(Q37134197)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

2 references

20 September 2020

6 November 2020

Mitochondrial mutations: newly discovered players in neuronal degeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

Douglass Matthew Turnbull

17 January 2020

main subject

mitochondrial disease

9 references

24 March 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

12 October 2019

20 September 2020

6 November 2020

7 references

24 March 2019

25 April 2019

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30 June 2019

2 August 2019

14 September 2019

12 October 2019

1 reference

2 August 2019

1 reference

14 September 2019

1 reference

12 October 2019

1 reference

1 reference

20 September 2020

1 reference

6 November 2020

series ordinal

2

1 reference

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17 January 2020

author name string

Nichola Z Lax

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Amy K Reeve

series ordinal

3

1 reference

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17 January 2020

publication date

1 December 2011

10 references

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25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

12 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

20 September 2020

6 November 2020

10 references

24 March 2019

25 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

12 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

20 September 2020

6 November 2020

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

6

1 reference

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17 January 2020

page(s)

645-658

1 reference

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Creative Commons Attribution-NonCommercial

17 January 2020

copyright license

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30 June 2019

2 August 2019

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12 October 2019

20 September 2020

6 November 2020

on focus list of Wikimedia project

ScienceSource

0 references

cites work

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14 September 2017

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14 September 2017

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14 September 2017

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Mitochondrial dysfunction is a converging point of multiple pathological pathways in amyotrophic lateral sclerosis

14 September 2017

1 reference

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

14 September 2017

1 reference

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14 September 2017

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14 September 2017

1 reference

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PINK1 is selectively stabilized on impaired mitochondria to activate Parkin

14 September 2017

1 reference

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Mitochondrial trafficking of APP and alpha synuclein: Relevance to mitochondrial dysfunction in Alzheimer's and Parkinson's diseases

14 September 2017

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The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons

14 September 2017

1 reference

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Mammalian macroautophagy at a glance

14 September 2017

1 reference

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Amyloid beta, mitochondrial structural and functional dynamics in Alzheimer's disease

14 September 2017

1 reference

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Amyloid-beta overproduction causes abnormal mitochondrial dynamics via differential modulation of mitochondrial fission/fusion proteins

14 September 2017

1 reference

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Molecular mechanisms of alpha-synuclein neurodegeneration

14 September 2017

1 reference

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Mitochondrial localization of alpha-synuclein protein in alpha-synuclein overexpressing cells

14 September 2017

1 reference

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Mitochondrial translocation of alpha-synuclein is promoted by intracellular acidification

14 September 2017

1 reference

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Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration

14 September 2017

1 reference

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Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

14 September 2017

1 reference

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Prevalence of mitochondrial DNA disease in adults

14 September 2017

1 reference

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DJ-1 gene deletion reveals that DJ-1 is an atypical peroxiredoxin-like peroxidase

14 September 2017

1 reference

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Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons

14 September 2017

1 reference

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Accumulation of amyloid precursor protein in the mitochondrial import channels of human Alzheimer's disease brain is associated with mitochondrial dysfunction.

14 September 2017

1 reference

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Mitochondrial reactive oxygen species and Ca2+ signaling

14 September 2017

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Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

14 September 2017

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High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

14 September 2017

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Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

14 September 2017

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Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration

14 September 2017

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14 September 2017

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

14 September 2017

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Mitochondrial DNA mutations in human colonic crypt stem cells

14 September 2017

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Role of Protein Aggregation in Mitochondrial Dysfunction and Neurodegeneration in Alzheimer's and Parkinson's Diseases

14 September 2017

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Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy

14 September 2017

1 reference

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Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants

14 September 2017

1 reference

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Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

14 September 2017

1 reference

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Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.

14 September 2017

1 reference

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OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.

14 September 2017

1 reference

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High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain

14 September 2017

1 reference

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Neuropathological features of mitochondrial disorders

14 September 2017

1 reference

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Mammalian TOR: a homeostatic ATP sensor

14 September 2017

1 reference

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

14 September 2017

1 reference

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Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

14 September 2017

1 reference

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Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

14 September 2017

1 reference

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Ubiquitin tag for sperm mitochondria

14 September 2017

1 reference

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Oxidative phosphorylation at the fin de siècle

14 September 2017

1 reference

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Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis

14 September 2017

1 reference

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Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade

14 September 2017

1 reference

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α-Synuclein in Lewy bodies

14 September 2017

1 reference

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Axoplasmic organelles at nodes of Ranvier. I. Occurrence and distribution in large myelinated spinal root axons of the adult cat.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Sequence and organization of the human mitochondrial genome

14 September 2017

1 reference

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Maternal inheritance of human mitochondrial DNA

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

MERRF: a clinicopathological study. Relationships between myoclonus epilepsies and mitochondrial myopathies

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Rapid evolution of animal mitochondrial DNA

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Histochemical localization of cytochrome oxidase in the hippocampus: Correlation with specific neuronal types and afferent pathways

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Neuropathology in Kearns-Sayre syndrome

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Mitochondrial complex I deficiency in Parkinson's disease

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Infantile Diffuse Cerebral Degeneration With Hepatic Cirrhosis

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

The PINK1-Parkin pathway is involved in the regulation of mitochondrial remodeling process.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

The distribution of mitochondrial activity in relation to optic nerve structure

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

Myoclonic Epilepsy and Ragged Red Fibers (MERRF) Syndrome: Selective Vulnerability of CNS Neurons Does Not Correlate with the Level of Mitochondrial tRNAlysMutation in Individual Neuronal Isolates

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757997

3 September 2018

Symbiosis and Evolution

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Mitochondrial dysfunction plays a key role in progressive axonal loss in Multiple Sclerosis

1 reference

12 December 2020

Increased autophagic degradation of mitochondria in Alzheimer disease

1 reference

12 December 2020

Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder

1 reference

12 December 2020

Identifiers

DOI

10.1177/1073858410385469

1 reference

18 August 2017

10.1177/1073858411385469

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22130639%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

PubMed publication ID

22130639

1 reference