Results 91 to 100 of about 459,773 (306)
ChIP-Seq of ZmSNAC1, ZmNAC23 and ZmNAC20
To explore the function of ZmSNAC1, ZmNAC23 and ZmNAC20 in salt stress resistance and plant development, the downstream target genes were explored by ChIP-Seq with ZmNACs-GFP transgenic maize plants (pooled leaves and roots at V1 stage)
can liu (4453648)
core +1 more source
Background Chromatin accessibility profiling assays such as ATAC-seq and DNase1-seq offer the opportunity to rapidly characterize the regulatory state of the genome at a single nucleotide resolution.
Thomas J. F. Pranzatelli +2 more
doaj +1 more source
This study identifies the HDAC6/GATA4/HtrA1 axis as a critical driver of cellular senescence in the inner ear. GATA4 nuclear translocation, facilitated by HDAC6 downregulation, transcriptionally activates HtrA1, promoting hair cell senescence, SASP, and audio‐vestibular dysfunction in models of Ménière's disease and age‐related audio‐vestibular ...
Na Zhang +16 more
wiley +1 more source
ChIPseqRUs: A pipeline for ChIP-seq preprocessing
<p>A preprocessing pipeline for ChIP-seq, including alignment, quality control, and visualization.</p ...
Loh, Yong-Hwee (5265370) +5 more
core +1 more source
TRMT6‐mediated m1A modification in CDK9 mRNA enhances its mRNA stability and translation efficiency, thereby increasing the protein levels of CDK9. Upregulated CDK9 promotes the progression of HCC by elevating the levels of oncogenic factors including p‐STAT3, MCL1, and BCL‐2. On the other hand, CDK9 phosphorylates TARDBP at Ser254 to activate HBV core
Rui Zhang +12 more
wiley +1 more source
Informative sequence-based models for fragment distributions in ChIP-seq, RNA-seq and ChIP-chip data [PDF]
Many high throughput sequencing protocols for RNA and DNA require that the polynucleic acid is fragmented so that the identity of a limited number of nucleic acids of one or both of the ends of the fragments can be determined by sequencing. The nucleic
Dyer, Nigel
core
vanrooij-lab/chip-seq-pipeline2: timmer-et-al-2024
<p>Scripts chip-seq pipeline used for Timmer et al.
Jin wook Lee, Soo Lee, J. Seth Strattan
core +1 more source
ChIP-seq of PbAP2R-2 and differential expression analysis between WT and pbap2r-2(-).
(A) Cross-fertilization assay among pbap2r-2(-), p48/45(-) and p47(-). The number of normal and abnormal ookinetes are indicated as white and grey bars, respectively. Error bars indicate the standard error of the mean (n = 3).
Izumi Kaneko (121023) +3 more
core +1 more source
Universal count correction for high-throughput sequencing.
We show that existing RNA-seq, DNase-seq, and ChIP-seq data exhibit overdispersed per-base read count distributions that are not matched to existing computational method assumptions.
Tatsunori B Hashimoto +2 more
doaj +1 more source

