The scientist’s investigation covers issues in Estrogen receptor, Stereochemistry, Estrogen receptor alpha, Ligand and Biochemistry. Her Estrogen receptor research incorporates themes from Receptor, Tamoxifen, Nuclear receptor, Estrogen and Binding site. The various areas that she examines in her Stereochemistry study include Molecule, Binding selectivity, Chemical synthesis, Double bond and Isostructural.
Her work is dedicated to discovering how Estrogen receptor alpha, Estrogen receptor beta are connected with Nuclear receptor coactivator 3 and Endocrinology and other disciplines. In her study, Estradiol binding, Ligand binding assay, Amino acid, Pharmacophore and Ligand efficiency is strongly linked to Cooperative binding, which falls under the umbrella field of Ligand. Her Biochemistry study incorporates themes from Promoter and Pyrazine.
Her primary scientific interests are in Estrogen receptor, Stereochemistry, Receptor, Ligand and Estrogen receptor alpha. She has researched Estrogen receptor in several fields, including Biochemistry, Estrogen and Cell biology. Her research integrates issues of Ligand, Structure–activity relationship, Chemical synthesis and Binding site in her study of Stereochemistry.
Her research investigates the link between Chemical synthesis and topics such as Molecular model that cross with problems in Docking. Kathryn E. Carlson combines subjects such as Endocrinology, Uterus, Estrogen receptor binding, Steric effects and Progesterone receptor with her study of Receptor. Her Estrogen receptor alpha study combines topics from a wide range of disciplines, such as Antiestrogen, Tamoxifen, Bazedoxifene and Cancer research.
Her scientific interests lie mostly in Estrogen receptor, Estrogen receptor alpha, Cancer research, Antiestrogen and Breast cancer. Her studies deal with areas such as Tamoxifen, Receptor, Ligand and Cell biology as well as Estrogen receptor. Her study focuses on the intersection of Receptor and fields such as Coactivator with connections in the field of Biochemistry.
Her Estrogen receptor alpha study incorporates themes from Fulvestrant, Stereochemistry, Pharmacology, Binding site and Bazedoxifene. Her studies in Stereochemistry integrate themes in fields like Protein structure, Reporter gene and Structure–activity relationship. Her Antiestrogen research focuses on Selective estrogen receptor modulator and how it relates to Potency and Isoliquiritigenin.
Her primary areas of study are Estrogen receptor alpha, Estrogen receptor, Tamoxifen, Pharmacology and Antiestrogen. Her Estrogen receptor alpha research integrates issues from Nuclear receptor and Signal transduction, Cell biology. Her Nuclear receptor study combines topics in areas such as Cell growth and Ligand.
As part of her studies on Estrogen receptor, Kathryn E. Carlson frequently links adjacent subjects like Endocrinology. Kathryn E. Carlson has included themes like Cancer, Receptor, Fulvestrant, Estrogen Receptor Antagonists and Estrogen in her Pharmacology study. The concepts of her Antiestrogen study are interwoven with issues in Agonist and Isoliquiritigenin.
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Estrogen receptor-β potency-selective ligands: Structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues
Marvin J. Meyers;Jun Sun;Kathryn E. Carlson;Gwendolyn A. Marriner.
Journal of Medicinal Chemistry (2001)
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
Gregory M. Anstead;Kathryn E. Carlson;John A. Katzenellenbogen.
Steroids (1997)
Studies on the uterine, cytoplasmic estrogen binding protein. Thermal stability and ligand dissociation rate. An assay of empty and filled sites by exchange.
John A. Katzenellenbogen;Howard J. Johnson;Kathryn E. Carlson.
Biochemistry (1973)
Synthesis and biological evaluation of a novel series of furans: Ligands selective for estrogen receptor α
Deborah S. Mortensen;Alice L. Rodriguez;Kathryn E. Carlson;Jun Sun.
Journal of Medicinal Chemistry (2001)
Altered Ligand Binding Properties and Enhanced Stability of a Constitutively Active Estrogen Receptor: Evidence That an Open Pocket Conformation Is Required for Ligand Interaction†
Kathryn E. Carlson;Inho Choi;Arvin Gee;Benita S. Katzenellenbogen.
Biochemistry (1997)
Pyrazolo[1,5-a]pyrimidines: Estrogen Receptor Ligands Possessing Estrogen Receptor β Antagonist Activity
Dennis R. Compton;Shubin Sheng;Kathryn E. Carlson;Natalie A. Rebacz.
Journal of Medicinal Chemistry (2004)
Efficient and highly selective covalent labeling of the estrogen receptor with [3H]tamoxifen aziridine
J A Katzenellenbogen;K E Carlson;D F Heiman;D W Robertson.
Journal of Biological Chemistry (1983)
Activating ESR1 Mutations Differentially Affect the Efficacy of ER Antagonists
Weiyi Toy;Hazel Weir;Pedram Razavi;Mandy Lawson.
Cancer Discovery (2017)
Coactivator peptides have a differential stabilizing effect on the binding of estrogens and antiestrogens with the estrogen receptor.
Arvin C. Gee;Kathryn E. Carlson;Paolo G. V. Martini;Benita S. Katzenellenbogen.
Molecular Endocrinology (1999)
11 beta-methoxy-, 11 beta-ethyl- and 17 alpha-ethynyl-substituted 16 alpha-fluoroestradiols: receptor-based imaging agents with enhanced uptake efficiency and selectivity.
Martin G. Pomper;Henry VanBrocklin;Andrea M. Thieme;Ralph D. Thomas.
Journal of Medicinal Chemistry (1990)
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