(Q33623490)

28 July 2017

title

Mapping pathological phenotypes in a mouse model of CDKL5 disorder (English)

1 reference

CDKL5 deficiency disorder

28 July 2017

main subject

1 reference

Dominika Farley

10

0 references

Yang Zhan

Yang Zhan

2

0 references

Enrico Castroflorio

Enrico Castroflorio

4

0 references

Alexei L. Vyssotski

Alexei L Vyssotski

9

0 references

Elisabetta Ciani

Elisabetta Ciani

11

0 references

Maurizio Giustetto

Maurizio Giustetto

13

0 references

Tommaso Pizzorusso

Tommaso Pizzorusso

12

0 references

author name string

Elena Amendola

1

1 reference

28 July 2017

Camilla Mattucci

3

1 reference

28 July 2017

Eleonora Calcagno

5

1 reference

28 July 2017

Claudia Fuchs

6

1 reference

28 July 2017

Giuseppina Lonetti

7

1 reference

28 July 2017

Davide Silingardi

8

1 reference

28 July 2017

Cornelius T Gross

14

1 reference

28 July 2017

language of work or name

English

0 references

publication date

16 May 2014

1 reference

28 July 2017

1 reference

28 July 2017

volume

9

1 reference

28 July 2017

issue

5

1 reference

28 July 2017

page(s)

e91613

1 reference

Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

16 May 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4023934/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice.

1 reference

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The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

21 June 2018

1 reference

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MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice

21 June 2018

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21 June 2018

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The role of MeCP2 in the brain.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023934

CDKL5, a protein associated with rett syndrome, regulates neuronal morphogenesis via Rac1 signaling

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023934

CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery

21 June 2018

1 reference

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Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes

21 June 2018

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Key clinical features to identify girls with CDKL5 mutations

21 June 2018

1 reference

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CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail

21 June 2018

1 reference

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21 June 2018

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RAS/ERK signaling promotes site-specific ribosomal protein S6 phosphorylation via RSK and stimulates cap-dependent translation

21 June 2018

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Seizures and electroencephalographic findings in CDKL5 mutations: case report and review

21 June 2018

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Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

21 June 2018

1 reference

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21 June 2018

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Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

21 June 2018

1 reference

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Dissecting MECP2 function in the central nervous system

21 June 2018

1 reference

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CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

21 June 2018

1 reference

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A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development

21 June 2018

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S6K1(-/-)/S6K2(-/-) mice exhibit perinatal lethality and rapamycin-sensitive 5'-terminal oligopyrimidine mRNA translation and reveal a mitogen-activated protein kinase-dependent S6 kinase pathway

21 June 2018

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21 June 2018

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 June 2018

1 reference

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 June 2018

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Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Early onset seizures and Rett-like features associated with mutations in CDKL5.

21 June 2018

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CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disorders.

21 January 2018

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Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model.

21 January 2018

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EEG gamma frequency and sleep-wake scoring in mice: comparing two types of supervised classifiers.

21 January 2018

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TrkA activation in the rat visual cortex by antirat trkA IgG prevents the effect of monocular deprivation

21 January 2018

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Presence of visual head tracking differentiates normal sighted from retinal degenerate mice

21 January 2018

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Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome

21 January 2018

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Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0091613

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0091613

Early environmental enrichment moderates the behavioral and synaptic phenotype of MeCP2 null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0091613

Dorsal telencephalon-specific expression of Cre recombinase in PAC transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0091613

High throughput production of mouse monoclonal antibodies using antigen microarrays

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24838000

12 December 2020

inferred from PubMed ID database lookup

Widespread recombinase expression using FLPeR (flipper) mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24838000

12 December 2020

inferred from PubMed ID database lookup

Temporal aspects of contrast visual evoked potentials in the pigmented rat: effect of dark rearing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24838000

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1371/JOURNAL.PONE.0091613

1 reference

28 July 2017

0 references

1 reference

28 July 2017

1 reference