The ubiquitin E3 ligase NOSIP modulates protein phosphatase 2A activity in craniofacial development.

Holoprosencephaly is a common developmental disorder in humans characterised by incomplete brain hemisphere separation and midface anomalies. The etiology of holoprosencephaly is heterogeneous with environmental and genetic causes, but for a majority of holoprosencephaly cases the genes associated w...

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Bibliographic Details
Main Authors: Meike Hoffmeister, Carola Prelle, Philipp Küchler, Igor Kovacevic, Markus Moser, Werner Müller-Esterl, Stefanie Oess
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4278855?pdf=render