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Year | Number of Results |
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2010 | 1 |
2011 | 1 |
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2022 | 2 |
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Page 1
Phase 1 study of anti-CD47 monoclonal antibody CC-90002 in patients with relapsed/refractory acute myeloid leukemia and high-risk myelodysplastic syndromes.
Ann Hematol. 2022 Mar;101(3):557-569. doi: 10.1007/s00277-021-04734-2. Epub 2022 Jan 4.
Ann Hematol. 2022.
PMID: 34981142
Free PMC article.
Clinical Trial.
Modulation of CD47-SIRPα innate immune checkpoint axis with Fc-function detuned anti-CD47 therapeutic antibody.
Narla RK, Modi H, Bauer D, Abbasian M, Leisten J, Piccotti JR, Kopytek S, Eckelman BP, Deveraux Q, Timmer J, Zhu D, Wong L, Escoubet L, Raymon HK, Hariharan K.
Narla RK, et al. Among authors: kopytek s.
Cancer Immunol Immunother. 2022 Feb;71(2):473-489. doi: 10.1007/s00262-021-03010-6. Epub 2021 Jul 10.
Cancer Immunol Immunother. 2022.
PMID: 34247273
Free PMC article.
Item in Clipboard
Investigation Into the Role of ERK in Tyrosine Kinase Inhibitor-Induced Neuropathy.
Belair DG, Sudak K, Connelly K, Collins ND, Kopytek SJ, Kolaja KL.
Belair DG, et al. Among authors: kopytek sj.
Toxicol Sci. 2021 May 27;181(2):160-174. doi: 10.1093/toxsci/kfab033.
Toxicol Sci. 2021.
PMID: 33749749
Clinical Trial.
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Effects of SCH 486757, a nociceptin-1 receptor agonist, on fertility and reproductive hormone levels in female CRL:CD®[SD] rats.
Enright BP, McIntyre BS, Barat SA, Treinen KA, Kopytek SJ.
Enright BP, et al. Among authors: kopytek sj.
Birth Defects Res B Dev Reprod Toxicol. 2012 Feb;95(1):12-22. doi: 10.1002/bdrb.20334. Epub 2011 Sep 15.
Birth Defects Res B Dev Reprod Toxicol. 2012.
PMID: 21922640
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Assessment of hydroxypropyl methylcellulose, propylene glycol, polysorbate 80, and hydroxypropyl-β-cyclodextrin for use in developmental and reproductive toxicology studies.
Enright BP, McIntyre BS, Thackaberry EA, Treinen KA, Kopytek SJ.
Enright BP, et al. Among authors: kopytek sj.
Birth Defects Res B Dev Reprod Toxicol. 2010 Dec;89(6):504-16. doi: 10.1002/bdrb.20273.
Birth Defects Res B Dev Reprod Toxicol. 2010.
PMID: 21058332
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Recommendations from a global cross-company data sharing initiative on the incorporation of recovery phase animals in safety assessment studies to support first-in-human clinical trials.
Sewell F, Chapman K, Baldrick P, Brewster D, Broadmeadow A, Brown P, Burns-Naas LA, Clarke J, Constan A, Couch J, Czupalla O, Danks A, DeGeorge J, de Haan L, Hettinger K, Hill M, Festag M, Jacobs A, Jacobson-Kram D, Kopytek S, Lorenz H, Moesgaard SG, Moore E, Pasanen M, Perry R, Ragan I, Robinson S, Schmitt PM, Short B, Lima BS, Smith D, Sparrow S, van Bekkum Y, Jones D.
Sewell F, et al. Among authors: kopytek s.
Regul Toxicol Pharmacol. 2014 Oct;70(1):413-29. doi: 10.1016/j.yrtph.2014.07.018. Epub 2014 Jul 29.
Regul Toxicol Pharmacol. 2014.
PMID: 25078890
Free article.
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