MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus
Author:
Funder
RGC
HKU
UGC
NSFC
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/132782/files/pdf
Reference66 articles.
1. Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus
2. Theories of cerebrospinal fluid dynamics and hydrocephalus: historical trend
3. Congenital Hydrocephalus in Genetically Engineered Mice
4. Loss of Dishevelleds Disrupts Planar Polarity in Ependymal Motile Cilia and Results in Hydrocephalus
5. SNX27 Deletion Causes Hydrocephalus by Impairing Ependymal Cell Differentiation and Ciliogenesis
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