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

Microarray analysis of the fetal hippocampus in the Emx2 mutant.

Developmental neuroscience - 1 Jan 2007

Skutella Thomas, Conrad Sabine, Hooge Jens, Bonin Michael, Alvarez-Bolado Gonzalo

Abstract excerpt

Deficiency in the transcription factor Emx2 causes a specific alteration of hippocampal development, which has been well analyzed morphologically. We are currently using microarrays and in situ hybridization to characterize gene expression in the Emx2 mutant hippocampus. In this report on our preliminary results for the fetal stage, we identify a group of genes for most of which a putative relation to Emx2...

Read the complete abstract on PubMed

Topics

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

Share to Dentate Gyrus
Share to Hippocampus
Share to Neovascularization, Physiologic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nervous System Malformations

Share to Neural Pathways

Share to Receptors, Notch

Share to Stem Cells

Share to Wnt Proteins

Source

Identifiers

PMID: 17148947
DOI: 10.1159/000096209

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Microarray analysis of the fetal hippocampus in the Emx2 mutant.PMID 17148947Read ↗

Emx1 and Emx2 cooperate to regulate cortical size, lamination, neuronal differentiation, development of cortical efferents, and thalamocortical pathfinding.Semantic proximity Read ↗

ECE2 regulates neurogenesis and neuronal migration during human cortical developmentSemantic proximity Read ↗

Lhx2 regulates the development of the forebrain hem system.Semantic proximity Read ↗

EMX2 transcriptionally regulates <i>Nfib</i> expression in neural progenitor cells during early cortical developmentSemantic proximity Read ↗

The lack of Emx2 causes impairment of Reelin signaling and defects of neuronal migration in the developing cerebral cortex.Semantic proximity Read ↗

Identification and characterization of a novel transcript down-regulated in Dlx1/Dlx2 and up-regulated in Pax6 mutant telencephalon.Semantic proximity Read ↗

Genetic analysis of anterior posterior expression gradients in the developing mammalian forebrain.Semantic proximity Read ↗

Cell autonomous and non-cell autonomous functions of Otx2 in patterning the rostral brain.Semantic proximity Read ↗

Emx2 and Pax6 control regionalization of the pre-neuronogenic cortical primordium.Semantic proximity Read ↗

Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers.Semantic proximity Read ↗

LIM-homeodomain gene Lhx2 regulates the formation of the cortical hem.Semantic proximity Read ↗

Agenesis of the Corpus Callosum Due to Defective Glial Wedge Formation in Lhx2 Mutant Mice.Semantic proximity Read ↗

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