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A mouse model of fragile X syndrome exhibits heightened arousal and/or emotion following errors or reversal of contingencies.
scientific article published on July 2008
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stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
A mouse model of fragile X syndrome exhibits heightened arousal and/or emotion following errors or reversal of contingencies
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
main subject
fragile X syndrome
1 reference
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inferred from title
author
David A. Levitsky
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4
1 reference
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Barbara J. Strupp
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5
object named as
B J Strupp
1 reference
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author name string
J Moon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
K T Ota
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
L L Driscoll
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
1 July 2008
1 reference
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
Developmental Psychobiology
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
50
1 reference
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
473-485
1 reference
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Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.
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Therapeutic implications of the mGluR theory of fragile X mental retardation
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The mGluR theory of fragile X mental retardation
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Differential impact of the FMR-1 full mutation on memory and attention functioning : a neuropsychological perspective.
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Do women with fragile X syndrome have problems in switching attention: preliminary findings from ERP and fMRI.
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Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach
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Fmr1 knockout mouse has a distinctive strain-specific learning impairment.
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Impaired sustained attention and error-induced stereotypy in the aged Ts65Dn mouse: a mouse model of Down syndrome and Alzheimer's disease.
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Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice
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Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
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Visuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotype
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A major gene affecting age-related hearing loss in C57BL/6J mice
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Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome
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Attentional dysfunction, impulsivity, and resistance to change in a mouse model of fragile X syndrome
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A neuropsychological profile of attention deficits in young males with fragile X syndrome.
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Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse
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Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children.
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Neural correlates of a reversal learning task with an affectively neutral baseline: an event-related fMRI study.
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7 January 2021
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Neural correlates of switching set as measured in fast, event-related functional magnetic resonance imaging
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7 January 2021
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Cognitive profile of rats exposed to lactational hyperphenylalaninemia: correspondence with human mental retardation
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7 January 2021
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Deficient cumulative learning: an animal model of retarded cognitive development.
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7 January 2021
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inferred from DOI database lookup
fMRI study of cognitive interference processing in females with fragile X syndrome.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence from two genetic syndromes for a dissociation between verbal and visual-spatial short-term memory.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Further delineation of the executive deficit in males with fragile-X syndrome.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.
1 reference
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDEV.20308
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/DEV.20308
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
PubMed publication ID
18551464
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18551464
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18551464%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
ResearchGate publication ID
5304390
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