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Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth

Loss of Foxc1 is associated with Dandy-Walker malformation, the most common human cerebellar malformation characterized by cerebellar hypoplasia and an enlarged posterior fossa and fourth ventricle. Although expressed in the mouse posterior fossa mesenchyme, loss of Foxc1 non-autonomously induces a...

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Enregistré dans:
Détails bibliographiques
Publié dans:eLife
Auteurs principaux: Haldipur, Parthiv, Gillies, Gwendolyn S, Janson, Olivia K, Chizhikov, Victor V, Mithal, Divakar S, Miller, Richard J, Millen, Kathleen J
Format: Artigo
Langue:Inglês
Publié: eLife Sciences Publications, Ltd 2014
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4281880/
https://ncbi.nlm.nih.gov/pubmed/25513817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.03962
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