1967, Scrittori d'Oriente 6, 265
Book
2003, ISBN 8817872180, 115
Book
1996, Muse pisane, ISBN 9788877419569, Volume 3, 250
Book
Music Score
Music Score
Immunity, ISSN 1074-7613, 2010, Volume 33, Issue 4, pp. 530 - 541
The sequence of microbial genomes made all potential antigens of each pathogen available for vaccine development. This increased by orders of magnitude...
T-CELL RESPONSES | HUMAN DENDRITIC CELLS | LYMPHOCYTE RESPONSES | PLASMODIUM-FALCIPARUM | IMMUNE-RESPONSES | MHC SUPERTYPES | PEPTIDE BINDING | IMMUNOLOGY | ANTIBODY-RESPONSES | DIFFERENT EPITOPES | PD-1 EXPRESSION | Vaccines - genetics | Animals | Humans | Computational Biology | Proteomics | Vaccines - immunology | T-Lymphocytes - immunology | Epitopes | Genomics - methods | Immunity, Cellular | Usage | Vaccines | T cells | Health aspects | Analysis | Antigenic determinants | Proteins | Smallpox | Microorganisms | Disease | Technological change | Genomes | Streptococcus infections
T-CELL RESPONSES | HUMAN DENDRITIC CELLS | LYMPHOCYTE RESPONSES | PLASMODIUM-FALCIPARUM | IMMUNE-RESPONSES | MHC SUPERTYPES | PEPTIDE BINDING | IMMUNOLOGY | ANTIBODY-RESPONSES | DIFFERENT EPITOPES | PD-1 EXPRESSION | Vaccines - genetics | Animals | Humans | Computational Biology | Proteomics | Vaccines - immunology | T-Lymphocytes - immunology | Epitopes | Genomics - methods | Immunity, Cellular | Usage | Vaccines | T cells | Health aspects | Analysis | Antigenic determinants | Proteins | Smallpox | Microorganisms | Disease | Technological change | Genomes | Streptococcus infections
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 10/2013, Volume 19, Issue 11, pp. 1508 - 1517
Background: Chronic cerebrospinal venous insufficiency (CCSVI) has been proposed as a possible cause of multiple sclerosis (MS). Objectives: The CoSMo study...
neurodegenerative disease | multiple sclerosis | circulatory system | Italy | multicentric study | prevalence study | Chronic cerebrospinal venous insufficiency | sonography | CCSVI | NEUROSCIENCES | CLINICAL NEUROLOGY | HEMODYNAMICS | ASSOCIATION | Prevalence | Humans | Middle Aged | Male | Spinal Cord - blood supply | Multiple Sclerosis - epidemiology | Case-Control Studies | Multiple Sclerosis - complications | Brain - blood supply | Venous Insufficiency - complications | Adult | Female | Venous Insufficiency - epidemiology
neurodegenerative disease | multiple sclerosis | circulatory system | Italy | multicentric study | prevalence study | Chronic cerebrospinal venous insufficiency | sonography | CCSVI | NEUROSCIENCES | CLINICAL NEUROLOGY | HEMODYNAMICS | ASSOCIATION | Prevalence | Humans | Middle Aged | Male | Spinal Cord - blood supply | Multiple Sclerosis - epidemiology | Case-Control Studies | Multiple Sclerosis - complications | Brain - blood supply | Venous Insufficiency - complications | Adult | Female | Venous Insufficiency - epidemiology
Journal Article
BMC Bioinformatics, ISSN 1471-2105, 11/2010, Volume 11, Issue 1, pp. 568 - 568
Background: MHC class II binding predictions are widely used to identify epitope candidates in infectious agents, allergens, cancer and autoantigens. The vast...
RECOGNITION | BIOCHEMICAL RESEARCH METHODS | IMMUNOGENIC EPITOPES | ALGORITHMS | REPERTOIRES | MHC CLASS-I | LIBRARIES | DATABASE | LIGANDS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | DISEASE | MATHEMATICAL & COMPUTATIONAL BIOLOGY | AFFINITIES | Genes, MHC Class II | Peptides - chemistry | Humans | Peptides - immunology | Epitopes - genetics | HLA-DR Antigens - chemistry | HLA-DQ Antigens - immunology | HLA-DR Antigens - genetics | Epitopes - immunology | HLA-DP Antigens - chemistry | HLA-DP Antigens - genetics | Peptides - metabolism | HLA-DQ Antigens - genetics | Alleles | HLA-DQ Antigens - chemistry | HLA-DR Antigens - immunology | Binding Sites | HLA-DP Antigens - immunology | Protein structure prediction | Histocompatibility antigens | Research | Analysis | HLA histocompatibility antigens | Protein binding | Studies | Algorithms | Ligands | Libraries | Autoimmune diseases | Experiments | Methods | Data bases
RECOGNITION | BIOCHEMICAL RESEARCH METHODS | IMMUNOGENIC EPITOPES | ALGORITHMS | REPERTOIRES | MHC CLASS-I | LIBRARIES | DATABASE | LIGANDS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | DISEASE | MATHEMATICAL & COMPUTATIONAL BIOLOGY | AFFINITIES | Genes, MHC Class II | Peptides - chemistry | Humans | Peptides - immunology | Epitopes - genetics | HLA-DR Antigens - chemistry | HLA-DQ Antigens - immunology | HLA-DR Antigens - genetics | Epitopes - immunology | HLA-DP Antigens - chemistry | HLA-DP Antigens - genetics | Peptides - metabolism | HLA-DQ Antigens - genetics | Alleles | HLA-DQ Antigens - chemistry | HLA-DR Antigens - immunology | Binding Sites | HLA-DP Antigens - immunology | Protein structure prediction | Histocompatibility antigens | Research | Analysis | HLA histocompatibility antigens | Protein binding | Studies | Algorithms | Ligands | Libraries | Autoimmune diseases | Experiments | Methods | Data bases
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 3, pp. 769 - 770
Conversely, TG-specific T cells were detectable out of season but were specifically downmodulated in the pollen season in nonallergic donors. [...]it seems...
Allergy and Immunology | nasal allergen challenge | house dust mite | T cells | Allergic rhinitis | nonallergic | ALLERGY | GRASS-POLLEN | IMMUNOLOGY | Pyroglyphidae | Epithelial Cells | Inflammation | Animals | Hypersensitivity | Dermatophagoides pteronyssinus | Studies | Food allergies | T cell receptors | Disease | Lymphocytes | Immunotherapy
Allergy and Immunology | nasal allergen challenge | house dust mite | T cells | Allergic rhinitis | nonallergic | ALLERGY | GRASS-POLLEN | IMMUNOLOGY | Pyroglyphidae | Epithelial Cells | Inflammation | Animals | Hypersensitivity | Dermatophagoides pteronyssinus | Studies | Food allergies | T cell receptors | Disease | Lymphocytes | Immunotherapy
Journal Article
BMC Bioinformatics, ISSN 1471-2105, 05/2005, Volume 6, Issue 1, pp. 132 - 132
Background: Many processes in molecular biology involve the recognition of short sequences of nucleic- or amino acids, such as the binding of immunogenic...
LIBRARIES | LIGANDS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TAP TRANSPORT | BIOCHEMICAL RESEARCH METHODS | PEPTIDE BINDING | CLASS-I MOLECULES | INDEPENDENT BINDING | PREDICTION | EPITOPES | Amino Acid Sequence | Computational Biology - methods | Data Interpretation, Statistical | Peptides - chemistry | Models, Statistical | Peptide Library | Algorithms | Models, Biological | Computer Simulation | Databases, Protein | Sensitivity and Specificity | Biology - methods | Programming Languages | Protein Binding | Software | Neural Networks (Computer)
LIBRARIES | LIGANDS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TAP TRANSPORT | BIOCHEMICAL RESEARCH METHODS | PEPTIDE BINDING | CLASS-I MOLECULES | INDEPENDENT BINDING | PREDICTION | EPITOPES | Amino Acid Sequence | Computational Biology - methods | Data Interpretation, Statistical | Peptides - chemistry | Models, Statistical | Peptide Library | Algorithms | Models, Biological | Computer Simulation | Databases, Protein | Sensitivity and Specificity | Biology - methods | Programming Languages | Protein Binding | Software | Neural Networks (Computer)
Journal Article
Human Vaccines & Immunotherapeutics, ISSN 2164-5515, 06/2017, Volume 13, Issue 6, pp. 1210 - 1212
Journal Article
Current Pharmaceutical Biotechnology, ISSN 1389-2010, 03/2016, Volume 17, Issue 3, p. 209
Journal Article
PLoS Computational Biology, ISSN 1553-734X, 04/2008, Volume 4, Issue 4, p. e1000048
The identification of MHC class II restricted peptide epitopes is an important goal in immunological research. A number of computational tools have been...
ACTIVATION | T-CELL RESPONSES | DATABASE | CRYSTAL-STRUCTURE | SEQUENCE | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | NETWORK-BASED PREDICTION | NEURAL-NETWORK | ALGORITHMS | PROTEINS | MOLECULES | Amino Acid Sequence | Sequence Analysis, Protein - methods | Genes, MHC Class II | HLA-D Antigens - chemistry | Algorithms | Peptides - chemistry | Molecular Sequence Data | Protein Binding | Epitope Mapping - methods | Binding Sites | Lymphocytes | Clinical trials | Experiments | Data bases | Binding sites | Methods
ACTIVATION | T-CELL RESPONSES | DATABASE | CRYSTAL-STRUCTURE | SEQUENCE | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | NETWORK-BASED PREDICTION | NEURAL-NETWORK | ALGORITHMS | PROTEINS | MOLECULES | Amino Acid Sequence | Sequence Analysis, Protein - methods | Genes, MHC Class II | HLA-D Antigens - chemistry | Algorithms | Peptides - chemistry | Molecular Sequence Data | Protein Binding | Epitope Mapping - methods | Binding Sites | Lymphocytes | Clinical trials | Experiments | Data bases | Binding sites | Methods
Journal Article
Science, ISSN 0036-8075, 2016, Volume 354, Issue 6310, pp. 354 - 358
The proteasome generates the epitopes presented on human leukocyte antigen (HLA) class I molecules that elicit CD8(+) T cell responses. Reports of...
COLLISION DISSOCIATION ETHCD | PROTEIN | SPECIFICITY | MULTIDISCIPLINARY SCIENCES | ANTIGEN PRESENTATION | CANCER-IMMUNOTHERAPY | MASS-SPECTROMETRY | Histocompatibility Antigens Class I - metabolism | Peptides - metabolism | Antigen Presentation | Humans | Peptides - immunology | Computational Biology | Protein Splicing | Cell Line, Tumor | Ligands | Proteasome Endopeptidase Complex - metabolism | CD8-Positive T-Lymphocytes - immunology | Epitopes, T-Lymphocyte - metabolism | Physiological aspects | Histocompatibility antigens | Peptides | Ubiquitin-proteasome system | HLA histocompatibility antigens | Antigens | Immunology | Lymphocytes | Abundance | Vaccines | Pools | Cancer
COLLISION DISSOCIATION ETHCD | PROTEIN | SPECIFICITY | MULTIDISCIPLINARY SCIENCES | ANTIGEN PRESENTATION | CANCER-IMMUNOTHERAPY | MASS-SPECTROMETRY | Histocompatibility Antigens Class I - metabolism | Peptides - metabolism | Antigen Presentation | Humans | Peptides - immunology | Computational Biology | Protein Splicing | Cell Line, Tumor | Ligands | Proteasome Endopeptidase Complex - metabolism | CD8-Positive T-Lymphocytes - immunology | Epitopes, T-Lymphocyte - metabolism | Physiological aspects | Histocompatibility antigens | Peptides | Ubiquitin-proteasome system | HLA histocompatibility antigens | Antigens | Immunology | Lymphocytes | Abundance | Vaccines | Pools | Cancer
Journal Article
Immunity, ISSN 1074-7613, 10/2013, Volume 39, Issue 4, pp. 758 - 769
The vast majority of currently licensed human vaccines work on the basis of long-term protective antibody responses. It is now conceivable that an...
B-CELLS | T-FOLLICULAR HELPER | COMMITMENT | BCL6 | PROTECTION | DYNAMICS | REGULATORS | IMMUNOLOGY | EXPRESSION | PROGRAM | LYMPHOCYTES | Germinal Center - immunology | Humans | Molecular Sequence Data | Gene Expression Profiling | T-Lymphocytes, Helper-Inducer - virology | HIV Infections - immunology | HIV Infections - pathology | Immunity, Humoral | T-Lymphocytes, Helper-Inducer - immunology | B-Lymphocytes - virology | HIV Antibodies - biosynthesis | T-Lymphocytes, Helper-Inducer - pathology | B-Lymphocytes - pathology | Amino Acid Sequence | Gene Expression | Receptors, CXCR5 - genetics | Signal Transduction | HIV Infections - virology | Germinal Center - pathology | Receptors, CXCR5 - immunology | HIV-1 - immunology | B-Lymphocytes - immunology | Antibodies, Neutralizing - biosynthesis | Germinal Center - virology | Receptors, CXCR3 - genetics | Receptors, CXCR3 - immunology | Immunologic Memory | Programmed Cell Death 1 Receptor - immunology | Programmed Cell Death 1 Receptor - genetics | Antigens | Hypotheses | Acquired immune deficiency syndrome--AIDS | Lymphocytes | Infections | Vaccines | Mutation | Gene expression | Viral infections | Immune system
B-CELLS | T-FOLLICULAR HELPER | COMMITMENT | BCL6 | PROTECTION | DYNAMICS | REGULATORS | IMMUNOLOGY | EXPRESSION | PROGRAM | LYMPHOCYTES | Germinal Center - immunology | Humans | Molecular Sequence Data | Gene Expression Profiling | T-Lymphocytes, Helper-Inducer - virology | HIV Infections - immunology | HIV Infections - pathology | Immunity, Humoral | T-Lymphocytes, Helper-Inducer - immunology | B-Lymphocytes - virology | HIV Antibodies - biosynthesis | T-Lymphocytes, Helper-Inducer - pathology | B-Lymphocytes - pathology | Amino Acid Sequence | Gene Expression | Receptors, CXCR5 - genetics | Signal Transduction | HIV Infections - virology | Germinal Center - pathology | Receptors, CXCR5 - immunology | HIV-1 - immunology | B-Lymphocytes - immunology | Antibodies, Neutralizing - biosynthesis | Germinal Center - virology | Receptors, CXCR3 - genetics | Receptors, CXCR3 - immunology | Immunologic Memory | Programmed Cell Death 1 Receptor - immunology | Programmed Cell Death 1 Receptor - genetics | Antigens | Hypotheses | Acquired immune deficiency syndrome--AIDS | Lymphocytes | Infections | Vaccines | Mutation | Gene expression | Viral infections | Immune system
Journal Article
Immunology, ISSN 0019-2805, 07/2018, Volume 154, Issue 3, pp. 394 - 406
Summary Major histocompatibility complex class II (MHC‐II) molecules are expressed on the surface of professional antigen‐presenting cells where they display...
immunogenic peptides | T‐cell epitope | affinity predictions | peptide–MHC binding | MHC binding specificity | T-cell epitope | MYCOBACTERIUM-TUBERCULOSIS | HLA-DR BINDING | SIZE | T-CELL EPITOPES | HLA-DR1 | NETWORKS | IMMUNOLOGY | peptide-MHC binding | PAN-SPECIFIC PREDICTION | Histocompatibility antigens | Peptides | Analysis | HLA histocompatibility antigens | T cells | Methods | Antigenic determinants | Binding | Major histocompatibility complex | Immune response | Helper cells | Predictions | Affinity | Lymphocytes T | Histocompatibility antigen HLA | Epitopes | Histocompatibility | Molecular chains | Original
immunogenic peptides | T‐cell epitope | affinity predictions | peptide–MHC binding | MHC binding specificity | T-cell epitope | MYCOBACTERIUM-TUBERCULOSIS | HLA-DR BINDING | SIZE | T-CELL EPITOPES | HLA-DR1 | NETWORKS | IMMUNOLOGY | peptide-MHC binding | PAN-SPECIFIC PREDICTION | Histocompatibility antigens | Peptides | Analysis | HLA histocompatibility antigens | T cells | Methods | Antigenic determinants | Binding | Major histocompatibility complex | Immune response | Helper cells | Predictions | Affinity | Lymphocytes T | Histocompatibility antigen HLA | Epitopes | Histocompatibility | Molecular chains | Original
Journal Article