Positive selection and high sensitivity test for MYD88 mutations using locked nucleic acid
Author:
Affiliation:
1. NeoGenomics Laboratories; Irvine CA USA
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Reference21 articles.
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2. Identification of critical residues of the MyD88 death domain involved in the recruitment of downstream kinases;Loiarro;J Biol Chem,2009
3. MYD88 L265P somatic mutation in Waldenström's macroglobulinemia;Treon;N Engl J Med,2012
4. Oncogenically active MYD88 mutations in human lymphoma;Ngo;Nature,2011
5. Prevalence and clinical significance of the MYD88 (L265P) somatic mutation in Waldenström's macroglobulinemia and related lymphoid neoplasms;Varettoni;Blood,2013
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1. Zanubrutinib for the treatment of MYD88 wild-type Waldenström macroglobulinemia: a substudy of the phase 3 ASPEN trial;Blood Advances;2020-12-07
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3. Detection of TERT promoter mutation in serum cell‐free DNA using wild‐type blocking PCR combined with Sanger sequencing in hepatocellular carcinoma;Journal of Medical Virology;2020-03
4. A head-to-head Phase III study comparing zanubrutinib versus ibrutinib in patients with Waldenström macroglobulinemia;Future Oncology;2018-09
5. Wild-type Blocking PCR Combined with Direct Sequencing as a Highly Sensitive Method for Detection of Low-Frequency Somatic Mutations;Journal of Visualized Experiments;2017-03-29
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