(Q51075210)

28 March 2018

title

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

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28 March 2018

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Dobkin C

1

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28 March 2018

Rabe A

2

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28 March 2018

Dumas R

3

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28 March 2018

El Idrissi A

4

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28 March 2018

Haubenstock H

5

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28 March 2018

Brown WT

6

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28 March 2018

language of work or name

English

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publication date

1 January 2000

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28 March 2018

language of work

Neuroscience

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28 March 2018

volume

100

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28 March 2018

issue

2

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28 March 2018

page(s)

423-429

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28 March 2018

Expression of FMR1, FXR1, and FXR2 genes in human prenatal tissues

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Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein

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Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1

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Analysis of neocortex in three males with the fragile X syndrome

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7 January 2021

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7 January 2021

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7 January 2021

Isolation of high molecular weight DNA for reliable genotyping of transgenic mice.

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7 January 2021

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

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7 January 2021

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7 January 2021

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

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7 January 2021

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7 January 2021

Contribution of the FMR1 gene mutation to human intellectual dysfunction

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7 January 2021

Genetic determinants of susceptibility to excitotoxic cell death: implications for gene targeting approaches

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7 January 2021

Five different genes, Eif4a1, Cd68, Supl15h, Sox15 and Fxr2h, are clustered in a 40 kb region of mouse chromosome 11.

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7 January 2021

Strain-dependent epithelial defects in mice lacking the EGF receptor

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7 January 2021

Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

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7 January 2021

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

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7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

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7 January 2021

Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms

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7 January 2021

A gene trap approach in mouse embryonic stem cells: the lacZ reported is activated by splicing, reflects endogenous gene expression, and is mutagenic in mice

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7 January 2021

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7 January 2021

Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype

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7 January 2021

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

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7 January 2021

Characterization of FMR1 proteins isolated from different tissues

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https://api.crossref.org/works/10.1016%2FS0306-4522%2800%2900292-X

7 January 2021

Alternative splicing in the fragile X gene FMR1.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2800%2900292-X

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2800%2900292-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2800%2900292-X

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%2FS0306-4522%2800%2900292-X

7 January 2021

DBA/2 and C57BL/6 mice differ in contextual fear but not auditory fear conditioning.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2800%2900292-X

7 January 2021

10.1016/S0306-4522(00)00292-X

Identifiers

DOI

1 reference

28 March 2018

1 reference

28 March 2018