Searching journal content for articles similar to Kotze et al. 4 (6): 352.

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  1. ...reconstruction (Banecki et al. 2024) by modeling multiple scHi-C maps simultaneously and leveraging their ordering, as determined by a TI method or the scHi-C experiment itself. Themethod incorporates the knowledge about cell order by adding metarestraints to the molecular dynamics simulation (MD; see Methods...
  2. ...polymorphism (RFLP) analysis 574 Genomic DNA was amplified by PCR using gene-specific primers and Diastar Taq DNA 575 polymerase (Solgent). The following primer pairs were used for PCR amplification: for 576 EFTUD2: 5′–AGAGTGGCTGTGATACCG–3′ (forward) and 5′–577 GAAGCACTAACAGTGAGGG–3′ (reverse); for KPNB1: 5...
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  3. ...(Toropainen et al. 2016). Coactivation of both AR and GR led to a substantial increase of hormone-regulated genes compared with DHT-only treatment (Fig. 3B), and only a small proportion of genes lost their hormone regulation upon DexDHT treatment. In support, RT-qPCR analyses performed in PC3-AR cells...
  4. ...beads. To focus on individual candidate genes predicted to be bound by the protein of interest, precipitated DNA can be analyzed using qPCR with primers designed specifically against the regulatory sequences of the GOIs. Alternatively, in ChIP-seq following precipitation, cross-links are reversed...
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  5. ...within the same FunFam. (*) Known cancer genes from CGC.Figure 2, B through D, provide illustrative examples of FIEs in three functional families in which mutations affected the same functional site in multiple paralogs, including those in the known cancer genes EGFR and RAC1. Although this study focused...
  6. ...PCR and high-throughput sequencing. No significant off-target effects were detected by this method (Supplemental Fig. S5). RNA-seq analysis of seven-gene-edited cells revealed increased expression of genes involved in DNA replication, repair pathways, p53 signaling, and cancer-related pathways...
  7. ..., it is worthwhile to exploit the ancestor estimation approach based on the prior information from the reference population, which avoids calculating multiple K values.Here, we propose an algorithmic framework, HITSNP, to screen feature SNPs from deep WGS and evaluate its ability in breed diversity estimation...
  8. ...to the reference with Burrows-Wheeler Aligner 0.7.18 (Li and Durbin 2010). Sequence Alignment Map (SAM) files were converted into Binary Alignment Maps (BAM) with SAMtools 1.18 (Danecek et al. 2021). Quality filter and removal of PCR duplicates were performed with SAMtools using the view and markdup functions...
  9. ...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...
  10. ...stem cell–derived SOD1E100G MNs and shows that dysregulation of VGF, INA, and PENK is a strong disease predictor across species and SOD1 mutations. Our study reveals MN population-specific gene expression and temporal disease-induced regulation that together provide a basis to explain ALS selective...
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