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by Balachandran, Vinod P and Luksza, Marta and Zhao, Julia N and Makarov, Vladimir and Moral, John Alec and Remark, Romain and Herbst, Brian and Askan, Gokce and Bhanot, Umesh and Senbabaoglu, Yasin and Wells, Daniel K and Cary, Charles Ian Ormsby and Grbovic-Huezo, Olivera and Attiyeh, Marc and Medina, Benjamin and Zhang, Jennifer and Loo, Jennifer and Saglimbeni, Joseph and Abu-Akeel, Mohsen and Zappasodi, Roberta and Riaz, Nadeem and Smoragiewicz, Martin and Kelley, Z. Larkin and Basturk, Olca and Gönen, Mithat and Levine, Arnold J and Allen, Peter J and Fearon, Douglas T and Merad, Miriam and Gnjatic, Sacha and Iacobuzio-Donahue, Christine A and Wolchok, Jedd D and DeMatteo, Ronald P and Chan, Timothy A and Greenbaum, Benjamin D and Merghoub, Taha and Leach, Steven D and Australian Pancreatic Canc Genom and Garvan Institute of Medical Research and Bankstown Hospital and St Vincent’s Hospital and Royal Adelaide Hospital and Royal North Shore Hospital and Envoi Pathology and QIMR Berghofer Medical Research Institute and Prince of Wales Hospital and University of Melbourne, Centre for Cancer Research and University of Queensland, Institute for Molecular Bioscience and Royal Prince Alfred Hospital, Chris O’Brien Lifehouse and Princess Alexandria Hospital and Fremantle Hospital and Liverpool Hospital and Austin Hospital and University of Glasgow and Johns Hopkins Medical Institutes and Flinders Medical Centre and Westmead Hospital and St John of God Healthcare and ARC-Net Centre for Applied Research on Cancer and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 11/2017, Volume 551, Issue 7681, pp. S12 - S16
Journal Article
Nature, ISSN 0028-0836, 09/2010, Volume 467, Issue 7315, pp. 591 - 595
Journal Article
Drug metabolism and disposition: the biological fate of chemicals, ISSN 0090-9556, 11/2018, Volume 46, Issue 11, pp. 1787 - 1795
Journal Article
Nature, ISSN 0028-0836, 09/2012, Volume 489, Issue 7417, pp. 526 - 532
Immune recognition of protein antigens relies on the combined interaction of multiple antibody loops, which provide a fairly large footprint and constrain the... 
SYSTEM | POTENT NEUTRALIZATION | EPITOPE | HEMAGGLUTININ | RECOGNITION | STRUCTURAL BASIS | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | BROAD | DELETIONS | INSERTIONS | Influenza A Virus, H1N1 Subtype - immunology | Orthomyxoviridae Infections - prevention & control | Complementarity Determining Regions - genetics | Influenza A virus - chemistry | Cross Reactions - genetics | Molecular Sequence Data | Crystallography, X-Ray | Antibody Specificity - genetics | Hemagglutinin Glycoproteins, Influenza Virus - immunology | Epitopes - immunology | Antibodies, Neutralizing - immunology | Antibody Specificity - immunology | Complementarity Determining Regions - chemistry | Conserved Sequence | Influenza A virus - immunology | Binding Sites | Hemagglutinin Glycoproteins, Influenza Virus - chemistry | Enzyme-Linked Immunosorbent Assay | Models, Molecular | Antigens, Viral - chemistry | Antibodies, Neutralizing - genetics | Cross Reactions - immunology | Influenza A Virus, H3N2 Subtype - immunology | Mutation - genetics | Antigens, Viral - immunology | Animals | Influenza A Virus, H3N2 Subtype - chemistry | Influenza Vaccines - immunology | Antibodies, Neutralizing - chemistry | Antibodies, Viral - chemistry | Complementarity Determining Regions - immunology | Antibodies, Viral - immunology | Protein Conformation | Epitopes - chemistry | Influenza A Virus, H1N1 Subtype - chemistry | Mice | Influenza A virus - classification | Orthomyxoviridae Infections - virology | Antibodies, Viral - genetics | Orthomyxoviridae Infections - immunology | Influenza viruses | Agglutinins | Viruses | Complementarity-determining regions | Research | Observations | Inactivation | Proteins | Infections | Binding sites
Journal Article
Pharmacogenomics, ISSN 1462-2416, 03/2010, Volume 11, Issue 3, pp. 349 - 356
Aims: Compared with other categories of drugs, such as antibiotics and NSAIDs, antiepileptic therapies are associated with a high incidence of Stevens Johnson... 
Oxcarbazepine | Stevens-Johnson syndrome | Toxic epidermal necrolysis | Antiepileptic drugs | Cutaneous adverse drug reactionn HLA susceptibility | Phenytoin | Lamotrigine | antiepileptic drugs | lamotrigine | MARKER | TAIWAN | CARBAMAZEPINE | phenytoin | cutaneous adverse drug reaction | toxic epidermal necrolysis | HLA-B LOCUS | ALLOPURINOL | ANTICONVULSANT HYPERSENSITIVITY SYNDROME | CUTANEOUS ADVERSE-REACTIONS | oxcarbazepine | CROSS-REACTIVITY | PHARMACOLOGY & PHARMACY | HLA susceptibility | JAPANESE PATIENTS | HLA-B-ASTERISK-1502 ALLELE | Stevens-Johnson Syndrome - immunology | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Male | HLA Antigens - genetics | Case-Control Studies | Young Adult | Stevens-Johnson Syndrome - chemically induced | Anticonvulsants - adverse effects | Drug-Related Side Effects and Adverse Reactions - genetics | Aged, 80 and over | Adult | Female | HLA-B15 Antigen | Child | HLA-B Antigens - genetics | Pharmacogenetics | Carbamazepine - analogs & derivatives | Genetic Association Studies | Risk Factors | Stevens-Johnson Syndrome - etiology | Stevens-Johnson Syndrome - genetics | Carbamazepine - adverse effects | Drug-Related Side Effects and Adverse Reactions - immunology | Phenytoin - adverse effects | Adolescent | Alleles | Taiwan | Triazines - adverse effects | Aged | Antibiotics
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2010, Volume 107, Issue 28, pp. 12658 - 12663
Influenza remains a serious public health threat throughout the world. Vaccines and antivirals are available that can provide protection from infection.... 
H1N1 subtype influenza A virus | Pandemics | Influenza A virus | Humans | Vaccination | Antibodies | Viruses | Orthomyxoviridae | Infections | Epitopes | Influenza matrix 2 protein | Pandemic | Monoclonal | MULTIDISCIPLINARY SCIENCES | EXTRACELLULAR DOMAIN | monoclonal | pandemic | NEUTRALIZING EPITOPE | influenza matrix 2 protein | M2 PROTEIN | CYTOMEGALOVIRUS GLYCOPROTEIN-B | MATRIX PROTEIN-2 | CONJUGATE VACCINES | IN-VIVO | ECTODOMAIN | MICE | MONOCLONAL-ANTIBODIES | Influenza A Virus, H1N1 Subtype - immunology | Cross Reactions - genetics | Influenza A virus - genetics | Molecular Sequence Data | Influenza A Virus, H5N1 Subtype - genetics | Influenza in Birds - immunology | Epitopes - immunology | Influenza in Birds - genetics | Disease Outbreaks | Antibodies - immunology | Influenza A virus - immunology | Influenza A Virus, H1N1 Subtype - genetics | Antibodies, Monoclonal - immunology | Birds | Cross Reactions - immunology | Epitopes - genetics | Antibodies, Monoclonal - genetics | Animals | Influenza Vaccines - immunology | Influenza Vaccines - genetics | Influenza A Virus, H5N1 Subtype - immunology | Influenza, Human - genetics | Antibodies - genetics | Mice | Influenza, Human - prevention & control | Influenza, Human - immunology | Prevention | Physiological aspects | Monoclonal antibodies | Care and treatment | Research | Influenza | Immunological memory | Memory cells | Genomes | Vaccines | Infection | Proteins | Disease resistance | Lymphocytes B | Influenza A | pandemics | Public health | Biological Sciences
Journal Article
Genetics, ISSN 0016-6731, 2014, Volume 196, Issue 1, pp. 321 - 347
Journal Article