(Q28710285)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

review article

2 references

20 September 2020

Mitochondrial DNA sequence variation and neurodegeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

20 September 2020

4 references

30 June 2019

2 August 2019

14 September 2019

20 September 2020

1 reference

2 August 2019

1 reference

14 September 2019

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Daniele Orsucci

3

1 reference

ORCID Public Data File 2021

author name string

Michelangelo Mancuso

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Gabriele Siciliano

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

language of work or name

English

0 references

publication date

1 September 2008

5 references

30 June 2019

2 August 2019

14 September 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

20 September 2020

6 references

30 June 2019

2 August 2019

14 September 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

20 September 2020

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

71-78

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases

19 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Harvesting the fruit of the human mtDNA tree

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Alzheimer's disease: genes, proteins, and therapy

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial DNA and human evolution

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

17 March 2017

1 reference

https://api.crossref.org/works/10.1186/1479-7364-3-1-71

Mitochondrial respiratory-chain diseases

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

mtDNA nt13708A variant increases the risk of multiple sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondria and neurodegeneration.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial diseases: a nosological update.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial dysfunction, oxidative stress and neurodegeneration.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial genomic contribution to mitochondrial dysfunction in Alzheimer's disease.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondria take center stage in aging and neurodegeneration

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

A "mitochondrial cascade hypothesis" for sporadic Alzheimer's disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial abnormalities in cybrid cell models of sporadic Alzheimer's disease worsen with passage in culture

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

The rotary machine in the cell, ATP synthase

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Alzheimer's disease cybrids replicate beta-amyloid abnormalities through cell death pathways

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondria in sporadic amyotrophic lateral sclerosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease.

3 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Early-onset familial parkinsonism due to POLG mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA from platelets of sporadic ALS patients restores normal respiratory functions in rho(0) cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: a hospital-based case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Motor neuron disease in a patient with a mitochondrial tRNAIle mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Parent-of-origin effect in multiple sclerosis: observations in half-siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

The power to detect disease associations with mitochondrial DNA haplogroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Genetic ancestry and the search for personalized genetic histories

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1479-7364-3-1-71

Lack of association between mtDNA haplogroups and Alzheimer's disease in Tuscany.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3525185

Mitochondrial DNA haplogroups and amyotrophic lateral sclerosis

27 November 2018

1 reference

12 December 2020

Mitochondrial dysfunction in Parkinson's disease

1 reference

12 December 2020

UCP2 and mitochondrial haplogroups as a multiple sclerosis risk factor

1 reference

12 December 2020

Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy

1 reference

12 December 2020

Mitochondrial DNA deletion mutation levels are elevated in ALS brains

1 reference

12 December 2020

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family

1 reference

12 December 2020

Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population

1 reference

12 December 2020

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

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

Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis

1 reference

12 December 2020

Does the mitochondrial genome play a role in the etiology of Alzheimer's disease?

1 reference

12 December 2020

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease

1 reference

12 December 2020

The mtDNA A8344G “MERRF” mutation is not a common cause of sporadic Parkinson disease in Italian population

1 reference

12 December 2020

Association of the 11778 mitochondrial DNA mutation and demyelinating disease

1 reference

12 December 2020

Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis

1 reference

12 December 2020

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis

1 reference

12 December 2020

Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians

1 reference

12 December 2020

Identifiers

DOI

10.1186/1479-7364-3-1-71

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

1041244900

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19129091%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

PubMed publication ID

19129091

2 references