Protecting the mitochondrial powerhouse. (Q38286869)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

review article

1 reference

title

Protecting the mitochondrial powerhouse (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

author

Morten Scheibye-Knudsen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Evandro F Fang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

5

Vilhelm A Bohr

1 reference

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24 February 2020

author name string

Deborah L Croteau

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

David M Wilson

4

1 reference

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24 February 2020

language of work or name

1 reference

11 December 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

published in

Trends in Cell Biology

1 reference

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24 February 2020

volume

25

1 reference

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24 February 2020

issue

3

1 reference

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24 February 2020

page(s)

158-170

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

A conserved endoplasmic reticulum membrane protein complex (EMC) facilitates phospholipid transfer from the ER to mitochondria

24 February 2020

cites work

1 reference

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Mitochondrial proteostasis in the control of aging and longevity

6 September 2017

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The intrinsic apoptosis pathway mediates the pro-longevity response to mitochondrial ROS in C. elegans

6 September 2017

1 reference

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Defective mitophagy in XPA via PARP-1 hyperactivation and NAD(+)/SIRT1 reduction.

6 September 2017

1 reference

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Ubiquitin is phosphorylated by PINK1 to activate parkin

6 September 2017

1 reference

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To be or not to be? How selective autophagy and cell death govern cell fate

6 September 2017

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Loss of iron triggers PINK1/Parkin-independent mitophagy

6 September 2017

1 reference

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Inheritance of the fittest mitochondria in yeast

6 September 2017

1 reference

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Accessorizing the human mitochondrial transcription machinery

6 September 2017

1 reference

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PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria

6 September 2017

1 reference

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

6 September 2017

1 reference

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The ATM protein kinase: regulating the cellular response to genotoxic stress, and more

6 September 2017

1 reference

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Mice deficient in Epg5 exhibit selective neuronal vulnerability to degeneration

6 September 2017

1 reference

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Mitochondrial deficiency in Cockayne syndrome

6 September 2017

1 reference

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Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability

6 September 2017

1 reference

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Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

6 September 2017

1 reference

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Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.

6 September 2017

1 reference

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Human mitochondrial DNA replication

6 September 2017

1 reference

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Autophagy modulation as a potential therapeutic target for diverse diseases

6 September 2017

1 reference

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Protective coupling of mitochondrial function and protein synthesis via the eIF2α kinase GCN-2

6 September 2017

1 reference

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Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy.

6 September 2017

1 reference

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Signaling the mitochondrial unfolded protein response

6 September 2017

1 reference

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Shining a light on xeroderma pigmentosum

6 September 2017

1 reference

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The interface of transcription and DNA replication in the mitochondria

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Mitochondrial dysfunction in ataxia-telangiectasia

6 September 2017

1 reference

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Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

6 September 2017

1 reference

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ER Tubules Mark Sites of Mitochondrial Division

6 September 2017

1 reference

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Human diseases with impaired mitochondrial protein synthesis

6 September 2017

1 reference

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Mre11 is expressed in mammalian mitochondria where it binds to mitochondrial DNA.

6 September 2017

1 reference

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Toxin models of mitochondrial dysfunction in Parkinson's disease.

6 September 2017

1 reference

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Aprataxin localizes to mitochondria and preserves mitochondrial function

6 September 2017

1 reference

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Mitochondrial oxidative stress causes mitochondrial fragmentation via differential modulation of mitochondrial fission–fusion proteins

6 September 2017

1 reference

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Making heads or tails of phospholipids in mitochondria

6 September 2017

1 reference

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6 September 2017

Mechanisms of mitophagy

1 reference

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6 September 2017

Autophagy and Metabolism

1 reference

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Role of tyrosyl-DNA phosphodiesterase (TDP1) in mitochondria

6 September 2017

1 reference

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Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.

6 September 2017

1 reference

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Collaboration and competition between DNA double‐strand break repair pathways

6 September 2017

1 reference

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Nix is critical to two distinct phases of mitophagy, reactive oxygen species-mediated autophagy induction and Parkin-ubiquitin-p62-mediated mitochondrial priming

6 September 2017

1 reference

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Core human mitochondrial transcription apparatus is a regulated two-component system in vitro.

6 September 2017

1 reference

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Discovery of a novel function for human Rad51: maintenance of the mitochondrial genome

6 September 2017

1 reference

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PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondria.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane

6 September 2017

1 reference

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Multi-system neurological disease is common in patients with OPA1 mutations

6 September 2017

1 reference

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Synergistic roles of the proteasome and autophagy for mitochondrial maintenance and chronological lifespan in fission yeast.

6 September 2017

1 reference

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PINK1 is selectively stabilized on impaired mitochondria to activate Parkin

6 September 2017

1 reference

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Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of aging

6 September 2017

1 reference

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Mitochondrial DNA repair and association with aging--an update

6 September 2017

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Nix is a selective autophagy receptor for mitochondrial clearance

6 September 2017

1 reference

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Pearson syndrome in the neonatal period: two case reports and review of the literature

6 September 2017

1 reference

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DNA Damage, Aging, and Cancer

6 September 2017

1 reference

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Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity

6 September 2017

1 reference

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Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy

6 September 2017

1 reference

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The pathogenesis of Friedreich ataxia and the structure and function of frataxin

6 September 2017

1 reference

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Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study

6 September 2017

1 reference

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Novel DNA mismatch-repair activity involving YB-1 in human mitochondria

6 September 2017

1 reference

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DNA repair in mammalian cells: Base excision repair: the long and short of it.

6 September 2017

1 reference

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Coenzyme Q deficiency triggers mitochondria degradation by mitophagy

6 September 2017

1 reference

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Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Dynamic compartmentalization of base excision repair proteins in response to nuclear and mitochondrial oxidative stress

6 September 2017

1 reference

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6 September 2017

1 reference

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Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation

6 September 2017

1 reference

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Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy

6 September 2017

1 reference

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Mechanisms and functions of DNA mismatch repair

6 September 2017

1 reference

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Mitochondrial disease: a practical approach for primary care physicians.

6 September 2017

1 reference

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MGMT: key node in the battle against genotoxicity, carcinogenicity and apoptosis induced by alkylating agents

6 September 2017

1 reference

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Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators

6 September 2017

1 reference

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DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1.

6 September 2017

1 reference

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The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates

6 September 2017

1 reference

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

6 September 2017

1 reference

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Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients

6 September 2017

1 reference

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OPA1 requires mitofusin 1 to promote mitochondrial fusion

6 September 2017

1 reference

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The molecular structure and contact relationships of cell membranes.

6 September 2017

1 reference

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Aging: a theory based on free radical and radiation chemistry

6 September 2017

1 reference

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Uncoupling protein-2 prevents neuronal death and diminishes brain dysfunction after stroke and brain trauma

6 September 2017

1 reference

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Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

6 September 2017

1 reference

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Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Superoxide activates mitochondrial uncoupling proteins

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Long-term clinical outcome in patients with glutathione synthetase deficiency

6 September 2017

1 reference

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Mitochondrial morphology during preimplantational human embryogenesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia

6 September 2017

1 reference

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Quality control by DNA repair

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Close contacts with the endoplasmic reticulum as determinants of mitochondrial Ca2+ responses

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Phospholipid synthesis in a membrane fraction associated with mitochondria

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Mouse and human mitochondrial nucleoid--detailed structure in relation to function

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Double strand break rejoining by mammalian mitochondrial extracts.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Stable Golgi-mitochondria complexes and formation of Golgi Ca(2+) gradients in pancreatic acinar cells.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Resistance to cerebral ischemic injury in UCP2 knockout mice: evidence for a role of UCP2 as a regulator of mitochondrial glutathione levels

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Repair of mitochondrial DNA after various types of DNA damage in Chinese hamster ovary cells

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

31 August 2018

Treating iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

MITOL regulates endoplasmic reticulum-mitochondria contacts via Mitofusin2.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

A vesicular transport pathway shuttles cargo from mitochondria to lysosomes.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Decreased expression of Drp1 and Fis1 mediates mitochondrial elongation in senescent cells and enhances resistance to oxidative stress through PINK1.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

MELAS: clinical features, muscle biopsy and molecular genetics

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Wilson disease: description of 282 patients evaluated over 3 decades

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5576887

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy

31 August 2018

1 reference

12 December 2020

The effect of α-tocopherol on essential fatty acid oxidation in liver mitochondria from vitamin E-deficient chicks

1 reference

12 December 2020

Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA

1 reference

12 December 2020

Mitochondrial protein import: from transport pathways to an integrated network

1 reference

12 December 2020

Increased oxidative damage is correlated to altered mitochondrial function in heterozygous manganese superoxide dismutase knockout mice

1 reference

12 December 2020

10.1016/J.TCB.2014.11.002

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

PubMed publication ID

25499735

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25499735%20AND%20SRC:MED&resulttype=core&format=json