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Development of potent monoclonal antibody auristatin conjugates for cancer therapy.
Nat Biotechnol. 2003 Jul;21(7):778-84. doi: 10.1038/nbt832. Epub 2003 Jun 1.
Nat Biotechnol. 2003.
PMID: 12778055
cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity.
Francisco JA, Cerveny CG, Meyer DL, Mixan BJ, Klussman K, Chace DF, Rejniak SX, Gordon KA, DeBlanc R, Toki BE, Law CL, Doronina SO, Siegall CB, Senter PD, Wahl AF.
Francisco JA, et al. Among authors: deblanc r.
Blood. 2003 Aug 15;102(4):1458-65. doi: 10.1182/blood-2003-01-0039. Epub 2003 Apr 24.
Blood. 2003.
PMID: 12714494
Free article.
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6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity.
Tsou HR, Mamuya N, Johnson BD, Reich MF, Gruber BC, Ye F, Nilakantan R, Shen R, Discafani C, DeBlanc R, Davis R, Koehn FE, Greenberger LM, Wang YF, Wissner A.
Tsou HR, et al. Among authors: deblanc r.
J Med Chem. 2001 Aug 16;44(17):2719-34. doi: 10.1021/jm0005555.
J Med Chem. 2001.
PMID: 11495584
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Determination of the substrate specificity of the phospholipase D from Streptomyces chromofuscus via an inorganic phosphate quantitation assay.
Martin SF, DeBlanc RL, Hergenrother PJ.
Martin SF, et al. Among authors: deblanc rl.
Anal Biochem. 2000 Feb 15;278(2):106-10. doi: 10.1006/abio.1999.4420.
Anal Biochem. 2000.
PMID: 10660451
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