IKAP/hELP1 downregulation in neuroblastoma cells causes enhanced cell adhesion mediated by contactin overexpression

A splicing mutation in the IKBKAP gene encoding the IKAP/hELP1 (IKAP) protein was found to be the major cause of Familial Dysautonomia (FD). This mutation affects both the normal development and survival of sensory and sympathetic neurons of the peripheral nervous system (PNS). To understand the FD...

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Bibliografiset tiedot
Päätekijät: Cohen-Kupiec, Rachel, Weinstein, Shiri, Kantor, Gal, Peer, Dan, Weil, Miguel
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Landes Bioscience 2010
Aiheet:
Research Paper
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3011265/
https://ncbi.nlm.nih.gov/pubmed/20671422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/cam.4.4.12923
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