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Published in 2020 at "Human Mutation"
DOI: 10.1002/humu.23974
Abstract: Minisatellites, also called variable number of tandem repeats (VNTRs), are a class of repetitive elements that may affect gene expression at multiple levels and have been correlated to disease. Their identification and role as expression…
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Keywords:
start site;
number;
repeat number;
expression ... See more keywords
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Published in 2018 at "Biochemical and biophysical research communications"
DOI: 10.1016/j.bbrc.2018.07.025
Abstract: In Saccharomyces cerevisiae, the ATP-dependent chromatin remodeler, Chd1p, globally affects nucleosome positioning at coding regions, where nucleosomes are specifically and directionally aligned with respect to the transcription start site (TSS). Various auxiliary domains of remodelers…
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Keywords:
start site;
chd1p;
h3k36ac;
transcription start ... See more keywords
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Published in 2019 at "Journal of molecular biology"
DOI: 10.1016/j.jmb.2019.04.045
Abstract: Transcription starts at genomic positions called transcription start sites (TSSs), producing RNAs, and is mainly regulated by genomic elements and transcription factors binding around these TSSs. This indicates that TSSs may be a better unit…
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Keywords:
transcription;
human mouse;
reference;
start sites ... See more keywords
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Published in 2021 at "Scientific Reports"
DOI: 10.1038/s41598-021-85173-x
Abstract: MicroRNAs (miRNAs) play important roles in post-transcriptional gene regulation and phenotype development. Understanding the regulation of miRNA genes is critical to understand gene regulation. One of the challenges to study miRNA gene regulation is the…
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Keywords:
condition specific;
mirna;
mirna tss;
specific mirna ... See more keywords
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Published in 2021 at "Briefings in Bioinformatics"
DOI: 10.1093/bib/bbz178
Abstract: Abstract Motivation MicroRNAs (miRNAs) are small noncoding RNAs that play important roles in gene regulation and phenotype development. The identification of miRNA transcription start sites (TSSs) is critical to understand the functional roles of miRNA…
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Keywords:
transcription;
annotation;
start sites;
mirna tsss ... See more keywords
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1
Published in 2022 at "Nucleic Acids Research"
DOI: 10.1093/nar/gkac1126
Abstract: Abstract Chromatin remodelers have been thought to be crucial in creating an accessible chromatin environment before transcription activation. However, it is still unclear how chromatin remodelers recognize and bind to the active regions. In this…
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Keywords:
syd brm;
chromatin remodelers;
spt6l;
chromatin ... See more keywords
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Published in 2022 at "Nucleic Acids Research"
DOI: 10.1093/nar/gkac826
Abstract: Abstract Eukaryotes have evolved multiple ATP-dependent chromatin remodelers to shape the nucleosome landscape. We recently uncovered an evolutionarily conserved SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin remodeler complex in plants reminiscent of the mammalian BAF subclass, which specifically…
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Keywords:
positioning transcription;
swi snf;
transcription;
nucleosome positioning ... See more keywords
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Published in 2019 at "Genome research"
DOI: 10.1101/gr.240861.118
Abstract: Retroelement integration into host genomes affects both genome structure and function. A goal of a considerable number of investigations is to elucidate host features that influence insertion site selection. The retrotransposon Ty3 of Saccharomyces cerevisiae…
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Keywords:
targeting frequency;
frequency;
rna polymerase;
start sites ... See more keywords
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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.1026847
Abstract: The transcriptional activity of Transposable Elements (TEs) has been involved in numerous pathological processes, including neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal lobar degeneration. The TE expression analysis from short-read sequencing technologies is,…
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Keywords:
level;
expression analysis;
expression;
transcription start ... See more keywords
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Published in 2022 at "Frontiers in Molecular Biosciences"
DOI: 10.3389/fmolb.2022.953048
Abstract: Cerebral cavernous malformations are clusters of aberrant vessels that can lead to severe neurological complications. Pathogenic loss-of-function variants in the CCM1, CCM2, or CCM3 gene are associated with the autosomal dominant form of the disease.…
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Keywords:
crispr cas9;
deletion;
cas9 genome;
using crispr ... See more keywords