about
A complex of BBS1 and NPHP7 is required for cilia motility in zebrafishThe microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis.NEK1 mutations cause short-rib polydactyly syndrome type majewskiDisruption of CEP290 microtubule/membrane-binding domains causes retinal degenerationAxonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarificationCep164 mediates vesicular docking to the mother centriole during early steps of ciliogenesisThe axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertilityDYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsReduction of meckelin leads to general loss of cilia, ciliary microtubule misalignment and distorted cell surface organization.Juvenile nephronophthisis and dysthyroidism: a rare associationThe Golgi and the centrosome: building a functional partnership.Methods for visual mining of genomic and proteomic data atlasesThe ciliary protein Ftm is required for ventricular wall and septal development.Macular dystrophy in Heimler syndrome.Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans.A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4.Various facets of vertebrate cilia: motility, signaling, and role in adult neurogenesis.IQCB1 and PDE6B mutations cause similar early onset retinal degenerations in two closely related terrier dog breedsNormal mammary development and function in mice with Ift88 deleted in MMTV- and K14-Cre expressing cellsThe primary cilium in different tissues-lessons from patients and animal models.Hedgehog signaling in the liver.RPGR: role in the photoreceptor cilium, human retinal disease, and gene therapy.Sperm flagella: comparative and phylogenetic perspectives of protein components.Cilia, adenomatous polyposis coli and associated diseases.The dynamic cytoskeleton of the developing male germ cell.Ciliary disorder of the skeleton.Hair curvature: a natural dialectic and review.Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.The pathogenesis of the clinical features of oral-facial-digital syndrome type I.Intravitreal Injection of Splice-switching Oligonucleotides to Manipulate Splicing in Retinal Cells.Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis.Alcohol-induced ciliary dysfunction targets the outer dynein arm.Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis.Lack of primary cilia primes shear-induced endothelial-to-mesenchymal transition.Pancreatic cyst development: insights from von Hippel-Lindau disease.Comparative study of the primary cilia in thyrocytes of adult mammals.Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration.Sensing the cilium, digital capture of ciliary data for comparative genomics investigations.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականին հրատարակուած գիտական յօդուած
@hyw
2009 թվականին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
The dynamic cilium in human diseases
@ast
The dynamic cilium in human diseases
@en
The dynamic cilium in human diseases
@en-gb
The dynamic cilium in human diseases
@nl
type
label
The dynamic cilium in human diseases
@ast
The dynamic cilium in human diseases
@en
The dynamic cilium in human diseases
@en-gb
The dynamic cilium in human diseases
@nl
prefLabel
The dynamic cilium in human diseases
@ast
The dynamic cilium in human diseases
@en
The dynamic cilium in human diseases
@en-gb
The dynamic cilium in human diseases
@nl
P2860
P356
P1433
P1476
The dynamic cilium in human diseases
@en
P2093
Anna D'Angelo
P2860
P2888
P356
10.1186/1755-8417-2-3
P407
P577
2009-01-01T00:00:00Z
P5875
P6179
1039522645