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This gene is one member of a family of nuclear RNA export factor genes.
In the nucleus, the exosome is required for the correct processing of several small nuclear RNA molecules.
Eukaryotes have three nuclear RNA polymerases, each with distinct roles and properties:
RP9 has been shown to interact with U2 small nuclear RNA auxiliary factor 1.
Caenorhabditis elegans nuclear RNA export factor 1 (nxf-1).
In 1965 he reported his observation that most nuclear RNA was non-coding, a view that was not widely accepted until years later.
Small nuclear RNA, or snRNA, is found in the nucleus of the cell.
Perhaps as many as 16% of pre-miRNAs may be altered through nuclear RNA editing.
Nuclear RNA export factor 2 is a protein that in humans is encoded by the NXF2 gene.
SnoRNAs are classified under small nuclear RNA in MeSH.
Small nuclear RNA (snRNP, or 'snurps'), joins with proteins to form spliceosomes.
The small nuclear RNA (snRNA) encoded by this gene is part of the U12-dependent minor spliceosome complex.
Pre-mRNA comprises the bulk of heterogeneous nuclear RNA (hnRNA).
Human nuclear cap-binding protein complex plays important role in the maturation of pre-mRNA and uracil-rich small nuclear RNA.
The genome integrates into the host genome and gets transcribed by host cell enzymes such as eukaryotic nuclear RNA polymerase II.
The hnRNPs are nucleic acid binding proteins and they complex with heterogeneous nuclear RNA (hnRNA).
U1 is a small nuclear RNA (snRNA) component of the spliceosome and is involved in pre-mRNA splicing.
In contrast to the high amount of genetic variation observed with the mitochondrial DNA marker, no genetic variation in a nuclear RNA marker was observed.
NS1 might also inhibit splicing of pre-mRNA by binding to a stem-bulge region in U6 small nuclear RNA (snRNA).
This therapy consists of modifying the U7 small nuclear RNA at the 5' end of the non-translated RNA to target regions within pre-mRNA.
The RNA found within each snRNP particle is known as small nuclear RNA, or snRNA, and is usually about 150 nucleotides in length.
FTO partially co-localizes with nuclear speckles, which supports the notion that mA in nuclear RNA is a major physiological substrate of FTO.
To the right is a diagram of a heterogeneous nuclear RNA (hnRNA), which is an unedited mRNA transcript, or pre-mRNAs.
An unusual guide snoRNA U85 was identified that functions in both 2'-O-ribose methylation and pseudouridylation of small nuclear RNA (snRNA) U5.
The splicing reaction is catalyzed by a large protein complex called the spliceosome assembled from proteins and small nuclear RNA molecules that recognize splice sites in the pre-mRNA sequence.