نتایج جستجو برای: myh9 gene

تعداد نتایج: 1141526  

Journal: :Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2010
Karina Althaus Andreas Greinacher

MYH-9 related platelet disorders belong to the group of inherited giant platelet disorders. The MYH-9 gene encodes the non-muscular myosin heavy chain IIA (NMMHCIIA), a cytoskeletal contractile protein. Several mutations in the MYH-9 gene lead to macrothrombocytopenia, and cytoplasmic inclusion bodies within leukocytes, while the number of megakaryocytes in the bone marrow is normal. Four overl...

Journal: :The Biochemical journal 2011
Inju Park Cecil Han Sora Jin Boyeon Lee Heejin Choi Jun Tae Kwon Dongwook Kim Jihye Kim Ekaterina Lifirsu Woo Jin Park Zee Yong Park Do Han Kim Chunghee Cho

Myosin II is an actin-binding protein composed of MHC (myosin heavy chain) IIs, RLCs (regulatory light chains) and ELCs (essential light chains). Myosin II expressed in non-muscle tissues plays a central role in cell adhesion, migration and division. The regulation of myosin II activity is known to involve the phosphorylation of RLCs, which increases the Mg2+-ATPase activity of MHC IIs. However...

2017

MYH9 gene mutation results in a spectrum of diseases, such as May -Heglin anomaly and Epstein syndrome, depending upon the type of isoforms involved [1]. This mutation is inherited as an autosomal dominant entity and the gene encodes for non-muscle myosin heavy chain IIA (NMMHC-IIA) which is a part of myosin superfamily. The exact incidence of this disease in different populations is yet to be ...

2013
Lívia M. Paranaíba Sibele N. de Aquino Andreia Bufalino Hercílio Martelli-Júnior Edgard Graner Luciano A. Brito Maria R. Passos-Bueno Ricardo-D. Coletta Mário S. Swerts

BACKGROUND AND OBJECTIVE Nonsyndromic cleft lip and/or palate (NSCL/P) is a complex disease associated with both genetic and environmental factors. One strategy for identifying of possible NSCL/P genetic causes is to evaluate polymorphic variants in genes involved in the craniofacial development. DESIGN We carried out a case-control analysis of 13 single nucleotide polymorphisms in 9 genes re...

2014
Nicholette D. Palmer Maggie C. Y. Ng Pamela J. Hicks Poorva Mudgal Carl D. Langefeld Barry I. Freedman Donald W. Bowden

Type 2 diabetes (T2D)-associated end-stage kidney disease (ESKD) is a complex disorder resulting from the combined influence of genetic and environmental factors. This study contains a comprehensive genetic analysis of putative nephropathy loci in 965 African American (AA) cases with T2D-ESKD and 1029 AA population-based controls extending prior findings. Analysis was based on 4,341 directly ge...

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