Searching journal content for articles similar to Arts et al. 13 (10): 2325.

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  1. ...the identification of tumor-essential genes and tumor-promoting mutations in vivo. Cell Rep 10: 1422–1432. ↵Baumer S, Baumer N, Appel N, Terheyden L, Fremerey J, Schelhaas S, Wardelmann E, Buchholz F, Berdel WE, Muller-Tidow C. 2015. Antibody-mediated delivery of anti–KRAS-siRNA in vivo overcomes therapy resistance...
  2. ...of genome-scale siRNA and cDNA arrayed libraries enable the comprehensive global analysis of gene function. However, the current repertoire of high-throughput detection methodologies has limited the scope of cellular phenotypes that can be studied. In this report, we describe the systematic identification...
  3. ...separately transfected HUVECs with a vector containing siRNA targeting the DOC1 gene (psiRNA-Neo-Doc1) and a vector containing a sequence (psiRNA-Neo-Control), which, after BLAST search, resulted in complementary binding only to the intronic sequence of the human Tyrosine Hydroxylase gene. Figure 6...
  4. ...or implicated to be causal, there is a need to prove the causality, a phase of gene discovery termed target validation. The gold standard for proving that a gene is causal is to knock in the particular allele or mutation responsible for the trait, or replace the defect with a “normal” allele to demonstrate...
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