(Q33348163)

26 July 2017

title

Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients (English)

1 reference

26 July 2017

21

Sofia A Oliveira

1 reference

26 July 2017

Helena Manso

4

0 references

Alexandra Rosa

Alexandra Rosa

1

0 references

Ricardo Taipa

Ricardo Taipa

12

0 references

Astrid M. Vicente

Astrid M Vicente

20

0 references

José M. Ferro

José M Ferro

19

0 references

author name string

Benedita V Fonseca

2

1 reference

26 July 2017

Tiago Krug

3

1 reference

26 July 2017

Liliana Gouveia

5

1 reference

26 July 2017

Isabel Albergaria

6

1 reference

26 July 2017

Gisela Gaspar

7

1 reference

26 July 2017

Manuel Correia

8

1 reference

26 July 2017

Miguel Viana-Baptista

9

1 reference

26 July 2017

Rita Moiron Simões

10

1 reference

26 July 2017

Amélia Nogueira Pinto

11

1 reference

26 July 2017

Carla Ferreira

13

1 reference

26 July 2017

João Ramalho Fontes

14

1 reference

26 July 2017

Mário Rui Silva

15

1 reference

26 July 2017

João Paulo Gabriel

16

1 reference

26 July 2017

Ilda Matos

17

1 reference

26 July 2017

Gabriela Lopes

18

1 reference

26 July 2017

publication date

1 July 2008

1 reference

26 July 2017

1 reference

26 July 2017

volume

9

1 reference

26 July 2017

page(s)

57

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-9-57

26 July 2017

exact match

0 references

cites work

The putative role of mitochondrial dysfunction in hypertension

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Harvesting the fruit of the human mtDNA tree

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

HmtDB, a human mitochondrial genomic resource based on variability studies supporting population genetics and biomedical research

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

The role of selection in the evolution of human mitochondrial genomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Mitochondrial DNA affinities at the Atlantic fringe of Europe

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Major genomic mitochondrial lineages delineate early human expansions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Diversity of mtDNA lineages in Portugal: not a genetic edge of European variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

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.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Classification of European mtDNAs from an analysis of three European populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2492853

Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Antiatherogenic mitochondrial genotype in patients with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Interaction of oxidative stress and inflammatory response in coronary plaque instability: important role of C-reactive protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Effect of alcohol and tobacco smoke on mtDNA damage and atherogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Phylogeography of mitochondrial DNA in western Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Genotype and haplotype association study of the STRK1 region on 5q12 among Japanese: a case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Sex differences in first-ever acute stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Mitochondrial haplogroup A is a genetic risk factor for atherothrombotic cerebral infarction in Japanese females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: evidence from a hospital-based case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

The power to detect disease associations with mitochondrial DNA haplogroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Tissue-specific deletion patterns of the mitochondrial genome with advancing age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Cardiovascular risk factors emerge after artificial selection for low aerobic capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-57

Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males

21 January 2018

1 reference

12 December 2020

Increased risk of stroke in patients with the A12308G polymorphism in mitochondria

1 reference

12 December 2020

Cerebrovascular disorders and genetic polymorphisms: mitochondrial DNA5178C is predominant in cerebrovascular disorders

1 reference

12 December 2020

Mitochondrial genotype associated with longevity

1 reference

12 December 2020

Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine

1 reference

12 December 2020

Mitochondrial genotype associated with French Caucasian centenarians

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-9-57

1 reference

Dimensions Publication ID

26 July 2017

1005008786

0 references

Fatcat ID

release_ywmpfgaq25c4hbyezjrgibszvy

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ywmpfgaq25c4hbyezjrgibszvy

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2492853

1 reference

26 July 2017

1 reference