Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: Insights into the cause of periventricular heterotopia

1 Jan 2005

Abstract excerpt

Periventricular heterotopia (PH) is a malformation of cortical development characterized by nodules of neurons, ectopically located along the lateral ventricles of the brain. Mutations in the vesicle transport ADP-ribosylation factor guanine exchange factor 2 gene (ARFGEF2) or the actin-binding Filamin A (FLNA) gene cause PH. Previous studies have shown that FLNA expression is developmentally regulated, with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cerebrospinal fluid and hydrocephalus
Share to Fetal and Pediatric Neurological Disorders
Share to Spinal Dysraphism and Malformations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16320251
DOI: 10.1002/cne.20806

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: Insights into the cause of periventricular heterotopiaPMID 16320251Read ↗

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopiaSemantic proximity Read ↗

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.Semantic proximity Read ↗

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.Semantic proximity Read ↗

A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-ASemantic proximity Read ↗

Periventricular Heterotopia: Shuttling of Proteins through Vesicles and Actin in Cortical Development and DiseaseSemantic proximity Read ↗

Filamin A in focus: unravelling the multifaceted roles of filamin A in neurodevelopment and neurological disordersSemantic proximity Read ↗

Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review.Semantic proximity Read ↗

Filamin A Regulates Neural Progenitor Proliferation and Cortical Size through Wee1-Dependent Cdk1 PhosphorylationSemantic proximity Read ↗

Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionSemantic proximity Read ↗

Afadin Loss Uncovers an Ectopic Neurogenic Niche and Reorganizes the Adult Ventricular-Subventricular ZoneSemantic proximity Read ↗

<i>Afadin</i> Loss Uncovers an Ectopic Neurogenic Niche and Reorganizes the Adult Ventricular-Subventricular ZoneSemantic proximity Read ↗

ARHGEF6-dependent cytoskeletal regulation underlies a conserved program of forebrain interneuron developmentSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.