Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis

Keyphrases

• Gain-of-function 100%
• Transcriptional Repressor 100%
• Signal Transducer 100%
• Autosomal Dominant 100%
• Bronchiectasis 100%
• Non-cystic Fibrosis Bronchiectasis 60%
• Phosphorylation 40%
• Genome Analysis 40%
• Gain-of-function mutation 40%
• Immunophenotyping 40%
• Switched Memory B Cells 40%
• CD8 T Cells 40%
• Cell-to-cell 20%
• B Cells 20%
• Genetic Analysis 20%
• Interferon-α (IFN-α) 20%
• Natural Killer Cells 20%
• Etiology 20%
• T Cell Subpopulations 20%
• Minor Change 20%
• CD4 T Cells 20%
• Early Use 20%
• Mutation Mutation 20%
• Suppurative 20%
• Immunodeficiency Diseases 20%
• Patient numbers 20%
• Sinopulmonary Infections 20%
• Memory B Cells 20%
• Chronic Suppurative Lung Disease 20%

Medicine and Dentistry

• Autosomal Dominant Inheritance 100%
• Bronchiectasis 100%
• STAT1 Protein 100%
• Cystic Fibrosis 60%
• Memory B Cell 60%
• Cytotoxic T-Cell 40%
• Gain of Function Mutation 40%
• Exome 40%
• Immunophenotyping 40%
• phosphorylation 40%
• B Cell 20%
• Disease Predisposition 20%
• Natural Killer Cell 20%
• Silo-Filler's Disease 20%
• Interferon 20%
• Genetic Analysis 20%
• T-Helper Cell 20%
• Immune Deficiency 20%
• Diseases 20%
• T Lymphocyte Subpopulation 20%
• Etiology 20%

Immunology and Microbiology

• STAT1 100%
• Autosomal Dominant Inheritance 100%
• Memory B Cell 60%
• Cytotoxic T-Cell 40%
• Gain of Function Mutation 40%
• Exome 40%
• phosphorylation 40%
• B Cell 20%
• interferon 20%
• Natural Killer Cell 20%
• Immunodeficiency 20%
• T-Helper Cell 20%
• T Lymphocyte Subpopulation 20%
• Lung 20%