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Absence of Platelet Phenotype in Mice Lacking the Motor Protein Myosin Va

Overview of attention for article published in PLOS ONE, January 2013
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Title
Absence of Platelet Phenotype in Mice Lacking the Motor Protein Myosin Va
Published in
PLOS ONE, January 2013
DOI 10.1371/journal.pone.0053239
Pubmed ID
Authors

Matthew T. Harper, Marion T. J. van den Bosch, Ingeborg Hers, Alastair W. Poole

Abstract

The motor protein myosin Va plays an important role in the trafficking of intracellular vesicles. Mutation of the Myo5a gene causes Griscelli syndrome type 1 in humans and the dilute phenotype in mice, which are both characterised by pigment dilution and neurological defects as a result of impaired vesicle transport in melanocytes and neuroendocrine cells. The role of myosin Va in platelets is currently unknown. Rab27 has been shown to be associated with myosin Va cargo vesicles and is known to be important in platelet dense granule biogenesis and secretion, a crucial event in thrombus formation. Therefore, we hypothesised that myosin Va may regulate granule secretion or formation in platelets.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 7%
Unknown 14 93%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 33%
Student > Bachelor 2 13%
Researcher 2 13%
Student > Master 1 7%
Student > Doctoral Student 1 7%
Other 0 0%
Unknown 4 27%
Readers by discipline Count As %
Agricultural and Biological Sciences 5 33%
Pharmacology, Toxicology and Pharmaceutical Science 1 7%
Biochemistry, Genetics and Molecular Biology 1 7%
Physics and Astronomy 1 7%
Medicine and Dentistry 1 7%
Other 2 13%
Unknown 4 27%