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Article

Gene deletion mutants reveal a role for semaphorin receptors of the plexin-B family in mechanisms underlying corticogenesis.

Molecular and cellular biology - 1 Feb 2010

Hirschberg A, Deng S, Korostylev A, Paldy E, Costa M R, Worzfeld T, Vodrazka P, Wizenmann A, Götz M, Offermanns S, Kuner R

Abstract excerpt

Semaphorins and their receptors, plexins, are emerging as key regulators of various aspects of neural and nonneural development. Semaphorin 4D (Sema4D) and B-type plexins demonstrate distinct expression patterns over critical time windows during the development of the murine neocortex. Here, analysis of mice genetically lacking plexin-B1 or plexin-B2 revealed the significance of Sema4D-plexin-B signaling in...

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Identifiers

PMID: 19948886
DOI: 10.1128/MCB.01458-09
PMCID: PMC2812242

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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.

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