L1CAM and its cell-surface mutants: new mechanisms and effects relevant to the physiology and pathology of neural cells

The L1 syndrome, a genetic disease that affects 1/30 000 newborn males, is sustained by numerous missense mutations of L1 cell adhesion molecule (L1CAM), an adhesion surface protein active also in transmembrane signaling, essential for the development and function of neurons. To investigate the cell...

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Detalles Bibliográficos
Autores principales: Tagliavacca, Luigina, Colombo, Federico, Racchetti, Gabriella, Meldolesi, Jacopo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557714/
https://www.ncbi.nlm.nih.gov/pubmed/22973895
http://dx.doi.org/10.1111/jnc.12015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557714/
https://www.ncbi.nlm.nih.gov/pubmed/22973895
http://dx.doi.org/10.1111/jnc.12015

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