Molecular biology, Genetics, Biochemistry, Gene and Cell culture are his primary areas of study. His research in Molecular biology intersects with topics in Mutation, Receptor, Ectodomain and Cytoplasm. His study explores the link between Cell culture and topics such as Myeloid that cross with problems in In vitro, Antibody-dependent cell-mediated cytotoxicity, Bone marrow, Interleukin and CD19.
His In vitro research integrates issues from Leukemia and Antigen. His study looks at the relationship between Leukemia and fields such as Tumor necrosis factor alpha, as well as how they intersect with chemical problems. Georg H. Fey has researched Antibody in several fields, including Programmed cell death and Virology.
His main research concerns Molecular biology, Antigen, Antibody, Cancer research and CD19. His Molecular biology study combines topics in areas such as Cell culture, Gene, Recombinant DNA, Antibody-dependent cell-mediated cytotoxicity and Immunotoxin. His Antibody-dependent cell-mediated cytotoxicity research includes elements of Immunoglobulin G and Avidity.
His study in Antigen is interdisciplinary in nature, drawing from both Phage display, Stem cell and Minimal residual disease. The study incorporates disciplines such as Virology, Natural killer cell, Cytolysis, Pseudomonas exotoxin and Lysis in addition to Antibody. His work carried out in the field of Cancer research brings together such families of science as Apoptosis, Leukemia, Immunology and Immunotherapy.
His scientific interests lie mostly in Cancer research, Immunotherapy, Antigen, Antibody and Immunology. His Cancer research research is multidisciplinary, relying on both T cell, Dual targeting and Cancer immunotherapy. His Immunotherapy research includes themes of Molecular biology and Immunotoxin.
Georg H. Fey has included themes like Antibody-dependent cell-mediated cytotoxicity, Fusion protein, Cytolysis, Cell cycle and Cell biology in his Molecular biology study. Georg H. Fey usually deals with Antigen and limits it to topics linked to Myeloid leukemia and Adoptive cell transfer, CD135, Stem cell and Chimeric antigen receptor. As a part of the same scientific study, he usually deals with the Antibody, concentrating on Lysis and frequently concerns with Cancer cell.
His primary scientific interests are in Molecular biology, Immunotherapy, Antibody, Antigen and Chimeric antigen receptor. The various areas that Georg H. Fey examines in his Molecular biology study include Cell, Cytokine and HLA-DR Antigen. The concepts of his Immunotherapy study are interwoven with issues in Cell cycle, Immunotoxin and Fusion protein.
His Antibody research entails a greater understanding of Immunology. His work in the fields of CD19 overlaps with other areas such as CD16. His Chimeric antigen receptor research incorporates elements of CD28, Transfection, RNA transfection and Cell biology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
T Cell-Specific siRNA Delivery Suppresses HIV-1 Infection in Humanized Mice
Priti Kumar;Hong Seok Ban;Sang Soo Kim;Haoquan Wu.
Cell (2008)
Human complement component C3: cDNA coding sequence and derived primary structure
M H de Bruijn;G H Fey.
Proceedings of the National Academy of Sciences of the United States of America (1985)
Susceptibility to SARS coronavirus S protein-driven infection correlates with expression of angiotensin converting enzyme 2 and infection can be blocked by soluble receptor.
Heike Hofmann;Martina Geier;Andrea Marzi;Mandy Krumbiegel.
Biochemical and Biophysical Research Communications (2004)
Transcription Factors Stat3 and Stat5b Are Present in Rat Liver Nuclei Late in an Acute Phase Response and Bind Interleukin-6 Response Elements
Juergen A. Ripperger;Stefan Fritz;Karin Richter;Gertrud M. Hocke.
Journal of Biological Chemistry (1995)
Sequence of rat liver alpha 2-macroglobulin and acute phase control of its messenger RNA.
M. R. Gehring;B. R. Shiels;W. Northemann;M. H. L. De Bruijn.
Journal of Biological Chemistry (1987)
A recombinant trispecific single‐chain Fv derivative directed against CD123 and CD33 mediates effective elimination of acute myeloid leukaemia cells by dual targeting
Markus Kügler;Christoph Stein;Christian Kellner;Kristin Mentz.
British Journal of Haematology (2010)
Exon/intron structure of the human ALL‐1 (MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias
I. Nilson;K. LöCHNER;G. Siegler;J. Greil.
British Journal of Haematology (1996)
Targeting of DEC-205 on human dendritic cells results in efficient MHC class II-restricted antigen presentation.
Katrin Birkholz;Michael Schwenkert;Christian Kellner;Stefanie Gross.
Blood (2010)
The acute lymphoblastic leukaemia cell line SEM with t(4;11) chromosomal rearrangement is biphenotypic and responsive to interleukin-7.
Johann Greil;Martin Gramatzki;Renate Burger;Rolf Marschalek.
British Journal of Haematology (1994)
Target cell-restricted apoptosis induction of acute leukemic T cells by a recombinant tumor necrosis factor-related apoptosis-inducing ligand fusion protein with specificity for human CD7
Edwin Bremer;Douwe F. Samplonius;Matthias Peipp;Linda van Genne.
Cancer Research (2005)
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