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DYX1C1 is required for axonemal dynein assembly and ciliary motilityPredicted protein interactions of IFITMs which inhibit Zika virus infectionLysophosphatidylinositol-acyltransferase-1 (LPIAT1) is required to maintain physiological levels of PtdIns and PtdInsP(2) in the mouseAbnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse modelAdenine nucleotide metabolism and a role for AMP in modulating flagellar waveforms in mouse spermThe Tribbles 2 (TRB2) pseudokinase binds to ATP and autophosphorylates in a metal-independent mannerRestoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vector.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 Spef2Exploring the elephant: histopathology in high-throughput phenotyping of mutant mice.High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.Computer-assisted image analysis of human cilia and Chlamydomonas flagella reveals both similarities and differences in axoneme structure.Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections.Control of cortex development by ULK4, a rare risk gene for mental disorders including schizophreniaDeciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry.Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.What have we learned from murine models of otitis media?Mammalian O-mannosylation pathway: glycan structures, enzymes, and protein substrates.Nucleoside diphosphate kinases (NDPKs) in animal development.Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.Microtubule Motors Drive Hedgehog Signaling in Primary Cilia.Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration.General and specific promotions of flagellar assembly by a flagellar nucleoside diphosphate kinase.De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.Host genetic background influences diverse neurological responses to viral infection in mice.POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disability.Understanding the aetiology and resolution of chronic otitis media from animal and human studies.Multiple roles of Ulk4 in neurogenesis and brain function.A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?Dentin Dysplasia in Notum Knockout Mice.Human and mouse microarrays-guided expression analysis of membrane protein trafficking-related genes in MDCK cells, a canine epithelial model for apical and basolateral differential protein targeting.The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
P2860
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P248
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P2860
description
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
artikull shkencor
@sq
artículu científicu espublizáu en 2012
@ast
im Jahr 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2012
@uk
مقالة علمية (نشرت عام 2012)
@ar
name
Congenital hydrocephalus in genetically engineered mice
@ast
Congenital hydrocephalus in genetically engineered mice
@en
Congenital hydrocephalus in genetically engineered mice
@nl
type
label
Congenital hydrocephalus in genetically engineered mice
@ast
Congenital hydrocephalus in genetically engineered mice
@en
Congenital hydrocephalus in genetically engineered mice
@nl
prefLabel
Congenital hydrocephalus in genetically engineered mice
@ast
Congenital hydrocephalus in genetically engineered mice
@en
Congenital hydrocephalus in genetically engineered mice
@nl
P2093
P2860
P921
P3181
P356
P1433
P1476
Congenital hydrocephalus in genetically engineered mice
@en
P2093
A. T. Sands
B. J. Payne
B. P. Zambrowicz
G. M. Hansen
R. W. Read
P2860
P304
P3181
P356
10.1177/0300985811415708
P50
P577
2012-01-01T00:00:00Z