Searching journal content for articles similar to Corbeil et al. 11 (7): 1198.

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  1. ...61-specific CD4+ T cells. (B) Intramodular connectivity versus GP33-specific CD8+ T cell kinetics correlation significance for acute-brown module genes. (C) Visualization of the acute-brown module genes. Large nodes represent hub genes with high connection densities (TOM > 0.5). (D,E) Expression...
  2. ...the env gene and one from the nef gene of HIV-1, which together constitute approximately 1.0 kb of sequence, were amplified by PCR and analyzed. HIV-1 variants from each region were resolved and excised from the gel; this was followed by direct sequencing of different viral variants. In 9 infected...
  3. ...in both CD4+ and CD8+ T-cells was sufficient to confer a protective phenotype against Salmonella infection through activation of the TMEVP3 locus (Gomez et al. 2013). Yet again, there remain many possible interpretations. A lncRNA gene whose primary function is exerted locally in cis will not be able...
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  4. ...by which progression of infect ion may be monitored are limited, increasing the value of a method that allows the direct identif ication of viral genes in host cells. The separation of single ceils for PCR was originally performed for the purpose of genetic analysis ~31~ and gene map- ping. ~32) Flow...
  5. ..., A. Krishnarao, C. Heid, B. Karger, and P.M. Williams. 1996. Quantitative competitive PCR: Analysis of amplified products of the HIV-1 gag gene by capillary electrophoresis with laser induced fluorescence detection. Anal. Biochem. (in press). GENOME METHODS Real Time Quantitative PCR Christian A...
  6. .... Quantitative assessment of HIV-1 DNA load by coamplification of HIV-1 gag and HLA-DQ-α genes. AIDS 5 : 683 – 691 . 17.. Nielson, K. , Mathur. E.J. Nielson, K. and Mathur. E.J. 1990 . Perfect match enhancer: Limits false priming events during amplification reactions. Strategies Mol. Biol. 3 : 17 . 18.. Kellogg...
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