What is he best known for?
The fields of study he is best known for:
- Gene
- Phosphorylation
- Apoptosis
Andrew C. Larner mainly focuses on Tyrosine phosphorylation, Molecular biology, Phosphorylation, Signal transduction and Cell biology.
His Tyrosine phosphorylation research includes themes of ROR1, Tyrosine kinase and Cancer research.
The Molecular biology study combines topics in areas such as STAT2, STAT3 and SH2 domain.
His study on Phosphorylation is mostly dedicated to connecting different topics, such as Transcription factor.
Andrew C. Larner works in the field of Signal transduction, focusing on STAT protein in particular.
His studies deal with areas such as Receptor tyrosine kinase and JAK-STAT signaling pathway as well as Protein tyrosine phosphatase.
His most cited work include:
- Enhanced DNA-binding activity of a Stat3-related protein in cells transformed by the Src oncoprotein (860 citations)
- Function of Mitochondrial Stat3 in Cellular Respiration (679 citations)
- Mitochondrial STAT3 supports Ras-dependent oncogenic transformation. (523 citations)
What are the main themes of his work throughout his whole career to date?
Andrew C. Larner focuses on Cell biology, Molecular biology, Tyrosine phosphorylation, Signal transduction and Transcription factor.
In his study, T-cell receptor, Programmed cell death and Apoptosis is strongly linked to Cytokine, which falls under the umbrella field of Cell biology.
RNA is closely connected to Transcription in his research, which is encompassed under the umbrella topic of Molecular biology.
His Tyrosine phosphorylation research integrates issues from Tyrosine kinase, Cancer research and Receptor tyrosine kinase.
His Signal transduction study results in a more complete grasp of Biochemistry.
Andrew C. Larner works mostly in the field of Transcription factor, limiting it down to concerns involving Interferon gamma and, occasionally, Phosphatase.
He most often published in these fields:
- Cell biology (51.14%)
- Molecular biology (42.05%)
- Tyrosine phosphorylation (38.64%)
What were the highlights of his more recent work (between 2010-2020)?
- Cell biology (51.14%)
- Mitochondrion (18.18%)
- STAT3 (20.45%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Mitochondrion, STAT3, Transcription factor and Electron Transport Complex I.
His study in the field of Wnt signaling pathway also crosses realms of Mitophagy.
The STAT3 study which covers Molecular biology that intersects with Serine.
His Transcription factor research incorporates themes from Adipose tissue, Endocrinology, Internal medicine, Signal transduction and STAT protein.
To a larger extent, Andrew C. Larner studies Biochemistry with the aim of understanding Signal transduction.
His research in Oxidative stress intersects with topics in Mitochondrial apoptosis-induced channel and Tyrosine phosphorylation.
Between 2010 and 2020, his most popular works were:
- Mitochondrial-targeted Signal Transducer and Activator of Transcription 3 (STAT3) Protects against Ischemia-induced Changes in the Electron Transport Chain and the Generation of Reactive Oxygen Species (155 citations)
- The Import of the Transcription Factor STAT3 into Mitochondria Depends on GRIM-19, a Component of the Electron Transport Chain (128 citations)
- Mitochondrial localized Stat3 promotes breast cancer growth via phosphorylation of serine 727. (112 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Mitochondrion, Cell biology, STAT3, Electron Transport Complex I and Transcription factor.
His study looks at the intersection of Mitochondrion and topics like STAT2 with STAT5, STAT6 and STAT1.
His Cell biology study typically links adjacent topics like Molecular biology.
Andrew C. Larner interconnects Cytoprotection, Oxidative phosphorylation and Electron transport chain in the investigation of issues within ATP–ADP translocase.
The various areas that Andrew C. Larner examines in his Mitochondrial transport study include Chaperone and Inner mitochondrial membrane.
His STAT protein study contributes to a more complete understanding of Phosphorylation.
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