(Q51978092)

19 April 2018

title

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome. (English)

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19 April 2018

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7

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author name string

Musumeci SA

1

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19 April 2018

Bosco P

2

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19 April 2018

Calabrese G

3

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19 April 2018

Bakker C

4

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19 April 2018

De Sarro GB

5

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19 April 2018

Elia M

6

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19 April 2018

Oostra BA

8

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19 April 2018

publication date

1 January 2000

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19 April 2018

published in

Epilepsia

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19 April 2018

volume

41

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19 April 2018

page(s)

19-23

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issue

1

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19 April 2018

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Transgenic mouse model for the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Paroxysmal discharges in the EL mouse, a genetic model of epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Mapping of two genes that influence susceptibility to audiogenic seizures in crosses of C57BL/6J and DBA/2J mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Sound-induced seizures in serotonin 5-HT2c receptor mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Amyotrophic lateral sclerosis in a patient with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Adult fragile X syndrome. Clinico-neuropathologic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Analysis of neocortex in three males with the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Neuroanatomy of fragile X syndrome: the temporal lobe

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01499.X

10.1111/J.1528-1157.2000.TB01499.X

21 January 2018

Identifiers

DOI

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19 April 2018

PubMed ID

10643918

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19 April 2018