(Q72148202)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

author name string

M Kishimoto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

M Hashiramoto

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

S Araki

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Y Ishida

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

T Kazumi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

E Kanda

6

1 reference

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24 October 2019

M Kasuga

7

1 reference

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24 October 2019

publication date

1 February 1995

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24 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

volume

38

1 reference

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24 October 2019

issue

2

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24 October 2019

page(s)

193-200

1 reference

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Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR) ]

24 October 2019

cites work

1 reference

12 December 2020

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

12 December 2020

Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation

1 reference

12 December 2020

The effects of metformin compared to the effects of phenformin on the lactate production and the metabolism of isolated parenchymal rat liver cell

1 reference

12 December 2020

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

1 reference

12 December 2020

Autoantibodies to glutamic acid decarboxylase in patients with IDDM and autoimmune thyroid disease

1 reference

12 December 2020

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

1 reference

12 December 2020

Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation

1 reference

12 December 2020

Maternal effect and familial aggregation in NIDDM. The CODIAB Study. CODIAB-INSERM-ZENECA Study Group

1 reference

12 December 2020

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

12 December 2020

Glucagon physiology and pathophysiology

1 reference

12 December 2020

Decreased mitochondrial gene expression in isolated islets of rats injected neonatally with streptozotocin

1 reference

12 December 2020

Physiology and pathophysiology of glucagon

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study

1 reference

12 December 2020

Congenital Susceptibility to NIDDM: Role of Intrauterine Environment

1 reference

12 December 2020

Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus

1 reference

12 December 2020

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

12 December 2020

Diabetes in identical twins. A study of 200 pairs

1 reference

12 December 2020

C-peptide Response to Glucagon: A Test for the Residual β-cell Function in Diabetes Mellitus

1 reference

12 December 2020

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the insulin receptor gene

1 reference

12 December 2020

A structurally abnormal insulin causing human diabetes

1 reference

12 December 2020

Type I diabetes mellitus. A chronic autoimmune disease

1 reference

12 December 2020

MELAS: clinical features, biochemistry, and molecular genetics

1 reference

12 December 2020

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

1 reference

12 December 2020

Glucose clamp technique: a method for quantifying insulin secretion and resistance

1 reference

12 December 2020

Effects of guanidine derivatives on mitochondrial function. I. Phenethylbiguanide inhibition of respiration in mitochondria from guinea pig and rat tissues

1 reference

12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

12 December 2020

Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene

1 reference

12 December 2020

A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

1 reference

12 December 2020

Association between polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus.

1 reference

12 December 2020

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

1 reference

12 December 2020

Importance of maternal history of non-insulin dependent diabetic patients

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

1 reference

12 December 2020

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

1 reference

12 December 2020

Studies of pancreatic alpha cell function in normal and diabetic subjects

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

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/BF00400094

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7713314%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference