Cargando…
B-Cell-Specific Myd88 L252P Expression Causes a Premalignant Gammopathy Resembling IgM MGUS
A highly recurrent somatic L265P mutation in the TIR domain of the signaling adapter MYD88 constitutively activates NF-κB. It occurs in nearly all human patients with Waldenström’s macroglobulinemia (WM), a B cell malignancy caused by IgM-expressing cells. Here, we introduced an inducible leucine to...
Autores principales: | Schmidt, Kristin, Sack, Ulrike, Graf, Robin, Winkler, Wiebke, Popp, Oliver, Mertins, Philipp, Sommermann, Thomas, Kocks, Christine, Rajewsky, Klaus |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747680/ https://www.ncbi.nlm.nih.gov/pubmed/33343574 http://dx.doi.org/10.3389/fimmu.2020.602868 |
Ejemplares similares
-
MYD88 Mutations: Transforming the Landscape of IgM Monoclonal Gammopathies
por: Alcoceba, Miguel, et al.
Publicado: (2022) -
Determination of MYD88(L265P) mutation fraction in IgM monoclonal gammopathies
por: Bagratuni, Tina, et al.
Publicado: (2022) -
Detection of MYD88 and CXCR4 mutations in cell-free DNA of patients with IgM monoclonal gammopathies
por: Bagratuni, Tina, et al.
Publicado: (2018) -
MYD88(L265P) Detection in IgM Monoclonal Gammopathies: Methodological Considerations for Routine Implementation
por: Ferrante, Martina, et al.
Publicado: (2021) -
Gamma-heavy chain monoclonal gammopathy with undetermined significance (MGUS)
por: Zushi, Yuriko, et al.
Publicado: (2019)