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Validation Strategy for Ultrasensitive Mutation Detection.
Debeljak M, Noë M, Riel SL, Haley LM, Norris AL, Anderson DA, Adams EM, Suenaga M, Beierl KF, Lin MT, Goggins MG, Gocke CD, Eshleman JR. Debeljak M, et al. Among authors: adams em. Mol Diagn Ther. 2018 Oct;22(5):603-611. doi: 10.1007/s40291-018-0350-z. Mol Diagn Ther. 2018. PMID: 29974360
FLT3 inhibitors added to induction therapy induce deeper remissions.
Levis M, Shi W, Chang K, Laing C, Pollner R, Gocke C, Adams E, Berisha F, Lameh J, Lesegretain A. Levis M, et al. Blood. 2020 Jan 2;135(1):75-78. doi: 10.1182/blood.2019002180. Blood. 2020. PMID: 31722002 Free article. Clinical Trial. No abstract available.
Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies.
Jiang L, Pallavajjala A, Huang J, Haley L, Morsberger L, Stinnett V, Hardy M, Park R, Ament C, Finch A, Shane A, Parish R, Nozari A, Long P, Adams E, Smith K, Parimi V, Dougaparsad S, Long L, Gocke CD, Zou YS. Jiang L, et al. J Mol Diagn. 2021 Apr;23(4):467-483. doi: 10.1016/j.jmoldx.2021.01.011. Epub 2021 Feb 10. J Mol Diagn. 2021. PMID: 33577993 Free article.
168 results