Myosin-9

Known as: Cellular Myosin Heavy Chain, Type A, Myosin Heavy Chain, Non-Muscle IIa, Non-Muscle Myosin Heavy Polypeptide 9 
Myosin-9 (1960 aa, ~227 kDa) is encoded by the human MYH9 gene. This protein is involved in both cell shape and cytokinesis.
National Institutes of Health

Papers overview

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2011
2011
Mammalian hibernation is a complex phenotype involving metabolic rate reduction, bradycardia, profound hypothermia, and a… (More)
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2011
2011
Myosin II is an actin-binding protein composed of MHC (myosin heavy chain) IIs, RLCs (regulatory light chains) and ELCs… (More)
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2010
2010
MYH9-related disease ( MYH9-RD) is an autosomal dominant thrombocytopenia with giant platelets variably associated with young… (More)
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Highly Cited
2010
Highly Cited
2010
MYH9 has been proposed as a major genetic risk locus for a spectrum of nondiabetic end stage kidney disease (ESKD). We use… (More)
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Highly Cited
2009
Highly Cited
2009
BACKGROUND Although MYH9 is strongly associated with biopsy-proven idiopathic and HIV-associated focal segmental… (More)
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Highly Cited
2008
Highly Cited
2008
Precise spatial and temporal regulation of cell adhesion and de-adhesion is critical for dynamic lymphocyte migration. Although a… (More)
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2007
2007
OBJECTIVE MYH9 disorders are characterised by giant platelets, thrombocytopenia, and Döhle body-like cytoplasmic granulocyte… (More)
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Highly Cited
2006
Highly Cited
2006
Nucleolin, originally described as a nuclear protein, was recently found to be expressed on the surface of endothelial cells… (More)
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Highly Cited
2003
Highly Cited
2003
The autosomal dominant macrothrombocytopenia with leukocyte inclusions, May-Hegglin anomaly, Sebastian syndrome, and Fechtner… (More)
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Highly Cited
2000
Highly Cited
2000
The autosomal dominant, giant-platelet disorders, May-Hegglin anomaly (MHA; MIM 155100), Fechtner syndrome (FTNS; MIM 153640) and… (More)
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