Carlson KE - Search Results

1

Adamantyl Antiestrogens with Novel Side Chains Reveal a Spectrum of Activities in Suppressing Estrogen Receptor Mediated Activities in Breast Cancer Cells.

Min J, Guillen VS, Sharma A, Zhao Y, Ziegler Y, Gong P, Mayne CG, Srinivasan S, Kim SH, Carlson KE, Nettles KW, Katzenellenbogen BS, Katzenellenbogen JA. Min J, et al. Among authors: carlson ke. J Med Chem. 2017 Jul 27;60(14):6321-6336. doi: 10.1021/acs.jmedchem.7b00585. Epub 2017 Jul 14. J Med Chem. 2017. PMID: 28657320 Free PMC article.

2

Iodohexestrols. II. Characterization of the binding and estrogenic activity of iodinated hexestrol derivatives, in vitro and in vivo.

Katzenellenbogen JA, Hsiung HM, Carlson KE, McGuire WL, Kraay RJ, Katzenellenbogen BS. Katzenellenbogen JA, et al. Among authors: carlson ke. Biochemistry. 1975 Apr 22;14(8):1742-50. doi: 10.1021/bi00679a029. Biochemistry. 1975. PMID: 164893

3

Antiestrogens and antiestrogen metabolites: preparation of tritium-labeled (+/-)-cis-3-[p-(1,2,3,4-tetrahydro-6-methoxy-2-phenyl-1-naphthyl)phenoxyl]-1,2-propanediol (U-23469) and characterization and synthesis of a biologically important metabolite.

Tatee T, Carlson KE, Katzenellenbogen JA, Robertson DW, Katzenellenbogen BS. Tatee T, et al. Among authors: carlson ke. J Med Chem. 1979 Dec;22(12):1509-17. doi: 10.1021/jm00198a015. J Med Chem. 1979. PMID: 536996

4

Estrogen photoaffinity labels. 2. Reversible binding and covalent attachment of photosensitive hexestrol derivatives to the uterine estrogen receptor.

Katzenellenbogen JA, Carlson KE, Johnson HJ Jr, Myers HN. Katzenellenbogen JA, et al. Among authors: carlson ke. Biochemistry. 1977 May 3;16(9):1970-6. doi: 10.1021/bi00628a034. Biochemistry. 1977. PMID: 870034

5

Characterization of trypsin-treated forms of the estrogen receptor from rat and lamb uterus.

Carlson KE, Sun LH, Katzenellenbogen JA. Carlson KE, et al. Biochemistry. 1977 Sep 20;16(19):4288-96. doi: 10.1021/bi00638a025. Biochemistry. 1977. PMID: 901772 No abstract available.

6

Chemical probes of estrogen action: affinity labeling.

Katzenellenbogen JA, Carlson KE, Johnson HJ Jr, Myers HN. Katzenellenbogen JA, et al. Among authors: carlson ke. J Toxicol Environ Health Suppl. 1976;1:205-30. J Toxicol Environ Health Suppl. 1976. PMID: 1033295

7

Donor-acceptor tetrahydrochrysenes, inherently fluorescent, high-affinity ligands for the estrogen receptor: binding and fluorescence characteristics and fluorometric assay of receptor.

Hwang KJ, Carlson KE, Anstead GM, Katzenellenbogen JA. Hwang KJ, et al. Among authors: carlson ke. Biochemistry. 1992 Nov 24;31(46):11536-45. doi: 10.1021/bi00161a035. Biochemistry. 1992. PMID: 1445887

8

Nonsteroidal estrogens bearing acyl azide functions: potential electrophilic and photoaffinity labeling agents for the estrogen receptor.

Pinney KG, Carlson KE, Katzenellenbogen JA. Pinney KG, et al. Among authors: carlson ke. Steroids. 1992 May;57(5):222-32. doi: 10.1016/0039-128x(92)90106-j. Steroids. 1992. PMID: 1488784

9

Synthesis of high affinity fluorine-substituted ligands for the androgen receptor. Potential agents for imaging prostatic cancer by positron emission tomography.

Liu A, Carlson KE, Katzenellenbogen JA. Liu A, et al. Among authors: carlson ke. J Med Chem. 1992 May 29;35(11):2113-29. doi: 10.1021/jm00089a024. J Med Chem. 1992. PMID: 1597861

10

Preparation and evaluation of 17-ethynyl-substituted 16 alpha-[18F]fluoroestradiols: selective receptor-based PET imaging agents.

VanBrocklin HF, Pomper MG, Carlson KE, Welch MJ, Katzenellenbogen JA. VanBrocklin HF, et al. Among authors: carlson ke. Int J Rad Appl Instrum B. 1992 Apr;19(3):363-74. doi: 10.1016/0883-2897(92)90122-f. Int J Rad Appl Instrum B. 1992. PMID: 1629026

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