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Rho-linked genes and neurological disorders
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Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
review article
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stated in
Europe PubMed Central
title
Rho-linked genes and neurological disorders
(English)
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Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
author name string
Nael Nadif Kasri
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
Linda Van Aelst
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
publication date
15 November 2007
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Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
published in
Pfluegers Archiv
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stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
volume
455
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stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
issue
5
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stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
page(s)
787-797
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
exact match
https://scigraph.springernature.com/pub.10.1007/s00424-007-0385-1
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Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking
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Rho GTPases, dendritic structure, and mental retardation
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FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.
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The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus
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Regulation of dendritic spine motility and stability by Rac1 and Rho kinase: evidence for two forms of spine motility
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Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor
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Structural plasticity and memory
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The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain
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PubMed Central
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Inhibition of dendritic spine morphogenesis and synaptic transmission by activity-inducible protein Homer1a
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30 September 2017
Structure-stability-function relationships of dendritic spines
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30 September 2017
ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics
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30 September 2017
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
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30 September 2017
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia
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Rocks: multifunctional kinases in cell behaviour
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30 September 2017
Loss of WAVE-1 causes sensorimotor retardation and reduced learning and memory in mice
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30 September 2017
Rho GTPases in cell biology
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30 September 2017
The WRP component of the WAVE-1 complex attenuates Rac-mediated signalling
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30 September 2017
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation
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30 September 2017
Function and regulation of CREB family transcription factors in the nervous system
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30 September 2017
Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck
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30 September 2017
Homer as both a scaffold and transduction molecule.
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30 September 2017
AMPA receptor trafficking and synaptic plasticity
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30 September 2017
Rho proteins, mental retardation and the cellular basis of cognition
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30 September 2017
p21-activated kinases: three more join the Pak.
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30 September 2017
Dendritic spines: structure, dynamics and regulation
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30 September 2017
From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS
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30 September 2017
The molecular biology of memory storage: a dialogue between genes and synapses
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Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway
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30 September 2017
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
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30 September 2017
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
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30 September 2017
Monogenic causes of X-linked mental retardation.
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30 September 2017
Morphological changes in dendritic spines associated with long-term synaptic plasticity
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30 September 2017
Abnormal development of dendritic spines in FMR1 knock-out mice
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30 September 2017
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.
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30 September 2017
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
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30 September 2017
Dendritic anomalies in disorders associated with mental retardation
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30 September 2017
Homer: a link between neural activity and glutamate receptor function
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30 September 2017
Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia.
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30 September 2017
PAK3 mutation in nonsyndromic X-linked mental retardation
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30 September 2017
Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase
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30 September 2017
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
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30 September 2017
p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.
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30 September 2017
Rho GTPases and signaling networks
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30 September 2017
Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
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30 September 2017
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits
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30 September 2017
Altered cortical synaptic morphology and impaired memory consolidation in forebrain- specific dominant-negative PAK transgenic mice
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28 June 2018
The X-linked mental retardation protein oligophrenin-1 is required for dendritic spine morphogenesis
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28 June 2018
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.
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28 June 2018
alphaPix stimulates p21-activated kinase activity through exchange factor-dependent and -independent mechanisms
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28 June 2018
LIM-kinase deleted in Williams syndrome.
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28 June 2018
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28 June 2018
Phosphorylation of actin-depolymerizing factor/cofilin by LIM-kinase mediates amyloid beta-induced degeneration: a potential mechanism of neuronal dystrophy in Alzheimer's disease.
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21 September 2018
Lim kinase regulates the development of olfactory and neuromuscular synapses
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21 September 2018
Glutamate receptor exocytosis and spine enlargement during chemically induced long-term potentiation.
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21 September 2018
Role of p21-activated kinase pathway defects in the cognitive deficits of Alzheimer disease.
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21 September 2018
Abnormal long-lasting synaptic plasticity and cognition in mice lacking the mental retardation gene Pak3.
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21 September 2018
Key role of the postsynaptic density scaffold proteins Shank and Homer in the functional architecture of Ca2+ homeostasis at dendritic spines in hippocampal neurons.
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21 September 2018
Homer expression in the Xenopus tadpole nervous system
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21 September 2018
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21 September 2018
Rapid and persistent modulation of actin dynamics regulates postsynaptic reorganization underlying bidirectional plasticity.
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21 September 2018
Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.
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21 September 2018
Control of dendritic development by theDrosophila fragile X-relatedgene involves the small GTPase Rac1
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21 September 2018
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21 September 2018
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
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21 September 2018
Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice.
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21 September 2018
Regulation of postsynaptic structure and protein localization by the Rho-type guanine nucleotide exchange factor dPix
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21 September 2018
Dendritic Spine "Dysgenesis" and Mental Retardation
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21 September 2018
Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology
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4 December 2018
Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?
1 reference
stated in
PubMed
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retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00424-007-0385-1
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
PMCID
3515081
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
PubMed ID
18004590
1 reference
stated in
Europe PubMed Central
PMCID
3515081
retrieved
14 August 2017
ResearchGate publication ID
5841590
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