James D. Marks mostly deals with Antibody, Molecular biology, Antigen, Phage display and Monoclonal antibody. James D. Marks has included themes like Polypeptide chain, Nucleic acid, Endocytosis and Virology in his Antibody study. The various areas that James D. Marks examines in his Molecular biology study include Mutant, Affinity maturation, Immunoglobulin light chain, Internalization and In vivo.
His studies deal with areas such as Receptor–ligand kinetics, In vitro and Genomic library as well as Antigen. His Phage display research includes elements of Red blood cell and Hybridoma technology. His Monoclonal antibody study combines topics from a wide range of disciplines, such as Immunohistochemistry and Epidermal growth factor.
James D. Marks spends much of his time researching Antibody, Molecular biology, Monoclonal antibody, Antigen and Virology. James D. Marks works in the field of Antibody, focusing on Epitope in particular. The study incorporates disciplines such as In vitro, Affinity maturation, Immunoglobulin light chain, Phage display and In vivo in addition to Molecular biology.
His work carried out in the field of Phage display brings together such families of science as Peptide library and Fusion protein. His Monoclonal antibody research incorporates elements of Cancer research and Neutralization. His Antigen research includes themes of Cell surface receptor and Cell culture.
His primary areas of investigation include Antibody, Monoclonal antibody, Molecular biology, Cancer research and Epitope. His study of Phage display is a part of Antibody. James D. Marks has researched Monoclonal antibody in several fields, including Recombinant DNA, Virology, Neutralization, Botulism and Antitoxin.
His study looks at the relationship between Molecular biology and topics such as In vivo, which overlap with Cancer cell. His Cancer research research is multidisciplinary, incorporating perspectives in Cell, Ephrin, Cancer, Immunology and Erythropoietin-producing hepatocellular receptor. As a part of the same scientific family, James D. Marks mostly works in the field of Epitope, focusing on Single-Chain Antibodies and, on occasion, Endopeptidase.
His main research concerns Antibody, Molecular biology, Epitope, Monoclonal antibody and In vivo. The Antibody study combines topics in areas such as Cancer research, Tumor microenvironment, Clostridium botulinum, Cancer immunotherapy and Botulism. His studies in Molecular biology integrate themes in fields like Biodistribution, Carcinogenesis, Toxin, Antigen and Microarray.
As part of one scientific family, James D. Marks deals mainly with the area of Epitope, narrowing it down to issues related to the Biochemistry, and often Ethylene glycol. His Monoclonal antibody research integrates issues from Antitoxin and Virology. His In vivo study combines topics in areas such as Immunoliposome, Pharmacokinetics, Liposome, Phage display and Drug.
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Methods for producing members of specific binding pairs
John Mccafferty;Anthony Richard Pope;Kevin Stuart Johnson;Hendricus Renerus Jacobus Mattheus Hoogenboom.
(1991)
By-passing immunization: Human antibodies from V-gene libraries displayed on phage
James D. Marks;Hennie R. Hoogenboom;Timothy P. Bonnert;John McCafferty.
Journal of Molecular Biology (1991)
Production of anti-self antibodies from antibody segment repertoires and displayed on phage
Andrew David Griffiths;Hendricus Renerus Jacobus Mattheus Hoogenboom;James David Marks;John Mccafferty.
(1992)
Human anti‐self antibodies with high specificity from phage display libraries.
A D Griffiths;M Malmqvist;J D Marks;J M Bye.
The EMBO Journal (1993)
Antibody targeting of long-circulating lipidic nanoparticles does not increase tumor localization but does increase internalization in animal models.
Dmitri B. Kirpotin;Daryl C. Drummond;Yi Shao;M. Refaat Shalaby.
Cancer Research (2006)
Multivalent and multispecific binding proteins, their manufacture and use
Kaspar-Philipp Holliger;Andrew David Griffiths;Hendricus Renerus Jacobus Matheus Hoogenboom;Magnus Malmqvist.
(1993)
By-passing immunization: building high affinity human antibodies by chain shuffling.
James D. Marks;Andrew D. Griffiths;Magnus Malmqvist;Tim P. Clackson.
Nature Biotechnology (1992)
Anti-HER2 immunoliposomes: enhanced efficacy attributable to targeted delivery.
John W Park;Keelung Hong;Dmitri B Kirpotin;Gail Colbern.
Clinical Cancer Research (2002)
The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops.
Ian M. Tomlinson;Gerald Walter;James D. Marks;Meirion B. Llewelyn.
Journal of Molecular Biology (1992)
High affinity restricts the localization and tumor penetration of single-chain fv antibody molecules.
Gregory P. Adams;Robert Schier;Adrian M. McCall;Heidi H. Simmons.
Cancer Research (2001)
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