The same major histocompatibility complex polymorphism involved in control of HIV influences peptide binding in the mouse H-2L^d system

Keyphrases

• Major Histocompatibility Complex 100%
• Polymorphism 100%
• Peptide Binding 100%
• HLA-B 40%
• High Affinity 20%
• T Cell Activation 20%
• Enhanced Stability 20%
• Binding Structure 20%
• Binding Capacity 20%
• Allelic Variants 20%
• Self-assembling Peptide 20%
• Specific Probe 20%
• Binding Stability 20%
• CD-8 20%
• Disease Control 20%
• T Cell Selection 20%
• Complex Product 20%
• B System 20%
• Peptide Stability 20%
• Peripheral T Cells 20%
• Through Effect 20%
• Antigen Processing 20%
• T Cell Repertoire 20%
• Peptide Structure 20%
• HIV Disease Progression 20%
• Human Polymorphism 20%
• Selection Behavior 20%

Biochemistry, Genetics and Molecular Biology

• T Cell 100%
• Mouse 100%
• Human Immunodeficiency Virus 100%
• Major Histocompatibility Complex Polymorphism 100%
• Allele 66%
• HLA-B 66%
• Antigen Presentation 33%
• Major Histocompatibility Complex 33%
• Cell Selection 33%
• Cell Activity 33%
• T Cell Receptor 33%
• CD8 33%

Neuroscience

• T Cell 100%
• Major Histocompatibility Complex 100%
• Human Immunodeficiency Virus 100%
• HLA-B 66%
• Behavior (Neuroscience) 33%
• Cell Activity 33%
• Cell Line 33%
• CD8 33%