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LRRK2 interactions with microtubules are independent of LRRK2-mediated Rab phosphorylation.

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Title: LRRK2 interactions with microtubules are independent of LRRK2-mediated Rab phosphorylation.
Authors: Malankhanova T; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Liu Z; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Xu E; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Bryant N; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Sung KW; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Li H; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., Strader S; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA., West AB; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA. andrew.west@duke.edu.
Source: EMBO reports [EMBO Rep] 2025 Jul; Vol. 26 (13), pp. 3445-3466. Date of Electronic Publication: 2025 May 27.
Publication Type: Journal Article
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 100963049 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-3178 (Electronic) Linking ISSN: 1469221X NLM ISO Abbreviation: EMBO Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: LRRK2 interactions with microtubules are independent of LRRK2-mediated Rab phosphorylation.
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  Data: <searchLink fieldCode="AU" term="%22Malankhanova+T%22">Malankhanova T</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Liu+Z%22">Liu Z</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Xu+E%22">Xu E</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Bryant+N%22">Bryant N</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Sung+KW%22">Sung KW</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Li+H%22">Li H</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22Strader+S%22">Strader S</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA.<br /><searchLink fieldCode="AU" term="%22West+AB%22">West AB</searchLink>; Duke Center for Neurodegeneration Research, Department of Pharmacology and Cancer Biology, Duke University, Durham, NC, USA. andrew.west@duke.edu.
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  Data: <searchLink fieldCode="JN" term="%22100963049%22">EMBO reports</searchLink> [EMBO Rep] 2025 Jul; Vol. 26 (13), pp. 3445-3466. <i>Date of Electronic Publication: </i>2025 May 27.
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        Value: 10.1038/s44319-025-00486-6
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      – TitleFull: LRRK2 interactions with microtubules are independent of LRRK2-mediated Rab phosphorylation.
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              Text: 2025 Jul
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