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.
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.
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.
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.
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.
Here we evaluate and discuss the expression levels of Raf-1 and MAPK (critical members of the MAPK cascade) and their activation status in matched HNPC and CRPC tumours and correlate expression levels with type 1 tyrosine kinase receptors, as well as their downstream targets, AR and AP-1, in the same cohort of patients.
We then discuss the expression signatures of key miRNAs in several cancers, highlighting the molecular pathways through which they may be acting to control cell proliferation, survival, and invasion.
