What is she best known for?
The fields of study she is best known for:
Her main research concerns Receptor, Biochemistry, Stereochemistry, Internal medicine and Endocrinology.
Her study in Receptor is interdisciplinary in nature, drawing from both Insulin receptor and Binding site.
Her study on Peptide, Enzyme inhibitor, Binding protein and Enzyme is often connected to Steroid as part of broader study in Biochemistry.
Her biological study spans a wide range of topics, including Agonist, Antagonist, IC50, Tachykinin receptor 1 and Chemical synthesis.
In the field of Internal medicine, her study on Thermogenin, Brown adipose tissue and Adipose tissue overlaps with subjects such as Gastric motility and Antrum.
Her Motilin study in the realm of Endocrinology interacts with subjects such as Monoaminergic.
Her most cited work include:
- Distinct Mechanism for Antidepressant Activity by Blockade of Central Substance P Receptors (932 citations)
- Receptor for motilin identified in the human gastrointestinal system. (359 citations)
- Azasteroids: structure-activity relationships for inhibition of 5.alpha.-reductase and of androgen receptor binding (351 citations)
What are the main themes of her work throughout her whole career to date?
Receptor, Stereochemistry, Biochemistry, Internal medicine and Endocrinology are her primary areas of study.
Her Receptor study combines topics from a wide range of disciplines, such as Binding site and Cell biology.
Her Stereochemistry research includes themes of In vitro, Chemical synthesis, Antagonist, Substance P and Trifluoromethyl.
Her research in Biochemistry focuses on subjects like Molecular biology, which are connected to Enzyme-linked receptor.
Particularly relevant to Neuropeptide Y receptor is her body of work in Internal medicine.
Her Endocrinology research integrates issues from Neuropeptide and Partial agonist.
She most often published in these fields:
- Receptor (47.73%)
- Stereochemistry (43.18%)
- Biochemistry (29.55%)
What were the highlights of her more recent work (between 1997-2010)?
- Stereochemistry (43.18%)
- Receptor (47.73%)
- Chemical synthesis (18.18%)
In recent papers she was focusing on the following fields of study:
Margaret A. Cascieri focuses on Stereochemistry, Receptor, Chemical synthesis, Agonist and In vitro.
Her Stereochemistry study incorporates themes from CCR2, Antagonist and Trifluoromethyl.
Her research investigates the connection with Receptor and areas like Endocrinology which intersect with concerns in Partial agonist.
Margaret A. Cascieri interconnects Bicyclic molecule, Substituent, Structure–activity relationship and Piperidine in the investigation of issues within Chemical synthesis.
Margaret A. Cascieri combines subjects such as Oral administration, Beta-3 adrenergic receptor, Adrenergic receptor and Lipolysis with her study of Agonist.
Her research integrates issues of Urea and Triazole derivatives in her study of In vitro.
Between 1997 and 2010, her most popular works were:
- Distinct Mechanism for Antidepressant Activity by Blockade of Central Substance P Receptors (932 citations)
- Receptor for motilin identified in the human gastrointestinal system. (359 citations)
- Peroxisome Proliferator-Activated Receptors γ and α Mediate in Vivo Regulation of Uncoupling Protein (UCP-1, UCP-2, UCP-3) Gene Expression (263 citations)
In her most recent research, the most cited papers focused on:
Margaret A. Cascieri mostly deals with Receptor, Agonist, Pharmacology, Internal medicine and Endocrinology.
Her Receptor research entails a greater understanding of Biochemistry.
Within one scientific family, Margaret A. Cascieri focuses on topics pertaining to Glucagon under Biochemistry, and may sometimes address concerns connected to Transmembrane domain and Glucagon-like peptide 1 receptor.
The various areas that Margaret A. Cascieri examines in her Agonist study include Chemical synthesis, Bioavailability, Lipolysis and Stereochemistry.
Her research ties Antagonist and Stereochemistry together.
Her biological study spans a wide range of topics, including Blockade, Gene and Peptide.
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