MYD88 L265P Mutation Detection by ddPCR: Recommendations for Screening and Minimal Residual Disease Monitoring
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-2950-5_5
Reference51 articles.
1. Ngo VN, Young RM, Schmitz R et al (2011) Oncogenically active MYD88 mutations in human lymphoma. Nature 470:115–119. https://doi.org/10.1038/nature09671
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3. Jeelall YS, Horikawa K (2011) Oncogenic MYD88 mutation drives Toll pathway to lymphoma. Immunol Cell Biol 89:659–660. https://doi.org/10.1038/icb.2011.31
4. de Groen RAL, Schrader AMR, Kersten MJ et al (2019) MYD88 in the driver’s seat of B-cell lymphomagenesis: from molecular mechanisms to clinical implications. Haematologica 104:2337–2348. https://doi.org/10.3324/haematol.2019.227272
5. Puente XS, Pinyol M, Quesada V et al (2011) Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature 475:101–105. https://doi.org/10.1038/nature10113
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