「r rna」の共起表現一覧(1語右で並び替え)
該当件数 : 102件
by any ribosomal proteins but by ribosomal RNA ( | rRNA), a ribozyme. |
al ribonucleate adenosine 2'-methyltransferase, | rRNA adenosine 2'-methylase, RNA-pentose methylase, |
Based on 16S | rRNA analysis, P. straminea has been placed in the P |
Based on 16S | rRNA analysis, P. putida has been placed in the P. p |
It will decrease | rRNA and other genes transcription but will increase |
from Hypsipetes than Iole is, whereas mtDNA 12S | rRNA and 16S rRNA sequence data places it actually c |
Binding between 5S | rRNA and TFIIIA serves to both repress further trans |
function in the modification of ribosomal RNA ( | rRNA) and transfer RNA (tRNA). |
e software package for phylogenetic analysis of | rRNA and other biological sequences. |
The RNA molecules ( | rRNA and tRNA) played an important role in the catal |
transcriptional modification of ribosomal RNAs ( | rRNA) and in some cases of small nuclear RNAs (sRNAs |
ue specific) and the lack of complementarity to | rRNA and SnRNA. |
However, the GC content of ribosomal RNA ( | rRNA) and transfer RNA (tRNA) genes in hyperthermoph |
ition to these, mitochondrial and chloroplastic | rRNA are also amplified. |
he 2'O-ribose methylation of 18S ribosomal RNA ( | rRNA) at residue A99 3 |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) at residue C3848.. Its is related to mouse sno |
he 2'O-ribose methylation of 18S ribosomal RNA ( | rRNA) at residue G436. |
de 2'O-ribose methylation of 28s ribosomal RNA ( | rRNA) at position U3797. |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) at residue G3923. |
e 2'-O-ribose methylation of 28s ribosomal RNA ( | rRNA) at residue A4531. |
'O-ribose methylation of the 28S ribosomal RNA ( | rRNA) at residue A3697 . |
cted to guide the 2'O-ribose methylation of 28S | rRNA C2279 . |
5.8S | rRNA can be used as a reference gene for miRNA detec |
ed identification methods are mainly based upon | rRNA derived phylogenetic conclusions. |
rRNA forms not only secondary but also tertiary stru | |
tures proteins, including RNases, and separates | rRNA from ribosomes, while phenol, isopropanol and w |
This structure is of the 5S | rRNA from the Escherichia coli 50S ribosomal subunit |
g f-AFLP, automated ribotyping, full-length 16S | rRNA gene sequencing and DNA-DNA hybridization. |
n to highly conserved primer binding sites, 16S | rRNA gene sequences contain hypervariable regions th |
As a result, 16S | rRNA gene sequencing has become prevalent in medical |
mes been included in the Rhizaria, based on 18S | rRNA gene sequencing, it has been concluded that the |
Based on 16S | rRNA gene sequences, it is most similar to S. perori |
ts at a specific site in the 28S ribosomal RNA ( | rRNA) genes of most insect genomes In order to inser |
ecause it a) is (due to the high copy number of | rRNA genes) easy to amplify even from small quantiti |
According to the comparisons of 16S | rRNA genes, Ignicoccus represents a new, deeply bran |
v., a unique halophilic archeon, with three 16s | rRNA genes, that grows only in defined medium with g |
oteins preferentially bind to its complementary | rRNA if it is present, rather than mRNA. |
equence and is located at the 3' end of the 16S | rRNA in the ribosome. |
s as a methylation guide for 18S ribosomal RNA ( | rRNA) in plants . |
18S | rRNA is the structural RNA for the small component o |
molecular biology the 5.8S ribosomal RNA (5.8S | rRNA) is a non-coding RNA component of the large sub |
5.8S | rRNA is also found in archaea. |
16S ribosomal RNA (or 16S | rRNA) is a component of the 30S subunit of prokaryot |
18S ribosomal RNA (abbreviated 18S | rRNA) is a part of the ribosomal RNA. |
18S | rRNA is a component of the small eukaryotic ribosoma |
rRNA is the one of the only genes present in all cel | |
5S ribosomal RNA (5S | rRNA) is a component of the large ribosomal subunit |
Eukaryotic 5S | rRNA is synthesised by RNA polymerase III, whereas m |
A reduced amount of | rRNA means that ribosomal proteins (r-proteins) will |
r, in one case it is far (3 kilobases) from the | rRNA methyltransferase gene. |
bonucleic acid-adenine (N6) methylase, ErmC 23S | rRNA methyltransferase, and S-adenosyl-L-methionine: |
attractive hypothesis in view of the fact that | rRNA methyltransferases can bind RNA, and therefore |
ure found upstream of genes predicted to encode | rRNA methyltransferases, possibly for 23S rRNA. |
m primers which amplify all RNA which is mostly | rRNA, miRNA microarray ligate an oligonucleotide to |
A 3D representation of a 5S | rRNA molecule. |
D is found in tRNA and | rRNA molecules as a nucleoside; the corresponding nu |
ol binds to A2451 and A2452 residues in the 23S | rRNA of the ribosome and inhibits peptide bond forma |
o guide 2'O-ribose methylation of the small 18S | rRNA on position A512. |
RNA situated between structural ribosomal RNAs ( | rRNA) on a common precursor transcript. |
o guide 2'O-ribose methylation of the large 28S | rRNA on residue U4276. |
Targets of (p)ppGpp include | rRNA operons, of which there are seven in Escherichi |
not predicted to guide to 2'O-methylation of a | rRNA or snRNA. |
Read from 5' to 3', this polycistronic | rRNA precursor transcript contains the 5' external t |
catalyze their own excision from mRNA, tRNA and | rRNA precursors in a wide range of organisms. |
In the nucleus it is involved in precursor | rRNA processing, where it cleaves the internal trans |
he 2'O-ribose methylation of 18S ribosomal RNA ( | rRNA) reside A590. |
he 2'O-ribose methylation of 18S ribosomal RNA ( | rRNA) residue C517. |
uide the 2'-O-methylation of 28S ribosomal RNA ( | rRNA) residue A-2634 . |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) residue C4506 . |
he 2'O-ribose methylation of 18S ribosomal RNA ( | rRNA) residue G601. |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) residue A3764 . |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) residue A4493 . |
he 2'O-ribose methylation of 28S ribosomal RNA ( | rRNA) residue G4020. |
Its function is thought to be in 5.8S | rRNA ribosome translocation. |
hael orders and families in accordance with 16S | rRNA sequence data". |
acement was eventually verified using mtDNA 12S | rRNA sequence data. |
Unique 16S | rRNA sequence. |
For this reason many thousands of | rRNA sequences are known and stored in specialized d |
Lemuridae has been dated to 26.1 ±3.3 mya while | rRNA sequences of mtDNA place the split at 24.9 ±3.6 |
rum pernix based on comparative analysis of 23S | rRNA sequences". |
y, thermophily and monophyly from environmental | rRNA sequences". |
Trees based on | rRNA show the Hartmannellidae as usually defined are |
The large 50S ribosomal subunit contains two | rRNA species (the 5S and 23S rRNAs). |
ous small noncoding RNA genes, such as tRNA, 5S | rRNA, SRP RNA and U6 snRNA genes , which are transcr |
Overall, 50S is generally monolithic and | rRNA structure is stabilized by proteins. |
ose methylation of the large 28S ribosomal RNA ( | rRNA) subunit on residue G4198 . |
snoRNAs and guides the pseudouridylation of 28S | rRNA subunit at position U4565. |
seudouridylation of the U372 residue in the 28S | rRNA subunit. |
ght be more proteins or transcripts involved in | rRNA than previously and/or that some snoRNAs have d |
c organisms shows distinct bands of 28s and 18s | rRNA, the 28s band being approximately twice as inte |
7 in Drosophila 28S and U1920 in Drosophila 18S | rRNA to pseudouridine . |
modification of uridine 3316 in Drosophila 28S | rRNA to pseudouridine |
roliferation and it may also be a regulator for | rRNA transcription. |
This binding causes a reduction in | rRNA transcription. |
c regions of rDNA (for small- and large-subunit | rRNA), variation among individual rDNA repeats can s |
are usually reserved for sections that code for | rRNA, whereas endolytic cleavage corresponds to tRNA |
es of this enzyme are S-adenosyl methionine and | rRNA, whereas its two products are S-adenosylhomocys |
es of this enzyme are S-adenosyl methionine and | rRNA, whereas its two products are S-adenosylhomocys |
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