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English
Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome.
scientific article published in June 2000
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
apoptotic process
1 reference
based on heuristic
inferred from title
author
Cord Brakebusch
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
J Dixon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
R Fässler
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
M J Dixon
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 June 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Human Molecular Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
1473-1480
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
10
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Identifiers
DOI
10.1093/HMG/9.10.1473
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed ID
10888597
1 reference
stated in
Europe PubMed Central
PubMed ID
10888597
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10888597%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
ResearchGate publication ID
12429739
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