Retrograde intraflagellar transport by cytoplasmic dynein-2 is required for outer segment extension in vertebrate photoreceptors but not arrestin translocation.
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The role of primary cilia in the development and disease of the retinaMolecular complexes that direct rhodopsin transport to primary ciliaDYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsRecombinant human cytoplasmic dynein heavy chain 1 and 2: observation of dynein-2 motor activity in vitroMutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophyThe intraflagellar transport dynein complex of trypanosomes is made of a heterodimer of dynein heavy chains and of light and intermediate chains of distinct functions.Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafishIn vivo cell biology in zebrafish - providing insights into vertebrate development and disease.Analysis of a zebrafish dync1h1 mutant reveals multiple functions for cytoplasmic dynein 1 during retinal photoreceptor development.The intraflagellar transport protein ift80 is essential for photoreceptor survival in a zebrafish model of jeune asphyxiating thoracic dystrophyThe Par-PrkC polarity complex is required for cilia growth in zebrafish photoreceptorsRetrograde intraciliary trafficking of opsin during the maintenance of cone-shaped photoreceptor outer segments of Xenopus laevis.A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies.Toward a better understanding of human eye disease insights from the zebrafish, Danio rerio.Dynein and intraflagellar transport.Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet-Biedl syndrome.Protein sorting, targeting and trafficking in photoreceptor cellsArl13b Interacts With Vangl2 to Regulate Cilia and Photoreceptor Outer Segment Length in Zebrafish.Photoreceptor outer segment as a sink for membrane proteins: hypothesis and implications in retinal ciliopathies.The Golgi matrix protein giantin is required for normal cilia function in zebrafish.Mutations in the Dynein1 Complex are Permissible for Basal Body Migration in Photoreceptors but Alter Rab6 LocalizationLoss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport.Operation profile of zebrafish guanylate cyclase-activating protein 3.The Arf GEF GBF1 and Arf4 synergize with the sensory receptor cargo, rhodopsin, to regulate ciliary membrane trafficking.Dynein motors: How AAA+ ring opening and closing coordinates microtubule binding and linker movement.
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Retrograde intraflagellar transport by cytoplasmic dynein-2 is required for outer segment extension in vertebrate photoreceptors but not arrestin translocation.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 27 May 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@en
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@nl
type
label
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@en
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@nl
prefLabel
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@en
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@nl
P2093
P2860
P356
P1476
Retrograde intraflagellar tran ...... ut not arrestin translocation.
@en
P2093
Brian D Perkins
Bryan L Krock
Ishara Mills-Henry
P2860
P304
P356
10.1167/IOVS.09-3828
P407
P577
2009-05-27T00:00:00Z