Because intelectin-1 mRNA is expressed in normal intestines (Tsuji et al, 2001), we also investigated expression of intelectin-1 in colon cancer.
We also investigated expression of the GA signalling components TaRht, TaGID1 and TaGID2: these genes were expressed in all tissues studied (Fig. 5D).
To further increase solvent production, we investigated expression of both native and heterologous chaperones in C. acetobutylicum.
We investigated expression of HIF-dependent growth factors and HIF-independent somatotrophic factors in term placenta in response to hypoxic ischemia.
We investigated expression of an efflux pump belonging to a class of membrane transporters that export toxic chemicals from cells to improve ethanol tolerance of Saccharomyces cerevisiae.
Because abnormalities of glutamatergic neurotransmission in psychiatric illness are likely not limited to glutamate receptor expression, we investigated expression of excitatory amino acid transporters (EAATs) in the striatum.
To understand how D2/SMG11 regulates cell expansion in spikelet hulls, we investigated expression of several known grain size genes involved in the regulation of cell expansion, including GS2, GL7, GLW7/SPL13, PGL1, PGL2, APG and SRS5.
The authors investigated expression of these TRP channels in the submandibular gland during early developmental stage in which the cell constitution is different, and discussed the function of TRP in the submandibular gland in early development.
Next we investigated expression of hBD1 in our patient cohort.
Initially, we investigated expression of HNF4α in the pancreas of Zucker diabetic fatty (ZDF) rats.
We also investigated expression of cell-type specific markers in P120 mutant retinas.
