What is she best known for?
The fields of study she is best known for:
Her primary areas of investigation include Epitope, Peptide sequence, Molecular biology, Biochemistry and Virology.
Her research in Epitope intersects with topics in T cell, Ligand binding assay and Viral protein.
Her study looks at the relationship between Peptide sequence and topics such as Major histocompatibility complex, which overlap with Cell.
Elisabetta Bianchi works in the field of Biochemistry, focusing on Peptide in particular.
Her Virology research is multidisciplinary, relying on both Turn, Gp41, Antigen, Peptidomimetic and Binding site.
In her study, which falls under the umbrella issue of Peptidomimetic, NS3, Protease and Stereochemistry is strongly linked to Product inhibition.
Her most cited work include:
- Aggregates from mutant and wild-type α-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of β-sheet and amyloid-like filaments (320 citations)
- Glucagon-Like Peptide 1/Glucagon Receptor Dual Agonism Reverses Obesity in Mice (316 citations)
- Solid Phase Synthesis of Peptide C-Terminal Thioesters by Fmoc/t-Bu Chemistry (251 citations)
What are the main themes of her work throughout her whole career to date?
Elisabetta Bianchi spends much of her time researching Peptide, Biochemistry, Virology, NS3 and Stereochemistry.
Her Peptide research incorporates themes from Amino acid, Peptide library, Cleavage and Receptor.
Much of her study explores Biochemistry relationship to Molecular biology.
Her Virology study combines topics from a wide range of disciplines, such as Epitope, Antibody, Gp41, Antigen and Immune system.
Her work focuses on many connections between NS3 and other disciplines, such as Serine protease, that overlap with her field of interest in Binding site.
Her Stereochemistry research integrates issues from Solid-phase synthesis, Protein design, Sequence and Polyamide.
She most often published in these fields:
- Peptide (34.11%)
- Biochemistry (28.68%)
- Virology (23.26%)
What were the highlights of her more recent work (between 2010-2021)?
- Receptor (11.63%)
- Internal medicine (9.30%)
- Endocrinology (9.30%)
In recent papers she was focusing on the following fields of study:
Her primary scientific interests are in Receptor, Internal medicine, Endocrinology, Glucagon and Peptide.
Her Glucagon research is multidisciplinary, incorporating elements of Agonist and Dipeptidyl peptidase.
Her research investigates the connection between Agonist and topics such as Oxyntomodulin that intersect with issues in Glucagon receptor.
Her Dipeptidyl peptidase study also includes fields such as
- Peptide library and Phage display most often made with reference to Glucagon-like peptide 1 receptor,
- Peptide analog which is related to area like Fatty liver.
Peptide is a subfield of Biochemistry that she studies.
Binding site is the focus of her Biochemistry research.
Between 2010 and 2021, her most popular works were:
- The Glucagon Receptor Is Involved in Mediating the Body Weight-Lowering Effects of Oxyntomodulin (85 citations)
- DPP‐IV‐resistant, long‐acting oxyntomodulin derivatives (68 citations)
- A PEGylated analog of the gut hormone oxyntomodulin with long-lasting antihyperglycemic, insulinotropic and anorexigenic activity. (38 citations)
In her most recent research, the most cited papers focused on:
Elisabetta Bianchi mostly deals with Internal medicine, Receptor, Endocrinology, Glucagon and Oxyntomodulin.
Her studies examine the connections between Internal medicine and genetics, as well as such issues in PEGylation, with regards to Glucagon-like peptide 1 receptor.
Her Glucagon study integrates concerns from other disciplines, such as Agonist and Dipeptidyl peptidase.
Elisabetta Bianchi combines subjects such as Hormone and Peptide hormone with her study of Dipeptidyl peptidase.
Her Endogeny research includes elements of Human serum albumin, Energy homeostasis, Anorectic and Peptide.
Her Glucagon receptor study incorporates themes from Antagonist and Mechanism of action.
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