Results 31 to 40 of about 17,107 (226)

Kinesin-2 family in vertebrate ciliogenesis [PDF]

open access: yesProceedings of the National Academy of Sciences, 2012
The differentiation of cilia is mediated by kinesin-driven transport. As the function of kinesins in vertebrate ciliogenesis is poorly characterized, we decided to determine the role of kinesin-2 family motors—heterotrimeric kinesin-II and the homodimeric Kif17 kinesin—in zebrafish cilia.
Chengtian, Zhao   +4 more
openaire   +2 more sources

Tethering of an E3 ligase by PCM1 regulates the abundance of centrosomal KIAA0586/Talpid3 and promotes ciliogenesis

open access: yeseLife, 2016
To elucidate the role of centriolar satellites in ciliogenesis, we deleted the gene encoding the PCM1 protein, an integral component of satellites. PCM1 null human cells show marked defects in ciliogenesis, precipitated by the loss of specific proteins ...
Lei Wang   +4 more
doaj   +1 more source

The small GTPase Rab29 is a common regulator of immune synapse assembly and ciliogenesis [PDF]

open access: yes, 2015
Acknowledgements We wish to thank Jorge Galán, Gregory Pazour, Derek Toomre, Giuliano Callaini, Joel Rosenbaum, Alessandra Boletta and Francesco Blasi for generously providing reagents and for productive discussions, and Sonia Grassini for technical ...
A Batista   +51 more
core   +1 more source

Length-dependent disassembly maintains four different flagellar lengths in Giardia. [PDF]

open access: yes, 2019
With eight flagella of four different lengths, the parasitic protist Giardia is an ideal model to evaluate flagellar assembly and length regulation. To determine how four different flagellar lengths are maintained, we used live-cell quantitative imaging ...
Aurrecoechea   +69 more
core   +2 more sources

Ciliogenesis: Polarity Proteins on the Move [PDF]

open access: yesCurrent Biology, 2004
The formation and maintenance of cilia and flagella require a selective and directed transport along the axoneme, a characteristic central bundle of microtubules. Recent evidence suggests an interesting link between the generation of cilia and the protein complexes that establish apico-basal cell polarity.
Bossinger, Olaf, Bachmann, André
openaire   +2 more sources

Robust interaction of IFT70 with IFT52–IFT88 in the IFT-B complex is required for ciliogenesis

open access: yesBiology Open, 2018
In the intraflagellar transport (IFT) machinery, the IFT-B and IFT-A complexes mediate anterograde and retrograde ciliary protein trafficking, respectively.
Ryota Takei   +2 more
doaj   +1 more source

A role for Tctex-1 (DYNLT1) in controlling primary cilium length [PDF]

open access: yes, 2011
The microtubule motor complex cytoplasmic dynein is known to be involved in multiple processes including endomembrane organization and trafficking, mitosis, and microtubule organization.
MacCarthy-Morrogh, LJ   +3 more
core   +2 more sources

VDAC3 and Mps1 negatively regulate ciliogenesis [PDF]

open access: yesCell Cycle, 2013
Centrosomes serve to organize new centrioles in cycling cells, whereas in quiescent cells they assemble primary cilia. We have recently shown that the mitochondrial porin VDAC3 is also a centrosomal protein that is predominantly associated with the mother centriole and modulates centriole assembly by recruiting Mps1 to centrosomes.
Shubhra, Majumder, Harold A, Fisk
openaire   +2 more sources

Nonredundant roles of DIAPHs in primary ciliogenesis [PDF]

open access: yesJournal of Biological Chemistry, 2021
Primary cilia are hubs for several signaling pathways, and disruption in cilia function and formation leads to a range of diseases collectively known as ciliopathies. Both ciliogenesis and cilia maintenance depend on vesicle trafficking along a network of microtubules and actin filaments toward the basal body.
Oliva Palander   +4 more
openaire   +2 more sources

RPGR protein complex regulates proteasome activity and mediates store-operated calcium entry [PDF]

open access: yes, 2018
Ciliopathies are a group of genetically heterogeneous disorders, characterized by defects in cilia genesis or maintenance. Mutations in the RPGR gene and its interacting partners, RPGRIP1 and RPGRIP1L, cause ciliopathies, but the function of their ...
Aguirre   +68 more
core   +3 more sources

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