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Page 1
SETBP1 overexpression acts in the place of class-defining mutations to drive FLT3-ITD-mutant AML.
Blood Adv. 2021 May 11;5(9):2412-2425. doi: 10.1182/bloodadvances.2020003443.
Blood Adv. 2021.
PMID: 33956058
Free PMC article.
Accelerated Development With Increased Bone Mass and Skeletal Response to Loading Suggest Receptor Activity Modifying Protein-3 as a Bone Anabolic Target.
Pacharne S, Livesey M, Kadmiel M, Wang N, Caron KM, Richards GO, Skerry TM.
Pacharne S, et al.
Front Endocrinol (Lausanne). 2022 Jan 12;12:807882. doi: 10.3389/fendo.2021.807882. eCollection 2021.
Front Endocrinol (Lausanne). 2022.
PMID: 35095771
Free PMC article.
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Molecular synergy underlies the co-occurrence patterns and phenotype of NPM1-mutant acute myeloid leukemia.
Dovey OM, Cooper JL, Mupo A, Grove CS, Lynn C, Conte N, Andrews RM, Pacharne S, Tzelepis K, Vijayabaskar MS, Green P, Rad R, Arends M, Wright P, Yusa K, Bradley A, Varela I, Vassiliou GS.
Dovey OM, et al. Among authors: pacharne s.
Blood. 2017 Oct 26;130(17):1911-1922. doi: 10.1182/blood-2017-01-760595. Epub 2017 Aug 23.
Blood. 2017.
PMID: 28835438
Free PMC article.
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Research resource: Haploinsufficiency of receptor activity-modifying protein-2 (RAMP2) causes reduced fertility, hyperprolactinemia, skeletal abnormalities, and endocrine dysfunction in mice.
Kadmiel M, Fritz-Six K, Pacharne S, Richards GO, Li M, Skerry TM, Caron KM.
Kadmiel M, et al. Among authors: pacharne s.
Mol Endocrinol. 2011 Jul;25(7):1244-53. doi: 10.1210/me.2010-0400. Epub 2011 May 12.
Mol Endocrinol. 2011.
PMID: 21566080
Free PMC article.
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