What is she best known for?
The fields of study she is best known for:
Her main research concerns Biochemistry, Internal medicine, Endocrinology, Metabolism and Amino acid.
Her work in Biochemistry addresses subjects such as Molecular biology, which are connected to disciplines such as Bone morphogenetic protein 2.
She has included themes like Leucine, Glutamine and Binding protein in her Internal medicine study.
Her research in Metabolism intersects with topics in Pyruvate carboxylase and Phosphorylation.
Her Amino acid study combines topics from a wide range of disciplines, such as Catabolism, Transaminase and Isozyme.
In Branched-chain amino acid, Susan M. Hutson works on issues like Mitochondrion, which are connected to Alanine and Transamination.
Her most cited work include:
- Obesity-related elevations in plasma leucine are associated with alterations in enzymes involved in branched-chain amino acid metabolism (320 citations)
- FGF21 is an endocrine signal of protein restriction (290 citations)
- A molecular model of human branched-chain amino acid metabolism. (282 citations)
What are the main themes of her work throughout her whole career to date?
Her primary scientific interests are in Biochemistry, Branched chain aminotransferase, Amino acid, Internal medicine and Endocrinology.
Her research in Leucine, Branched-chain amino acid, Transamination, Enzyme and Mitochondrion are components of Biochemistry.
The various areas that Susan M. Hutson examines in her Branched-chain amino acid study include Enzyme complex and Glutamate dehydrogenase.
Her Branched chain aminotransferase research incorporates themes from Molecular biology, Cysteine, Alanine, Stereochemistry and Isozyme.
Her research investigates the connection between Amino acid and topics such as Kinase that intersect with problems in Maple syrup urine disease.
Her Internal medicine study incorporates themes from Glutamine and Phosphorylation.
She most often published in these fields:
- Biochemistry (65.22%)
- Branched chain aminotransferase (34.78%)
- Amino acid (28.26%)
What were the highlights of her more recent work (between 2011-2020)?
- Leucine (24.64%)
- Biochemistry (65.22%)
- Internal medicine (26.81%)
In recent papers she was focusing on the following fields of study:
Susan M. Hutson spends much of her time researching Leucine, Biochemistry, Internal medicine, Endocrinology and Amino acid.
Her study in Leucine is interdisciplinary in nature, drawing from both PI3K/AKT/mTOR pathway and Signal transduction.
Her study in Catabolism, Branched chain aminotransferase, mTORC1 and Enzyme falls under the purview of Biochemistry.
The study incorporates disciplines such as Temporal cortex, Excitotoxicity, Molecular biology, Dementia with Lewy bodies and Alanine in addition to Branched chain aminotransferase.
Susan M. Hutson interconnects Function and Phosphorylation in the investigation of issues within Internal medicine.
Her research investigates the connection with Amino acid and areas like Kinase which intersect with concerns in Allosteric regulation and Maple syrup urine disease.
Between 2011 and 2020, her most popular works were:
- FGF21 is an endocrine signal of protein restriction (290 citations)
- BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1 (248 citations)
- Branched-Chain Amino Acids and Brain Metabolism. (60 citations)
In her most recent research, the most cited papers focused on:
Her main research concerns Biochemistry, Amino acid, Leucine, Metabolism and mTORC1.
She combines subjects such as Kinase and Valine with her study of Leucine.
Internal medicine and Endocrinology are the subject areas of her Metabolism study.
Her study on Starvation and Endocrine system is often connected to Eukaryotic initiation factor and Ketogenic diet as part of broader study in Internal medicine.
Her mTORC1 research focuses on T cell and how it connects with Branched chain aminotransferase, Lymphocyte, Cyclosporin a and PI3K/AKT/mTOR pathway.
Her biological study spans a wide range of topics, including Wild type, Transaminase, Cell growth and Isocitrate dehydrogenase.
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