Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases (Q30645106)

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English	Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases	scientific article

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scholarly article

1 reference

Europe PubMed Central

17 August 2017

6 references

30 June 2019

20 June 2019

14 September 2019

23 July 2020

10 September 2020

5 July 2021

Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases (English)

1 reference

Europe PubMed Central

17 August 2017

genetic variation

1 reference

14 September 2019

genetic predisposition to disease

1 reference

23 July 2020

energy metabolism

1 reference

5 July 2021

author name string

Douglas C Wallace

1

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Europe PubMed Central

17 August 2017

language of work or name

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publication date

10 June 2013

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Europe PubMed Central

17 August 2017

19 July 2013

6 references

30 June 2019

20 June 2019

14 September 2019

23 July 2020

10 September 2020

5 July 2021

Philosophical Transactions of the Royal Society B

6 references

Europe PubMed Central

17 August 2017

30 June 2019

20 June 2019

14 September 2019

23 July 2020

5 July 2021

368

1 reference

Europe PubMed Central

17 August 2017

1622

1 reference

Europe PubMed Central

17 August 2017

20120267

1 reference

Europe PubMed Central

17 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

5 references

Europe PubMed Central

30 June 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

23 July 2020

Europe PubMed Central

5 July 2021

copyright status

0 references

The origin of membrane bioenergetics

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Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition

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Deep mitochondrial introgression and hybridization among ecologically divergent vole species.

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14 July 2018

A disproportionate role for mtDNA in Dobzhansky-Muller incompatibilities?

1 reference

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14 July 2018

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

1 reference

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14 July 2018

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

1 reference

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14 July 2018

Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans.

1 reference

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14 July 2018

Bioenergetic origins of complexity and disease

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Energetics and genetics across the prokaryote-eukaryote divide

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14 July 2018

Genetic Variance in Uncoupling Protein 2 in Relation to Obesity, Type 2 Diabetes, and Related Metabolic Traits: Focus on the Functional -866G>A Promoter Variant (rs659366)

1 reference

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14 July 2018

The energetics of genome complexity

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14 July 2018

Mitochondrial-nuclear epistasis affects fitness within species but does not contribute to fixed incompatibilities between species of Drosophila

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14 July 2018

Sequencing of 50 human exomes reveals adaptation to high altitude

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14 July 2018

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

1 reference

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14 July 2018

Genetic evidence for high-altitude adaptation in Tibet

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Colloquium paper: bioenergetics, the origins of complexity, and the ascent of man.

1 reference

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14 July 2018

Climate shaped the worldwide distribution of human mitochondrial DNA sequence variation

1 reference

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14 July 2018

The polymorphisms of UCP1 genes associated with fat metabolism, obesity and diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Mitochondria as chi.

1 reference

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Worldwide human relationships inferred from genome-wide patterns of variation

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14 July 2018

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Molecular evolution of the cytochrome c oxidase subunit 5A gene in primates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

An enhanced MITOMAP with a global mtDNA mutational phylogeny

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Adaptive selection of mitochondrial complex I subunits during primate radiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Rapid electrostatic evolution at the binding site for cytochrome c on cytochrome c oxidase in anthropoid primates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Production of homoplasmic xenomitochondrial mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Effects of purifying and adaptive selection on regional variation in human mtDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Functional respiratory chain analyses in murid xenomitochondrial cybrids expose coevolutionary constraints of cytochrome b and nuclear subunits of complex III.

1 reference

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14 July 2018

The function of genomes in bioenergetic organelles

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Climatic influences on basal metabolic rates among circumpolar populations

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Mutation analysis of peroxisome proliferator-activated receptor-gamma coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Expression of Rattus norvegicus mtDNA in Mus musculus cells results in multiple respiratory chain defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Mitochondrial DNA variation in human evolution and disease

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency

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14 July 2018

The evolutionary genetics of speciation

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14 July 2018

A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis

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14 July 2018

The DNA revolution in population genetics

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14 July 2018

Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids

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14 July 2018

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

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14 July 2018

Sequence and organization of the human mitochondrial genome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Structure and evolution of organelle genomes.

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14 July 2018

Mitochondrial DNA sequences of primates: Tempo and mode of evolution

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14 July 2018

Mitochondrial DNA and human evolution

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14 July 2018

Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685467

14 July 2018

Effects of UCP2 and UCP3 variants on the manifestation of overweight in Korean children

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

A common polymorphism in the promoter of UCP2 is associated with obesity and hyperinsulenemia in northern Indians

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

A Gly482Ser missense mutation in the peroxisome proliferator-activated receptor gamma coactivator-1 is associated with altered lipid oxidation and early insulin secretion in Pima Indians

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

The influence of basal metabolic rate on blood pressure among indigenous Siberians

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https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

Basal metabolic rate in the Yakut (Sakha) of Siberia

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

Elevated male European and female African contributions to the genomes of African American individuals

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21 January 2018

Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA.

1 reference

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21 January 2018

A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease

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https://api.crossref.org/works/10.1098%2FRSTB.2012.0267

21 January 2018

Accelerated evolution of the electron transport chain in anthropoid primates.

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21 January 2018

Origin of life on earth.

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25 November 2018

Evolution of nuclear- and mitochondrial-encoded subunit interaction in cytochrome c oxidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/23754818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coadaptive evolution in cytochrome c oxidase: 9 of 13 subunits show accelerated rates of nonsynonymous substitution in anthropoid primates

1 reference

https://pubmed.ncbi.nlm.nih.gov/23754818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23754818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the Origin of Species by Means of Natural Selection, or the Preservation of Favoured Races in the Struggle for Life

1 reference

https://pubmed.ncbi.nlm.nih.gov/23754818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1098/RSTB.2012.0267

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

ResearchGate publication ID

0 references

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