(Q34660403)

3 August 2017

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title

Mitochondrial diabetes mellitus. (English)

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3 August 2017

Maassen JA

1

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3 August 2017

Janssen GM

series ordinal

2

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3 August 2017

Lemkes HH

series ordinal

3

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3 August 2017

1 May 2002

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Journal of Endocrinological Investigation

3 August 2017

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3 August 2017

25

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3 August 2017

5

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3 August 2017

477-484

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https://scigraph.springernature.com/pub.10.1007/bf03344042

3 August 2017

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cites work

Mitochondrial diseases in man and mouse

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https://api.crossref.org/works/10.1007%2FBF03344042

Sequence and organization of the human mitochondrial genome

21 January 2018

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Molecular basis of mitochondrial DNA disease

21 January 2018

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A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03344042

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03344042

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

21 January 2018

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Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

21 January 2018

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03344042

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

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Mitochondrial DNA mutations in diseases of energy metabolism

21 January 2018

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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

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https://api.crossref.org/works/10.1007%2FBF03344042

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

21 January 2018

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Maternally inherited diabetes and deafness: a new diabetes subtype

21 January 2018

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

21 January 2018

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

21 January 2018

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Maternally inherited diabetes and deafness: a multicenter study

21 January 2018

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Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

21 January 2018

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Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

21 January 2018

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Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome

21 January 2018

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Importance of maternal history of non-insulin dependent diabetic patients

21 January 2018

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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

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

21 January 2018

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Insulin resistance in mitochondrial gene mutation.

21 January 2018

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

21 January 2018

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Genomic organization and chromosomal assignment of the human beta1, 4-N-acetylgalactosaminyltransferase gene. Identification of multiple transcription units

21 January 2018

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

21 January 2018

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High prevalence of mitochondrial diabetes mellitus in Japanese patients with major risk factors.

21 January 2018

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

21 January 2018

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

21 January 2018

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Functional and molecular mitochondrial abnormalities associated with a C --> T transition at position 3256 of the human mitochondrial genome. The effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03344042

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

21 January 2018

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Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03344042

Detection of Mitochondrial DNA Deletions in Human Skin Fibroblasts of Patients with Pearson's Syndrome by Two-color Fluorescence In Situ Hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344042

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/10.1007%2FBF03344042

Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344042

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344042

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344042

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

21 January 2018

1 reference

12 December 2020

Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys)

1 reference

12 December 2020

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

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12 December 2020

Renal failure from mitochondrial cytopathies

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12 December 2020

Clinical, physiological, and histological features in a kindred with the T3271C melas mutation

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12 December 2020

On possible genetic and epigenetic modes of diabetes transmission

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12 December 2020

Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine tRNA

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12 December 2020

Mitochondrial gene mutations in gestational diabetes mellitus

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12 December 2020

Mitochondrial diabetes: investigation and identification of a novel mutation

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12 December 2020

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

1 reference

12 December 2020

Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

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12 December 2020

Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus

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12 December 2020

Nonrandom tissue distribution of mutant mtDNA

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12 December 2020

A G-to-A substitution at nucleotide position 3316 in mitochondrial DNA is associated with Japanese non-insulin-dependent diabetes mellitus

1 reference

12 December 2020

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

1 reference

12 December 2020

Role of mitochondrial calcium in metabolism-secretion coupling in nutrient-stimulated insulin release

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12 December 2020

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

1 reference

12 December 2020

The T-C(8356) mitochondrial DNA mutation in a Japanese family

1 reference

12 December 2020

Association between HLA and islet cell antibodies in diabetic patients with a mitochondrial DNA mutation at base pair 3243

1 reference

12 December 2020

Mitochondrial DNA point mutation at nucleotide pair 3316 in a Japanese family with heterogeneous phenotypes of diabetes

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12 December 2020

Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria

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12 December 2020

Role of mitochondria in oxidative stress and ageing

1 reference

12 December 2020

PPARalpha and PPARgamma activators direct a distinct tissue-specific transcriptional response via a PPRE in the lipoprotein lipase gene

1 reference

12 December 2020

The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate

1 reference

12 December 2020

A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes

1 reference

12 December 2020

(R)-alpha-lipoic acid reverses the age-associated increase in susceptibility of hepatocytes to tert-butylhydroperoxide both in vitro and in vivo

1 reference

12 December 2020

Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family

1 reference

12 December 2020

Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulin-dependent diabetes mellitus

1 reference

12 December 2020

Diabetes mellitus associated with the 3243 mitochondrial tRNA(Leu)(UUR) mutation: insulin secretion and sensitivity

1 reference

12 December 2020

A Caucasian Family with the 3271 Mutation in Mitochondrial DNA

1 reference

12 December 2020

Mitochondrial DNA 3394 mutation in the NADH dehydrogenase subunit 1 associated with non-insulin-dependent diabetes mellitus

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03344042

1 reference

Dimensions Publication ID

3 August 2017

1004145941

0 references

Fatcat ID

release_le3rju35wbhz5o37g5sdoejq3q

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/le3rju35wbhz5o37g5sdoejq3q

24 November 2022

mapped directly with Wikidata item

1 reference