Webb19 sep. 2024 · Plectin is a giant cytoskeletal crosslinker and intermediate filament stabilizing protein. Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies.The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy … WebbAn in situ proximity ligation assay confirmed that FUS-plectin interactions take place in the cytoplasm of cells. Furthermore, plectin deficient cells showed an altered subcellular localization of FUS and a deregulated expression of mRNAs bound to FUS. Our results show that plectin is important for normal FUS localization and function.
Plectin mutation analysis and expression across several cancers.
Webb14 okt. 2008 · Description. A form of epidermolysis bullosa, a genodermatosis characterized by recurrent blistering, fragility of the skin and mucosal epithelia, and erosions caused by minor mechanical trauma. EBS5C is an autosomal recessive disorder characterized by severe skin blistering at birth and congenital pyloric atresia. Death … Webb30 apr. 1996 · Plectin, a 500-kDa intermediate filament binding protein, has been proposed to provide mechanical strength to cells and tissues by acting as a cross-linking element … headboard how to
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Webb15 sep. 2013 · Plectin is a versatile cytolinker of the plakin family conferring cell resilience to mechanical stress in stratified epithelia and muscles. It acts as a critical organizer of the cytoskeletal system by tethering various intermediate filament (IF) networks through its C-terminal IF-binding domain (IF … WebbPlectin Plectin, also referred to as IFAP 300 or HD1, is a 500-kDa plakin family member. It is particularly important for hemidesmosome function in epithelial tissues, and as a … Webb12 nov. 2024 · 经蛋白组学分析,靶向肽PTP是通过与胰腺癌发生时误定位在细胞膜表面上的plectin-1特异性结合实现靶向作用的。 然而,胰腺癌在遗传上是非常复杂的,肿瘤的质量是由患者的63个基因改变和12个核心信号通路的异常引起的,在不同癌症患者的肿瘤生物标志物表达中存在异质性。 head board image code