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  1. ...after repression of each cCRE. A one-way ANOVA with a Dunnett's post hoc test was used to compare gene expression. (F–K) RT-qPCR for MYH6 (F), MYH7 (G), NPPA (H), NPPB (I), TNNT2 (J), and ATP2A2 (K) 15 days following activation of each cCRE in human iPSC-CMs ±1 µM ET-1 for 72 h. A two-way ANOVA...
  2. ...the PDB helps predict putative rare driver events in lung tumors. By extending the analysis with high-quality structural models from AlphaFold using The Encyclopedia of Domains (TED), we find a significant increase in the diversity of both genes and functional families with postduplication FIEs in lung...
  3. ....5; FDR ≤0.01) in D1 ΔXp cells compared to both WT clones and WT EV clones (Fig. 2E). Of note, we did not notice such an increase in expression for Jpx, Ftx, and Rlim in RT-qPCR analysis (Supplemental Fig. S2C). Additionally, the expression of Chic1(log2 FC > 3; FDR ≤0.01), a gene located in the adjacent...
  4. ...coding gene expression with qPCR-validated targets. Our findings demonstrate that quantifying mRNA fragments from sRNA-seq experiments provides a reliable approach to investigate microRNA–mRNA interactions when total RNA-seq is unavailable.The analysis of gene expression is a cornerstone of functional...
  5. ...single-gene RNAPII elongation rate estimates, we implemented several improvements in our computational pipeline, including relying on wave front estimation as described above. Additionally, several other new method features, such as improved background correction and the removal of PCR duplicates, also...
  6. .... 2021). Quality filter and 397 removal of PCR duplicates were performed with SAMtools using the view and markdup functions, 398 respectively. Mapped, filtered, and deduplicated reads were counted into genomic windows of 399 Sadu Murari et al., Page 18 1Mb using the intersect function from BEDTools 2...
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  7. ...Cell type–specific gene regulatory atlas prioritizes drug targets and repurposable medicines in Alzheimer's disease Yunxiao Ren1,2, Ming Hu3,4, Yang E. Li5, Andrew A. Pieper6,7,8,9,10,11, Jeffrey Cummings12 and Feixiong Cheng1,2,4,13 1Cleveland Clinic Genome Center, Cleveland Clinic Research...
  8. ...of the Austrian Academy of Sciences, 1090 Vienna, Austria; 11Eric and Wendy Schmidt Center, The Broad Institute of MIT and Harvard, Cambridge, MA 02141, USA Corresponding author: valentina.boeva@inf.ethz.chAbstractGene signature scoring is integral to single-cell RNA sequencing (scRNA-seq) data analysis...
  9. ...using the NEB Ultra II directional RNA library prep kit with sample purification beads (NEB E7765), with 10–14 PCR cycles (determined empirically to achieve the minimum number of cycles per library). Libraries were then sequenced on an Illumina HiSeq 2000 in single-end mode, except for the 12 h time...
  10. ...) Gene expression measured after CRISPRi of the caPeak21014 region. Compared with a pool of nontargeting control gRNAs, a pool of gRNAs targeted to the enhancer led to lower expression of RALGPS2. Each point represents the mean of three qPCR replicates for an independently transfected well. Lines...
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