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Disease Info Card
Zinc Deficiency Disorder
Information about Zinc Deficiency Disorder: 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 Zinc Deficiency Disorder
Most recent studies have shown that Zinc Deficiency Disorder shares some biological mechanisms with acrodermatitis-enteropathica, anemia, deficiency-diseases, dermatitis, dermatologic-disorders, diabetes-mellitus, diarrhea, growth-disorders, growth-retardation, infective-disorder, inflammation, iron-deficiency, malabsorption-syndrome, malignant-neoplasms, malnutrition, neoplasms, pregnancy-complications.
Among the many pathways, these few ones have gauged particular interests from scientists studying Zinc Deficiency Disorder, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Division, Cell Proliferation, Cytokine Production, Excretion, Hypersensitivity, Immune Response, Inflammatory Response, Intestinal Absorption, Lactation, Localization, Mating, Parturition, Pathogenesis, Secretion, Spermatogenesis, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Zinc Deficiency Disorder, such as ACE, ALB, CASP3, CAT, CD4, CP, CRP, IGF1, IL2, IL6, INS, JUN, MCAT, NFKB1, SLC30A1, SLC39A4, SOD1, TNF. 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.