J A Katzenellenbogen - JoVE Visualize

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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 1, 1992

Fluorine-18-labeled androgens: radiochemical synthesis and tissue distribution studies on six fluorine-substituted androgens, potential imaging agents for prostatic cancerA Liu, C S Dence, M J Welch, et al.

Endocrinology|October 3, 2000

Conformational changes and coactivator recruitment by novel ligands for estrogen receptor-alpha and estrogen receptor-beta: correlations with biological character and distinct differences among SRC coactivator family membersD M Kraichely, J Sun, J A Katzenellenbogen, et al.

Chemistry & Biology|April 18, 2001

The estrogen receptor: a structure-based approach to the design of new specific hormone-receptor combinationsR Tedesco, J A Thomas, B S Katzenellenbogen, et al.

The Journal of Biological Chemistry|August 16, 1996

Identification of amino acids in the hormone binding domain of the human estrogen receptor important in estrogen bindingK Ekena, K E Weis, J A Katzenellenbogen, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1980

Receptor-binding radiopharmaceuticals for imaging breast tumors: estrogen-receptor interactions and selectivity of tissue uptake of halogenated estrogen analogsJ A Katzenellenbogen, K E Carlson, D F Heiman, et al.

Journal of Protein Chemistry|October 1, 1996

Haloenol lactones as inactivators and substrates of aldehyde dehydrogenaseN Mukerjee, M Dryjanski, W Dai, et al.

The Journal of Biological Chemistry|February 21, 1997

Different residues of the human estrogen receptor are involved in the recognition of structurally diverse estrogens and antiestrogensK Ekena, K E Weis, J A Katzenellenbogen, et al.

Bioorganic & Medicinal Chemistry|July 15, 2000

Acyclic amides as estrogen receptor ligands: synthesis, binding, activity and receptor interactionS R Stauffer, J Sun, B S Katzenellenbogen, et al.

Bioorganic & Medicinal Chemistry Letters|June 8, 2001

Synthesis and evaluation of hexahydrochrysene and tetrahydrobenzofluorene ligands for the estrogen receptorR Tedesco, M K Youngman, S R Wilson, et al.

Journal of Medicinal Chemistry|February 1, 1982

Antiestrogen basicity--activity relationships: a comparison of the estrogen receptor binding and antiuterotrophic potencies of several analogues of (Z)-1,2-diphenyl-1-[4-[2-(dimethylamino)ethoxy]phenyl]-1-butene (tamoxifen, Nolvadex) having altered basicityD W Robertson, J A Katzenellenbogen, J R Hayes, et al.

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Showing results (61-70 of 199) with videos related to

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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 1, 1992

Fluorine-18-labeled androgens: radiochemical synthesis and tissue distribution studies on six fluorine-substituted androgens, potential imaging agents for prostatic cancerA Liu, C S Dence, M J Welch, et al.

Endocrinology|October 3, 2000

Conformational changes and coactivator recruitment by novel ligands for estrogen receptor-alpha and estrogen receptor-beta: correlations with biological character and distinct differences among SRC coactivator family membersD M Kraichely, J Sun, J A Katzenellenbogen, et al.

Chemistry & Biology|April 18, 2001

The estrogen receptor: a structure-based approach to the design of new specific hormone-receptor combinationsR Tedesco, J A Thomas, B S Katzenellenbogen, et al.

The Journal of Biological Chemistry|August 16, 1996

Identification of amino acids in the hormone binding domain of the human estrogen receptor important in estrogen bindingK Ekena, K E Weis, J A Katzenellenbogen, et al.

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1980

Receptor-binding radiopharmaceuticals for imaging breast tumors: estrogen-receptor interactions and selectivity of tissue uptake of halogenated estrogen analogsJ A Katzenellenbogen, K E Carlson, D F Heiman, et al.

Journal of Protein Chemistry|October 1, 1996

Haloenol lactones as inactivators and substrates of aldehyde dehydrogenaseN Mukerjee, M Dryjanski, W Dai, et al.

The Journal of Biological Chemistry|February 21, 1997

Different residues of the human estrogen receptor are involved in the recognition of structurally diverse estrogens and antiestrogensK Ekena, K E Weis, J A Katzenellenbogen, et al.

Bioorganic & Medicinal Chemistry|July 15, 2000

Acyclic amides as estrogen receptor ligands: synthesis, binding, activity and receptor interactionS R Stauffer, J Sun, B S Katzenellenbogen, et al.

Bioorganic & Medicinal Chemistry Letters|June 8, 2001

Synthesis and evaluation of hexahydrochrysene and tetrahydrobenzofluorene ligands for the estrogen receptorR Tedesco, M K Youngman, S R Wilson, et al.

Journal of Medicinal Chemistry|February 1, 1982

Antiestrogen basicity--activity relationships: a comparison of the estrogen receptor binding and antiuterotrophic potencies of several analogues of (Z)-1,2-diphenyl-1-[4-[2-(dimethylamino)ethoxy]phenyl]-1-butene (tamoxifen, Nolvadex) having altered basicityD W Robertson, J A Katzenellenbogen, J R Hayes, et al.

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