What is she best known for?
The fields of study she is best known for:
- Enzyme
- Biochemistry
- Internal medicine
Her primary scientific interests are in Receptor, Biochemistry, Internal medicine, Cell biology and Agonist.
Her Receptor research integrates issues from Signal transduction and Secretin receptor.
Her Secretin receptor research is multidisciplinary, incorporating elements of Pharmacophore and Secretin receptor family.
Her Internal medicine study combines topics in areas such as Gastroenterology, Chondrocyte and Endocrinology.
The study incorporates disciplines such as Homologous desensitization, Internalization, Cell growth and Transmembrane domain in addition to Cell biology.
Her Glucagon-like peptide 1 receptor study combines topics from a wide range of disciplines, such as Enzyme-linked receptor, Allosteric regulation and Ligand.
Her most cited work include:
- Seven Transmembrane Receptors as Shapeshifting Proteins: The Impact of Allosteric Modulation and Functional Selectivity on New Drug Discovery (494 citations)
- Study of recurrence after surgical resection of intraductal papillary mucinous neoplasm of the pancreas. (430 citations)
- International Union of Pharmacology. XXXV. The Glucagon Receptor Family (393 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of study are Receptor, Biochemistry, Cholecystokinin receptor, Internal medicine and G protein-coupled receptor.
Her Receptor research is multidisciplinary, incorporating perspectives in Secretin receptor, Peptide and Cell biology.
The Secretin receptor study combines topics in areas such as Secretin receptor family and G protein.
Laurence J. Miller studied Biochemistry and Biophysics that intersect with Transmembrane domain.
Laurence J. Miller has researched Cholecystokinin receptor in several fields, including Binding site, Affinity labeling, Stereochemistry, Acinar cell and Allosteric regulation.
Her Internal medicine study integrates concerns from other disciplines, such as Gastroenterology and Endocrinology.
She most often published in these fields:
- Receptor (59.06%)
- Biochemistry (38.46%)
- Cholecystokinin receptor (26.30%)
What were the highlights of her more recent work (between 2012-2021)?
- Receptor (59.06%)
- G protein-coupled receptor (22.33%)
- Cell biology (17.62%)
In recent papers she was focusing on the following fields of study:
Laurence J. Miller mainly investigates Receptor, G protein-coupled receptor, Cell biology, Biophysics and Biochemistry.
Her research investigates the connection between Receptor and topics such as Peptide that intersect with problems in Extracellular.
Her G protein-coupled receptor research incorporates elements of Secretin receptor, Function, Transmembrane protein, Transmembrane domain and Binding site.
Her research integrates issues of RAMP1, Membrane protein, Calcitonin receptor and Cell membrane in her study of Cell biology.
Her Biophysics course of study focuses on Ligand and Stereochemistry and Protein structure.
Her biological study deals with issues like Pharmacology, which deal with fields such as Endogeny.
Between 2012 and 2021, her most popular works were:
- Phase-plate cryo-EM structure of a class B GPCR–G-protein complex (277 citations)
- Phase-plate cryo-EM structure of a biased agonist-bound human GLP-1 receptor-Gs complex. (159 citations)
- Phase-plate cryo-EM structure of a biased agonist-bound human GLP-1 receptor-Gs complex. (159 citations)
In her most recent research, the most cited papers focused on:
- Enzyme
- Biochemistry
- Amino acid
Her primary areas of investigation include Receptor, Cell biology, G protein-coupled receptor, Transmembrane domain and Functional selectivity.
Receptor is a subfield of Biochemistry that Laurence J. Miller explores.
Her Cell biology study incorporates themes from RAMP1, Calcitonin receptor and Cell membrane.
Her work deals with themes such as Heterotrimeric G protein, Tetrazine, Binding site and Transmembrane protein, which intersect with G protein-coupled receptor.
Her research investigates the link between Functional selectivity and topics such as Glucagon-like peptide 1 receptor that cross with problems in Bioinformatics.
Her Agonist research focuses on subjects like Ligand, which are linked to Protein structure.
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