To predict the co-expressed genes, we also examined the relationships among genes that are putatively regulated by OsSMF1 by RAN analysis.
To further evaluate ERBB2 inhibition of these genes, we also treated cells from a new batch of iPSC-derived cardiomyocytes with additional ERBB2 inhibitors, neratinib, afatinib and poziotinib.
In five genes we also examined 100 kb upstream of each gene, but only the portions strongly conserved between humans and mice.
In addition to essential metabolic genes, we also analysed the dispensability of inter-compartmental metabolite transporters since the mechanism of photorespiration is quite intricate, involving three major organelles, chloroplast, mitochondrion and peroxisome.
For the CYP2D6 and CYP2C19 genes, we also modeled the putative metabolism status of the subjects as follows.
In addition to using constitutive expression of Pax3 and Pax7 to explore the role of these genes, we also used dominant-negative versions [15], [30].
In addition to the HOXA genes, we also observed discrepancies between cancer cell lines and clinical specimens in the expression of several homeobox genes that were analyzed.
In addition to a conservation of sequence similarity in PMT genes, we also demonstrated that the basic function of C. neoformans Pmt enzymes is likely similarly conserved.
In addition to the common set of up-regulated genes, we also identified a cluster that displayed a general down-regulation.
Additionally, since tropT and tropI genes are in direct 3' proximity to all teleost myod genes, we also assessed their location in human and chicken genomes.
Concomitant to investigating the genetic features of LMW-GS genes, we also succeeded in placing polymorphic microsatellite markers in the vicinities of Xiaoyan 54 Glu-3 loci.
