Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.
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Primary cilia in the developing and mature brainCFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in miceNEK1 variants confer susceptibility to amyotrophic lateral sclerosisThe impact of spinal cord nerve roots and denticulate ligaments on cerebrospinal fluid dynamics in the cervical spineCFAP157 is a murine downstream effector of FOXJ1 that is specifically required for flagellum morphogenesis and sperm motility.Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vector.NHERF1/EBP50 is an organizer of polarity structures and a diagnostic marker in ependymomaNeural Tissue Motion Impacts Cerebrospinal Fluid Dynamics at the Cervical Medullary Junction: A Patient-Specific Moving-Boundary Computational Model.MR assessment of pediatric hydrocephalus: a road map.Loss of Mpdz impairs ependymal cell integrity leading to perinatal-onset hydrocephalus in mice.Loss of Dishevelleds disrupts planar polarity in ependymal motile cilia and results in hydrocephalus.Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cellsMechanosensory Genes Pkd1 and Pkd2 Contribute to the Planar Polarization of Brain Ventricular Epithelium.Cerebrospinal fluid biomarkers of infantile congenital hydrocephalusMutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.Enhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2.Flow induced by ependymal cilia dominates near-wall cerebrospinal fluid dynamics in the lateral ventricles.Pathogenic implications of cerebrospinal fluid barrier pathology in neuromyelitis optica.Primary cilia in neurodevelopmental disorders.Structure and function of the ependymal barrier and diseases associated with ependyma disruption.Planar Organization of Multiciliated Ependymal (E1) Cells in the Brain Ventricular Epithelium.Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.PTPRQ as a potential biomarker for idiopathic normal pressure hydrocephalusA mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice.Primary cilia proteins: ciliary and extraciliary sites and functions.Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.SrGAP3 knockout mice display enlarged lateral ventricles and specific cilia disturbances of ependymal cells in the third ventricle.Clinical phenotype and current diagnostic criteria for primary ciliary dyskinesia.Clinical analysis of patients with primary ciliary dyskinesia in mainland China.The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in miceStrain-specific differences in brain gene expression in a hydrocephalic mouse model with motile cilia dysfunction
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P2860
Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Riding the wave of ependymal c ...... in primary ciliary dyskinesia.
@en
type
label
Riding the wave of ependymal c ...... in primary ciliary dyskinesia.
@en
prefLabel
Riding the wave of ependymal c ...... in primary ciliary dyskinesia.
@en
P2860
P356
P1476
Riding the wave of ependymal c ...... in primary ciliary dyskinesia.
@en
P2093
P2860
P304
P356
10.1002/JNR.23238
P577
2013-05-17T00:00:00Z