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  1. ...collaborative study to assess a set of reference reagents for HIV-1 PCR. J. Virol. Methods 37 : 23 – 42 . 6.. Feature Article. 1991 . Guidelines for a quality assurance program for DNA analysis. Crime Laboratory Digest 18 : 44 – 75 . 7.. Kitchin, P.A. , Bootman. J.S. Kitchin, P.A. and Bootman. J.S. 1993...
  2. ...DS4, and KIR3DL2 exons 1–5 within the tA01 haplotype, forming the tA01-del9-hybd1 haplotype (Fig. 3G; Norman et al. 2009; Pyo et al. 2013).Real-time quantitative polymerase chain reaction (qPCR) was used to further verify CNVs in the KIR framework genes in 11 HPRC samples (HG002, HG00733, HG00741, HG...
  3. ..., including those relevant to angiogenesis and inflammation as well as to changes in chemokine- and cytokine-related signaling (Table 3). Quantification of 20 genes associated with chemokine and cytokine response as well as endothelial function confirmed the close association between qRT-PCR and m...
  4. ...in nonhuman primates are, in general, poor predictors of human defense reactions in clinical trials, which can lead to fatal outcomes (Suntharalingam et al. 2006). Possible reasons include molecular differences in downstream signaling cascades or simply poor cross-reactivity of detection kits and assays...
  5. ...by Bowtie. For both sequencing and ChIP-seq, only reads that mapped uniquely to hg18 with, at most, three mismatches were kept. MethylC-seq reads were mapped as previously described (Lister et al. 2009). RNA-seq reads were mapped by the TopHat program. For non-RNA libraries, PCR duplicates were removed...
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