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Disease Info Card
Purine-nucleoside Phosphorylase Deficiency
Information about Purine-nucleoside Phosphorylase Deficiency: 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 Purine-nucleoside Phosphorylase Deficiency
Most recent studies have shown that Purine-nucleoside Phosphorylase Deficiency shares some biological mechanisms with adenosine-deaminase-deficiency, anemia, anemia-hemolytic, ataxia, autoimmune-reaction, autoimmunity, congenital-combined-immunodeficiency, developmental-delay-(disorder), hypouricaemia, immunologic-deficiency-syndromes, infective-disorder, lesch-nyhan-syndrome, lymphoma, lymphopenia, malignant-neoplasms, metabolic-diseases, primary-immune-deficiency-disorder, severe-combined-immunodeficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Purine-nucleoside Phosphorylase Deficiency, and have been seen in publications frequently: Cell Cycle, Cell Division, Cell Maturation, Cell Proliferation, Cytolysis, Excretion, Guanine Salvage, Hypersensitivity, Immune Response, Lymphocyte Differentiation, Lymphocyte Proliferation, Mating, Mitochondrial Dna Repair, Pathogenesis, Protein Phosphorylation, Secretion, T Cell Mediated Immunity, T Cell Proliferation, Transport, V(d)j Recombination
Quite a number of genes have been found to play important roles in Purine-nucleoside Phosphorylase Deficiency, such as ADA, ADK, AHCY, APRT, CD4, DCK, DNTT, HPRT1, IL2, IL5, LBR, MTA2, OTC, PNP, PPY, UMPS. 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.