Searching journal content for articles similar to Fan et al. 14 (5): 878.

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  1. ...FANTOM5 (Kawaji et al. 2014) or DBTSS (Suzuki et al. 2015). However, for genes expressed at a low level, whole- experiments might not have enough coverage to reliably pinpoint TSS(s).Several databases provide comprehensive DNA methylation data derived from high-throughput sequencing, including single...
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  2. ...information into a motif finding algorithm. In addition to further refining location studies for transcription factors, this method holds promise for the high-throughput screening of promoters, SNP regions, and epigenetic modifications for factor binding. Gene expression is mediated by the interaction...
  3. .... ↵ Fan, J.B., Yeakley, J.M., Bibikova, M., Chudin, E., Wickham, E., Chen, J., Doucet, D., Rigault, P., Zhang, B., Shen, R., et al. 2004 . A versatile assay for high-throughput gene expression profiling on universal array matrices. Genome Res. 14 : 878 -885. ↵ Fingeroth, J.D. 1990 . Comparative structure...
  4. ...of differentially expressed genes (Log2FC > 0.5, adj. P < 0.05) in Wnt-ON versus Wnt-OFF.CTCF and beta-catenin come into physical proximity upon Wnt activationA comparison of beta-catenin and LEF1 data (Zambanini et al. 2022) and CTCF -wide binding profiles revealed—as the motifs indicated—that RUW sites could also...
  5. ..., Zibo Zhao5, Avani P. Shah5, Katherine Novitzky6, Eileen McAnarney6, Michael-C. Keogh6, Ali Shilatifard5, Uttiya Basu4, Martha L. Bulyk3,7 and B. Franklin Pugh1,2 1Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park...
  6. ...binding assay. Both genomic regions contain equally strong matches to the octamer site (ATGCA[A/T]AT, 4C!T inboth regions) and two FOXO1binding sites (TTGTTT) (Fig. 5A). These oligonucleotides map to in vivo regions of POU5F1 binding and are located upstream of ERMN and RAB5A genes. We performed a series...
  7. ...) for characterization of innate immune response and to The Jackson Laboratory ( JAX) for gene expression analysis. In addition to these four study arms, phenotyping efforts were also performed using different sets of mice at the ORNL and Tel Aviv University (TAU) breeding facilities. Here we present the first genetic...
  8. ...and assayed their activity in electroporated retinas. A minimal basal promoter including the first 35 bp upstream of the TATA box of the bovine Rho gene and containing a single CRX site fails to drive any expression in electroporated mouse retinas (Supplemental Fig. S6D). Addition of a synthetic 50-bp DNA...
  9. ...-occurring (Fig. 1C), but similar average distances (4–5 kb) between satDNA arrays and the closest annotated element were observed for all three addressed sequence types (genes, satDNAs, TEs) (Supplemental Table S7).Having obtained a general overview of the T. freemani satellitome, we next focused on the in...
  10. ...individually by PCR. Here we present a high-throughput 3C approach, 3C-Carbon Copy (5C), that employs microarrays or quantitative DNA sequencing using 454-technology as detection methods. We applied 5C to analyze a 400-kb region containing the human β-globin locus and a 100-kb conserved gene desert region. We...
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