In summary, our results showed that participation of NK cell subsets in ALL killing is dependent on respective expression levels and expression clusters of KIR and other receptors.
The present study aimed to quantify and compare the in vivo expression of genes pld (phospholipase D), cpp (CP40), nanH (neuraminidase H), sodC (superoxide dismutase C) and spaC (adhesin) using qRT-PCR, with the respective expression in vitro.
We analyzed the respective expression level of Rae-1δ and Rae-1ε transcripts in vivo.
We then compared the respective expression of RAE-1δ and RAE-1ε transcripts and proteins in C57BL/6 cell lines and neurospheres obtained from the SVZ (Fig. 2C).
Of particular interest is the close clustering of hESC-ECs and HUVECs, indicating a high degree of similarity between their respective expression profiles.
In order to further evaluate the status of NTS and NTSR1 in breast cancer we studied their respective expression in 106 IDCs.
In contrast, unsupervised classification approaches, achieve clustering of genes based on their respective expression profiles but are not intended to filter out uninformative genes.
The goals of our study were thus to characterize the in vivo and in vitro expression of each gene and to elucidate the mechanisms underlying their respective expression.
Plasmids carrying genes of these EvpC mutants were used to transform an E. tarda ΔevpC mutant and their respective expression and secretion of EvpC were anlaysed.
In the transgenic condition hepatocytes overexpressed IgEGF, yet livers presented no detectable tumor, so that respective expression profiles were considered to present a pre-tumor state.
The detailed list of the identified proteins with their theoretical molecular weights, pIs, number of matched peptides and their respective expression profiles are reported in Table S1.
