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

Year Number of Results
1991 2
1992 2
1993 2
1994 1
1996 3
1997 2
1998 6
1999 4
2000 4
2001 3
2002 2
2003 6
2004 3
2005 4
2006 7
2007 3
2008 2
2009 6
2010 4
2011 1
2012 1
2013 3
2014 1
2015 3
2016 2
2017 5
2018 5
2019 4
2020 6
2021 2
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Search Results

93 results
Results by year
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Page 1
RUNX1-targeted therapy for AML expressing somatic or germline mutation in RUNX1.
Mill CP, Fiskus W, DiNardo CD, Qian Y, Raina K, Rajapakshe K, Perera D, Coarfa C, Kadia TM, Khoury JD, Saenz DT, Saenz DN, Illendula A, Takahashi K, Kornblau SM, Green MR, Futreal AP, Bushweller JH, Crews CM, Bhalla KN. Mill CP, et al. Among authors: bushweller jh. Blood. 2019 Jul 4;134(1):59-73. doi: 10.1182/blood.2018893982. Epub 2019 Apr 25. Blood. 2019. PMID: 31023702 Free PMC article.
TNF-α signaling regulates RUNX1 function in endothelial cells.
Whitmore HAB, Amarnani D, O'Hare M, Delgado-Tirado S, Gonzalez-Buendia L, An M, Pedron J, Bushweller JH, Arboleda-Velasquez JF, Kim LA. Whitmore HAB, et al. Among authors: bushweller jh. FASEB J. 2021 Feb;35(2):e21155. doi: 10.1096/fj.202001668R. Epub 2020 Nov 2. FASEB J. 2021. PMID: 33135824 Free PMC article.
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D, Ratajczak J, Resende IC, Haworth C, Hock R, Loh M, Felix C, Roy DC, Busque L, Kurnit D, Willman C, Gewirtz AM, Speck NA, Bushweller JH, Li FP, Gardiner K, Poncz M, Maris JM, Gilliland DG. Song WJ, et al. Among authors: bushweller jh. Nat Genet. 1999 Oct;23(2):166-75. doi: 10.1038/13793. Nat Genet. 1999. PMID: 10508512
CBF--a biophysical perspective.
Bushweller JH. Bushweller JH. Semin Cell Dev Biol. 2000 Oct;11(5):377-82. doi: 10.1006/scdb.2000.0182. Semin Cell Dev Biol. 2000. PMID: 11105902 Review.
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