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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

Related topics

Related topics

13 relations
Angiogenic ProcessCell MovementCytokinesisCytoskeletal Gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Direct Interaction Between CD163 N-Terminal Domain and MYH9 C-Terminal Domain Contributes to Porcine Reproductive and Respiratory Syndrome Virus Internalization by Permissive Cells
Porcine reproductive and respiratory syndrome virus (PRRSV) has a highly restricted tropism for cells of the monocyte-macrophage… 
2016
2016
Major vault protein regulates cell growth/survival signaling through oxidative modifications.
2015
2015
In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress
African Americans have a disproportionate risk for developing nephropathy. This disparity has been attributed to coding variants… 
2014
2014
The collagen receptor DDR1 co-localizes with the non-muscle myosin IIA in mice inner ear and contributes to the cytoarchitecture and stability of motile cells
Discoidin domain receptor 1 (DDR1) is a tyrosine kinase receptor activated by native collagen. DDRs regulate cell adhesion… 
2013
2013
Establishment of Mouse Model of MYH9 Disorders: Heterozygous R702C Mutation Provokes Macrothrombocytopenia with Leukocyte Inclusion Bodies, Renal Glomerulosclerosis and Hearing Disability
Nonmuscle myosin heavy chain IIA (NMMHCIIA) encoded by MYH9 is associated with autosomal dominantly inherited diseases called… 
2011
2011
Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells
Summary MYH9-related disease (MYH9-RD) is an autosomal-dominant thrombocytopenia caused by mutations in the gene for the heavy… 
2011
2011
Distinct functional effects for dynamin 3 during megakaryocytopoiesis.
Dynamin 3 (DNM3) is a member of a family of motor proteins that participate in a number of membrane rearrangements such as… 
2006
2006
Signaling via the Angiotensin-Converting Enzyme Results in the Phosphorylation of the Nonmuscle Myosin Heavy Chain IIA
The phosphorylation of the short C-terminal cytoplasmic domain of the somatic angiotensin-converting enzyme (ACE) is involved in… 
Highly Cited
2004
Highly Cited
2004
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO…
Highly Cited
2003
Highly Cited
2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.
May-Hegglin anomaly (MHA), Fechtner syndrome (FTNS), Sebastian syndrome (SBS), and Epstein syndrome (EPS) are a group of rare… 
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