「Methylation」の共起表現一覧(1語右で並び替え)
該当件数 : 134件
| Figure 2: DNA | methylation analysis methods not based on methylation-s |
| modifications, such as protein acetylation, | methylation and ubiquitinylation. |
| It is used in organic synthesis for | methylation and occasionally as a precipitating agent. |
| y binding to coactivators increases histone | methylation and enhances the accessibility of promoter |
| Differential | methylation and phosphorylation of coilin likely influe |
| ting is an epigenetic process that involves | methylation and histone modifications in order to achie |
| ic and reversible inhibitor of nucleic acid | methylation, and as such is widely used in biochemical |
| ng via histone modifications - acetylation, | methylation and phosphorylation. |
| n, for their "pioneering discoveries on DNA | methylation and its role in gene expression." |
| r, for their "pioneering discoveries on DNA | methylation and its role in gene expression." |
| O-methyl transferase) catalyzing the B-ring | methylation and S-Adenosyl-L-methyl-3H methionine being |
| The ability to learn more about | methylation and TF binding sites on a genome wide scale |
| Methylation and demethylation of histones turns the gen | |
| ression, binding, modification (such as DNA | methylation), and other related applications. |
| ablishment of the relationships between DNA | methylation and cancer (Jones and Laird), the roles of |
| ibition or alterations in the status of DNA | methylation are responsible for the carcinogenic potent |
| The Illumina | Methylation Assay using the Infinium II platform uses " |
| arried out, DamID can be subject to plasmid | methylation biases. |
| High pressure can be used to accelerate | methylation by dimethyl carbonate. |
| They can be degraded either by | methylation by catechol-O-methyltransferases (COMT) or |
| It is considered to act on the | methylation cycle methylation cycle which may have a de |
| The | methylation cycle causes a transfer of a methyl group ( |
| myelopathy is caused by disruptions in the | methylation cycle. |
| ls with alkylating agents that mainly cause | methylation damage. |
| MethDB is a database for DNA | methylation data. |
| PubMeth: a cancer | methylation database combining text-mining and expert a |
| ethionine synthase enzyme is disrupted, the | methylation decreases and myelination of the spinal cor |
| remodeling of epigenetic marks, such as DNA | methylation, during mammalian development. |
| A twofold | methylation forms the bis-lactim. |
| mals and is thought to act as a 2'-O-ribose | methylation guide for ribosomal RNA. |
| mals and is thought to act as a 2'-O-ribose | methylation guide for ribosomal RNA. |
| Oryza sativa and is predicted to acts as a | methylation guide for 25S ribosomal RNA in plants . |
| mals and is thought to act as a 2'-O-ribose | methylation guide for ribosomal RNA. |
| sativa genome and is proposed to acts as a | methylation guide for 18S ribosomal RNA in plants . |
| sativa genome and is predicted to acts as a | methylation guide for 25S ribosomal RNA in plants . |
| C/D box small nucleolar RNA that acts as a | methylation guide for 18S ribosomal RNA in plants. |
| opsis thaliana and is proposed to acts as a | methylation guide for 18S ribosomal RNA (rRNA) in plant |
| mals and is thought to act as a 2'-O-ribose | methylation guide for ribosomal RNA. |
| C/D box snoRNAs have been shown to act as | methylation guides for a number of RNA targets. |
| Several genes control | methylation in Neurospora and mutation of the DNA methy |
| ons to our understanding of the role of DNA | methylation in the control of gene expression." |
| ons to our understanding of the role of DNA | methylation in the control of gene expression." |
| Histone | methylation is generally associated with transcriptiona |
| Histone | methylation is the modification of certain amino acids |
| DNA | methylation is often utilized to silence and regulate g |
| thereby disproving the theory that histone | methylation is permanent once and for all. |
| the fetus, however, there is evidence that | methylation is increased during pregnancy and that it c |
| ther with similar modifications such as DNA | methylation it is part of the epigenetic code. |
| ass the entire human genome, it can measure | methylation level at 27,578 CpG dinucloeotides in 14,49 |
| and pyrosequencing, this method quantifies | methylation levels at specific loci within the genome. |
| This region regulates CpG | methylation levels of somatically acquired differential |
| Methylation may also be linked to cancer development as | |
| DNA | methylation may be necessary for normal growth from emb |
| Methylation occurs on carbon nr 5. | |
| This | methylation occurs on cytosine residues. |
| The | methylation occurs through alternating reductive and ox |
| e has very little repeated DNA, half of the | methylation occurs in repeated DNA including transposon |
| Methylation of uracil produces thymine. | |
| The resistance mechanism is | methylation of the 23s binding site. |
| However, | methylation of some lysine and arginine residues of his |
| snoRNA R38 guides the | methylation of 2'-O-ribose sites in 28S rRNA. |
| Thioflavin S results from the | methylation of dehydrothiotoluidine with sulfonic acid. |
| methylation of lysine 9 of histone H3) which target the | |
| The | methylation of both 2' hydroxy-groups is shown on the d |
| NORD48 is predicted to guide the 2'O-ribose | methylation of 28S rRNA C2279 . |
| It is predicted to guide 2'O-ribose | methylation of the large 28S rRNA on residue U4276. |
| ORD100 is predicted to guide the 2'O-ribose | methylation of 18S ribosomal RNA (rRNA) at residue G436 |
| U35 is predicted to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) residue C4506 . |
| Histamine N-methyltransferase catalyzes the | methylation of histamine in the presence of S-adenosylm |
| U103 is predicted to guide the 2'O-ribose | methylation of 18S ribosomal RNA (rRNA) residue G601. |
| HBII-43 is predicted to guide 2'O-ribose | methylation of 28s ribosomal RNA (rRNA) at position U37 |
| Examples include | methylation of lysine 4 of histone 3 (H3K4), and argini |
| Methionine is likely responsible for the | methylation of the hydroxyl group on the aromatic ring |
| It is predicted to guide 2'O-ribose | methylation of 18S ribosomal RNA(rRNA) at residue A166 |
| Thioflavin T is obtained by the | methylation of dehydrothiotoluidine with methanol in th |
| ORD111 is predicted to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) at residue G392 |
| It is predicted to guide 2'O-ribose | methylation of ribosomal RNA (rRNA) 28S at residue C386 |
| U15 is predicted to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) residue A3764 . |
| cq and is predicted to guide the 2'O-ribose | methylation of U4 snRNA C8 . |
| U38 is predicted to guides the | methylation of 2'-O-ribose residues in 28S ribosomal RN |
| U29 is proposed to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) residue A4493 . |
| U102 is predicted to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) residue G4020. |
| cially available; it may be prepared by the | methylation of 1,8-diaminonaphthalene with iodomethane |
| It is predicted to guide the 2'-O-ribose | methylation of 28s ribosomal RNA (rRNA) at residue A453 |
| U62 is predicted to guide the 2'O-ribose | methylation of 18S ribosomal RNA (rRNA) reside A590. |
| esponsible for both de novo and maintenance | methylation of tumor suppressor genes. |
| NORD37 is predicted to guide the 2'O-ribose | methylation of the 28S ribosomal RNA (rRNA) at residue |
| lso be synthesized on a laboratory scale by | methylation of imidazole at the pyridine-like nitrogen |
| yl form of vitamin B12 that is required for | methylation of homocysteine. |
| nate in vivo binding site, resulting in the | methylation of neighboring GATCs. |
| II-234 and is predicted to guide 2'O-ribose | methylation of the small 18S rRNA on position A512. |
| Methylation of the transcriptional coactivator CBP by P | |
| rginine N-methyltransferase-4 (PRMT4/CARM1) | methylation of arginine residues within proteins plays |
| h snoRNAs are predicted to guide 2'O-ribose | methylation of the large 28S ribosomal RNA (rRNA) subun |
| ls and is predicted to guide the 2'O-ribose | methylation of 18S ribosomal RNA (rRNA) residue C517. |
| Further modifications include the possible | methylation of the 2' hydroxy-groups of the first 2 rib |
| l nucleolar ribonucleoprotein that mediates | methylation of pre-ribosomal RNAs. |
| urity in MDMA which has been synthesized by | methylation of MDA using methylating reagents such as m |
| ic E. coli is controlled by Dam through the | methylation of the two GATC sites proximal and distal t |
| .. Its is predicted to guide the 2'O-ribose | methylation of 18S ribosomal RNA (rRNA) at residue A99 |
| Methylation of Ada protein converts it into a self tran | |
| ls and is predicted to guide the 2'O-ribose | methylation of 28S ribosomal RNA (rRNA) at residue C384 |
| Methylation of CpG sites within the promoters of genes | |
| ligand to their periplasmic domains and by | methylation of specific glutamate residues on their cyt |
| initiated against alkylation, particularly | methylation, of guanine or thymine nucleotides or phosp |
| play an important role in epigenetics; the | methylation of specific lysines of certain histones in |
| Methylation often occurs on nucleic bases in DNA or ami | |
| ation by processes such as phosphorylation, | methylation, or glycosylation. |
| lantation embryos has been shown to disrupt | methylation patterns at imprinted loci and plays a cruc |
| lls must have their original biparental DNA | methylation patterns erased and re-established based on |
| , 17), demonstrating the inheritance of DNA | methylation patterns (18), and isolating the first vert |
| terochromatin and possessing unique histone | methylation patterns. |
| acetylation as well as other modifications ( | methylation, phosphorilation, ubiquitination) may frame |
| this intermediate to methionine, through a | methylation reaction carried out by methionine synthase |
| yme S-adenosylmethionine (SAM) is used in a | methylation reaction, SAH is produced. |
| by binding to the enzymes that catalyse the | methylation reaction, DNA methyltransferases; and titra |
| lmethionine (SAM) , a cofactor used in many | methylation reactions. |
| e nucleotide polymorphisms, analysis of DNA | methylation, relative mRNA quantification, chromosomal |
| ating agents are compounds that can inhibit | methylation, resulting in the expression of the previou |
| ooped out to search for the nearest d(GATC) | methylation site to the mismatch, which could be up to |
| Methylation specific oligonucleotide microarray was dev | |
| some isoschizomers allows identification of | methylation state of the restriction site while isolati |
| Methylation Statistics | |
| hemist, Irvine worked on the application of | methylation techniques to carbohydrates, and isolated t |
| tro, but it is still more active at de novo | methylation than other DNMTs. |
| (Schizosaccharomyces) have very little DNA | methylation, the model filamentous fungus Neurospora cr |
| For many years histone | methylation was thought to be a permanent modification. |
| cause diverse changes in the pattern of DNA | methylation, which may provide a link between chromatin |
| Methylation with trimethylaluminium affords hexamethyl | |
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|