Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects (Q73676308)

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scientific article published on 01 September 1999

Language	Label	Description	Also known as
English	Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects	scientific article published on 01 September 1999

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

M Fukuda

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

S Nakano

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

N Imaizumi

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

M Kitazawa

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

M Nishizawa

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

T Kigoshi

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K Uchida

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 September 1999

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Journal of Diabetes and its Complications

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

13

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

5-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

277-283

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Mitochondrial diabetes mellitus: a review

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA and Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Maternally inherited diabetes and deafness: a new diabetes subtype

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Stimulation by D-glucose of mitochondrial oxidative events in islet cells

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Circadian rhythm of blood pressure in normotensive NIDDM subjects. Its relationship to microvascular complications.

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Oxidative damage to mitochondrial DNA and its relationship to ageing

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Oxidative damage to mitochondrial DNA and its relationship to diabetic complications

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial medicine

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?

1 reference

https://api.crossref.org/works/10.1016%2FS1056-8727%2899%2900060-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1056-8727(99)00060-4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10765002%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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