「his tone」の共起表現(2語右で並び替え)

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UTX has been linked with	histone demethylation, a potential means of regulatin
	Histone deacetylases act via the formation of large m
It has	histone deacetylase activity and represses transcript
It possesses	histone deacetylase activity and represses transcript
ylline in vitro can restore the reduced HDAC (	histone deacetylase) activity that is induced by oxid
on of nucleosomes from free histones and DNA (	histone chaperone activity).
re typically silenced or downregulated due to	histone deacetylase activity.
receptor interacting domains and an intrinsic	histone acetyltransferase activity.
These histones of the	histone octamer all contain N-terminal tails that ema
	Histone acetylation/deacetylation alters chromosome s
The opposing enzymatic activities of	histone acetyltransferases and histone deacetylases,
ine residues restoring the positive charge to	histone proteins and hence the tie between histone an
cally, butyrate treatment of cells results in	histone hyperacetylation, and butyrate itself inhibit
CDK3 can phosphorylate	histone H1 and interacts with an unknown type of cycl
hromatin by binding to coactivators increases	histone methylation and enhances the accessibility of
	Histone acetylation and deacetylation, catalyzed by m
udies provided inspiration for the eukaryotic	histone code and underlie the modern study of epigene
teract with some basal transcription factors,	histone acetyltransferases, and methyltransferases.
am was based on DNA sequences of both nuclear	histone H3 and mitochondrial cytochrome-c oxidase I (
are sequestered by the addition of the linker	histone (H1), and various length of "linker" DNA (~0-
Two specific JmjC	histone demethylases are PHF8 and KIAA1718.
	Histone tails are normally positively charged due to
	Histone acetylation as well as other modifications (m
-loop binding protein (SLBP - also termed the	histone hairpin binding protein, or HBP).
Structural determinants of	histone recognition by readers, writers and erasers o
The MITR protein lacks the	histone deacetylase catalytic domain.
cell, neutralizes the positive charges on the	histone by changing amines into amides and decreases
makrishnan is also known for his past work on	histone and chromatin structure.
See nucleosome,	histone and chromatin.
This gene is found in the small	histone gene cluster on chromosome 6p22-p21.3.
repression and to interact with components of	histone deacetylase co-repressor complexes including
	Histone acetylase coactivators increase the rate of a
found that N-terminal regions of Gli1 recruit	histone deacetylase complexes via SuFu, which are inv
gh the C-terminal domain, also interacts with	histone deacetylase complexes.
binds specifically to mononulceosomes and the	histone H2A/H2B dimer, but not to the H3/H4 tetramer
-terminus of Spt16 (a common feature of known	histone chaperones) does not prevent Spt16 from formi
Very recently two families of	histone demethylating enzymes were discovered.
Panobinostat inhibits multiple	histone deacetylase enzymes, a mechanism leading to a
an HDAC inhibitor, inhibiting the function of	histone deacetylase enzymes, thereby favoring an acet
e protein encoded by this gene belongs to the	histone deacetylase/acuc/apha family and is a compone
This gene product belongs to the	histone deacetylase family.
e protein encoded by this gene belongs to the	histone deacetylase/acuc/apha family.
gene has sequence homology to members of the	histone deacetylase family.
ene is intronless and encodes a member of the	histone H1 family.
coded by this gene belongs to class II of the	histone deacetylase/acuc/apha family.
ncoded by this gene belongs to class I of the	histone deacetylase/acuc/apha family.
ses and the acetoin utilization proteins, the	histone deacetylases form an ancient protein superfam
1996, Allis and colleagues discovered that a	histone acetyltransferase from Tetrahymena was the ho
It interacts with chromatin, the	histone methyltransferase G9a (responsible for the mo
equences are enriched for the heterochromatic	histone modification H3K9me3.
Other	histone modifications have similar or opposite effect
	Histone H4, Hsp70, melanocortin-4-receptor).
The critical concept of the	Histone Code Hypothesis is that the histone modificat
ould then propagate across the surface of the	histone octamer in a wave-like manner, resulting in t
essential vehicle for determining the role of	histone acetylation in chromatin structure and functi
genetic process that involves methylation and	histone modifications in order to achieve monoallelic
it replaces 1 or both copies of conventional	histone H3 in the (H3-H4)2 tetrameric core of the nuc
	Histone acetyltransferases including CBP histone acet
(INN) or gavinostat (originally ITF2357) is a	histone deacetylase inhibitor with potential anti-inf
Zolinza was the first	histone deacetylase inhibitor approved by the U.S. Fo
known as SNDX-275 and MS-275, is a benzamide	histone deacetylase inhibitor undergoing clinical tri
Mocetinostat (MGCD0103) is a benzamide	histone deacetylase inhibitor undergoing clinical tri
and the University of Tokyo found it to be a	histone deacetylase inhibitor with effects similar to
	Histone deacetylase inhibitors (HDI) have a broad spe
The linker	histone, H1, interacts with linker DNA between nucleo
Other	histone proteins involved: H1 H2A H3 H4
A	histone gene is a gene that codes for histone protein
	Histone methylation is generally associated with tran
	Histone H2B is one of the 5 main histone proteins inv
	Histone methylation is the modification of certain am
	Histone H1.5 is a protein that in humans is encoded b
In general,	histone acetylation is linked to transcriptional acti
The	Histone Code is a hypothesis that the transcription o
A	histone octamer is an octamer of the histones found a
The mRNAs of metazoan	histone genes lack polyadenylation and a poly-A tail,
ay of the Non-coding RNA ANRIL and Methylated	Histone H3 Lysine 27 by Polycomb CBX7 in Transcriptio
mono- and di-methylated lysines, specifically	histone 3, lysines 4 and 9 (H3K4 and H3K9).
e for the sequence of RNA's and proteins, the	Histone Code may ultimately be responsible for the ep
Many of the	histone tail modifications correlate very well to chr
Acetylation of	histone core particles modulates chromatin structure
ed into heterochromatin and possessing unique	histone methylation patterns.
Polyuridylation of a	histone mRNA promotes its degradation, involving the
	Histone deacetylases remove those acetyl groups, incr
For details of gene expression regulation by	histone modifications see table below.
	Histone deacetylases, such as HDAC11, control DNA exp
group of RNAs that can be polyuridylated are	histone mRNAs that lack a poly(A) tail.
tein-protein interaction for example with the	histone acetyltransferase TIP60 (HIV-1 Tat interactin
Allis was the first to mechanistically link	histone acetylation to transcription activation.
emethylase, converting specific trimethylated	histone residues to the dimethylated form.
These positive charges help the	histone tails to interact with and bind to the negati
emethylase, converting specific trimethylated	histone residues to the dimethylated form, and as a t
nc atom in the binding pocket of Zn-dependent	histone deacetylase to block its activity.
with Hir1p and Hir2p, the two corepressors of	histone gene transcription characterized in the yeast
The	Histone 3' UTR stem-loop is an RNA element involved i
For many years	histone methylation was thought to be a permanent mod
ate 2005 the Jumonji domain-containing (JmjC)	histone demethylases were discovered which are able t
methylation of lysine 9 of	histone H3) which target the genomic region for heter
molecule involved in the splicing of metazoan	histone pre-mRNAs, which are spliced by a different m
MT1), but does not affect the interactions of	histone methyltransferases with KCNQ1OT1.

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