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Page 1
Overview on the application of transcription profiling using selected nephrotoxicants for toxicology assessment.
Kramer JA, Pettit SD, Amin RP, Bertram TA, Car B, Cunningham M, Curtiss SW, Davis JW, Kind C, Lawton M, Naciff JM, Oreffo V, Roman RJ, Sistare FD, Stevens J, Thompson K, Vickers AE, Wild S, Afshari CA. Kramer JA, et al. Among authors: curtiss sw. Environ Health Perspect. 2004 Mar;112(4):460-4. doi: 10.1289/ehp.6673. Environ Health Perspect. 2004. PMID: 15033596 Free PMC article. Review.
Identification of putative gene based markers of renal toxicity.
Amin RP, Vickers AE, Sistare F, Thompson KL, Roman RJ, Lawton M, Kramer J, Hamadeh HK, Collins J, Grissom S, Bennett L, Tucker CJ, Wild S, Kind C, Oreffo V, Davis JW 2nd, Curtiss S, Naciff JM, Cunningham M, Tennant R, Stevens J, Car B, Bertram TA, Afshari CA. Amin RP, et al. Environ Health Perspect. 2004 Mar;112(4):465-79. doi: 10.1289/ehp.6683. Environ Health Perspect. 2004. PMID: 15033597 Free PMC article.
Acute lymphoid and gastrointestinal toxicity induced by selective p38alpha map kinase and map kinase-activated protein kinase-2 (MK2) inhibitors in the dog.
Morris DL, O'Neil SP, Devraj RV, Portanova JP, Gilles RW, Gross CJ, Curtiss SW, Komocsar WJ, Garner DS, Happa FA, Kraus LJ, Nikula KJ, Monahan JB, Selness SR, Galluppi GR, Shevlin KM, Kramer JA, Walker JK, Messing DM, Anderson DR, Mourey RJ, Whiteley LO, Daniels JS, Yang JZ, Rowlands PC, Alden CL, Davis JW 2nd, Sagartz JE. Morris DL, et al. Among authors: curtiss sw. Toxicol Pathol. 2010 Jun;38(4):606-18. doi: 10.1177/0192623310367807. Epub 2010 May 6. Toxicol Pathol. 2010. PMID: 20448081
Revolution through genomics in investigative and discovery toxicology.
Rodi CP, Bunch RT, Curtiss SW, Kier LD, Cabonce MA, Davila JC, Mitchell MD, Alden CL, Morris DL. Rodi CP, et al. Among authors: curtiss sw. Toxicol Pathol. 1999 Jan-Feb;27(1):107-10. doi: 10.1177/019262339902700120. Toxicol Pathol. 1999. PMID: 10367683 Review.
Design, synthesis, and biological evaluation of 3-[4-(2-hydroxyethyl)piperazin-1-yl]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one, a potent, orally active, brain penetrant inhibitor of phosphodiesterase 5 (PDE5).
Hughes RO, Rogier DJ, Jacobsen EJ, Walker JK, Macinnes A, Bond BR, Zhang LL, Yu Y, Zheng Y, Rumsey JM, Walgren JL, Curtiss SW, Fobian YM, Heasley SE, Cubbage JW, Moon JB, Brown DL, Acker BA, Maddux TM, Tollefson MB, Mischke BV, Owen DR, Freskos JN, Molyneaux JM, Benson AG, Blevis-Bal RM. Hughes RO, et al. Among authors: curtiss sw. J Med Chem. 2010 Mar 25;53(6):2656-60. doi: 10.1021/jm901781q. J Med Chem. 2010. PMID: 20196613
Informatics and data mining tools and strategies for the human connectome project.
Marcus DS, Harwell J, Olsen T, Hodge M, Glasser MF, Prior F, Jenkinson M, Laumann T, Curtiss SW, Van Essen DC. Marcus DS, et al. Among authors: curtiss sw. Front Neuroinform. 2011 Jun 27;5:4. doi: 10.3389/fninf.2011.00004. eCollection 2011. Front Neuroinform. 2011. PMID: 21743807 Free PMC article.
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