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Recent studies indicate that CXCR7 may regulate other pathways including epidermal growth factor receptor (EGFR)/extracellular regulated kinase (ERK) axis, AKT pathway and mTOR signaling.
CreA protein of A. cellulolyticus may regulate other transcription factors involving cellulase and hemicellulase production as T. reesei; however, no transcription factors other than CreA of A. cellulolyticus have been investigated.
There is a possibility, however, that MOR may regulate other events upstream of PKC and Src activation as well.
On the other hand, there have been numerous reports that suggest dystrophin may regulate other cellular targets [11], e.g. ec-coupling and Ca2+ homeostasis (e.g. [12] [16]), mitochondrial function [17], motor protein interaction [18], [19] or gene transcription 20, 21.
However, we suspected that some NHRs may regulate other lipid metabolism pathways that may compensate for the fat-6;fat-7 defects and therefore improve the fat-6;fat-7 growth and fat storage defects.
However, genes in the IRMA network may regulate other genes in the genome.
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The MbnI ECF sigma factor may then interact with RNA polymerase to either upregulate or inhibit Mbn biosynthesis and transport and may also regulate other operons that are highly expressed at low copper, such as the sMMO operon.
Some sequences, similar to the SSE, exist in the gene promoter regions of the rat, mouse, and human, suggesting that RNF10 may also regulate other gene expressions.
TCF7L2 may also regulate other β-cell functions essential for maintaining GSIS.
Previous reports have suggested that NPAS2 may directly regulate other genes in the circadian regulatory system.
This cytokine recruits circulating memory T cells in the synovial membrane and may up regulate other pro-inflammatory cytokines [ 14, 15].
Related(20)
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