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  1. ...corresponding to DNA molecules with full-6mApT congregation within an LD (Fig. 5H) and across adjacent LDs (Fig. 5I), respectively. (H) Full-6mApT congregation within an LD. (I) Full-6mApT congregation across adjacent LDs.We also analyzed human chromatin in vitro methylated by AMT1 complex or M.EcoGII (Fig. 6D...
  2. ...in chromatin. Small DNA fragments excised from accessible DNA sequences (typically regulatory elements) are isolated and sequenced. However, the rest of the is excluded from the analysis because it is still present as very long DNA molecules. Consequently, the signal and relative amounts of each accessible...
  3. ...buffer overnight at 37°C, and DNA was precipitated using ethanol. The 4C libraries were multiplexed and single-end 1 × 150-bp sequencing was performed on the Illumina MiSeq.RNA-seq experimental procedureTotal RNA was extracted from U2OS cells with or without MYC induction in duplicate, using the RNeasy...
  4. ...L. The polymerase was then inactivated for 3 min at 65°C. MDA-amplified DNA clean-up was performed with 1:1.3 (v/v) ratio AMPure XP beads (Beckman Coulter A63881) immediately before the de-branching step. To screen nuclei for those with the most even -wide amplification, multiplexed PCR primers were designed...
  5. ...cohort among PDAC patients. Finally, we identify and validate the casein kinase CSNK1A1 (also known as CK1alpha or CK1a) as an APA-regulated therapeutic target in PDAC. Knockdown or pharmacological inhibition of CSNK1A1 attenuates PDAC cell proliferation and clonogenic growth. Our single-cancer analysis...
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