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2017 6
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2019 4
2020 2
2021 1
2024 0

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Multiplex assessment of protein variant abundance by massively parallel sequencing.
Matreyek KA, Starita LM, Stephany JJ, Martin B, Chiasson MA, Gray VE, Kircher M, Khechaduri A, Dines JN, Hause RJ, Bhatia S, Evans WE, Relling MV, Yang W, Shendure J, Fowler DM. Matreyek KA, et al. Nat Genet. 2018 Jun;50(6):874-882. doi: 10.1038/s41588-018-0122-z. Epub 2018 May 21. Nat Genet. 2018. PMID: 29785012 Free PMC article.
Mutagenesis-based protein structure determination.
Chiasson M, Fowler DM. Chiasson M, et al. Nat Genet. 2019 Jul;51(7):1072-1073. doi: 10.1038/s41588-019-0461-4. Nat Genet. 2019. PMID: 31253976 No abstract available.
Applying Multiplex Assays to Understand Variation in Pharmacogenes.
Chiasson M, Dunham MJ, Rettie AE, Fowler DM. Chiasson M, et al. Clin Pharmacol Ther. 2019 Aug;106(2):290-294. doi: 10.1002/cpt.1468. Epub 2019 May 30. Clin Pharmacol Ther. 2019. PMID: 31145826 Free PMC article. No abstract available.
Interrogation of CYP2D6 Structural Variant Alleles Improves the Correlation Between CYP2D6 Genotype and CYP2D6-Mediated Metabolic Activity.
Dalton R, Lee SB, Claw KG, Prasad B, Phillips BR, Shen DD, Wong LH, Fade M, McDonald MG, Dunham MJ, Fowler DM, Rettie AE, Schuetz E, Thornton TA, Nickerson DA, Gaedigk A, Thummel KE, Woodahl EL. Dalton R, et al. Clin Transl Sci. 2020 Jan;13(1):147-156. doi: 10.1111/cts.12695. Epub 2019 Oct 25. Clin Transl Sci. 2020. PMID: 31536170 Free PMC article.
13 results