What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Immune system
His primary scientific interests are in Inflammation, Immunology, Cell biology, Leukocyte Rolling and Cell adhesion.
His biological study spans a wide range of topics, including LDL receptor, Endocrinology and Pathology.
His studies deal with areas such as Molecular biology and Endothelium as well as Immunology.
His Cell biology research incorporates themes from Cell, Foam cell and Actin cytoskeleton.
Klaus Ley combines subjects such as E-selectin, Lymphocyte function-associated antigen 1, L-selectin, Selectin and Venule with his study of Leukocyte Rolling.
His Cell adhesion study combines topics from a wide range of disciplines, such as Extracellular, Intercellular Adhesion Molecule-1, Cell adhesion molecule and Integrin.
His most cited work include:
- Monocyte and Macrophage Dynamics During Atherogenesis (386 citations)
- Interleukin-17 Signaling in Inflammatory, Kupffer Cells, and Hepatic Stellate Cells Exacerbates Liver Fibrosis in Mice (364 citations)
- Selectins in T-cell recruitment to non-lymphoid tissues and sites of inflammation. (362 citations)
What are the main themes of his work throughout his whole career to date?
Klaus Ley spends much of his time researching Immunology, Cell biology, Inflammation, Molecular biology and Leukocyte Rolling.
Immunology and In vivo are frequently intertwined in his study.
His studies in Cell biology integrate themes in fields like Adhesion, Cell adhesion, Integrin and Chemotaxis.
His Inflammation study incorporates themes from Tumor necrosis factor alpha, Endocrinology and Pathology.
His Molecular biology study integrates concerns from other disciplines, such as P-selectin glycoprotein ligand-1, P-selectin and Granulocyte.
His study focuses on the intersection of Leukocyte Rolling and fields such as Selectin with connections in the field of E-selectin, Glycoprotein and Biochemistry.
He most often published in these fields:
- Immunology (43.89%)
- Cell biology (26.09%)
- Inflammation (28.16%)
What were the highlights of his more recent work (between 2015-2021)?
- Immunology (43.89%)
- Inflammation (28.16%)
- Cell biology (26.09%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Immunology, Inflammation, Cell biology, Immune system and Cell.
His Immunology research focuses on Disease and how it connects with Immunity.
His study looks at the relationship between Inflammation and fields such as Apolipoprotein E, as well as how they intersect with chemical problems.
His work carried out in the field of Cell biology brings together such families of science as Chemokine, Integrin and Chemotaxis.
The Integrin study combines topics in areas such as Adhesion, Cancer research, Lymphocyte and Ligand.
The various areas that he examines in his Cell study include Glycocalyx and Phenotype, Gene, RNA, Mass cytometry.
Between 2015 and 2021, his most popular works were:
- Integrin-based therapeutics: biological basis, clinical use and new drugs (199 citations)
- Single-Cell RNA-Seq Reveals the Transcriptional Landscape and Heterogeneity of Aortic Macrophages in Murine Atherosclerosis (192 citations)
- Oxidized phospholipids are proinflammatory and proatherogenic in hypercholesterolaemic mice (163 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Immune system
His scientific interests lie mostly in Immunology, Cell biology, Inflammation, Cell and Integrin.
His study ties his expertise on Macrophage together with the subject of Immunology.
His Cell biology research is multidisciplinary, incorporating elements of Chemokine, Interleukin 21 and Natural killer T cell.
The study incorporates disciplines such as Phagocytosis, LDL receptor, Pathology, Apolipoprotein E and In vivo in addition to Inflammation.
His biological study deals with issues like CX3CR1, which deal with fields such as Intravital microscopy.
His research in Integrin intersects with topics in Cancer research, Lymphocyte homing receptor, Lymphocyte, Transmembrane domain and Topology.
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