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Page 1
Bcr-Abl inhibition as a modality of CML therapeutics.
Buchdunger E, Matter A, Druker BJ. Buchdunger E, et al. Biochim Biophys Acta. 2001 Aug 31;1551(1):M11-8. doi: 10.1016/s0304-419x(01)00022-1. Biochim Biophys Acta. 2001. PMID: 11553417 Review. No abstract available.
Selective inhibition of the platelet-derived growth factor signal transduction pathway by a protein-tyrosine kinase inhibitor of the 2-phenylaminopyrimidine class.
Buchdunger E, Zimmermann J, Mett H, Meyer T, Müller M, Regenass U, Lydon NB. Buchdunger E, et al. Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2558-62. doi: 10.1073/pnas.92.7.2558. Proc Natl Acad Sci U S A. 1995. Retraction in: Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):12069. doi: 10.1073/pnas.95.20.12069-a PMID: 7708684 Free PMC article. Retracted.
A potent protein-tyrosine kinase inhibitor which selectively blocks proliferation of epidermal growth factor receptor-expressing tumor cells in vitro and in vivo.
Lydon NB, Mett H, Mueller M, Becker M, Cozens RM, Stover D, Daniels D, Traxler P, Buchdunger E. Lydon NB, et al. Among authors: buchdunger e. Int J Cancer. 1998 Mar 30;76(1):154-63. doi: 10.1002/(sici)1097-0215(19980330)76:1<154::aid-ijc24>3.0.co;2-b. Int J Cancer. 1998. Retraction in: Int J Cancer. 1999 May 17;81(4):669. doi: 10.1002/(sici)1097-0215(19990517)81:4<669::aid-ijc27>3.0.co;2-c PMID: 9533776 Retracted.
64 results