(Q38168700)

English

The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex disease

scientific article published on 04 December 2013

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 August 2017

The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

David N. Cooper

2

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

author name string

Martin P Horan

1

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

language of work or name

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based on heuristic

inferred from title

publication date

4 December 2013

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Europe PubMed Central

PubMed publication ID

30 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

133

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

435-458

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

https://scigraph.springernature.com/pub.10.1007/s00439-013-1402-4

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21 January 2018

Humanin: a novel central regulator of peripheral insulin action

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Upregulation of the mitochondrial Lon Protease allows adaptation to acute oxidative stress but dysregulation is associated with chronic stress, disease, and aging.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Neuronal cell death in Alzheimer's disease and a neuroprotective factor, humanin

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Unravelling the role of Humanin

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Oxidative damage targets complexes containing DNA methyltransferases, SIRT1, and polycomb members to promoter CpG Islands

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Defective quality control mechanisms and accumulation of damaged mitochondria link Gaucher and Parkinson diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A mitochondrial protein compendium elucidates complex I disease biology

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial dysfunction in some oxidative stress-related genetic diseases: Ataxia-Telangiectasia, Down Syndrome, Fanconi Anaemia and Werner Syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

The mitochondrial genotype can influence nuclear gene expression in yeast.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Amelioration of neurodegenerative diseases by cell death-induced cytoplasmic delivery of humanin.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

DNA damage in telomeres and mitochondria during cellular senescence: is there a connection?

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

SIRT1 deacetylates the DNA methyltransferase 1 (DNMT1) protein and alters its activities

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Changes of haematic parameters, redox status and mitochondrial complex activity in the heart and liver of broilers fed with different density diets under low ambient temperature.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Decreased insulin-stimulated ATP synthesis and phosphate transport in muscle of insulin-resistant offspring of type 2 diabetic parents

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

mtDNA mutations increase tumorigenicity in prostate cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A case-control study of peripheral blood mitochondrial DNA copy number and risk of renal cell carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Long noncoding RNAs are generated from the mitochondrial genome and regulated by nuclear-encoded proteins

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Frequency and pattern of heteroplasmy in the complete human mitochondrial genome.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Cytonuclear coevolution: the genomics of cooperation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

High-resolution mapping of DNA hypermethylation and hypomethylation in lung cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in Aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial haplotypes associated with biomarkers for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

The mitochondrial genome encodes abundant small noncoding RNAs

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Natural selection of mitochondria during somatic lifetime promotes healthy aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspring

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Germline mitochondrial DNA mutations aggravate ageing and can impair brain development

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

An enhanced MITOMAP with a global mtDNA mutational phylogeny

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Linking functional decline of telomeres, mitochondria and stem cells during ageing

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Telomere dysfunction induces metabolic and mitochondrial compromise.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Selection of cancer cells with repressed mitochondria triggers colon cancer progression

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Up-regulation of the ATPase inhibitory factor 1 (IF1) of the mitochondrial H+-ATP synthase in human tumors mediates the metabolic shift of cancer cells to a Warburg phenotype.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A targeted antioxidant reveals the importance of mitochondrial reactive oxygen species in the hypoxic signaling of HIF-1alpha.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Frequent epigenetic inactivation of RASSF2 in thyroid cancer and functional consequences

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A novel diagnostic tool reveals mitochondrial pathology in human diseases and aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Epigenetic silencing mediates mitochondria stress-induced longevity

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial copy number and risk of breast cancer: a pilot study

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Oxidative damage and mitochondrial decay in aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Uncoupling protein 2 impacts endothelial phenotype via p53-mediated control of mitochondrial dynamics

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial telomerase protects cancer cells from nuclear DNA damage and apoptosis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A novel role for mitochondria in regulating epigenetic modification in the nucleus

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Changes of mitochondria in atherosclerosis: possible determinant in the pathogenesis of the disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Inhibition of excessive mitochondrial fission reduced aberrant autophagy and neuronal damage caused by LRRK2 G2019S mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A common mutation of the MYH gene is associated with increased DNA oxidation and age-related diseases.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Atypical early onset of diabetes, deafness and lung cancer in a male patient with mitochondrial mutations in peripheral mononuclear cells

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Charcot-Marie-Tooth hereditary neuropathy due to a mitochondrial ATP6 mutation.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial gene replacement in primate offspring and embryonic stem cells

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Towards germline gene therapy of inherited mitochondrial diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Evidence for in vivo production of Humanin peptide, a neuroprotective factor against Alzheimer's disease-related insults

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

DNA methylation status of nuclear-encoded mitochondrial genes underlies the tissue-dependent mitochondrial functions

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Polymorphic mutations in mouse mitochondrial DNA regulate a tumor phenotype

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial copy number is associated with colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA copy number is associated with breast cancer risk

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Associations of mitochondrial haplogroups b4 and e with biliary atresia and differential susceptibility to hydrophobic bile Acid.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Harvesting the fruit of the human mtDNA tree

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial-nuclear epistasis: implications for human aging and longevity

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Premature ageing in mice expressing defective mitochondrial DNA polymerase

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA haplogroups associated with age-related macular degeneration.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondria and tumor progression in ulcerative colitis.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

The ageing systemic milieu negatively regulates neurogenesis and cognitive function.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondria as chi.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

A mitochondrial bioenergetic etiology of disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA copy number, but not haplogroup, confers a genetic susceptibility to leprosy in Han Chinese from Southwest China

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondria are targets for peroxisome-derived oxidative stress in cultured mammalian cells

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Oxidative stress response elicited by mitochondrial dysfunction: implication in the pathophysiology of aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Study of insulin resistance in cybrid cells harboring diabetes-susceptible and diabetes-protective mitochondrial haplogroups

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Circulating humanin levels are associated with preserved coronary endothelial function

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Reactive oxygen species regulate angiogenesis and tumor growth through vascular endothelial growth factor

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Decreased mitochondrial DNA content in blood samples of patients with stage I breast cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial regulation of cancer associated nuclear DNA methylation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Association of mitochondrial DNA copy number in peripheral blood leukocytes with risk of esophageal adenocarcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Lysine acetylation: codified crosstalk with other posttranslational modifications

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial inverted repeats strongly correlate with lifespan: mtDNA inversions and aging

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial bioenergetic deficit precedes Alzheimer's pathology in female mouse model of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA damage can promote atherosclerosis independently of reactive oxygen species through effects on smooth muscle cells and monocytes and correlates with higher-risk plaques in humans.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Reduced mitochondrial DNA copy number in Chinese patients with osteosarcoma.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Humanin, a cytoprotective peptide, is expressed in carotid atherosclerotic [corrected] plaques in humans

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial-nuclear interactions: compensatory evolution or variable functional constraint among vertebrate oxidative phosphorylation genes?

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

S14G-humanin improves cognitive deficits and reduces amyloid pathology in the middle-aged APPswe/PS1dE9 mice.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Association of mitochondrial DNA variations with lung cancer risk in a Han Chinese population from southwestern China

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Induction of a tumor-associated activating mutation in protein tyrosine phosphatase Ptpn11 (Shp2) enhances mitochondrial metabolism, leading to oxidative stress and senescence

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

The impact of reactive oxygen species and genetic mitochondrial mutations in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Mitochondrial DNA haplogroup H as a risk factor for idiopathic dilated cardiomyopathy in Spanish population

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1402-4

21 January 2018

Association between mitochondrial DNA content in leukocytes and colorectal cancer risk: a case-control analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autophagy deficiency leads to protection from obesity and insulin resistance by inducing Fgf21 as a mitokine

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial energetics is impaired in vivo in aged skeletal muscle.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA haplogroups and age-related maculopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioenergetic flux, mitochondrial mass and mitochondrial morphology dynamics in AD and MCI cybrid cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene polymorphisms that protect mice from colitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-synuclein transmission and mitochondrial toxicity in primary human foetal enteric neurons in vitro.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired mitochondrial respiration and decreased fatigue resistance followed by severe muscle weakness in skeletal muscle of mitochondrial DNA mutator mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frailty and mortality are not influenced by mitochondrial DNA haplotypes in the very old.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MFN2 mutations cause compensatory mitochondrial DNA proliferation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of MnSOD enzymatic activity by Sirt3 connects the mitochondrial acetylome signaling networks to aging and carcinogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in disease and aging.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA haplogroup M is associated with late onset of hepatocellular carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational hotspots in the mitochondrial genome of lung cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomerase does not counteract telomere shortening but protects mitochondrial function under oxidative stress

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations and essential hypertension (Review).

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The creation of cybrids harboring mitochondrial haplogroups in the Taiwanese population of ethnic Chinese background: an extensive in vitro tool for the study of mitochondrial genomic variations

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quaternary protein modeling to predict the function of DNA variation found in human mitochondrial cytochrome c oxidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue-specific differences in mitochondrial activity and biogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA nucleotide changes in primary congenital glaucoma patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of European mtDNAs from an analysis of three European populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA damage is uncommon in cancer but can promote aggressive behaviour.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial dysfunction in neurodegenerative diseases and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease genetics: Double danger from mitochondrial mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RECQL4 and p53 potentiate the activity of polymerase γ and maintain the integrity of the human mitochondrial genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutations of mitochondrial DNA in aging and cancer progression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of mitochondrial genome depletion by a novel cDNA in renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/24305784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-013-1402-4

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

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