Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24563813)
Watch
English
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
title
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author
Sjoerd Wanrooij
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Johannes N Spelbrink
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Petri Luoma
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Gert van Goethem
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Christine van Broeckhoven
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Anu Suomalainen
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
language of work or name
English
0 references
publication date
4 June 2004
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Nucleic Acids Research
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
32
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
3053-3064
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
cites work
Premature ageing in mice expressing defective mitochondrial DNA polymerase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
TWINKLE Has 5' -> 3' DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Composition and dynamics of human mitochondrial nucleoids
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Hypervariable sites in the mtDNA control region are mutational hotspots
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Role of adenine nucleotide translocator 1 in mtDNA maintenance
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
EMBOSS: the European Molecular Biology Open Software Suite
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Sequence and organization of the human mitochondrial genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Altered thymidine metabolism due to defects of thymidine phosphorylase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Mitochondrial disease in superoxide dismutase 2 mutant mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
24 March 2017
Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classification
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
MtDNA mutations in aging and apoptosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mutations in DNA polymerase gamma cause error prone DNA synthesis in human mitochondrial disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Active site mutation in DNA polymerase gamma associated with progressive external ophthalmoplegia causes error-prone DNA synthesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Identification of conserved residues contributing to the activities of adenovirus DNA polymerase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mitochondrial genetics and disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mitochondrial disease in mouse results in increased oxidative stress
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
DNA double-strand breaks caused by replication arrest
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Protein binding to a single termination-associated sequence in the mitochondrial DNA D-loop region
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
In organello footprint analysis of human mitochondrial DNA: human mitochondrial transcription factor A interactions at the origin of replication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Transcription and replication of animal mitochondrial DNAs.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
A sensitive genetic assay for the detection of cytosine deamination: determination of rate constants and the activation energy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Mitochondrial genetics and human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
27 September 2017
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
30 May 2018
Structural elements highly preserved during the evolution of the D-loop-containing region in vertebrate mitochondrial DNA.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
30 May 2018
Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
28 November 2018
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
28 November 2018
Mammalian mitochondrial DNA replicates bidirectionally from an initiation zone
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
28 November 2018
Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
28 November 2018
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=434440
retrieved
28 November 2018
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Response: The mitochondrial DNA replication bubble has not burst
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The mitochondrial DNA replication bubble has not burst
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mitochondrial disorders come full circle
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Yeast ARMs (DNA at-risk motifs) can reveal sources of genome instability
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Lack of WRN results in extensive deletion at nonhomologous joining ends
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15181170
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/NAR/GKH634
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PMC publication ID
434440
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed publication ID
15181170
1 reference
stated in
Europe PubMed Central
PMC publication ID
434440
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15181170%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
ResearchGate publication ID
8526088
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit