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Disease Info Card
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Information about Multiple Acyl Coenzyme A Dehydrogenase 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 Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Most recent studies have shown that Multiple Acyl Coenzyme A Dehydrogenase Deficiency shares some biological mechanisms with adenocarcinoma, atrophy, carcinoma, celiac-disease, hiv-infections, leukemia, lung-neoplasms, lymphoma, malignant-neoplasm-of-breast, malignant-neoplasms, malignant-paraganglionic-neoplasm, malignant-squamous-cell-neoplasm, mammary-neoplasms, neoplasm-metastasis, neoplasms, nervousness, sarcoma, skin-neoplasms, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Multiple Acyl Coenzyme A Dehydrogenase Deficiency, and have been seen in publications frequently: Cell Adhesion, Cell Cycle, Cell Death, Cell Differentiation, Cell Growth, Cell Proliferation, Dna Replication, Endocytosis, Excretion, Glycosylation, Immune Response, Localization, Methylation, Mitosis, Pathogenesis, Proteolysis, Secretion, Translation, Transport, Virulence
Quite a number of genes have been found to play important roles in Multiple Acyl Coenzyme A Dehydrogenase Deficiency, such as CD34, CEACAM5, CEACAM7, CHKA, CHKB, DES, ENO2, ETFA, GFAP, KRT20, KRT7, MUC1, PSG2, PTPRC, S100A1, S100B, TNFRSF8, TP53, VIM. 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.