Role of innate responses to viruses in the genesis of IgA Nephropathy

对病毒的先天反应在 IgA 肾病发生中的作用

• 批准号: 8195576
• 负责人: STEVEN N EMANCIPATOR
• 金额: --
• 依托单位: LOUIS STOKES CLEVELAND VA MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-04-01 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8195576
• 关键词: Accounting; Acute; Affect; Animal Model; Antibody Formation; Antigen-Antibody Complex; Antigens; Binding; Cell physiology; Cells; Chronic; Chronic Kidney Failure; Clinical; Data; Deposition; Development; Dialysis procedure; Disease; Double-Stranded RNA; End stage renal failure; Event; Exhibits; Exposure to; Functional disorder; Genetic; Glomerular Mesangial Cell; Glomerulonephritis; HIV; Health; Healthcare; Hepatitis C; IFNAR1 gene; IgA receptor; Immune; Immune Complex Glomerulonephritis; Immune response; Immunity; Immunization; Immunoglobulin A; In Vitro; Individual; Infection; Intravenous; Kidney; Kidney Diseases; Kidney Transplantation; Label; Lead; Life; Link; Measurable; Mediating; Military Personnel; Minority; Morbidity - disease rate; Mucosal Immunity; Mucous Membrane; Mus; Nature; Nephritis; Outcome; Parainfluenza; Pathogenesis; Pathway interactions; Patients; Penetration; Population; Prevalence; Publishing; Recombinant Interferon; Renal glomerular disease; Reporting; Respiratory System; Respiratory tract structure; Role; Route; Sendai virus; Signal Transduction Pathway; Source; Stimulus; System; Testing; Treatment Cost; Veterans; Viral; Virion; Virus; Virus Diseases; Virus Replication; Wild Type Mouse; Work; chemokine; common treatment; cytokine; effective therapy; experience; gastrointestinal; glomerular function; in vivo; insight; macrophage; male; mesangial cell; mortality; mouse model; novel; novel therapeutics; parainfluenza virus; pathogen; patient population; podocyte; public health relevance; receptor; research study; respiratory; response; sensor; social