(Q28574630)

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861382%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

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

2 references

31 January 2017

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14 February 2020

0 references

0 references

1 reference

8

1 reference

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14 February 2020

author name string

Qian Chen

1

2 references

31 January 2017

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14 February 2020

Yong-Chuan Zhu

2

2 references

31 January 2017

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14 February 2020

Jing Yu

3

2 references

31 January 2017

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14 February 2020

Sheng Miao

4

2 references

31 January 2017

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14 February 2020

Jing Zheng

5

2 references

31 January 2017

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14 February 2020

Li Xu

6

2 references

31 January 2017

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14 February 2020

Yang Zhou

7

2 references

31 January 2017

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14 February 2020

Chi Zhang

9

2 references

31 January 2017

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14 February 2020

Jiong Tao

10

2 references

31 January 2017

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14 February 2020

Zhi-Qi Xiong

11

2 references

31 January 2017

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14 February 2020

language of work or name

English

0 references

publication date

1 September 2010

1 reference

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14 February 2020

published in

Journal of Neuroscience

2 references

31 January 2017

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14 February 2020

volume

30

2 references

31 January 2017

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14 February 2020

issue

38

2 references

31 January 2017

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14 February 2020

page(s)

12777-12786

1 reference

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Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

14 February 2020

cites work

1 reference

12 December 2020

Dendritic anomalies in disorders associated with mental retardation

1 reference

12 December 2020

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

1 reference

12 December 2020

Efficient gene transfer into the embryonic mouse brain using in vivo electroporation

1 reference

12 December 2020

Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors

1 reference

12 December 2020

Rho proteins, mental retardation and the cellular basis of cognition

1 reference

12 December 2020

Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity

1 reference

12 December 2020

Signalling and crosstalk of Rho GTPases in mediating axon guidance.

1 reference

12 December 2020

Trk receptors: roles in neuronal signal transduction

1 reference

12 December 2020

Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome

1 reference

12 December 2020

PDGF alpha- and beta-receptors activate unique and common signal transduction pathways

1 reference

12 December 2020

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

1 reference

12 December 2020

Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation

1 reference

12 December 2020

The role of the Rho GTPases in neuronal development

1 reference

12 December 2020

CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients.

1 reference

12 December 2020

TrkB binds and tyrosine-phosphorylates Tiam1, leading to activation of Rac1 and induction of changes in cellular morphology

1 reference

12 December 2020

FilGAP, a Rho- and ROCK-regulated GAP for Rac binds filamin A to control actin remodelling

1 reference

12 December 2020

Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation

1 reference

12 December 2020

Neurotrophin-regulated signalling pathways

1 reference

12 December 2020

Requirement of TORC1 for late-phase long-term potentiation in the hippocampus

1 reference

12 December 2020

Polarized signaling endosomes coordinate BDNF-induced chemotaxis of cerebellar precursors.

1 reference

12 December 2020

Endocytic trafficking of Rac is required for the spatial restriction of signaling in cell migration

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Neuropathology of Rett syndrome

1 reference

12 December 2020

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

1 reference

12 December 2020

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

12 December 2020

Neurotrophins regulate dendritic growth in developing visual cortex

1 reference

12 December 2020

Selective dendritic alterations in the cortex of Rett syndrome

1 reference

12 December 2020

Axonal origin and purity of growth cones isolated from fetal rat brain.

1 reference

12 December 2020

Involvement of phosphatidylinositide 3'-kinase and Rac in platelet-derived growth factor-induced actin reorganization and chemotaxis

1 reference

12 December 2020

Platelet-derived growth factor (PDGF)-induced actin rearrangement is deregulated in cells expressing a mutant Y778F PDGF beta-receptor

1 reference

12 December 2020

Rho GTPases and the actin cytoskeleton

1 reference

12 December 2020

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

12 December 2020

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

12 December 2020

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

12 December 2020

Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region

1 reference

12 December 2020

Regulation of the small GTP-binding protein Rho by cell adhesion and the cytoskeleton

1 reference

12 December 2020

10.1523/JNEUROSCI.1102-10.2010

Identifiers

DOI

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861382%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20861382%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

2 references

31 January 2017