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English
X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
title
X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
main subject
Rett syndrome
0 references
author
Rodney Samaco
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Janine M. LaSalle
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
author name string
Daniel Braunschweig
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Thomas Simcox
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
publication date
28 April 2004
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
published in
Human Molecular Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
volume
13
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
issue
12
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
page(s)
1275-1286
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Identifiers
DOI
10.1093/HMG/DDH142
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
PubMed ID
15115765
1 reference
stated in
Europe PubMed Central
PubMed ID
15115765
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15115765%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
ResearchGate publication ID
8589051
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