulated gene expression maintaining the glucose-responsive state of beta-cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

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/10.1080%2F07853890510007188

Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Mouse models for mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

UKPDS 21: low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243bp in UK Caucasian type 2 diabetic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

A genetic approach to understanding auditory function

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

Altered beta-cell characteristics in impaired glucose tolerant carriers of a GAA trinucleotide repeat polymorphism in the frataxin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

21 January 2018

Mitochondrial Deafness

1 reference

https://api.crossref.org/works/10.1080%2F07853890510007188

10.1080/07853890510007188

21 January 2018

Identifiers

DOI

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12 August 2017

1 reference