「rn a」の共起表現(1語左が「the」) - Weblio英語共起表現検索

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共起表現

「rn a」の共起表現一覧(1語左が「the」)

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The primer is allowed to anneal to the	RNA and reverse transcriptase is used to synthesize
In this environment, the	RNA started to replicate.
here are two major approaches to understand the	RNA accumulation in meiocytes: 1) RNA-seq and 2) Mi
iation of DNA transcription, the capping of the	RNA transcript, and attachment to the spliceosome f
othetical lipid-based structure that, under the	RNA world hypothesis, could have confined RNA in an
A pre-cell allowed the	RNA to remain in close proximity with other RNA mol
In other cases, the	RNA molecules are the actual functional products.
s a possible functional association between the	RNA and the protein.
Further analysis has shown that the	RNA is well conserved and highly expressed in cyano
fragments that were formerly hybridized to the	RNA fragment.
However, it is unknown if the	RNA is used by phages.
ly(A) tail can also recruit RNases that cut the	RNA in two.
naturally occurring pseudoknot is found in the	RNA component of human telomerase.
can recruit another protein complex, called the	RNA polymerase.
oop (the stem-loop closest to the 5' end of the	RNA) has significant covariation in support of its
He and his group discovered that the	RNA molecule alone was sufficient for the observed
Because of the	RNA motif's consistent gene association and a possi
ver, the genetic data, complex structure of the	RNA and the failure to detect a protein involved in
gulatory subunit cyclin C are components of the	RNA polymerase II holoenzyme complex, which phospho
e splicing, a process by which the exons of the	RNA produced by transcription of a gene are reconne
Upon ingestion, it binds to the	RNA polymerase II enzyme, effectively causing cytol
exonuclease activity and serves to degrade the	RNA primers used to initiate DNA synthesis.
on including the Miller-Urey experiment and the	RNA World.
in, which causes a conformational change in the	RNA molecule.
de an easy way of digital quantification of the	RNA transcript abundances in biological samples.
Patricia Thomas, developer of the	RNA blot which then became known as the northern bl
ng interactions in helices and destabilizes the	RNA structure.
e Rev response element (RRE) is a region in the	RNA molecule of the HIV env gene.
Specifically, it inhibits the assembly of the	RNA polymerase II transcription complex and DNA pol
InvR has been shown to bind the	RNA chaperone Hfq in vitro and Hfq is required for
Gpp associates with the promoter it affects the	RNA polymerase enzyme's ability to bind and initiat
the repressor protein physically obstructs the	RNA polymerase from transcribing the genes.
ops with loops L3 and L4 that interact with the	RNA target.
Because the 5' end of the	RNA molecule ends in a phosphate group, the bond fo
Dicer catalyzes the first step in the	RNA interference pathway and initiates formation of
nucleotide identity are present throughout the	RNA motif, and many contain short runs of adenosine
ed domain which assists in the formation of the	RNA polymerase holoenzyme, or may operate through a
of RNase P and the enzymatic properties of the	RNA subunit of that enzyme.
general transcription factors that make up the	RNA polymerase II preinitiation complex.
Only four instances of the	RNA were detected, and all are in the bacterial phy
After digestion of the	RNA, a single stranded DNA (ssDNA) is left and beca
general transcription factors that make up the	RNA polymerase II preinitiation complex.
on signal and thus allows for the export of the	RNA even if its introns aren't spliced out.
general transcription factors that make up the	RNA polymerase II preinitiation complex.
y cDNA is created with labelled primers for the	RNA sequence of interest to act as the probe in the
Since the	RNA could be in the 5' UTRs of protein-coding genes
methyl group (-CH3) to the 2'-O position in the	RNA backbone.
This complex cleaves the	RNA between the polyadenylation sequence and the GU
bout 200 adenine units to the new 3' end of the	RNA molecule using ATP as a precursor.
has also been adopted by some adherents of the	RNA world model.
initiation by stabilizing the formation of the	RNA polymerase holoenzyme enabling faster clearance
This has relevance for prebiotic studies of the	RNA world and DNA world hypothesis for the origin o
lation is the control of gene expression at the	RNA level, therefore between the transcription and
Upon ingestion, it binds to the	RNA polymerase II enzyme which completely prevents
n intron, and the snRNP subunits bring fold the	RNA so that the 5' and 3' ends of the intron are jo
ted into Xenopus oocytes to ultimately find the	RNA species that induced the expression of sodium-g
are cis-regulatory elements functioning at the	RNA level, since bacterial cis-regulatory RNAs typi
ing the course of his studies he discovered the	RNA sequence necessary for ribosome binding and the
computationally predicts the structures of the	RNA input sequences rather than requiring experimen
x) is a multi-protein complex consisting of the	RNA helicase Mtr4, a poly(A) polymerase (PAP) (eith
the 5' UTR, so it is not inconceivable that the	RNA has a role as a cis-regulatory element.
rial, resulting in a starting milestone for the	RNA world hypothesis, which speculates about furthe
nd the formation of a channel through which the	RNA can enter the cell.
t of the nucleus and into the cytosol where the	RNA is degraded, for example by the exosome complex
mi-1 RNAs known, it is also unknown whether the	RNA structure might extend further in the 5′ or 3′
s; for example, in the protein-bound state, the	RNA could form an intrinsic transcription terminati
As a result, the	RNA is cleaved at an internal processing site (IPS)
ved stem-loops whose terminal loops contain the	RNA sequence ACGR, where R represents either A or G
coming ribosome pauses because of a knot in the	RNA, then the polypeptide can have time to fold int
es and in several contexts sequestration of the	RNA transcript occurs in eukaryotes but not in prok
The phosphorylated 5' end of the	RNA strand enters a conserved basic surface pocket
f its molecule and nonspecific affinity for the	RNA molecules on its other end, which allows it to
hoto-regulation of the translation of psbA, the	RNA encoding for the photoisystem II core protein D
er protein content than the bacterial ones, the	RNA cores from all three lineages are homologous --
ot followed by a poly-Uracil sequence cause the	RNA polymerase to pause, but it will typically cont
ID), a transcription factor that is part of the	RNA polymerase II holoenzyme, interacts with promot
ated, were the chromatin expands and occurs the	RNA transcription and DNA replication.

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