Presynaptic FMR1 genotype influences the degree of synaptic connectivity in a mosaic mouse model of fragile X syndrome. (Q45192998)

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29 December 2019

title

Presynaptic FMR1 genotype influences the degree of synaptic connectivity in a mosaic mouse model of fragile X syndrome (English)

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29 December 2019

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Jesse E Hanson

1

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29 December 2019

Daniel V Madison

series ordinal

2

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language of work or name

English

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publication date

1 April 2007

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29 December 2019

published in

Journal of Neuroscience

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29 December 2019

volume

27

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29 December 2019

issue

15

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29 December 2019

page(s)

4014-4018

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FMRP expression as a potential prognostic indicator in fragile X syndrome.

29 December 2019

cites work

1 reference

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Epilepsy and EEG findings in males with fragile X syndrome.

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

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The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation

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

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Deficits in trace fear memory and long-term potentiation in a mouse model for fragile X syndrome.

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Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons

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Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse model

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Age-dependent and selective impairment of long-term potentiation in the anterior piriform cortex of mice lacking the fragile X mental retardation protein.

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Skewed X inactivation of the normal allele in fully mutated female carriers determines the levels of FMRP in blood and the fragile X phenotype.

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Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses

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Fragile X syndrome and autism at the intersection of genetic and neural networks

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The functional nature of synaptic circuitry is altered in area CA3 of the hippocampus in a mouse model of Down's syndrome

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A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases

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

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Non-invasive sexing of preimplantation stage mammalian embryos.

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12 December 2020

10.1523/JNEUROSCI.4717-06.2007

Identifiers

DOI

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