What is she best known for?
The fields of study she is best known for:
Debbie L. Hay mainly focuses on Receptor, Receptor activity-modifying protein, Calcitonin gene-related peptide, Calcitonin receptor and Internal medicine.
Her biological study spans a wide range of topics, including Signal transduction, Neuroscience, Pharmacology and Bioinformatics.
The various areas that Debbie L. Hay examines in her Receptor activity-modifying protein study include Agonist, G protein-coupled receptor, RAMP2 and Receptor Activity-Modifying Protein 1.
Her research integrates issues of Calcitonin and Cell biology in her study of Calcitonin gene-related peptide.
Her Calcitonin receptor study frequently intersects with other fields, such as CALCRL.
Internal medicine is closely attributed to Endocrinology in her study.
Her most cited work include:
- Oxyntomodulin inhibits food intake in the rat. (295 citations)
- GPCR modulation by RAMPs (200 citations)
- Pharmacological discrimination of calcitonin receptor - receptor activity modifying protein complexes (158 citations)
What are the main themes of her work throughout her whole career to date?
Her main research concerns Receptor, Calcitonin gene-related peptide, Calcitonin receptor, Receptor activity-modifying protein and RAMP1.
Debbie L. Hay has researched Receptor in several fields, including Calcitonin, Endocrinology and Pharmacology.
As a part of the same scientific family, Debbie L. Hay mostly works in the field of Calcitonin gene-related peptide, focusing on Amylin and, on occasion, Peptide hormone.
Her Calcitonin receptor study which covers Enzyme-linked receptor that intersects with Interleukin-21 receptor.
Her Receptor activity-modifying protein research is multidisciplinary, relying on both Plasma protein binding, Stereochemistry and CALCRL.
Her RAMP1 research incorporates elements of Protein structure, RAMP2 and Receptor Activity-Modifying Protein 1.
She most often published in these fields:
- Receptor (66.87%)
- Calcitonin gene-related peptide (58.12%)
- Calcitonin receptor (42.50%)
What were the highlights of her more recent work (between 2018-2021)?
- Receptor (66.87%)
- Calcitonin gene-related peptide (58.12%)
- Calcitonin (25.63%)
In recent papers she was focusing on the following fields of study:
Receptor, Calcitonin gene-related peptide, Calcitonin, G protein-coupled receptor and Cell biology are her primary areas of study.
Debbie L. Hay studied Receptor and Amylin that intersect with Ligand.
Her Calcitonin gene-related peptide study combines topics from a wide range of disciplines, such as Photophobia, Endocrinology and Pharmacology.
Debbie L. Hay regularly links together related areas like Receptor activity-modifying protein in her G protein-coupled receptor studies.
Her work in Receptor activity-modifying protein addresses issues such as Receptor Activity-Modifying Protein 1, which are connected to fields such as Internalization.
Her research in RAMP1 tackles topics such as RAMP2 which are related to areas like RAMP3, CALCRL and Corticotropin-releasing hormone receptor 1.
Between 2018 and 2021, her most popular works were:
- Molecular studies of CGRP and the CGRP family of peptides in the central nervous system. (31 citations)
- Structure and Dynamics of Adrenomedullin Receptors AM1 and AM2 Reveal Key Mechanisms in the Control of Receptor Phenotype by Receptor Activity-Modifying Proteins. (29 citations)
- New Insights into the Regulation of CGRP-Family Receptors. (18 citations)
In her most recent research, the most cited papers focused on:
- Gene
- Amino acid
- Biochemistry
Debbie L. Hay mainly investigates Receptor, G protein-coupled receptor, Cell biology, Receptor activity-modifying protein and Adrenomedullin.
She studies Receptor, namely Calcitonin gene-related peptide.
The subject of her Calcitonin gene-related peptide research is within the realm of Internal medicine.
In her work, Calcitonin and Cell signaling is strongly intertwined with Calcitonin receptor, which is a subfield of Cell biology.
Her Receptor activity-modifying protein research is multidisciplinary, incorporating perspectives in RAMP1, Amino acid peptide and Receptor Activity-Modifying Protein 1.
Her RAMP1 study combines topics in areas such as Internalization, RAMP3, RAMP2 and CALCRL.
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