Kadwell SH - Search Results

1

Discovery of novel quinoline-based estrogen receptor ligands using peptide interaction profiling.

Hoekstra WJ, Patel HS, Liang X, Blanc JB, Heyer DO, Willson TM, Iannone MA, Kadwell SH, Miller LA, Pearce KH, Simmons CA, Shearin J. Hoekstra WJ, et al. Among authors: kadwell sh. J Med Chem. 2005 Mar 24;48(6):2243-7. doi: 10.1021/jm040154f. J Med Chem. 2005. PMID: 15771467

2

Correlation between in vitro peptide binding profiles and cellular activities for estrogen receptor-modulating compounds.

Iannone MA, Simmons CA, Kadwell SH, Svoboda DL, Vanderwall DE, Deng SJ, Consler TG, Shearin J, Gray JG, Pearce KH. Iannone MA, et al. Among authors: kadwell sh. Mol Endocrinol. 2004 May;18(5):1064-81. doi: 10.1210/me.2003-0432. Epub 2004 Feb 19. Mol Endocrinol. 2004. PMID: 14976226

3

Expression, purification, and characterization of the human receptor activator of NF-kappaB ligand (RANKL) extracellular domain.

Willard D, Chen WJ, Barrett G, Blackburn K, Bynum J, Consler T, Hoffman C, Horne E, Iannone MA, Kadwell S, Parham J, Ellis B. Willard D, et al. Protein Expr Purif. 2000 Oct;20(1):48-57. doi: 10.1006/prep.2000.1278. Protein Expr Purif. 2000. PMID: 11035950

4

Comparison of the biochemical and kinetic properties of the type 1 receptor tyrosine kinase intracellular domains. Demonstration of differential sensitivity to kinase inhibitors.

Brignola PS, Lackey K, Kadwell SH, Hoffman C, Horne E, Carter HL, Stuart JD, Blackburn K, Moyer MB, Alligood KJ, Knight WB, Wood ER. Brignola PS, et al. Among authors: kadwell sh. J Biol Chem. 2002 Jan 11;277(2):1576-85. doi: 10.1074/jbc.M105907200. Epub 2001 Nov 5. J Biol Chem. 2002. PMID: 11696537 Free article.

5

Production and characterization of an estrogen receptor beta subtype-specific mouse monoclonal antibody.

Su JL, McKee DD, Ellis B, Kadwell SH, Wisely GB, Moore LB, Triantafillou JA, Kost TA, Fuqua S, Moore JT. Su JL, et al. Among authors: kadwell sh. Hybridoma. 2000 Dec;19(6):481-7. doi: 10.1089/027245700750053977. Hybridoma. 2000. PMID: 11152400

6

The characterization of novel, dual ErbB-2/EGFR, tyrosine kinase inhibitors: potential therapy for cancer.

Rusnak DW, Affleck K, Cockerill SG, Stubberfield C, Harris R, Page M, Smith KJ, Guntrip SB, Carter MC, Shaw RJ, Jowett A, Stables J, Topley P, Wood ER, Brignola PS, Kadwell SH, Reep BR, Mullin RJ, Alligood KJ, Keith BR, Crosby RM, Murray DM, Knight WB, Gilmer TM, Lackey K. Rusnak DW, et al. Among authors: kadwell sh. Cancer Res. 2001 Oct 1;61(19):7196-203. Cancer Res. 2001. PMID: 11585755

7

Production of baculovirus-expressed recombinant proteins in wave bioreactors.

Kadwell SH, Hardwicke PI. Kadwell SH, et al. Methods Mol Biol. 2007;388:247-66. doi: 10.1007/978-1-59745-457-5_12. Methods Mol Biol. 2007. PMID: 17951774

8

Expression cloning and receptor pharmacology of human calcitonin receptors from MCF-7 cells and their relationship to amylin receptors.

Chen WJ, Armour S, Way J, Chen G, Watson C, Irving P, Cobb J, Kadwell S, Beaumont K, Rimele T, Kenakin T. Chen WJ, et al. Mol Pharmacol. 1997 Dec;52(6):1164-75. doi: 10.1124/mol.52.6.1164. Mol Pharmacol. 1997. PMID: 9396787

9

17 beta-(N-tert-butylcarbamoyl)-4-aza-5 alpha-androstan-1-en-3-one is an active site-directed slow time-dependent inhibitor of human steroid 5 alpha-reductase 1.

Tian G, Stuart JD, Moss ML, Domanico PL, Bramson HN, Patel IR, Kadwell SH, Overton LK, Kost TA, Mook RA Jr, et al. Tian G, et al. Among authors: kadwell sh. Biochemistry. 1994 Mar 1;33(8):2291-6. doi: 10.1021/bi00174a041. Biochemistry. 1994. PMID: 8117686

10

Structure of the Tie2 RTK domain: self-inhibition by the nucleotide binding loop, activation loop, and C-terminal tail.

Shewchuk LM, Hassell AM, Ellis B, Holmes WD, Davis R, Horne EL, Kadwell SH, McKee DD, Moore JT. Shewchuk LM, et al. Among authors: kadwell sh. Structure. 2000 Nov 15;8(11):1105-13. doi: 10.1016/s0969-2126(00)00516-5. Structure. 2000. PMID: 11080633 Free article.

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