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Disease Info Card
Usual Interstitial Pneumonitis
Information about Usual Interstitial Pneumonitis: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Usual Interstitial Pneumonitis
Most recent studies have shown that Usual Interstitial Pneumonitis shares some biological mechanisms with bronchiolitis, bronchiolitis-obliterans-organizing-pneumonia, dyspnea, extrinsic-allergic-alveolitis, fibrosis, hamman-rich-syndrome, idiopathic-interstitial-pneumonias, inflammation, lung-diseases, lung-diseases-interstitial, malignant-neoplasm-of-lung, malignant-neoplasms, nonspecific-interstitial-pneumonia, organising-pneumonia, pneumonia, pneumonia-interstitial, pulmonary-fibrosis, sarcoidosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Usual Interstitial Pneumonitis, and have been seen in publications frequently: Aging, Angiogenesis, Cell Death, Cell Differentiation, Cell Growth, Cell Proliferation, Coagulation, Excretion, Fibroblast Activation, Fibroblast Proliferation, Hypersensitivity, Immune Response, Inflammatory Response, Localization, Methylation, Pathogenesis, Regeneration, Secretion, Tissue Remodeling, Wound Healing
Quite a number of genes have been found to play important roles in Usual Interstitial Pneumonitis, such as ALB, CRP, DLC1, FN1, HP, IFNG, IL4, IL6, MUC1, NCKIPSD, PIAS2, SFTPC, SLC22A3, TNF, TSC22D3, VEGFA. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.