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Arl13b

  • RESEARCH ARTICLE
    EFA6A, an exchange factor for Arf6, regulates early steps in ciliogenesis
    Mariagrazia Partisani, Carole L. Baron, Rania Ghossoub, Racha Fayad, Sophie Pagnotta, Sophie Abélanet, Eric Macia, Frédéric Brau, Sandra Lacas-Gervais, Alexandre Benmerah, Frédéric Luton, Michel Franco
    Journal of Cell Science 2021 134: jcs249565 doi: 10.1242/jcs.249565 Published 22 January 2021

    Summary: A novel fusion machinery comprising EFA6A, Arf6 and Arl13B controls the coordinated fusion of ciliary vesicles docked at the distal appendages of the mother centriole.

  • RESEARCH ARTICLE
    Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration
    Jesús Muñoz-Estrada, Russell J. Ferland
    Journal of Cell Science 2019 132: jcs230680 doi: 10.1242/jcs.230680 Published 4 September 2019

    Summary: The Joubert syndrome-causing protein, Ahi1, acts as a gatekeeper in regulating primary cilia protein composition and length. Ahi1 also regulates Arl13b stability, Shh signaling and cell migration.

  • RESEARCH ARTICLE
    The unusual flagellar-targeting mechanism and functions of the trypanosome ortholog of the ciliary GTPase Arl13b
    Yiliu Zhang, Yameng Huang, Amrita Srivathsan, Teck Kwang Lim, Qingsong Lin, Cynthia Y. He
    Journal of Cell Science 2018 131: jcs219071 doi: 10.1242/jcs.219071 Published 5 September 2018

    Highlighted Article: All roads lead to cilia – how the essential flagellar enrichment of Arl13 is achieved in trypanosome cells using a fundamentally different strategy compared with that of animal cells.

  • RESEARCH ARTICLE
    The Joubert syndrome protein ARL13B binds tubulin to maintain uniform distribution of proteins along the ciliary membrane
    Ekaterina Revenkova, Qing Liu, G. Luca Gusella, Carlo Iomini
    Journal of Cell Science 2018 131: jcs212324 doi: 10.1242/jcs.212324 Published 4 May 2018

    Summary: The Joubert syndrome protein ARL13B binds tubulin to maintain uniform distribution of proteins along the ciliary membrane.

  • RESEARCH ARTICLE
    Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E
    Shohei Nozaki, Yohei Katoh, Masaya Terada, Saki Michisaka, Teruki Funabashi, Senye Takahashi, Kenji Kontani, Kazuhisa Nakayama
    Journal of Cell Science 2017 130: 563-576; doi: 10.1242/jcs.197004

    Summary: Mutations in the genes encoding ARL13B and INPP5E are causative for Joubert syndrome. ARL13B interacts with INPP5E and regulates IFT-A-mediated retrograde protein trafficking within cilia.

  • RESEARCH ARTICLE
    Arl13b and the non-muscle myosin heavy chain IIA are required for circular dorsal ruffle formation and cell migration
    Cristina Casalou, Cecília Seixas, Ana Portelinha, Petra Pintado, Mafalda Barros, José S. Ramalho, Susana S. Lopes, Duarte C. Barral
    Journal of Cell Science 2014 127: 2709-2722; doi: 10.1242/jcs.143446

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