(Q57365640)

T. Tuomi

7

0 references

Tina Rönn

T. Rönn

1

0 references

Charlotte Ling

C. Ling

11

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Leif Groop

9

L. Groop

0 references

Bo Isomaa

8

B. Isomaa

0 references

Peter Almgren

5

P. Almgren

0 references

author name string

P. Poulsen

2

0 references

J. Holmkvist

4

0 references

P. Nilsson

6

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A. Vaag

https://scigraph.springernature.com/pub.10.1007/s00125-008-1018-8

10

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publication date

17 May 2008

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published in

Diabetologia

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volume

51

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issue

7

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page(s)

1159-1168

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exact match

0 references

cites work

Genome-wide association studies provide new insights into type 2 diabetes aetiology

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00125-008-1018-8

Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00125-008-1018-8

Genomic organization and promoter regulation of human cytochrome c oxidase subunit VII heart/muscle isoform (COX7AH)

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00125-008-1018-8

Longitudinal data analysis for discrete and continuous outcomes

21 January 2018

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The association between total energy intake and early mortality: data from the Malmö Diet and Cancer Study

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Age-dependent impact of zygosity and birth weight on insulin secretion and insulin action in twins

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Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status

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12 December 2020

MethPrimer: designing primers for methylation PCRs

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Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.

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Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation

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Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase

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DNA methylation profiling of human chromosomes 6, 20 and 22

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Gene expression profile in skeletal muscle of type 2 diabetes and the effect of insulin treatment

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Transcriptional profiling of aging in human muscle reveals a common aging signature

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12 December 2020

Role of DNA methylation in the regulation of cell function: autoimmunity, aging and cancer

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12 December 2020

On the determination of basal glucose production rate in patients with type 2 (non-insulin-dependent) diabetes mellitus using primed-continuous 3-3H-glucose infusion.

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Tissue specificity of methylation of cytosines in regulatory regions of four genes located in the locus FXYD5-COX7A1 of human chromosome 19: correlation with their expression level

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Europium as a label in time-resolved immunofluorometric assays

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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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Regression analysis for correlated data

1 reference

12 December 2020

The intrauterine environment as reflected by birth size and twin and zygosity status influences insulin action and intracellular glucose metabolism in an age- or time-dependent manner

1 reference

12 December 2020

Epigenetic differences arise during the lifetime of monozygotic twins

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12 December 2020

Classifying diabetes according to the new WHO clinical stages

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Metabolic consequences of a family history of NIDDM (the Botnia study): evidence for sex-specific parental effects.

1 reference

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The epigenetic basis of twin discordance in age-related diseases

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12 December 2020

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

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Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M

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12 December 2020

Insulin-regulated mitochondrial gene expression is associated with glucose flux in human skeletal muscle

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12 December 2020

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

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12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

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12 December 2020

Heritability of insulin secretion, peripheral and hepatic insulin action, and intracellular glucose partitioning in young and old Danish twins

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12 December 2020

Genetic and nongenetic determinants of skeletal muscle glucose transporter 4 messenger ribonucleic acid levels and insulin action in twins

1 reference

12 December 2020

Impact of the peroxisome proliferator activated receptor-gamma coactivator-1beta (PGC-1beta) Ala203Pro polymorphism on in vivo metabolism, PGC-1beta expression and fibre type composition in human skeletal muscle

1 reference

12 December 2020

Mitochondrial dysfunction in the elderly: possible role in insulin resistance

1 reference

12 December 2020

Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes

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12 December 2020

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

1 reference

12 December 2020

CpG islands in vertebrate genomes

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12 December 2020

Epigenetics and aging: the targets and the marks

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Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle

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12 December 2020

Quantitative DNA methylation analysis based on four-dye trace data from direct sequencing of PCR amplificates

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12 December 2020

The mammalian epigenome

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12 December 2020

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

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12 December 2020

Blot hybridisation analysis of genomic DNA

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12 December 2020

BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing.

1 reference

12 December 2020

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

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12 December 2020

Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1

1 reference

12 December 2020

The International HapMap Project

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

DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING

1 reference

12 December 2020