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pathway Info Card
Response To Rapamycin
Information about Response To Rapamycin: 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 Response To Rapamycin
Most recent studies have shown that Response To Rapamycin shares some biological mechanisms with autophagy, cell-cycle, cell-cycle-arrest, cell-death, cell-growth, cell-proliferation, drug-export, endocytosis, gene-silencing, hypersensitivity, localization, macroautophagy, mitochondrial-genome-maintenance, programmed-cell-death, ribosome-biogenesis, sporulation, telomere-maintenance, translation, transport, virulence.
Among the many pathways, these few ones have gauged particular interests from scientists studying Response To Rapamycin, and have been seen in publications frequently: autophagy, cell-cycle, cell-cycle-arrest, cell-death, cell-growth, cell-proliferation, drug-export, endocytosis, gene-silencing, hypersensitivity, localization, macroautophagy, mitochondrial-genome-maintenance, programmed-cell-death, ribosome-biogenesis, sporulation, telomere-maintenance, translation, transport, virulence
Quite a number of genes have been found to play important roles in Response To Rapamycin, such as AKT1, BBS9, CCND1, CDKN1A, CDKN1B, EIF4EBP1, FKBP1A, GOLPH3, HMOX1, JUN, MTOR, MYC, NOS3, NPR1, PSMC4, RORC, RPS6, RPTOR, SLC22A1, ZFP36. 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 pathway. Plesae stay updated.