Phenotypic analysis of Myo10 knockout (Myo10) mice lacking full-length (motorized) but not brain-specific headless myosin X

scientific article published in Scientific Reports

Phenotypic analysis of Myo10 knockout (Myo10) mice lacking full-length (motorized) but not brain-specific headless myosin X is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41598-018-37160-Y
P932PMC publication ID6345916
P698PubMed publication ID30679680

P50authorLaura MacheskyQ21264247
Richard StangeQ90096014
Hyun-Woo JeongQ91211630
Ralf H AdamsQ42126165
Cornelius FaberQ43120057
P2093author name stringMartin Bähler
Peter J Hanley
Boris V Skryabin
Sandra Bachg
Nina Nagelmann
Anne C Bachg
Markus Horsthemke
Emma Woodham
Tim Klasen
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Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new playersQ38883845
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A microtubule-binding myosin required for nuclear anchoring and spindle assembly.Q52560093
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Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation.Q47139973
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Multiple roles of filopodial dynamics in particle capture and phagocytosis and phenotypes of Cdc42 and Myo10 deletionQ48623666
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P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)597
P577publication date2019-01-24
P1433published inScientific ReportsQ2261792
P1476titlePhenotypic analysis of Myo10 knockout (Myo10tm2/tm2) mice lacking full-length (motorized) but not brain-specific headless myosin X
P478volume9

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Q94465899Tunneling Nanotubes and the Eye: Intercellular Communication and Implications for Ocular Health and Diseasecites workP2860

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