What is he best known for?
The fields of study he is best known for:
His main research concerns Programmed cell death, Cell biology, Immune system, Autophagy and Immunology.
His Programmed cell death research is within the category of Apoptosis.
The various areas that Oliver Kepp examines in his Cell biology study include Secretion and Growth factor.
His studies deal with areas such as Cancer cell and Autocrine signalling as well as Immune system.
His study in Autophagy is interdisciplinary in nature, drawing from both Adenosine triphosphate and Intrinsic apoptosis.
His Immunology research is multidisciplinary, incorporating perspectives in Cancer and Cancer research.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012 (1734 citations)
- Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012 (1734 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Cell biology, Programmed cell death, Immunogenic cell death, Cancer research and Autophagy.
His Cell biology research includes themes of Apoptosis and Biochemistry.
His Programmed cell death research integrates issues from Inflammation, Cell and Neuroscience.
The various areas that Oliver Kepp examines in his Immunogenic cell death study include Extracellular, Dendritic cell, Calreticulin and Immune checkpoint.
He combines subjects such as Cancer cell, Cancer, Immunotherapy, Immunology and Lung cancer with his study of Cancer research.
His Autophagy study combines topics in areas such as Transcription factor and Phosphorylation.
He most often published in these fields:
- Cell biology (103.66%)
- Programmed cell death (78.03%)
- Immunogenic cell death (55.15%)
What were the highlights of his more recent work (between 2019-2021)?
- Immunogenic cell death (55.15%)
- Cancer research (55.15%)
- Cell biology (103.66%)
In recent papers he was focusing on the following fields of study:
Oliver Kepp mostly deals with Immunogenic cell death, Cancer research, Cell biology, Immune system and Autophagy.
His Immunogenic cell death study also includes fields such as
- Immunogenicity, Cell and Flow cytometry most often made with reference to Calreticulin,
- Transcription and related DNA.
The study incorporates disciplines such as Malignant cells, Cancer cell, Dendritic cell, Programmed cell death and Immunotherapy in addition to Cancer research.
His work on Endoplasmic reticulum as part of general Cell biology study is frequently connected to Context, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
His Immune system study integrates concerns from other disciplines, such as RNA, Cetuximab and Antigen.
His research integrates issues of Protein kinase B and Phosphorylation in his study of Autophagy.
Between 2019 and 2021, his most popular works were:
- Consensus guidelines for the definition, detection and interpretation of immunogenic cell death (106 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) (38 citations)
- Mitophagy: An Emerging Role in Aging and Age-Associated Diseases. (35 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Cancer research, Immunogenic cell death, Immune system, Cell biology and Autophagy.
His Cancer research course of study focuses on Calreticulin and Cancer cell and Immunogenicity.
His Immune system research includes elements of Photothermal ablation and Antigen.
Oliver Kepp has included themes like Cellular homeostasis, Mitochondrial DNA and Mitophagy in his Cell biology study.
Programmed cell death is closely connected to Mitochondrial fission in his research, which is encompassed under the umbrella topic of Mitophagy.
Oliver Kepp interconnects Phosphatase, Serine, Phosphorylation and Mutant in the investigation of issues within Autophagy.
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