(Q41088487)

26 September 2017

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title

Maternally inherited diabetes and deafness: a new diabetes subtype (English)

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26 September 2017

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J A Maassen

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26 September 2017

T Kadowaki

series ordinal

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26 September 2017

publication date

1 April 1996

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26 September 2017

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26 September 2017

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26 September 2017

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26 September 2017

page(s)

375-382

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Human liver glucokinase gene: cloning and sequence determination of two alternatively spliced cDNAs

26 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

The glucokinase glucose sensor in human pancreatic islet tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Maternal inheritance of human mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF00400668

Mitochondrial DNA mutations in human degenerative diseases and aging

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF00400668

Mitochondrial DNA mutations in diseases of energy metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Importance of maternal history of non-insulin dependent diabetic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

Ion Channels and Insulin Secretion

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF00400668

Insulin resistance in mitochondrial gene mutation.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF00400668

Diabetes mellitus in Kearns-Sayre syndrome

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF00400668

Does the mitochondrial DNA play a role in the pathogenesis of diabetes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00400668

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%2FBF00400668

Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia

21 January 2018

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12 December 2020

Noninvasive diagnosis of the MELAS syndrome from blood DNA

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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

Mild familial diabetes with dominant inheritance

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12 December 2020

A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance

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12 December 2020

An autosomal locus predisposing to deletions of mitochondrial DNA

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12 December 2020

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

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12 December 2020

Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene

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12 December 2020

Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene

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12 December 2020

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

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12 December 2020

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

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12 December 2020

On possible genetic and epigenetic modes of diabetes transmission

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12 December 2020

The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan

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12 December 2020

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus

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12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

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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

Mitochondrial gene mutations and diabetes mellitus

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12 December 2020

Linkage of type 2 diabetes to the glucokinase gene

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12 December 2020

Transient insulin-dependent diabetes mellitus in an HIV-infected patient receiving didanosine.

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12 December 2020

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

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12 December 2020

Diseases of the mitochondrial DNA.

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12 December 2020

Mutation in the mitochondrial tRNA(leu) at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies.

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12 December 2020

Mutations in the insulin receptor gene

1 reference

12 December 2020

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

1 reference

12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

12 December 2020

A genome-wide search for human type 1 diabetes susceptibility genes

1 reference

12 December 2020

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

1 reference

12 December 2020

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

1 reference

12 December 2020

Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes

1 reference

12 December 2020

Congestive heart failure in mitochondrial diabetes mellitus

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00400668

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26 September 2017

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