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The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complexThe tiny eukaryote Ostreococcus provides genomic insights into the paradox of plankton speciationThe intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assemblyCombined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseNovel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesDisruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromeCharacterization of mouse IFT complex BRadial spoke proteins of Chlamydomonas flagellaDNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary DyskinesiaIFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment.Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeletonGlobal genetic analysis in mice unveils central role for cilia in congenital heart diseaseA dynein light intermediate chain, D1bLIC, is required for retrograde intraflagellar transport.Functional analysis of an individual IFT protein: IFT46 is required for transport of outer dynein arms into flagella.The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiationArf4 is required for Mammalian development but dispensable for ciliary assemblyIFT25 links the signal-dependent movement of Hedgehog components to intraflagellar transportSpatial distribution of intraflagellar transport proteins in vertebrate photoreceptorsCiliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochleaDistinct functions for IFT140 and IFT20 in opsin transportPolycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney diseasePrimary cilia regulate proliferation of amplifying progenitors in adult hippocampus: implications for learning and memoryLocalization of transient receptor potential ion channels in primary and motile cilia of the female murine reproductive organsIFT20 is required for opsin trafficking and photoreceptor outer segment developmentA dynein light chain is essential for the retrograde particle movement of intraflagellar transport (IFT)PDGFRalphaalpha signaling is regulated through the primary cilium in fibroblastsProteomic analysis of a eukaryotic ciliumLoss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degenerationThe Chlamydomonas reinhardtii BBSome is an IFT cargo required for export of specific signaling proteins from flagella.Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella.Intraflagellar transport is required for polarized recycling of the TCR/CD3 complex to the immune synapse.Intraflagellar transport protein IFT20 is essential for male fertility and spermiogenesis in miceThe cytoplasmic tail of fibrocystin contains a ciliary targeting sequenceRor2 signaling regulates Golgi structure and transport through IFT20 for tumor invasivenessPrimary cilia regulate branching morphogenesis during mammary gland development.Differential light chain assembly influences outer arm dynein motor function.Intraflagellar transport and cilia-dependent diseases.Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease.Oda5p, a novel axonemal protein required for assembly of the outer dynein arm and an associated adenylate kinase.NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
@en
հետազոտող
@hy
name
Gregory J Pazour
@nl
Gregory J Pazour
@sl
Gregory J. Pazour
@en
Gregory J. Pazour
@es
type
label
Gregory J Pazour
@nl
Gregory J Pazour
@sl
Gregory J. Pazour
@en
Gregory J. Pazour
@es
prefLabel
Gregory J Pazour
@nl
Gregory J Pazour
@sl
Gregory J. Pazour
@en
Gregory J. Pazour
@es
P106
P1153
6603731355
P21
P31
P496
0000-0002-6285-8796