What is he best known for?
The fields of study he is best known for:
Cell biology, Molecular biology, Microinjection, Biochemistry and Cell culture are his primary areas of study.
His studies in Cell biology integrate themes in fields like Gene product, Antibody and Microfilament.
The concepts of his Molecular biology study are interwoven with issues in cDNA library, Gene expression and Cytoplasm.
His study in Microinjection is interdisciplinary in nature, drawing from both Phospholipase A2, Macropinosome, Oncogene and Nucleolus.
His Cell culture study combines topics in areas such as Cell growth, RNA, Antisense RNA, DNA synthesis and Cell cycle.
As a part of the same scientific family, James R. Feramisco mostly works in the field of Phosphorylation, focusing on CREB and, on occasion, Regulation of gene expression, Signal transduction and DNA-binding protein.
His most cited work include:
- Activation of cAMP and mitogen responsive genes relies on a common nuclear factor (685 citations)
- Microinjection of the ras oncogene protein into PC12 cells induces morphological differentiation (617 citations)
- Induction of membrane ruffling and fluid-phase pinocytosis in quiescent fibroblasts by ras proteins (580 citations)
What are the main themes of his work throughout his whole career to date?
James R. Feramisco mainly focuses on Cell biology, Molecular biology, Biochemistry, Microinjection and Signal transduction.
While the research belongs to areas of Cell biology, he spends his time largely on the problem of Microfilament, intersecting his research to questions surrounding Actin.
The concepts of his Molecular biology study are interwoven with issues in Protein phosphatase 2, Cell culture, Gene expression, DNA synthesis and Cell cycle.
The various areas that James R. Feramisco examines in his Cell culture study include Oncogene and Cell division.
His work deals with themes such as Fibroblast and Antibody, which intersect with Microinjection.
As part of the same scientific family, James R. Feramisco usually focuses on Protein kinase A, concentrating on Peptide and intersecting with Stereochemistry, Serine and Amino acid.
He most often published in these fields:
- Cell biology (48.44%)
- Molecular biology (37.50%)
- Biochemistry (21.09%)
What were the highlights of his more recent work (between 2001-2020)?
- Molecular biology (37.50%)
- Cell biology (48.44%)
- Adenylyl cyclase (4.69%)
In recent papers he was focusing on the following fields of study:
James R. Feramisco spends much of his time researching Molecular biology, Cell biology, Adenylyl cyclase, Internal medicine and Cancer research.
James R. Feramisco interconnects Autophagy-related protein 13, Cyclin-dependent kinase 2, Protein kinase C, Signal transduction and Forskolin in the investigation of issues within Molecular biology.
His Cell biology study frequently links to other fields, such as Macrophage.
His Adenylyl cyclase research focuses on Protein kinase B and how it relates to Protein phosphatase 2, Dephosphorylation and Pleckstrin homology domain.
His Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Genetically modified mouse.
His Cancer research study combines topics in areas such as Mutation, Gene mutation and Regulation of gene expression.
Between 2001 and 2020, his most popular works were:
- DNase expression allows the pathogen group A Streptococcus to escape killing in neutrophil extracellular traps. (527 citations)
- Nkx2-5 Pathways and Congenital Heart Disease: Loss of Ventricular Myocyte Lineage Specification Leads to Progressive Cardiomyopathy and Complete Heart Block (361 citations)
- Minimally modified LDL binds to CD14, induces macrophage spreading via TLR4/MD-2, and inhibits phagocytosis of apoptotic cells. (349 citations)
In his most recent research, the most cited papers focused on:
His primary areas of study are Cell biology, Phagocytosis, Macrophage, Innate immune system and Kinase.
He has researched Cell biology in several fields, including RNA splicing and SR protein.
His Phagocytosis research integrates issues from TLR2, TLR4, CD14 and Chinese hamster ovary cell.
His study in Macrophage is interdisciplinary in nature, drawing from both Cytoskeleton, Intracellular, Cell membrane and Phosphoinositide 3-kinase.
His Innate immune system study incorporates themes from Pathogen, Microbiology, Chemotaxis, Neutrophil clearance and Virulence.
His Kinase research includes themes of Molecular biology and Signal transduction, Focal adhesion.
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