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1 ivation, and increased polyubiquitination of TNF receptor-associated factors.
2                                              TNF receptor-associated factor 1 (TRAF1) is a unique TRA
3                       One of these proteins, TNF receptor-associated factor 1 (TRAF1), is highly regu
4                  AITR associates with TRAF1 (TNF receptor-associated factor 1), TRAF2, and TRAF3, and
5 osome-linked IAP, Bcl-2, Bcl-x(L), Bfl-1/A1, TNF receptor-associated factor 1, and cellular Fas-assoc
6                   The tumor necrosis factor (TNF) receptor-associated factor 1 (TRAF1) is a member of
7 bitor of apoptosis protein (c-IAP1), c-IAP2, TNF receptor-associated factor-1 (TRAF-1), TRAF-2, B-cel
8 romosome-linked IAP (XIAP), Bcl-2, Bfl-1/A1, TNF receptor-associated factor-1 (TRAF1), and Fas-associ
9 or necrosis factor (TNF) family members, and TNF receptor-associated factor-1 (TRAF1).
10 s (SAPKs, Jun NH2-terminal kinases) requires TNF receptor associated factor 2 (TRAF2).
11 B-inducing kinase-IKK was interrupted at the TNF receptor associated factor 2 and NF-kappa B-inducing
12 eptor 1-TNF receptor associated death domain-TNF receptor associated factor 2 NF-kappa B-inducing kin
13 , TNF receptor 2 (TNF-R2) interacts with the TNF receptor associated factors 2/1 (TRAF2/TRAF1) hetero
14 ding of CD154 (gp39, CD40L) to CD40 recruits TNF receptor- associated factor 2 (TRAF2) and TRAF3 to t
15 am of receptor-interacting protein (RIP) and TNF receptor- associated factor 2.
16 induces IRAK1 sumoylation in the presence of TNF receptor-associated factor 2 (TRAF2) and intracellul
17 B and JNK activity associated with increased TNF receptor-associated factor 2 (TRAF2) and NF-kappaB e
18             We examined the contributions of TNF receptor-associated factor 2 (TRAF2) and TRAF3 to CD
19          The death domain kinase RIP and the TNF receptor-associated factor 2 (TRAF2) are essential e
20 of the Fn14-TRAF domain site or depletion of TNF receptor-associated factor 2 (TRAF2) expression by s
21                                              TNF receptor-associated factor 2 (TRAF2) is a signal-tra
22   In addition, we also demonstrated that the TNF receptor-associated factor 2 (TRAF2) plays little ro
23                   Furthermore, we found that TNF receptor-associated factor 2 (TRAF2) recruitment is
24                    Both CD40 and CD120b bind TNF receptor-associated factor 2 (TRAF2) upon ligand sti
25                                              TNF receptor-associated factor 2 (TRAF2) was identified
26  we discovered that GAPDH interacts with the TNF receptor-associated factor 2 (TRAF2), a protein requ
27  and CD160 engagement induced recruitment of TNF receptor-associated factor 2 (TRAF2), but not TRAF3,
28 ptosis signal-regulating kinase 1 (ASK1) and TNF receptor-associated factor 2 (TRAF2), regulation of
29 aling by TRANCE-R appears to be dependent on TNF receptor-associated factor 2 (TRAF2), since JNK indu
30 aprolin (TTP) is Lys-63-polyubiquitinated by TNF receptor-associated factor 2 (TRAF2), suggesting a r
31 wn to be important for CD40 association with TNF receptor-associated factor 2 (TRAF2), TRAF3, and TRA
32                      One gene in particular, TNF receptor-associated factor 2 (TRAF2)-inhibiting prot
33 s and c-Jun NH(2)-terminal kinases) requires TNF receptor-associated factor 2 (TRAF2).
34 d to the TNF receptor 1 (TNF-R1) complex via TNF receptor-associated factor 2 (TRAF2).
35 K) is the recruitment to the TNF receptor of TNF receptor-associated factor 2 (TRAF2).
36  c-jun N-terminal kinase (JNK/SAPK) requires TNF receptor-associated factor 2 (TRAF2).
37 cells, along with the selective reduction of TNF receptor-associated factor 2 and impairment in the a
38 e/IkappaBalpha kinase was interrupted at the TNF receptor-associated factor 2 and NF-kappaB-inducing
39        Overexpression of a dominant negative TNF receptor-associated factor 2 construct, lacking the
40 d IL-6, and the cytoplasmic adaptor molecule TNF receptor-associated factor 2 is involved in both R-8
41  Tumor necrosis factor alpha (TNF-alpha) and TNF receptor-associated factor 2 protein were moderately
42 40 ligation, and inhibits the recruitment of TNF receptor-associated factor 2 to the CD40.
43 e essential for GAPDH-mediated activation of TNF receptor-associated factor 2 ubiquitination.
44                        Cbl-b associates with TNF receptor-associated factor 2 upon CD40 ligation, and
45 at beta-arrestin-1 is associated with TRAF2 (TNF receptor-associated factor 2), an adaptor protein of
46 osis protein 1, Bcl-2, Bcl-xL, survivin, and TNF receptor-associated factor 2), proliferation (cyclin
47 F-alpha induced the ubiquitination of TRAF2 (TNF receptor-associated factor 2), which interacts with
48 ter gene expression activated by TNF, TNFR1, TNF receptor-associated factor 2, and NF-kappaB-inducing
49 eptor, TNF receptor-associated death domain, TNF receptor-associated factor 2, NF-kappa B-inducing ki
50 e activated by receptor-interacting protein, TNF receptor-associated factor 2, NF-kappaB-inducing kin
51  IKK-beta, TNF receptor-associated factor 6, TNF receptor-associated factor 2, receptor-interacting p
52 ulin were related to increased expression of TNF receptor-associated factor 2, the product of an NF-k
53     These data suggest that TNFR1, through a TNF receptor-associated factor 2-NF-kappaB signaling pat
54 rs or dominant-negative forms of p38 MAPK or TNF receptor-associated factor 2.
55 level of cIAP1 and, in some cases, cIAP2 and TNF receptor-associated factor 2.
56 eptor 1/TNF receptor-associated death domain/TNF receptor-associated factor 2/NF-kappaB-inducing kina
57 cytoplasmic domain of CD40, while binding of TNF receptor-associated factors 2 and 3 is dispensable,
58 microscopy revealed that JAB1 interacts with TNF receptor-associated-factor 2 (TRAF2).
59                       Tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2) and receptor-i
60                      Tumour-necrosis factor (TNF) receptor-associated factor 2 (TRAF2) is a key compo
61                       Tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2) is a key media
62                       Tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2) is an adaptor
63                       Tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2) is an intracel
64  molecules, including tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2).
65 h the adapter protein tumor necrosis factor (TNF) receptor-associated factor 2 (TRAF2).
66 paB regulator, TRAF2 (tumor necrosis factor (TNF) receptor-associated factor 2), as an oncogene that
67 (E2) Ubc13 for binding to the RING domain of TNF-receptor associated factor 2 (TRAF2), thereby inhibi
68                                              TNF-receptor-associated factor 2 (TRAF2), an E3 ubiquiti
69 RADD (TNF receptor-associated death domain), TNF receptor-associated factor-2 (TRAF-2), the Ser/Thr k
70 ptor proteins, including the docking protein TNF receptor-associated factor-2 (TRAF-2), which is beli
71          The subcellular localization of the TNF receptor-associated factor-2 (TRAF2) adaptor protein
72                        In particular, Bcl-2, TNF receptor-associated factor-2 (TRAF2), and TRAF4 were
73                     Because hCG also blocked TNF receptor-associated factor-2 and NF-kappaB-inducing
74  both knockdowns reduce expression of TRAF2 (TNF receptor-associated factor-2) protein, and small int
75 IP (receptor-interacting protein), or TRAF2 (TNF receptor-associated factor-2) were caused by apoptog
76 hibitor of apoptosis-1), cIAP-2, and TRAF-2 (TNF receptor-associated factor-2)) in an NF-kappaB-depen
77 tor 1, TNF receptor-associated death domain, TNF receptor-associated factor-2, NF-kappaB-inducing kin
78 tor 1, TNF receptor-associated death domain, TNF receptor-associated factor-2, NF-kappaB-inducing kin
79  by TNF receptor-associated death domain and TNF receptor-associated factor-2.
80                  In this study, we show that TNF receptor associated factor 3 (TRAF3) plays a critica
81 as used to explore the in vivo expression of TNF receptor-associated factor 3 (TRAF-3), a putative si
82              PTPN22 directly associated with TNF receptor-associated factor 3 (TRAF3) and promotes TR
83 D88 as a prototypical adaptor, we identified TNF receptor-associated factor 3 (TRAF3) as a new compon
84                           Here we identified TNF receptor-associated factor 3 (TRAF3) as a regulator
85 vely regulated by the full-length isoform of TNF receptor-associated factor 3 (Traf3) as formation of
86                          The adaptor protein TNF receptor-associated factor 3 (TRAF3) is a critical r
87                          The adaptor protein TNF receptor-associated factor 3 (TRAF3) regulates signa
88 athway signaling by promoting degradation of TNF receptor-associated factor 3 (Traf3), a potent inhib
89 , but not RANKL, increased OCP expression of TNF receptor-associated factor 3 (TRAF3), an adapter pro
90 d the effect of selective deletion in TEC of TNF receptor-associated factor 3 (TRAF3), an inhibitor o
91 volves degradation of an inhibitory protein, TNF receptor-associated factor 3 (TRAF3), but how this s
92  inhibiting Lys(63)-linked ubiquitination of TNF receptor-associated factor 3 (TRAF3).
93 ine kinase RICK, which was then able to bind TNF receptor-associated factor 3 (TRAF3).
94                       Tumor necrosis factor (TNF) receptor-associated factor 3 (TRAF3) regulates both
95 onstrate that loss of tumor necrosis factor (TNF) receptor-associated factor 3 (TRAF3) results in con
96 in and failed to bind tumor necrosis factor (TNF) receptor-associated factor 3 (TRAF3), a TBK1 comple
97 uniparental disomy in tumor necrosis factor (TNF) receptor-associated factor 3 and TNFalpha-induced p
98                  LTbetaR, not HveA, recruits TNF receptor-associated factor-3 (TRAF3), and LIGHT-indu
99  induces IDO and involves the recruitment of TNF receptor-associated factor-3 to the Toll-like recept
100 uous degradation by a tumor necrosis factor (TNF) receptor-associated factor-3 (TRAF3)-dependent E3 u
101                                  We identify TNF receptor associated factor 4 (TRAF4) as a novel Drap
102 f p47(phox) and recovered the orphan adapter TNF receptor-associated factor 4 (TRAF4).
103 ownstream gene-TRAF4 (tumor necrosis factor [TNF] receptor associated-factor 4)-that functions in cel
104     Here, we identify tumor necrosis factor (TNF)-receptor-associated factor-4 (TRAF4) as a new targe
105            The cytoplasmic signaling protein TNF receptor-associated factor 5 (TRAF5) has been implic
106 is inhibited by dominant negative mutants of TNF receptor-associated factor 5 (TRAF5), TRAF6, NF-kapp
107                           p62 interacts with TNF receptor associated factor 6 (TRAF6) and is required
108  found to activate NF-kappaB in concert with TNF receptor associated factor 6 (TRAF6), we propose tha
109 l analyses revealed that DAB2 interacts with TNF receptor-associated factor 6 (TRAF6) and attenuates
110                                              TNF receptor-associated factor 6 (TRAF6) associates with
111 NKL-induced NF-kappaB activation and delayed TNF receptor-associated factor 6 (TRAF6) deubiquitinatio
112 completely understood, but ubiquitination of TNF receptor-associated factor 6 (TRAF6) has recently be
113                                              TNF receptor-associated factor 6 (TRAF6) is an adaptor p
114                                              TNF receptor-associated factor 6 (TRAF6) is an adaptor p
115                                              TNF receptor-associated factor 6 (TRAF6) is identified a
116                                              TNF receptor-associated factor 6 (TRAF6), a verified tar
117     Upon LPS challenge, CREBH interacts with TNF receptor-associated factor 6 (TRAF6), an E3 ubiquiti
118                This study demonstrates that, TNF receptor-associated factor 6 (TRAF6), an E3 ubiquiti
119                     This activation requires TNF receptor-associated factor 6 (TRAF6), and U(L)37 con
120 urthermore, NOSTRIN interacted directly with TNF receptor-associated factor 6 (TRAF6), leading to the
121 1 receptor-associated protein kinase (IRAK), TNF receptor-associated factor 6 (TRAF6), phosphatidylin
122 rectly interacting with the TRAF-C domain of TNF receptor-associated factor 6 (TRAF6), resulting in i
123 thin a recently identified binding motif for TNF receptor-associated factor 6 (TRAF6).
124 se 1, IL-1 receptor-associated kinase 4, and TNF receptor-associated factor 6 (TRAF6).
125 1 receptor-associated kinase 1 (IRAK-1), and TNF receptor-associated factor 6 (TRAF6).
126 -1 receptor-associated kinase 1 (IRAK-1) and TNF receptor-associated factor 6 (TRAF6).
127  Lys-34 and required the E3 ubiquitin ligase TNF receptor-associated factor 6 after stimulation of ce
128 se-pair with sequences in the 3' UTRs of the TNF receptor-associated factor 6 and IL-1 receptor-assoc
129 ys-63-linked polyubiquitination at Lys-34 by TNF receptor-associated factor 6 and is thereby activate
130 nd prevents the dissociation of, IRAK-IRAK-4-TNF receptor-associated factor 6 from the TLR signaling
131 ion of IL-1 receptor-associated kinase 1 and TNF receptor-associated factor 6 protein levels.
132 ependent upon binding of the adapter protein TNF receptor-associated factor 6 to the cytoplasmic doma
133 ase) and subsequently integrates with TRAF6 (TNF receptor-associated factor 6) and/or c-fos signaling
134 ukin-1 receptor-associated kinase)1/4-TRAF6 (TNF receptor-associated factor 6), leading to integrin a
135 d expression of the signal transducer TRAF6 (TNF receptor-associated factor 6), leading us to conside
136 e system of IKK complex activation by TRAF6 (TNF receptor-associated factor 6), we show that these pe
137 AK1, TAB1 (TAK1 binding protein), and TRAF6 (TNF receptor-associated factor 6).
138  involving MyD88, IL-1R-associated kinase 1, TNF receptor-associated factor 6, and IkappaB kinase and
139 ts of myeloid differentiation protein, IRAK, TNF receptor-associated factor 6, and NF-kappaB-inducing
140 otein interactions with IKK-alpha, IKK-beta, TNF receptor-associated factor 6, TNF receptor-associate
141 leukin (IL)-1 receptor-associated kinase and TNF receptor-associated factor 6, two key adaptor/scaffo
142 luding MyD88, IL-1R-associated kinase 4, and TNF receptor-associated factor 6, while it inhibited the
143 terleukin-1 receptor-activated kinase-1, and TNF receptor-associated factor 6.
144 isolated NASPs act either via or upstream of TNF receptor-associated factor 6.
145 t signaling by disrupting the recruitment of TNF receptor-associated factor 6/c-Src complex to lipid
146 the molecular adaptor tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6) exhibit a spec
147                       Tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6) is a key media
148                      Tumour-necrosis factor (TNF) receptor-associated factor 6 (TRAF6) is the only TR
149 es demonstrated that tumour necrosis factor (TNF) receptor-associated factor 6 (TRAF6) plays a key ro
150 estigated the role of tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6), an adaptor pr
151    Here we show that tumour necrosis factor (TNF) receptor-associated factor 6 (TRAF6), an adaptor pr
152 d kinase (IRAK-1) and tumor-necrosis factor (TNF) receptor-associated factor 6 (TRAF6), which are kno
153    We also found that tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6), which mediate
154 luding IL-1 receptor-associated kinase 4 and TNF-receptor associated factor 6.
155 he CINC promoter by IL-17 in IEC-6 cells was TNF receptor-associated factor-6 (TRAF6), but not TRAF2,
156 r gene activity was 16-fold higher following TNF receptor-associated factor-6 transfection after IL-1
157 ly interacts with IL-1R-associated kinase-1, TNF receptor-associated factor-6, TGF-beta-activated kin
158  cells, is dependent upon a MyD88-dependent, TNF receptor-associated factor-6-independent signaling p
159 l survival by hindering interactions between TNF-receptor-associated factors, blocking their negative
160              We have identified a Drosophila TNF-receptor-associated factor, DTRAF1, by screening for
161 te that cells lacking TRAF3, a member of the TNF receptor-associated factor family, are defective in
162    Here we identified mutations in TRAF3IP1 (TNF Receptor-Associated Factor Interacting Protein 1) in
163 mary gland identified tumor necrosis factor (TNF) receptor-associated factor-interacting protein (TRI
164 eptor, TNF receptor-associated death domain, TNF receptor-associated factor, NF-kappaB-inducing kinas
165 paB activation pathways, including the TRAF (TNF receptor-associated factor) proteins, IKK, NF-kappaB
166                          The adaptor protein TNF receptor associated factor (TRAF) 3 is required for
167      NOPO is the Drosophila homolog of human TNF receptor associated factor (TRAF)-interacting protei
168 aling (SOCS) 3, B-cell CLL/lymphoma (BCL) 3, TNF receptor-associated factor (TRAF) 1, and TNFAIP3-int
169 ation and proteasome-mediated degradation of TNF receptor-associated factor (TRAF) 2 and TRAF6, which
170  of c-IAP1 is blocked upon coexpression with TNF receptor-associated factor (TRAF) 2, and this is ach
171  receptor-associated kinase (IRAK) 4, IRAK1, TNF receptor-associated factor (TRAF) 6, TGF-beta-activa
172       TRAF1/2 and cIAP1/2 are members of the TNF receptor-associated factor (TRAF) and the inhibitor
173                                          The TNF receptor-associated factor (TRAF) family of molecule
174               In this report we identify the TNF receptor-associated factor (TRAF) family of signal t
175 act directly with signaling molecules of the TNF receptor-associated factor (TRAF) family to activate
176           Through their interaction with the TNF receptor-associated factor (TRAF) family, members of
177 ng association with adaptor molecules of the TNF receptor-associated factor (TRAF) family.
178                                              TNF receptor-associated factor (TRAF) proteins associate
179 is: inhibitor of apoptosis(IAP)-1 and X-IAP, TNF receptor-associated factor (TRAF)-2, and factors OX4
180 rm prolactin receptors (PRLR-S), constrained TNF receptor-associated factor (TRAF)-dependent innate i
181 n-canonical K63-linked polyubiquitination of TNF receptor-associated factor (TRAF)-family adapter pro
182 sponsible for noncanonical ubiquitination of TNF receptor-associated factor (TRAF)-family adapter pro
183  HVEM activates NF-kappaB and AP-1 through a TNF receptor-associated factor (TRAF)-mediated mechanism
184  antiapoptotic factors Bcl-xL, A1/Bfl-1, and TNF receptor-associated factor (TRAF)1, all of which are
185 xpressing in B lymphocytes either Bcl-2 or a TNF receptor-associated factor (TRAF)2 mutant lacking th
186 receptor-associated death domain (TRADD), DN-TNF receptor-associated factor (TRAF)2, DN-receptor-inte
187 ein caused a shift in CD40 signaling through TNF receptor-associated factors (TRAF), including the TR
188 ransformation, binds tumour necrosis factor (TNF) receptor associated factor (TRAF) 1 and TRAF3 and t
189 e that IHPK2 binds to tumor necrosis factor (TNF) receptor-associated factor (TRAF) 2 and interferes
190                       Tumor necrosis factor (TNF) receptor-associated factor (TRAF) 2 is an intracell
191 g by deubiquitinating tumor necrosis factor (TNF) receptor-associated factor (TRAF) 2, TRAF6, and NEM
192 ction is initiated by tumor necrosis factor (TNF) receptor-associated factor (TRAF) adapter proteins,
193         Intracellular tumor necrosis factor (TNF) receptor-associated factor (TRAF) adapter proteins,
194 nd is a member of the tumor necrosis factor (TNF) receptor-associated factor (TRAF) family of putativ
195       A member of the tumor necrosis factor (TNF) receptor-associated factor (TRAF) family was identi
196                       Tumor necrosis factor (TNF) receptor-associated factor (TRAF) proteins associat
197 -kappaB, and binds to tumor necrosis factor (TNF)-receptor-associated factor (TRAF) proteins, but the
198 s on the ubiquitin-conjugating enzyme Ubc13, TNF receptor-associated factor TRAF2, the protein kinase
199              Furthermore, recruitment of the TNF-receptor-associated factor TRAF6 and activation of t
200                  A family of proteins called TNF receptor associated factors (TRAFs) plays key roles
201 gnal transducers for TNFRs are the family of TNF receptor associated factors (TRAFs).
202 JNK) pathways through their interaction with TNF receptor-associated factors (TRAFs) and NF-kappaB-in
203 F) family receptor in its ability to recruit TNF receptor-associated factors (TRAFs) and TNF receptor
204                                              TNF receptor-associated factors (TRAFs) are recruited to
205 , the most recently identified member of the TNF receptor-associated factors (TRAFs) family of protei
206 mily members, including CD40, is mediated by TNF receptor-associated factors (TRAFs) that interact wi
207 its ligand initiates signaling by recruiting TNF receptor-associated factors (TRAFs) to the CD40 cyto
208  are believed to be mediated in part through TNF receptor-associated factors (TRAFs), a family of cyt
209 lecule CD40 and its signaling intermediates, TNF receptor-associated factors (TRAFs), in diet-induced
210     The CD30 cytoplasmic tail interacts with TNF receptor-associated factors (TRAFs), which have been
211 d to be delivered through mediators known as TNF receptor-associated factors (TRAFs).
212                       Tumor necrosis factor (TNF) receptor-associated factors (TRAFs) are critical si
213                       Tumor necrosis factor (TNF) receptor-associated factors (TRAFs) are cytoplasmic
214         Intracellular tumor necrosis factor (TNF) receptor-associated factors (TRAFs) are key element
215                       Tumor necrosis factor (TNF) receptor-associated factors (TRAFs) are mediators o
216  in part, by engaging tumor necrosis factor (TNF) receptor-associated factors (TRAFs), which also med
217                      Tumour necrosis factor (TNF)-receptor-associated factors (TRAFs) form a family o
218  membrane to the nucleus through cytoplasmic TNF-receptor-associated factors (TRAFs).
219 these bacteria resulted in the activation of TNF receptor associated factors, two recently described

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