Mitochondrial gene defects in patients with NIDDM (Q72134564)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

title

Mitochondrial gene defects in patients with NIDDM (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

author name string

A Majid

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

M Brockington

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

R Morgan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

A Rees

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

A E Harding

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

A H Barnett

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

publication date

1 April 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

volume

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

page(s)

372-376

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

24 October 2019

cites work

1 reference

12 December 2020

Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

1 reference

12 December 2020

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage studies on NIDDM and the insulin and insulin-receptor genes

1 reference

12 December 2020

Association between a restriction fragment length polymorphism at the liver/islet cell (GluT 2) glucose transporter and familial Type 2 (non-insulin-dependent) diabetes mellitus

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 mutations and diabetes mellitus

1 reference

12 December 2020

Progressive ocular myopathy with ovarian insufficiency and diabetes mellitus. Report of a case

1 reference

12 December 2020

Diabetes Mellitus in Twins

1 reference

12 December 2020

Diabetes in identical twins. A study of 200 pairs

1 reference

12 December 2020

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

1 reference

12 December 2020

Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child

1 reference

12 December 2020

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

1 reference

12 December 2020

Mitochondrial myopathy

1 reference

12 December 2020

Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia

1 reference

12 December 2020

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

1 reference

12 December 2020

Mitochondrial gene mutations and diabetes mellitus

1 reference

12 December 2020

Detection of mutations in insulin-receptor gene in NIDDM patients by analysis of single-stranded conformation polymorphisms

1 reference

12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

12 December 2020

The clinical features of mitochondrial myopathy

1 reference

12 December 2020

Report of the committee on human mitochondrial DNA.

1 reference

12 December 2020

Importance of maternal history of non-insulin dependent diabetic patients

1 reference

12 December 2020

Isolation, subunit composition, and site of synthesis of human cytochrome c oxidase

1 reference

12 December 2020

Further evidence for a predominantly maternal transmission of maturity-onset type diabetes

1 reference

12 December 2020

Duplications of mitochondrial DNA in mitochondrial myopathy

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/BF00408473

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8063037 AND SRC:MED&resulttype=core&format=json

24 October 2019

1 reference