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Mitochondrial DNA variants in inclusion body myositis.
scientific article published in December 2000
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
title
Mitochondrial DNA variants in inclusion body myositis
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
main subject
mitochondrial DNA
0 references
author
Ralph Martins
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author name string
C C Kok
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
A Boyt
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
S Gaudieri
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
V Askanas
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
M Dalakas
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
L Kiers
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
F Mastaglia
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
M Garlepp
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
publication date
1 December 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
604-611
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polymyositis, dermatomyositis and inclusion-body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inclusion body myositis and myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes of autoinvasive cells in polymyositis and inclusion body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ragged red fibers in normal aging and inflammatory myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in human degenerative diseases and aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA and Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal locus predisposing to deletions of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inclusion body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial DNA clone is associated with increased risk for Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A comparison of single nucleotide primer extension with mispairing PCR-RFLP in detecting a point mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome oxidase deficiency in Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Branching pattern in the evolutionary tree for human mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA haplotype predicts deafness risk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HLA associations with inclusion body myositis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900144-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(00)00144-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
11053689
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11053689
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11053689%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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