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1 (activating transcription factor 6) or XBP1 (X-box-binding protein 1).
2 factors C/EBP homologous protein and spliced X box-binding protein 1.
3 regulatory factor-1, nucleophosmin, and the X-box binding protein-1.
4 y of the UPR and governs expression of XBP1 (X-box binding protein 1), a key transcription factor tha
5 UPR by promoting the nuclear localization of X-box binding protein 1, a transcription factor central
6 ER, regulates the expression and activity of X-box binding protein 1, a transcription factor required
7 revealed upregulation of the spliced form of X-box binding protein-1s, a potent transcription factor
8 hol alone increased messenger RNA of spliced X box-binding protein 1 and decreased SERCA, which were
9 fusion resulted in up-regulations of spliced X-box binding protein 1 and activating transcription fac
10 of HCV E1 and/or E2 also induced splicing of X-box binding protein 1 and transactivation of the unfol
14 smic reticulum kinase, inositol-requiring 1A/X box binding protein 1, and activating transcription fa
15 1 do not repress Pax5 mRNA and do not induce X-box binding protein 1, and mu secreted mRNA normally,
16 mphocyte inducer of maturation program 1 and X-box binding protein 1, are not up-regulated in secreti
17 breast cancers, including GATA-3, LIV-1, and X-box binding protein 1, did not show a similar pattern
18 ves the messenger RNA (mRNA) encoding XBP-1 (X-box-binding protein 1), enabling splicing and producti
19 eficiency, B cell-specific CD79a-Cre x XBP1 (X-box binding protein-1) floxed mice (XBP1-conditional k
22 bition of FAS also induces the processing of X-box binding protein-1, indicating that the IRE1 arm of
23 VEGF, high glucose, or H2O2 up-regulated the X-box binding protein-1/inositol-requiring protein-1 (IR
24 B cells fail to efficiently induce Blimp-1, X box-binding protein-1, J chain, or secretory Ig mu tra
25 oniae augmented inositol-requiring protein 1/X-box binding protein 1-mediated production of autophagy
26 y quantifying UPR target gene expression and X-box binding protein 1 messenger RNA (mRNA) splicing.
27 Transient expression of ERdj4 and ERdj5 in X-box binding protein 1(-/-) mouse embryonic fibroblasts
28 ha endoriboneclease activities, which led to X-box binding protein 1 mRNA cleavage, an ER stress mark
29 alpha, DNA damage-inducible transcript 3 and X-box binding protein-1 mRNA levels were reduced in both
31 homologous protein), and not parallel XBP1 (X box-binding protein 1) or ATF6 pathways, using siRNA a
32 ose-regulated protein 78 (Grp78) and spliced X-box binding protein-1 (sXBP-1) mRNA levels were reduce
33 se-regulated protein 78 (GRP78), the spliced X-box-binding protein 1 (sXBP-1), the glucose-regulated
34 1alpha resulted in the generation of spliced X-box binding protein 1 (sXBP1) and upregulation of lipi
35 ing enzyme 1alpha (IRE1alpha)-active spliced X-box binding protein 1 (sXBP1) axis and instrumental to
36 location of the transcription factor spliced X-box binding protein-1 (sXBP1) is selectively impaired
38 (AID) and transcription factors (Blimp-1 and X-box binding protein 1) that are critical to the B cell
39 s led to downregulation of AID, Blimp-1, and X-box binding protein 1, thereby inhibiting CSR, SHM, an
40 teins and activating a transcription factor, X-box-binding protein 1, through endonucleolytic cleavag
42 ctor 4 (ATF-4), ATF-6, and a spliced form of X-box binding protein 1, were up-regulated in PBMCs from
44 antly, B7-2 engagement induced expression of X-box binding protein 1 (XBP-1) and spliced XBP1, eviden
45 e-induced maturation protein 1 (Blimp-1) and X-box binding protein 1 (XBP-1) are required for plasma
48 embryonic fibroblasts that are deficient for X-box binding protein 1 (XBP-1), a key transcription fac
49 mas of several IL-4-induced genes, including X-box binding protein 1 (XBP-1), a regulator of the UPR.
50 potential role for a CREB/ATF family member, X-box binding protein 1 (XBP-1), in trans-activating the
51 ull synergistic IFN-beta production requires X-box binding protein 1 (XBP-1), this UPR-regulated tran
52 ted IgM in the endoplasmic reticulum (ER) of X-box binding protein 1 (XBP-1)-deficient B cells has be
53 ced resistance to ER stress dependent on the X-box binding protein 1 (XBP-1)/inositol requiring enzym
55 R chaperone protein BiP, the spliced form of X-box binding protein-1 (Xbp-1) mRNA, and the transcript
58 is directly induced by the spliced (active) X-box binding protein-1 (XBP-1s), a transcription factor
60 sential role in plasma cell differentiation, X-box-binding protein 1 (XBP-1), also activates the tran
63 of carbonic anhydrase VI (CA-VI), and active X-box-binding protein-1 (Xbp-1) were all induced signifi
65 re we show that p85alphaalpha interacts with X-box-binding protein-1 (XBP-1), a transcriptional media
68 , the only known role of the spliced form of X-box-binding protein-1 (XBP-1s) in metabolic processes
69 ndent messenger RNA splicing (activation) of X-box-binding protein-1 (XBP-1s) to inflammation in peri
71 tol-requiring enzyme 1-dependent splicing of X box binding protein 1 (XBP1) mRNA, activation of activ
72 highlighted the importance of IRE1alpha and X box binding protein 1 (XBP1), key members of this path
73 vated expression of the transcription factor X box-binding protein 1 (XBP1) in DC appears to play a d
74 folded protein response transcription factor X-box binding protein 1 (XBP1) in liver regeneration usi
75 e present study, we investigated the role of X-box binding protein 1 (XBP1) in retinal adhesion molec
76 ere we report that developmental ablation of X-Box binding protein 1 (XBP1) in the nervous system, a
77 beta activates the ER stress response factor X-box binding protein 1 (XBP1) in transgenic flies and i
81 panning 858 nucleotides in the 3' UTR of the X-box binding protein 1 (XBP1) mRNA that regulates its c
82 ain Ig binding protein (BiP) and splicing of X-box binding protein 1 (XBP1) mRNA, but no lung fibrosi
83 ctivity causes sequence-specific cleavage of X-box binding protein 1 (XBP1) mRNA, resulting in upregu
84 me 1alpha (IRE1alpha) is activated to splice X-box binding protein 1 (XBP1) mRNA, thereby increasing
88 he RNase-inactive IRE1alpha or the activated X-box binding protein 1 (XBP1), the canonical IRE1alpha
90 , we developed transgenic mice expressing an X-box binding protein 1 (XBP1)-luciferase construct that
94 protein response (UPR) transcription factor X-box binding protein-1 (Xbp1) in intestinal epithelial
97 us podocyte-specific genetic inactivation of X-box binding protein-1 (Xbp1), a transcription factor a
98 ector of the UPR is the transcription factor X-box binding protein-1 (XBP1), which is expressed on ER
99 nase-like ER kinase (PERK), up-regulation of X-box-binding protein 1 (XBP1) and glucose-regulated pro
100 PRNP promoter, is regulated by ER stress and X-box-binding protein 1 (XBP1) but not by activating tra
101 ng enzyme 1 (IRE1) and its downstream target X-box-binding protein 1 (XBP1) drive B-cell differentiat
102 ies are required to splice the mRNA encoding X-box-binding protein 1 (XBP1) for terminal differentiat
104 iring enzyme 1 alpha (IRE1alpha) to initiate X-box-binding protein 1 (Xbp1) mRNA splicing in adult pr
107 element (ERSE)-luciferase reporter activity, X-box-binding protein 1 (XBP1) splicing, and immunoglobu
108 nts of ER stress response mediators, such as X-box-binding protein 1 (XBP1), confer genetic risk for
109 mponents, including the transcription factor X-box-binding protein 1 (XBP1), is increased following e
114 IKKbeta phosphorylates the spliced form of X-Box Binding Protein 1 (XBP1s) and increases the activi
115 p38 MAPK) phosphorylates the spliced form of X-box binding protein 1 (Xbp1s) on its Thr48 and Ser61 r
117 ing of mice induces up-regulation of spliced X-box binding protein 1 (XBP1s), which regulates the end
119 he physiological role of the spliced form of X-box-binding protein 1 (XBP1s), a key transcription fac
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