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1 s to the mammalian transcriptional regulator Yin Yang 1 (YY1) and other members of the GLI-Kruppel fa
2 Here, we identify the transcription factor Yin Yang 1 (YY1) as a critical regulator of oligodendroc
4 acts, we identified the transcription factor Yin Yang 1 (YY1) as the protein that binds to this conse
5 vealed that the sequence contains a putative Yin Yang 1 (YY1) binding site overlapped with a putative
6 ce-specific DNA-binding transcription factor Yin Yang 1 (YY1) binds to and recruits the histone H4 (A
8 ubiquitously expressed transcription factor Yin Yang 1 (YY1) contributes to enhancer-promoter struct
11 Here, we show that the transcription factor Yin Yang 1 (YY1) in brown adipose tissue activates the c
14 n binding sites for the transcription factor Yin Yang 1 (YY1) in their proximal promoters, but the ph
15 s report, we describe the phosphorylation of Yin Yang 1 (YY1) in vitro and in vivo by CK2alpha (casei
32 he Gli-Krueppel-related transcription factor Yin Yang 1 (YY1) showed the most dramatic transactivatio
33 edicted binding site for the cellular factor Yin Yang 1 (YY1) that overlaps with GC box 2 was also id
36 PI-0052 inhibits the transcription repressor Yin Yang 1 (YY1) which regulates TRAIL resistance and ne
37 ity shift assays (EMSAs), we now report that Yin Yang 1 (YY1), a multifunctional protein that can act
38 ranscription factors screened, we found that Yin Yang 1 (YY1), a repressor of sarcomeric gene express
39 We identify another zinc finger protein, Yin Yang 1 (YY1), at the base of looping interactions be
40 e found rs7647481A nonrisk allele binding of Yin Yang 1 (YY1), confirmed by allele-specific chromatin
41 hat the binding of the transcription factor, Yin Yang 1 (YY1), to hs3 and to the mu E1 site of the in
42 ts the overexpressed transcription repressor Yin Yang 1 (YY1), which negatively regulates Fas and DR5
52 es we demonstrate that transiently expressed yin yang 1 protein (YY1) inhibits the SREBP-mediated act
53 overexpression leads to reduced occupancy of Yin Yang 1 transcription factor at the promoter region o
57 ansducers and activators of transcription 5, Yin Yang 1, CCAAT/enhancer binding protein, and the gluc
59 ed domain that is also present at the end of Yin Yang 1-associated protein-related protein (YARP) and
61 iction that the -74 T allele created a novel Yin-Yang 1 (YY-1) binding site adjacent to an existing o
62 mics, we identified the transcription factor yin-yang 1 (YY1) as a common target of mTOR and PGC-1alp
63 We show that the ubiquitously expressed TF Yin-Yang 1 (YY1) binds to both gene regulatory elements
64 lar proliferation and differentiation, while Yin-Yang 1 (YY1) has been shown to control the expressio
65 e direct role of the transcription repressor yin-yang 1 (YY1) in the regulation of resistance to CH-1
66 he ubiquitous autosomal transcription factor Yin-Yang 1 (YY1) in the transcriptional activation of Xi
70 and activity of the transcription repressor Yin-Yang 1 (YY1) that negatively regulates Fas transcrip
71 previously reported that the nuclear factor Yin-Yang 1 (YY1), a ubiquitous DNA-binding protein, is a
72 cells was associated with the creation of a Yin-Yang 1 binding site that overlapped a STAT motif inv
75 inactivation of the transcription repressor yin-yang 1 DNA binding activity to the silencer region o
77 we report that the zinc-finger protein YY-1 (Yin-Yang 1) can bind to multiple elements within the hum
78 Complex B contains the nuclear factor YY1 (Yin-Yang 1), whose function is to down-regulate ASRF act
80 l. demonstrate that the transcription factor Yin Yang-1 (YY1) regulates proliferation in three-dimens
81 g tagged SNAP(c) subunits is associated with Yin Yang-1 (YY1), a factor implicated in both activation
82 he ubiquitous mammalian transcription factor Yin Yang-1 and is encoded by pleiohomeotic, a known memb
83 ism within the promoter abolished binding of yin yang-1, which is identified as a negative regulator
84 lator of mouse embryonic stem cells (mESCs), Yin-yang 2 (YY2), that is controlled by the translation
85 hed Thulium doped fibre laser (TDFL) with a 'Yin-Yang' all-fibre cavity scheme based on a combination
86 opens an avenue to systematically study the yin-yang balance and its health implications with the us
87 TCM) has effectively relied on the theory of yin-yang balance in diagnoses and treatments of diseases
91 an adaptive pathway displaying a dichotomic yin yang characteristic; it initially contributes in saf
92 ng with DNA methyltransferases (DNMTs) in a "Yin-Yang" complex targeted to chromatin and enhanced by
93 hese findings provide strong evidence that a yin-yang coupling mechanism generates concerted, antisym
96 distinct human populations suggests that the yin yang haplotypes are likely to predate the African di
100 red disulfide bonds, this study develops the yin-yang hypothesis for signal transmission through the
102 alian transcription repressor-activator YY1 (Yin-Yang I), has now been identified in the 3' region.
103 attempted to define the physical meaning of yin-yang in TCM by correlating it with biochemical proce
104 infectious agents, orchestrate fibrosis in a yin-yang interaction with hepatic stellate cells, and ar
107 TPP1 in telomere maintenance, and support a yin-yang model in which TPP1 and POT1 function as a unit
111 ever, coalescent simulation reveals that the yin yang phenomenon can be explained by strictly neutral
115 s report of KaiC repression that there is a "yin-yang" regulation of gene expression whereby kaiA ove
116 that APPL isoforms function as an integrated Yin-Yang regulator of adiponectin signaling and mediate
118 Here we report further evidence of this yin-yang relationship by demonstrating that O-GlcNAc tra
120 ication is demonstrated for the example of a yin-yang-shaped gold-coated iHWG fabricated within an al
122 us, vertebrate SerRS and c-Myc is a pair of 'Yin-Yang' transcriptional regulator for proper developme
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