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SMARCE1 deficiency generates a targetable mSWI/SNF dependency in clear cell meningioma.
St Pierre R, Collings CK, Samé Guerra DD, Widmer CJ, Bolonduro O, Mashtalir N, Sankar A, Liang Y, Bi WL, Gerkes EH, Ramesh V, Qi J, Smith MJ, Meredith DM, Kadoch C. St Pierre R, et al. Among authors: bolonduro o. Nat Genet. 2022 Jun;54(6):861-873. doi: 10.1038/s41588-022-01077-0. Epub 2022 Jun 9. Nat Genet. 2022. PMID: 35681054
Recurrent SMARCB1 Mutations Reveal a Nucleosome Acidic Patch Interaction Site That Potentiates mSWI/SNF Complex Chromatin Remodeling.
Valencia AM, Collings CK, Dao HT, St Pierre R, Cheng YC, Huang J, Sun ZY, Seo HS, Mashtalir N, Comstock DE, Bolonduro O, Vangos NE, Yeoh ZC, Dornon MK, Hermawan C, Barrett L, Dhe-Paganon S, Woolf CJ, Muir TW, Kadoch C. Valencia AM, et al. Among authors: bolonduro o. Cell. 2019 Nov 27;179(6):1342-1356.e23. doi: 10.1016/j.cell.2019.10.044. Epub 2019 Nov 20. Cell. 2019. PMID: 31759698 Free PMC article.
Herlyn Werner Wunderlich Syndrome: Varying Presentations.
Raju R, Abuzeid OM, Bolonduro O, Akinpeloye A, Ashraf M, Abuzeid MI. Raju R, et al. Among authors: bolonduro o. J Minim Invasive Gynecol. 2015 Nov-Dec;22(6S):S153. doi: 10.1016/j.jmig.2015.08.567. Epub 2015 Oct 15. J Minim Invasive Gynecol. 2015. PMID: 27678869 No abstract available.
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