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Gene|August 26, 1998
YAC/STS map of 15Mb of Xp21.3-p11.3, at 100kb resolution, with refined comparisons of genetic distances and DMD structureR Nagaraja, C Jermak, M Trusgnich, et al.Journal of the American Chemical Society|August 19, 2007
Systematic exploration of the structural features of yatakemycin impacting DNA alkylation and biological activityMark S Tichenor, Karen S MacMillan, John D Trzupek, et al.Prehospital Emergency Care|July 23, 2005
Noninvasive fireground assessment of carboxyhemoglobin levels in firefightersDavid C Cone, Donald S MacMillan, Carin Van Gelder, et al.Plant Physiology|December 1, 1984
Subcellular Localizations of Two Dolichos biflorus LectinsM E Etzler, S Macmillan, S Scates, et al.Bioorganic & Medicinal Chemistry Letters|February 23, 2010
Synthesis and evaluation of duocarmycin SA analogs incorporating the methyl 1,2,8,8a-tetrahydrocyclopropa[c]oxazolo[2,3-e]indol-4-one-6-carboxylate (COI) alkylation subunitKristopher E Boyle, Karen S MacMillan, David A Ellis, et al.Genome Research|January 1, 1997
4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndromeG Porta, S MacMillan, R Nagaraja, et al.NAM Journal|June 30, 2026
GenoITS: Implementation of an Integrated Testing Strategy workflow for genotoxicity using QSAR-based toolsJosé Luis Vallés-Pardo, Eva Serrano-Candelas, Addel Goya-Jorge, et al.Magma (New York, N.Y.)|August 24, 1999
1H spectroscopic imaging of acute head injury--evidence of diffuse axonal injuryJ M Wild, C S Macmillan, J M Wardlaw, et al.Tetrahedron|February 18, 2010
Synthesis and Preliminary Evaluation of Duocarmycin Analogues Incorporating the 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[2,3-e]indol-4-one (CNI) and 1,2,11,11a-Tetrahydrocyclopropa[c]naphtho[1,2-e]indol-4-one (iso-CNI) Alkylation SubunitsCarla M Gauss, Akiyuki Hamasaki, Jay P Parrish, et al.Journal of Medicinal Chemistry|May 2, 2009
Potent cytotoxic C-11 modified geldanamycin analoguesZong-Qiang Tian, Zhan Wang, Karen S MacMillan, et al.Pageof 9