(Q46687091)

24 December 2017

title

Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns (English)

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24 December 2017

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17

Francis S Collins

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24 December 2017

1

Karen L Mohlke

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24 December 2017

14

Jaakko Tuomilehto

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24 December 2017

11

Narisu Narisu

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24 December 2017

16

Michael Boehnke

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24 December 2017

2

Anne U Jackson

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24 December 2017

15

Richard N Bergman

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24 December 2017

author name string

Laura J Scott

3

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24 December 2017

Erin C Peck

4

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24 December 2017

Yong D Suh

5

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24 December 2017

Peter S Chines

6

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24 December 2017

Richard M Watanabe

7

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24 December 2017

Thomas A Buchanan

8

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24 December 2017

Karen N Conneely

9

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24 December 2017

Michael R Erdos

10

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24 December 2017

Sareena Enloe

12

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24 December 2017

Timo T Valle

13

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24 December 2017

publication date

15 November 2005

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24 December 2017

published in

Human Genetics

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24 December 2017

volume

118

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24 December 2017

issue

2

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24 December 2017

page(s)

245-254

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24 December 2017

Long-Term Prospective Evaluation of Offspring of Diabetic Mothers

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-005-0046-4

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

21 January 2018

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Longitudinal data analysis for discrete and continuous outcomes

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Mammalian mitochondrial D-loop region structural analysis: identification of new conserved sequences and their functional and evolutionary implications

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12 December 2020

Are oxidative stress-activated signaling pathways mediators of insulin resistance and beta-cell dysfunction?

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12 December 2020

Mapping genes in diabetes. Genetic epidemiological perspective

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12 December 2020

Prevalence of Diabetes Mellitus and Impaired Glucose Tolerance in the Middle-Aged Population of Three Areas in Finland

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12 December 2020

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

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12 December 2020

Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and Childhood

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12 December 2020

Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification

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12 December 2020

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

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12 December 2020

The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits

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12 December 2020

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

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12 December 2020

Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001

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12 December 2020

Mitochondrial DNA variations in patients with Type 2 (non-insulin dependent) diabetes mellitus and a Welsh control population. Mutation in brief no. 239. Online

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12 December 2020

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

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12 December 2020

Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland

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12 December 2020

Biochemistry and molecular cell biology of diabetic complications

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12 December 2020

Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes

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12 December 2020

The presence of a common mitochondrial DNA variant is associated with fasting insulin levels in Europeans in Auckland.

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12 December 2020

Global burden of diabetes, 1995-2025: prevalence, numerical estimates, and projections

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12 December 2020

Mitochondrial function in normal and diabetic beta-cells

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12 December 2020

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

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12 December 2020

Major genomic mitochondrial lineages delineate early human expansions

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12 December 2020

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

1 reference

12 December 2020

Paleolithic and neolithic lineages in the European mitochondrial gene pool

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12 December 2020

Phylogeography of mitochondrial DNA in western Europe

1 reference

12 December 2020

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

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12 December 2020

Maternal transmission of diabetes.

1 reference

12 December 2020

A common mitochondrial DNA variant is associated with insulin resistance in adult life.

1 reference

12 December 2020

Congenital Susceptibility to NIDDM: Role of Intrauterine Environment

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12 December 2020

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

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12 December 2020

Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes.

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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

Mitochondrial DNA variation in human evolution and disease

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12 December 2020

Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study

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12 December 2020

Phylogenetic network for European mtDNA.

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12 December 2020

Increased expression of mitochondrial-encoded genes in skeletal muscle of humans with diabetes mellitus

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12 December 2020

Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes

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12 December 2020

New mitochondrial DNA homoplasmic mutations associated with Japanese patients with type 2 diabetes

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12 December 2020

Classification of European mtDNAs from an analysis of three European populations

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12 December 2020

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

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12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

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12 December 2020

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

12 December 2020

Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin dependent) diabetes mellitus.

1 reference

12 December 2020

Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes.

1 reference

12 December 2020

Correction: no evidence of an association between the T16189C mtDNA variant and late onset dementia (Gibson et al).

1 reference

12 December 2020

Analysis of a polycytosine tract and heteroplasmic length variation in the mitochondrial DNA D-loop of patients with diabetes, MELAS syndrome and race-matched controls.

1 reference

12 December 2020

A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14

1 reference

12 December 2020

A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes

1 reference

12 December 2020

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

12 December 2020

Altered glycolytic and oxidative capacities of skeletal muscle contribute to insulin resistance in NIDDM

1 reference

12 December 2020

Diabetes mellitus associated with the 3243 mitochondrial tRNA(Leu)(UUR) mutation: insulin secretion and sensitivity

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

A bidirectional origin of replication maps to the major noncoding region of human mitochondrial DNA.

1 reference

12 December 2020

10.1007/S00439-005-0046-4

Identifiers

DOI

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24 December 2017

1 reference

24 December 2017