S and shifting of the peptide signals by different RNA fragments masses are annotated and highlighted as bold letter. Proposed schematic illustration structures for peptide-RNA cross-links along with and without cross-link product of 152 Da mass are shown on the right side of each corresponding spectrum. Fragmentation of RNA refers as yr1, xr1, wr1 and yr2 by McLuckey et al. (61). E, Mapping of ML

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Arch: some methodological issues. World Health Stat. Q., 44(3), 145-9. Khawaja, N. P., Tayyeb, R., Malik, N. (2004). Awareness and practices of contraception among Pakistani women attending a tertiary care hospital. J. Obstet. Gynaecol., 24(5), 564-7. http://dx.doi.org/10.1080/01443610410001722662 Kitzinger, J. (1995). Qualitative research. Introducing focus groups. BMJ, 311(7000), 299-302. http

Tream of the 5'LTR Existence of the host-viral chimeric transcripts that originate from a host promoter and include 5'LTR could be useful for identifying ongoing transcription upstream of the 5'LTR independently of the site of viral integration. Therefore, we next devised an assay, which determines the ratio between transcripts containing LTR sequences and those containing sequences present solely

Ng the mean background fluorescence multiplied by the area of the cell measured. Cathepsin L2 was significantly more abundant in sym hemocytes (1.79-fold; ***two-tailed unequal variance t test, p value 0.0001; error bars represent standard error of the mean (S.E.)).were more abundant in sym hemocytes (Tables II and III). Although linked to other cellular pathways, cathepsins are proteases activate

Ng the mean background fluorescence multiplied by the area of the cell measured. Cathepsin L2 was significantly more abundant in sym hemocytes (1.79-fold; ***two-tailed unequal variance t test, p value 0.0001; error bars represent standard error of the mean (S.E.)).were more abundant in sym hemocytes (Tables II and III). Although linked to other cellular pathways, cathepsins are proteases activate

G human lung cells [145]. Lee and co-workers have explored the application of another biological pore, listeriolysin O (LLO), from the pathogenic bacterium Listeria monocytogenes, as a delivery vehicle for macromolecules such as proteins into cells both in vitro and in vivo [40,96?8,146?48]. These studies exploited that a relatively high proton concentration (pH range of 4.9?.7) triggers the membr