City to activate complement [101]. The frequency of deficient or non-functional MASP-2 ranges from 2 to 19 in different populations with the highest values in Africans [102]. We speculate that relative MBL excess in the setting of relatively low C4 levels or deficient MASP-2 may lead to MBL-mediated enhanced viral infections in clinical settings. Thus, we propose that MBL, C4 and MASP-2, among o

S) were enriched through the use of SCX, IEF (in an OFFGEL apparatus) or HILIC and analyzed by mass spectrometry. MS spectra for putative arginine methylated peptides were manually verified for the presence of a 1:1 methyl-SILAC pair. An example methyl-SILAC pair is shown. For each separation method, the total number of Meth-R sites identified as well as the novel ones is indicated; B, Meth-R-cont

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Nding gendered influences on women's reproductive health in Pakistan: moving beyond the autonomy paradigm. Soc. Sci. Med., 68(7), 1349-56. http://dx.doi.org/10.1016/j.socscimed.2009.01.025 National Institute of Population Studies (NIPS) Islamabad Pakistan Macro International Inc. USA (June 2008). Pakistan Demographic and Health Survey 2006-07. Patton, M. Q. (1999). Enhancing the quality and credib

R 15.4 cells. To do so, we designed a modified quantitative RTPCR (RT-qPCR). Our modified method, herein named RT-DNA-qPCR (RT-DqPCR), is based on the fact that molar ratio between two genes in genomic DNA is equal (see Supplemental text 1). In short, RT-DqPCR involves normalization of values obtained by amplification of cDNA to those obtained by amplification of genomic DNA with the same primer p

R 15.4 cells. To do so, we designed a modified quantitative RTPCR (RT-qPCR). Our modified method, herein named RT-DNA-qPCR (RT-DqPCR), is based on the fact that molar ratio between two genes in genomic DNA is equal (see Supplemental text 1). In short, RT-DqPCR involves normalization of values obtained by amplification of cDNA to those obtained by amplification of genomic DNA with the same primer p