(Q36918606)

17 August 2017

title

Specific polymorphic variation in the mitochondrial genome and increased in-hospital mortality after severe trauma (English)

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17 August 2017

3

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17 August 2017

Jeffrey A Canter

1

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17 August 2017

Patrick R Norris

series ordinal

2

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17 August 2017

Judith M Jenkins

series ordinal

4

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17 August 2017

John A Morris

series ordinal

5

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17 August 2017

language of work or name

English

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publication date

1 September 2007

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17 August 2017

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17 August 2017

volume

246

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17 August 2017

issue

3

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17 August 2017

page(s)

406-11; discussion 411-4

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Cardiac uncoupling and heart rate variability stratify ICU patients by mortality: a study of 2088 trauma patients.

17 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial Oxidative Stress and Mitochondrial DNA

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial formation of reactive oxygen species

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial respiratory-chain diseases

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Genetic associations in large versus small studies: an empirical assessment

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Natural selection shaped regional mtDNA variation in humans

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA variation in human evolution and disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Human mitochondrial complex I in health and disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial diseases in man and mouse

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

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.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Classification of European mtDNAs from an analysis of three European populations

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial oxidative phosphorylation changes in the life span. Molecular aspects and physiopathological implications

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

The staged celiotomy for trauma. Issues in unpacking and reconstruction

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial DNA sequence variation in human evolution and disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Sequence and organization of the human mitochondrial genome

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Normal oxidative damage to mitochondrial and nuclear DNA is extensive

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Mitochondrial oxidative phosphorylation defects in Parkinson's disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1959353

Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?

4 September 2018

1 reference

12 December 2020

Mitochondrial DNA polymorphism: its role in longevity of the Irish population

1 reference

12 December 2020

A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects

1 reference

12 December 2020

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women

1 reference

12 December 2020

Reduced heart rate variability: an indicator of cardiac uncoupling and diminished physiologic reserve in 1,425 trauma patients

1 reference

12 December 2020

Gene expression profiles differentiate between sterile SIRS and early sepsis

1 reference

12 December 2020

Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations

1 reference

12 December 2020

mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish

1 reference

12 December 2020

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes

1 reference

12 December 2020

Mitochondrial DNA in aging and disease

1 reference

12 December 2020

Mitochondrial genotype associated with longevity

1 reference

12 December 2020

Mitochondrial genotype associated with French Caucasian centenarians

1 reference

12 December 2020

10.1097/SLA.0B013E3181469955

Identifiers

DOI

1 reference

17 August 2017

0 references

1 reference