(Q36379639)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

The effect of an mGluR5 inhibitor on procedural memory and avoidance discrimination impairments in Fmr1 KO mice (English)

1 reference

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20 January 2020

2

1 reference

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20 January 2020

Laurens Bosman

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

M F Vinueza Veloz

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

R Willemsen

3

1 reference

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20 January 2020

A Cupido

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

S K E Koekkoek

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

J W Potters

7

1 reference

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20 January 2020

B A Oostra

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C I De Zeeuw

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

language of work or name

English

0 references

publication date

19 January 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

Genes, Brain and Behavior

20 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

11

1 reference

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20 January 2020

issue

3

1 reference

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20 January 2020

page(s)

325-331

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice

20 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Motor deficits in neurofibromatosis type 1 mice: the role of the cerebellum.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Potential therapeutic interventions for fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Genetic dissection of the function of hindbrain axonal commissures

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Dissociation of social and nonsocial anxiety in a mouse model of fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

The anxiolytic and analgesic properties of fenobam, a potent mGlu5 receptor antagonist, in relation to the impairment of learning

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

The state of synapses in fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

FMR1: a gene with three faces

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Fenobam: a clinically validated nonbenzodiazepine anxiolytic is a potent, selective, and noncompetitive mGlu5 receptor antagonist with inverse agonist activity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

The mGluR theory of fragile X mental retardation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

The RNA binding protein FMRP: new connections and missing links.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

FMR1 and the fragile X syndrome: human genome epidemiology review

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

FRAXA and FRAXE: the results of a five year survey

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Vasopressin and oxytocin in brain areas of rats with high or low behavioral performance.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Fragile X mice develop sensory hyperreactivity to auditory stimuli

28 June 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Prevalence of the fragile X syndrome in African-Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome: a prospective ten-year follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Internalization of ionotropic glutamate receptors in response to mGluR activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

EFFECT OF AMYGDALOID LESIONS ON AVOIDANCE BEHAVIOR AND VISUAL DISCRIMINATION IN CATS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Role of olivary electrical coupling in cerebellar motor learning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Profiling Fragile X Syndrome in males: strengths and weaknesses in cognitive abilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2011.00763.X

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3491868

Bilateral alteration in stepping pattern after unilateral motor cortex injury: A new test strategy for analysis of skilled limb movements in neurological mouse models

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22257369

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1601-183X.2011.00763.X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22257369%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

22257369

1 reference