Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model
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ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transportPrimary cilia in the developing and mature brainKIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeCiliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse modelmTORC1 signaling and primary cilia are required for brain ventricle morphogenesisHippocampal and cortical primary cilia are required for aversive memory in mice.Primary cilia signaling mediates intraocular pressure sensation.Regulation of fibroblast lipid storage and myofibroblast phenotypes during alveolar septation in miceThe BBSome Controls Energy Homeostasis by Mediating the Transport of the Leptin Receptor to the Plasma Membrane.tPA Deficiency in Mice Leads to Rearrangement in the Cerebrovascular Tree and Cerebroventricular Malformations.BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking.Diffusion tensor imaging detects early brain microstructure changes before and after ventriculoperitoneal shunt in children with high intracranial pressure hydrocephalus.CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.Neural stem cells: are they the hope of a better life for patients with fetal-onset hydrocephalus?Primary cilia in neurodevelopmental disorders.Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.VEGF: a potential target for hydrocephalus.Mutant IDH1 Disrupts the Mouse Subventricular Zone and Alters Brain Tumor Progression.Gene Therapeutic Reversal of Peripheral Olfactory Impairment in Bardet-Biedl Syndrome.Motile and non-motile cilia in human pathology: from function to phenotypes.Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease.Role of hemoglobin and iron in hydrocephalus after neonatal intraventricular hemorrhage.Genetic and Stress-Induced Loss of NG2 Glia Triggers Emergence of Depressive-like Behaviors through Reduced Secretion of FGF2.Dusp16 Deficiency Causes Congenital Obstructive Hydrocephalus and Brain Overgrowth by Expansion of the Neural Progenitor Pool.Primary cilium regulates CaV1.2 expression through Wnt signaling.Oligodendroglia-lineage cells in brain plasticity, homeostasis and psychiatric disorders.Cell Junction Pathology of Neural Stem Cells Is Associated With Ventricular Zone Disruption, Hydrocephalus, and Abnormal Neurogenesis.The APC/C cofactor Cdh1 prevents replicative stress and p53-dependent cell death in neural progenitors.[Primary cilia control different steps of brain development].Group II metabotropic glutamate receptor interactions with NHERF scaffold proteins: Implications for receptor localization in brain.Diverse application of MRI for mouse phenotyping.
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P2860
Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model
description
2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2012
@ast
im Dezember 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2012/12/01)
@sk
vědecký článek publikovaný v roce 2012
@cs
wetenschappelijk artikel (gepubliceerd op 2012/12/01)
@nl
наукова стаття, опублікована в грудні 2012
@uk
مقالة علمية (نشرت في ديسمبر 2012)
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name
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@ast
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@en
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
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type
label
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@ast
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@en
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@nl
prefLabel
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@ast
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@en
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@nl
P2093
P2860
P50
P921
P3181
P356
P1433
P1476
Abnormal development of NG2+PD ...... us in a ciliopathy mouse model
@en
P2093
Calvin S. Carter
Charles C. Searby
Daniel R. Thedens
Darryl Y. Nishimura
Kevin Bugge
Martin D. Cassell
Qihong Zhang
Ruth E. Swiderski
Thomas O. Moninger
Timothy W. Vogel
P2860
P2888
P304
P3181
P356
10.1038/NM.2996
P407
P577
2012-12-01T00:00:00Z
P5875
P6179
1053588843