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English
Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
title
Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
main subject
overexpression
1 reference
based on heuristic
inferred from title
author
Rachel A Burt
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
Joseph A Gogos
series ordinal
3
object named as
Joseph A Gogos
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
author name string
Kimberly L Stark
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
Maria Karayiorgou
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
publication date
11 June 2009
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
published in
The International Journal of Neuropsychopharmacology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
volume
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
issue
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
page(s)
983-989
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
cites work
Microduplication and triplication of 22q11.2: a highly variable syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lower prepulse inhibition in children with the 22q11 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BAC to the future: the use of bac transgenic mice for neuroscience research
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene encoding proline dehydrogenase modulates sensorimotor gating in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The murine VpreB1 and VpreB2 genes both encode a protein of the surrogate light chain and are co-expressed during B cell development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mammalian brain high-affinity L-proline transporter is enriched preferentially in synaptic vesicles in a subpopulation of excitatory nerve terminals in rat forebrain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sensorimotor gating deficits in adults with autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autistic disorder and 22q11.2 duplication.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural variation of chromosomes in autism spectrum disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1461145709000492
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S1461145709000492
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
Fatcat ID
release_oiksg2lhhrejnpywvjix4n4f3i
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/oiksg2lhhrejnpywvjix4n4f3i
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed publication ID
19519974
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19519974
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19519974%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 January 2020
ResearchGate publication ID
26286071
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