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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2008 1
2009 2
2010 1
2011 1
2012 1
2014 2
2015 2
2018 1
2020 1
2021 1
2022 2
2023 0
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16 results
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Page 1
ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine.
Rahmani NE, Ramachandra N, Sahu S, Gitego N, Lopez A, Pradhan K, Bhagat TD, Gordon-Mitchell S, Pena BR, Kazemi M, Rao K, Giricz O, Maqbool SB, Olea R, Zhao Y, Zhang J, Dolatshad H, Tittrea V, Tatwavedi D, Singh S, Lee J, Sun T, Steidl U, Shastri A, Inoue D, Abdel-Wahab O, Pellagatti A, Gavathiotis E, Boultwood J, Verma A. Rahmani NE, et al. Among authors: maqbool sb. Blood Cancer J. 2021 Sep 21;11(9):157. doi: 10.1038/s41408-021-00541-0. Blood Cancer J. 2021. PMID: 34548471 Free PMC article.
RNASeq in C. elegans Following Manganese Exposure.
Parmalee NL, Maqbool SB, Ye B, Calder B, Bowman AB, Aschner M. Parmalee NL, et al. Among authors: maqbool sb. Curr Protoc Toxicol. 2015 Aug 6;65:11.20.1-11.20.17. doi: 10.1002/0471140856.tx1120s65. Curr Protoc Toxicol. 2015. PMID: 26250396 Free PMC article.
Direct, genome-wide assessment of DNA mutations in single cells.
Gundry M, Li W, Maqbool SB, Vijg J. Gundry M, et al. Among authors: maqbool sb. Nucleic Acids Res. 2012 Mar;40(5):2032-40. doi: 10.1093/nar/gkr949. Epub 2011 Nov 15. Nucleic Acids Res. 2012. PMID: 22086961 Free PMC article.
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder.
Berko ER, Suzuki M, Beren F, Lemetre C, Alaimo CM, Calder RB, Ballaban-Gil K, Gounder B, Kampf K, Kirschen J, Maqbool SB, Momin Z, Reynolds DM, Russo N, Shulman L, Stasiek E, Tozour J, Valicenti-McDermott M, Wang S, Abrahams BS, Hargitai J, Inbar D, Zhang Z, Buxbaum JD, Molholm S, Foxe JJ, Marion RW, Auton A, Greally JM. Berko ER, et al. Among authors: maqbool sb. PLoS Genet. 2014 May 29;10(5):e1004402. doi: 10.1371/journal.pgen.1004402. eCollection 2014. PLoS Genet. 2014. PMID: 24875834 Free PMC article.
16 results