Inger Sandlie mostly deals with Neonatal Fc receptor, Receptor, Molecular biology, Antibody and Immunoglobulin G. Her Neonatal Fc receptor research includes themes of Human serum albumin, Albumin, Biochemistry and Histidine. Her research investigates the connection between Biochemistry and topics such as Complement system that intersect with issues in Peptide sequence.
Her work in Receptor addresses issues such as MHC class I, which are connected to fields such as Residue, Recombinant DNA and Receptor recycling. Inger Sandlie combines subjects such as Mutation, Mutant, Expression vector, Fusion protein and Epitope with her study of Molecular biology. Her research combines Cell biology and Antibody.
Her primary areas of investigation include Molecular biology, Antibody, Cell biology, Antigen and Neonatal Fc receptor. The study incorporates disciplines such as Recombinant DNA, Mutation, Mutant, Peptide sequence and Peptide in addition to Molecular biology. The Antibody study combines topics in areas such as Immune system and Virology.
Her Cell biology course of study focuses on Complement system and Hapten. Her Neonatal Fc receptor study combines topics in areas such as Receptor, Biochemistry, Albumin and Histidine. Her study looks at the relationship between Albumin and fields such as Intracellular, as well as how they intersect with chemical problems.
Her primary areas of study are Cell biology, Antigen, Albumin, Major histocompatibility complex and Epitope. Inger Sandlie interconnects Immunoglobulin G, Complement system, Classical complement pathway, Receptor and Transduction in the investigation of issues within Cell biology. Her Antigen research incorporates themes from Antibody and Immune system.
Inger Sandlie mostly deals with Monoclonal antibody in her studies of Antibody. Her Albumin research integrates issues from Pharmacokinetics and Intracellular. She studied Major histocompatibility complex and T-cell receptor that intersect with Computational biology, Periplasmic space, Protein structure, Chaperone and Biochemistry.
The scientist’s investigation covers issues in Cell biology, Immune system, Complement system, Intracellular and Plasma protein binding. Her Cell biology study combines topics from a wide range of disciplines, such as Immunoglobulin G, Virus, Fc receptor, Transduction and Classical complement pathway. Her studies deal with areas such as Endothelial stem cell, Cellular Assay, Albumin, Genetically modified mouse and Serum albumin as well as Immunoglobulin G.
Inger Sandlie has included themes like Epitope and Antibody in her Immune system study. She has researched Antibody in several fields, including Biophysics, Bivalent, Immune tolerance, Antigen and DNA origami. Her studies in Complement system integrate themes in fields like Transgene, Cell membrane, Viral replication, Antibody receptor and Effector.
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Therapeutic antibodies for human diseases at the dawn of the twenty-first century
Ole Henrik Brekke;Inger Sandlie.
Nature Reviews Drug Discovery (2003)
Competition for FcRn-mediated transport gives rise to short half-life of human IgG3 and offers therapeutic potential
Nigel M. Stapleton;Jan Terje Andersen;Jan Terje Andersen;Annette M. Stemerding;Stefania P. Bjarnarson.
Nature Communications (2011)
Versatile vectors for transient and stable expression of recombinant antibody molecules in mammalian cells
Lars Norderhaug;Tove Olafsen;Terje E Michaelsen;Inger Sandlie.
Journal of Immunological Methods (1997)
Unraveling the Interaction between FcRn and Albumin: Opportunities for Design of Albumin-Based Therapeutics
Kine Marita Knudsen Sand;Kine Marita Knudsen Sand;Malin C. Bern;Malin C. Bern;Jeannette Nilsen;Jeannette Nilsen;Hanna Theodora Noordzij;Hanna Theodora Noordzij.
Frontiers in Immunology (2015)
The structural requirements for complement activation by IgG: does it hinge on the hinge?
Ole Henrik Brekke;Terje E. Michaelsen;Inger Sandlie.
Immunology Today (1995)
Neonatal Fc receptor for IgG (FcRn) regulates cross-presentation of IgG immune complexes by CD8-CD11b+ dendritic cells.
Kristi Baker;Shuo-Wang Qiao;Timothy T. Kuo;Victoria G. Aveson.
Proceedings of the National Academy of Sciences of the United States of America (2011)
Cross-species Binding Analyses of Mouse and Human Neonatal Fc Receptor Show Dramatic Differences in Immunoglobulin G and Albumin Binding
Jan Terje Andersen;Muluneh Bekele Daba;Gøril Berntzen;Terje Einar Michaelsen;Terje Einar Michaelsen.
Journal of Biological Chemistry (2010)
Structure-based mutagenesis reveals the albumin-binding site of the neonatal Fc receptor.
Jan Terje Andersen;Bjørn Dalhus;Jason Cameron;Muluneh Bekele Daba;Muluneh Bekele Daba.
Nature Communications (2012)
Lysine 322 in the human IgG3 C(H)2 domain is crucial for antibody dependent complement activation.
John E Thommesen;Terje E Michaelsen;Geir Åge Løset;Inger Sandlie.
Molecular Immunology (2000)
Aglycosylated IgG variants expressed in bacteria that selectively bind FcγRI potentiate tumor cell killing by monocyte-dendritic cells
Sang Taek Jung;Sai T. Reddy;Tae Hyun Kang;M. Jack Borrok.
Proceedings of the National Academy of Sciences of the United States of America (2010)
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