Ohta et al. (2005) discussed the expression of aldehyde dehydrogenase in Escherichia coli, and a cloned enzyme showed similarity to NAD (P -dependent aldehyde dehydrogenase.
And, we discussed the expression of all MIKCc genes here in accord with thirteen clades identified in our study.
As discussed, the expression of ADHD in adults is to some extent different from that in children and the diagnostic descriptions of some of the features need to be adapted to adult expressions of the disorder.
In the following sections, we discuss the expression of only a subset of drought-regulated genes and gene family members.
In the following section, we further discuss the expression of MOh toxins according to their protein families.
In discussing the expression of the induced mutations, the importance of dominant mutations and of heterozygous effects of deletions and other recessives is pointed out.
We discuss the expression of the Pax2/5/8 gene family during development of the heart, endostyle, pharynx, and sensory organs, and provide new insights that reconcile previous conflicting hypotheses about the homology of the ascidian atrial primordia and the vertebrate otic placode.
In this review, we discuss the expression of DISC1, DBZ, and SGK1 in oligodendrocytes, their roles in the regulation of oligodendrocyte function, possible interactions of DISC1 and DBZ in relation to SZ, and the activation of the SGK1 signaling cascade in relation to MDD.
Prior studies have discussed the expression pattern of miRNA found in liver fibrosis samples between previous and present study.
Similarly, in networks exhibiting sequential and combinatorial stripe formation, as will be discussed, the expression patterns of the other genes closely follow those reported for short [30] and intermediate [12], [13], [31] germ-band arthropods respectively (Figs. 1H I, S2B C, and S3B C).
In addition, few gene expression studies have discussed the expression profile of pig prohormone or prohormone convertase genes.
