HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness (Q57420557)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

0 references

1 reference

1 reference

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

author name string

E H van Essen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

B O Roep

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J J Jansen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J M Van den Ouweland

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

H H Lemkes

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J A Maassen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

publication date

1 December 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

841-847

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Mitochondrial diabetes mellitus: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

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/10.1046%2FJ.1464-5491.2000.00379.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Islet cell antibodies in diabetes mellitus associated with a mitochondrial tRNA(Leu(UUR)) gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

A combination of HLA-DQ beta Asp57-negative and HLA DQ alpha Arg52 confers susceptibility to insulin-dependent diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

Ten-year follow-up study of islet-cell antibodies and childhood diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2000.00379.X

10.1046/J.1464-5491.2000.00379.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11168326%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference