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On the other hand, it has also been reported that expression of MeCP2 inhibited dendritic spine development in rat hippocampal slice cultures (Cheng et al., 2014).
It has been reported that expression of FGFR3 might mark a tumorigenic subpopulation in RMS.
Recently it has been reported that expression of p53 is required for the acute and chronic loss of salivary function following irradiation [17].
It has previously been reported that expression levels of proteins within a complex are significantly more correlated across tissue types than would be expected by chance [16], [55].
It has been reported that expression of antioxidant genes generally increases in the younger queens [36] and high demand for oxygen during embryonic development leads to increased level of ROS and thus increasing oxidative damage [37], [38].
It has been reported that expression of the intracellular domain of the wnt co-receptor LRP6 is sufficient to stabilize β-catenin and activate LEF/TCF-dependent transcription in the absence of a wnt ligand [35], [36].
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Actually, it was reported that expression of cbh1 was abolished by homologous recombination, pcbh1-gus in T. reesei PC-3-7 (Rahman et al. 2009).
It is reported that expression levels of DnaK gene in A. acidoterrestris were up-regulated rapidly under heat and acid stresses, and played significant roles for the survival of A. acidoterrestris in heat and acid conditions (Jiao et al. 2015).
It was reported that expression of cyanase from Suaeda aegyptiaca can be induced by salt stress, and analysis of upstream noncoding sequence revealed an ethylene-responsive element (ATTTAAAA) in Arabidopsis thaliana and Oryza sativa [26].
Moreover, it was reported that expression of EPO was influenced by single-nucleotide polymorphisms (SNPs) in the EPO gene [ 56].
It was reported that expression of S129D mutant α-synuclein in Drosophila significantly enhances the toxicity (34).
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