Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains (Q35946513)

11 August 2017

Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains (English)

1 reference

11 August 2017

1 reference

Marek Vrbacky

10

0 references

Petr Pecina

object named as

Petr Pecina

9

0 references

Ivan Mikšík

object named as

Ivan Miksik

7

0 references

Zdenek Drahota

object named as

Zdenek Drahota

11

0 references

Alena Pecinová

1 reference

ORCID Public Data File 2021

author name string

Michal Pravenec

1

1 reference

11 August 2017

Masaya Hyakukoku

2

1 reference

11 August 2017

Josef Houstek

3

1 reference

11 August 2017

Vaclav Zidek

4

1 reference

11 August 2017

Vladimir Landa

5

1 reference

11 August 2017

Petr Mlejnek

6

1 reference

11 August 2017

Kristyna Dudová-Mothejzikova

8

1 reference

11 August 2017

Alena Vojtiskova

12

1 reference

11 August 2017

Tomas Mracek

13

1 reference

11 August 2017

Ludmila Kazdova

14

1 reference

11 August 2017

Olena Oliyarnyk

15

1 reference

11 August 2017

Jiaming Wang

16

1 reference

11 August 2017

Christopher Ho

17

1 reference

11 August 2017

Nathan Qi

18

1 reference

11 August 2017

Ken Sugimoto

19

1 reference

11 August 2017

Theodore Kurtz

20

1 reference

11 August 2017

10 August 2007

1 reference

11 August 2017

1 reference

11 August 2017

17

1 reference

11 August 2017

1319-1326

1 reference

11 August 2017

9

1 reference

Impaired fasting glucose and impaired glucose tolerance: implications for care

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Systematic identification of human mitochondrial disease genes through integrative genomics

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Molecular mechanisms of mitochondrial diabetes (MIDD).

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Mitochondrial dysfunction and type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Impaired mitochondrial activity in the insulin-resistant offspring of patients with type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

A Novel Class of Tests for the Detection of Mitochondrial DNA–Mutation Involvement in Diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Processing of gene expression data generated by quantitative real-time RT-PCR.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Impaired noradrenaline-induced lipolysis in white fat of aP2-Ucp1 transgenic mice is associated with changes in G-protein levels.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Maternal transmission of diabetes.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Transgenic rescue of defective Cd36 ameliorates insulin resistance in spontaneously hypertensive rats

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

EMBOSS: the European Molecular Biology Open Software Suite

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

SEAVIEW and PHYLO_WIN: two graphic tools for sequence alignment and molecular phylogeny

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Is human Type 2 diabetes maternally inherited? Insights from an animal model

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Transgenic and recombinant resistin impair skeletal muscle glucose metabolism in the spontaneously hypertensive rat.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Y-chromosome transfer induces changes in blood pressure and blood lipids in SHR.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Quantitation of muscle glycogen synthesis in normal subjects and subjects with non-insulin-dependent diabetes by 13C nuclear magnetic resonance spectroscopy.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950900

Skeletal muscle mitochondrial functions, mitochondrial DNA copy numbers, and gene transcript profiles in type 2 diabetic and nondiabetic subjects at equal levels of low or high insulin and euglycemia

24 September 2018

1 reference

12 December 2020

A high-yield preparative method for isolation of rat liver mitochondria

1 reference

12 December 2020

Palmitate and glucose oxidation by diaphragm of rats with fructose-induced hypertriglyceridemia

1 reference

12 December 2020

Supersonic congenics?

1 reference

12 December 2020

Noninsulin-dependent diabetes mellitus as a mitochondrial genomic disease

1 reference

12 December 2020

Inheritance of a mitochondrial DNA defect and impaired glucose tolerance in BHE/Cdb rats

1 reference

12 December 2020

Identifiers

DOI

10.1101/GR.6548207

1 reference

11 August 2017

1 reference

11 August 2017

1 reference