(Q35076945)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

review article

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title

Of mice and the fragile X syndrome (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

R Frank Kooy

series ordinal

1

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6 August 2017

publication date

1 March 2003

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

19

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

148-154

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

Fragile X syndrome at the turn of the century.

1 November 2019

cites work

1 reference

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7 January 2021

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

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7 January 2021

Postmortem examination of two fragile X brothers with an FMR1 full mutation

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7 January 2021

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

1 reference

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7 January 2021

Characterization of the full fragile X syndrome mutation in fetal gametes.

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https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

1 reference

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7 January 2021

A decade of molecular studies of fragile X syndrome

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7 January 2021

Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes.

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7 January 2021

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7 January 2021

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

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7 January 2021

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

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7 January 2021

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

1 reference

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7 January 2021

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

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7 January 2021

Transgenic mouse model for the fragile X syndrome.

1 reference

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7 January 2021

Mildly impaired water maze performance in male Fmr1 knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Introduction of aFMR1 transgene in the fragile X knockout mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse

1 reference

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7 January 2021

Place navigation impaired in rats with hippocampal lesions

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Molecular mechanisms of memory acquisition, consolidation and retrieval

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

The neurobiology of startle

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Fragile X mice develop sensory hyperreactivity to auditory stimuli

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

The fragile X syndrome and other fragile site disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Macroorchidism in FMR1 knockout mice is caused by increased Sertoli cell proliferation during testicular development.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Neurodevelopmental effects of the FMR-1 full mutation in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Brain studies of mouse models for neurogenetic disorders using in vivo magnetic resonance imaging (MRI).

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Analysis of neocortex in three males with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Abnormal development of dendritic spines in FMR1 knock-out mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

FMRP involvement in formation of synapses among cultured hippocampal neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

A synaptic model of memory: long-term potentiation in the hippocampus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Long-term potentiation in the hippocampus of fragile X knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Altered synaptic plasticity in a mouse model of fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Evidence that fragile X mental retardation protein is a negative regulator of translation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

The fragile X mental retardation protein inhibits translation via interacting with mRNA

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Modifier genes in mice and humans

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Trinucleotide repeats (CGG)22TGG(CGG)43TGG(CGG)21 from the fragile X gene remain stable in transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Instability of a (CGG)98 repeat in the Fmr1 promoter.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Knockout mouse model for Fxr2: a model for mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Restoring the phenotype of fragile X syndrome: insight from the mouse model

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

Hippocampal lesions cause learning deficits in inbred mice in the Morris water maze and conditioned-fear task.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2803%2900017-9

7 January 2021

10.1016/S0168-9525(03)00017-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615009%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference