What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Cell biology, Tetraspanin, CD81, Integrin and Membrane protein.
Eric Rubinstein has researched Cell biology in several fields, including Transmembrane domain and Transmembrane protein.
His study on CD82 is often connected to APH-1 as part of broader study in Tetraspanin.
His CD81 research is multidisciplinary, incorporating perspectives in Molecular biology, Digitonin, CD151 and Circumsporozoite protein.
His Integrin research focuses on Transfection and how it relates to Raji cell, Fibronectin, Laminin, HLA-DR and Antigen-presenting cell.
He is studying Integral membrane protein, which is a component of Membrane protein.
His most cited work include:
- Severely Reduced Female Fertility in CD9-Deficient Mice (531 citations)
- The tetraspanin CD63 regulates ESCRT-independent and -dependent endosomal sorting during melanogenesis. (412 citations)
- CD9, CD63, CD81, and CD82 are components of a surface tetraspan network connected to HLA-DR and VLA integrins (339 citations)
What are the main themes of his work throughout his whole career to date?
Cell biology, Tetraspanin, CD81, Molecular biology and Integrin are his primary areas of study.
Eric Rubinstein studied Cell biology and Transmembrane protein that intersect with Signal transduction.
His Tetraspanin research is multidisciplinary, incorporating elements of Plasma protein binding, Cell migration, Membrane protein and Cancer research.
His research investigates the connection between CD81 and topics such as Receptor that intersect with issues in Intracellular and Immunology.
The various areas that he examines in his Molecular biology study include Cell culture, Antigen, Platelet activation and Antibody, Monoclonal antibody.
His work is dedicated to discovering how Integrin, Transmembrane domain are connected with Digitonin and Compartmentalization and other disciplines.
He most often published in these fields:
- Cell biology (77.84%)
- Tetraspanin (78.44%)
- CD81 (44.31%)
What were the highlights of his more recent work (between 2016-2020)?
- Cell biology (77.84%)
- Tetraspanin (78.44%)
- Notch signaling pathway (12.57%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Tetraspanin, Notch signaling pathway, CD81 and Receptor.
While working on this project, Eric Rubinstein studies both Cell biology and ADAM10.
Eric Rubinstein has included themes like Cancer research, Cell migration, Gene knockdown, T cell and Monoclonal antibody in his Tetraspanin study.
His biological study deals with issues like Endoplasmic reticulum, which deal with fields such as Tissue homeostasis, Signal transduction, Molecular biology, Transfection and Cell culture.
His studies examine the connections between CD81 and genetics, as well as such issues in Membrane, with regards to Viral protein, Flow cytometry, Viral replication and Budding.
Eric Rubinstein works mostly in the field of Receptor, limiting it down to concerns involving Virology and, occasionally, Plasmodium and Malaria.
Between 2016 and 2020, his most popular works were:
- Structural Basis for Regulated Proteolysis by the α-Secretase ADAM10 (63 citations)
- Plasmodium P36 determines host cell receptor usage during sporozoite invasion (40 citations)
- Plasmodium P36 determines host cell receptor usage during sporozoite invasion (40 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Cell biology, Notch signaling pathway, Tetraspanin, ADAM10 and Ectodomain.
Eric Rubinstein interconnects Endocytosis and WW domain in the investigation of issues within Cell biology.
His study in Endocytosis is interdisciplinary in nature, drawing from both T cell, Immune system, Antigen presentation, Antigen and Endosome.
His work deals with themes such as Phenotype, Cancer research and CD44, which intersect with Tetraspanin.
His study of ADAM10 brings together topics like Membrane protein, Cell adhesion molecule, Amyloid precursor protein secretase and Proteolysis.
His Intracellular research incorporates themes from Extracellular, Internalization and Notch proteins.
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