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English
MNGIE: from nuclear DNA to mitochondrial DNA.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
MNGIE: from nuclear DNA to mitochondrial DNA
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
main subject
mitochondrial DNA
0 references
author
Ichizo Nishino
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Antonella Spinazzola
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
author name string
M Hirano
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 January 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
11
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
7-10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
cites work
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
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%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THYMIDINE CATABOLISM BY NORMAL AND LEUKEMIC HUMAN LEUKOCYTES.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thymidine phosphorylase, 2-deoxy-D-ribose and angiogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900159-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(00)00159-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
11166160
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11166160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
ResearchGate publication ID
12164250
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