What is he best known for?
The fields of study he is best known for:
Ola Larsson mainly investigates Cell biology, EIF4E, mTORC1, Cell growth and Endocrinology.
His Cell biology research integrates issues from Cell culture, Cell and Transcriptome.
His research in EIF4E intersects with topics in Carcinogenesis, Translational regulation, Phosphorylation and Protein biosynthesis.
His Phosphorylation study deals with Epithelial–mesenchymal transition intersecting with Cancer research.
His studies in Protein biosynthesis integrate themes in fields like RNA and Gene expression.
His work in the fields of Endocrinology, such as Adipose tissue, intersects with other areas such as Immunoglobulin M.
His most cited work include:
- Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages (569 citations)
- mTORC1-Mediated Cell Proliferation, But Not Cell Growth, Controlled by the 4E-BPs (528 citations)
- mTORC1 Controls Mitochondrial Activity and Biogenesis through 4E-BP-Dependent Translational Regulation (433 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Cell biology, Cancer research, Translation, Molecular biology and PI3K/AKT/mTOR pathway.
His study in Cell biology is interdisciplinary in nature, drawing from both EIF4E, Messenger RNA and Eukaryotic translation.
His Translation research incorporates elements of Regulation of gene expression, Polysome and Protein biosynthesis.
His Regulation of gene expression study combines topics from a wide range of disciplines, such as Transcriptome and Computational biology.
He works mostly in the field of Molecular biology, limiting it down to concerns involving RNA and, occasionally, Translational efficiency.
Ola Larsson has researched Signal transduction in several fields, including Endocrinology and Internal medicine.
He most often published in these fields:
- Cell biology (31.08%)
- Cancer research (26.35%)
- Translation (20.27%)
What were the highlights of his more recent work (between 2016-2020)?
- Cancer research (26.35%)
- Cell biology (31.08%)
- Translation (20.27%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Cancer research, Cell biology, Translation, PI3K/AKT/mTOR pathway and Gene expression.
His work carried out in the field of Cancer research brings together such families of science as Cancer cell, Cancer, Pancreatic cancer, mTORC1 and Kinase.
Ola Larsson interconnects Eukaryotic translation and Antigen presentation in the investigation of issues within Cell biology.
His Translation study incorporates themes from Regulation of gene expression, In vitro, Polysome and Protein biosynthesis.
His PI3K/AKT/mTOR pathway study combines topics in areas such as EIF4E, Protein kinase B, Transcription and eIF4A.
His work on Transcriptome and Gene expression profiling as part of general Gene expression research is frequently linked to Estrogen receptor alpha, bridging the gap between disciplines.
Between 2016 and 2020, his most popular works were:
- mTOR Controls Mitochondrial Dynamics and Cell Survival via MTFP1 (115 citations)
- A Unique ISR Program Determines Cellular Responses to Chronic Stress (63 citations)
- mTOR-sensitive translation: Cleared fog reveals more trees. (45 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Cell biology, Translation, Transcriptome, mTORC1 and PI3K/AKT/mTOR pathway.
His Cell biology research is multidisciplinary, incorporating perspectives in Immunoprecipitation, Alphavirus, Eukaryotic translation, Tristetraprolin and Adipose tissue.
His Translation research includes themes of Carcinogenesis, Mechanistic target of rapamycin, Protein biosynthesis, Glutamine and In vivo.
The various areas that Ola Larsson examines in his Transcriptome study include Regulation of gene expression, Computational biology and Polysome.
His mTORC1 research incorporates themes from Phagocytosis, TFEB, Lysosome, Antigen presentation and Endosome.
His PI3K/AKT/mTOR pathway research includes elements of Autophagy, EIF4E and Untranslated region.
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