We explored the expression of PDE3 isoenzymes and the concentrations of cAMP in the tissue.
This study explored the expression of DNA mismatch repair (MMR) proteins in a range of oral biopsies.
In the present study, we explored the expression of uPAR/suPAR in common biopsy-proven kidney diseases and the relationship between suPAR and staging of type 2 diabetic nephropathy (DN).
Methods: We explored the expression of PDE III in postmortem human brain tissue followed by a series of experiments examining the effects of cilostazol on Aβ metabolism in transgenic mice (Tg-SwDI mice) as a model of cerebrovascular β-amyloidosis, as well as cultured neurons.
Accordingly we explored the expression level of differentiation associated genes by RT-qPCR.
To further elucidate the ancestral state of G6pdx expression, we explored the expression profile of the X-linked G6pd gene in rat spermatogenesis.
While we explored the expression of P. falciparum MSP1-19 in Chlamydomonas, we also extended our system to production of other malaria candidate vaccine antigens.
Recent studies have explored the expression signatures in peripheral blood mononuclear cells (PBMC) and in CD4+ T cells of human T1D and T2D subjects [20], [21].
We then explored the expression of target proteins known to regulate mechanisms of apoptosis induction or resistance such as the caspases and the poly (ADP-ribose) polymerase (PARP) by western blot analysis (Figure 4B, a).
More extensive analysis of the R. flavefaciens FD-1 genome [24] indicated that it harbours the largest number of dockerin-containing components known so far, and explored the expression of cellulolytic enzymes via functional microarray analysis.
We also explored the expression of genes (Mtf-1, DD104, Kaz1, A2M, Cath and Ft) that had been previously associated with the immune system [24] but that appeared to show no differential expression in the microarray.
