Published Application/Species/Sample/Dilution | Reference |
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- western blot knockout validation; mouse; loading ...; fig 1c
| Heimsath E, Yim Y, Mustapha M, Hammer J, Cheney R. Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. Sci Rep. 2017;7:17354 pubmed publisher
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| Balta E, Hardt R, Liang J, Kirchgessner H, Orlik C, Jahraus B, et al. Spatial oxidation of L-plastin downmodulates actin-based functions of tumor cells. Nat Commun. 2019;10:4073 pubmed publisher
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| So C, Seres K, Steyer A, Mönnich E, Clift D, Pejkovska A, et al. A liquid-like spindle domain promotes acentrosomal spindle assembly in mammalian oocytes. Science. 2019;364: pubmed publisher
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| Sun Y, Yang Y, Keller K. Myosin-X Silencing in the Trabecular Meshwork Suggests a Role for Tunneling Nanotubes in Outflow Regulation. Invest Ophthalmol Vis Sci. 2019;60:843-851 pubmed publisher
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| Bachg A, Horsthemke M, Skryabin B, Klasen T, Nagelmann N, Faber C, et al. Phenotypic analysis of Myo10 knockout (Myo10tm2/tm2) mice lacking full-length (motorized) but not brain-specific headless myosin X. Sci Rep. 2019;9:597 pubmed publisher
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| Wang B, Pan J, Yu H, Xiong L, Zhao K, Xiong S, et al. Lack of Myosin X Enhances Osteoclastogenesis and Increases Cell Surface Unc5b in Osteoclast-Lineage Cells. J Bone Miner Res. 2019;34:939-954 pubmed publisher
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| Uhl J, Gujarathi S, Waheed A, Gordon A, Freed E, Gousset K. Myosin-X is essential to the intercellular spread of HIV-1 Nef through tunneling nanotubes. J Cell Commun Signal. 2019;13:209-224 pubmed publisher
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| Robinson McCarthy L, McCarthy K, Raaben M, Piccinotti S, Nieuwenhuis J, Stubbs S, et al. Reconstruction of the cell entry pathway of an extinct virus. PLoS Pathog. 2018;14:e1007123 pubmed publisher
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| Tokuo H, Bhawan J, Coluccio L. Myosin X is required for efficient melanoblast migration and melanoma initiation and metastasis. Sci Rep. 2018;8:10449 pubmed publisher
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| Santhana Kumar K, Neve A, Guerreiro Stucklin A, Kuzan Fischer C, Rushing E, Taylor M, et al. TGF-? Determines the Pro-migratory Potential of bFGF Signaling in Medulloblastoma. Cell Rep. 2018;23:3798-3812.e8 pubmed publisher
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| Wang X, Li J, Xu X, Zheng J, Li Q. miR-129 inhibits tumor growth and potentiates chemosensitivity of neuroblastoma by targeting MYO10. Biomed Pharmacother. 2018;103:1312-1318 pubmed publisher
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| El Hayek S, Yang Q, Abbassi L, FitzHarris G, Clarke H. Mammalian Oocytes Locally Remodel Follicular Architecture to Provide the Foundation for Germline-Soma Communication. Curr Biol. 2018;28:1124-1131.e3 pubmed publisher
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| Kroon J, Schaefer A, van Rijssel J, Hoogenboezem M, van Alphen F, Hordijk P, et al. Inflammation-Sensitive Myosin-X Functionally Supports Leukocyte Extravasation by Cdc42-Mediated ICAM-1-Rich Endothelial Filopodia Formation. J Immunol. 2018;200:1790-1801 pubmed publisher
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| Lehtimäki J, Fenix A, Kotila T, Balistreri G, Paavolainen L, Varjosalo M, et al. UNC-45a promotes myosin folding and stress fiber assembly. J Cell Biol. 2017;216:4053-4072 pubmed publisher
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| Tasca A, Astleford K, Lederman A, Jensen E, Lee B, Gopalakrishnan R, et al. Regulation of Osteoclast Differentiation by Myosin X. Sci Rep. 2017;7:7603 pubmed publisher
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| Buccitelli C, Salgueiro L, Rowald K, Sotillo R, Mardin B, Korbel J. Pan-cancer analysis distinguishes transcriptional changes of aneuploidy from proliferation. Genome Res. 2017;27:501-511 pubmed publisher
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| Makowska K, Hughes R, White K, Wells C, Peckham M. Specific Myosins Control Actin Organization, Cell Morphology, and Migration in Prostate Cancer Cells. Cell Rep. 2015;13:2118-25 pubmed publisher
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| Caltagarone J, Ma S, Sorkin A. Dopamine transporter is enriched in filopodia and induces filopodia formation. Mol Cell Neurosci. 2015;68:120-30 pubmed publisher
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| Snyder J, Rochelle L, Marion S, Lyerly H, Barak L, Caron M. Lgr4 and Lgr5 drive the formation of long actin-rich cytoneme-like membrane protrusions. J Cell Sci. 2015;128:1230-40 pubmed publisher
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