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1 digm in which AIF can substitute for caspase executioners.
2 is setting function as downstream cell-death executioners.
3  well known as the core apoptotic cell death executioner, acts in early responses to neuronal injury
4                                          The executioners are members of a family of proteases founde
5                              BHRF1 bound the Executioner Bak and, when cells were cultured without cy
6 ision-making process, by functioning both as executioner by damaging the biomolecules, or as savior b
7                              Thus, no single executioner caspase (nor a combination of caspase-3 and
8 ucing factor (AIF) nuclear translocation and executioner caspase 3 activation, in NBD rats.
9 neration, of the cleaved form of the central executioner caspase 3 is inhibited.
10         Given the presence of unusually long executioner caspase 3' UTRs in many metazoans, translati
11 post-mitochondrial signaling responsible for executioner caspase activation is controversial.
12 ints, including mitochondrial fragmentation, executioner caspase activation, and DNA damage, it is as
13                            During apoptosis, executioner caspase activity has been considered a point
14  neuronal degeneration is independent of the executioner caspase CED-3, but instead requires the acti
15                              Caspase-6 is an executioner caspase found directly regulated by p53, and
16 and its linker to determine the mechanism of executioner caspase inhibition by XIAP.
17  death: at the level of p53/CEP-1 and at the executioner caspase level.
18 rus that attacks lepidopterans, codes for an executioner caspase synthesized by 9 h after infection o
19                              Caspase-7 is an executioner caspase that plays a key role in apoptosis,
20 l other DNA viruses, ascoviruses code for an executioner caspase, apparently involved in a novel cyto
21 ection, and the data further showed that the executioner caspase, caspase 3, does not become activate
22                            Activation of the executioner caspase, caspase 3, is essential for many fo
23           In contrast, autoactivation of the executioner caspase-3 and -6 zymogens was not detected.
24 epeat domain (BIR2) to inhibit the apoptotic executioner caspase-3 and -7.
25 e EFES is homologous to a loop unique to the executioner caspase-3 and caspase-7 that are targeted by
26              IGF-I blocked activation of the executioner caspase-3 and the intrinsic initiator caspas
27 ivation concomitantly with activation of the executioner caspase-3 as the final step in the toxic cas
28 he apoptogen cytochrome c, and activation of executioner caspase-3 were determined by Western blottin
29     To dissect the nonredundant roles of the executioner caspase-3, -6, and -7 in orchestrating apopt
30                                    Apoptotic executioner caspase-3, -6, and -7, but not the inflammat
31 the proteolytic activation of the downstream executioner caspase-3.
32 d (iv) activation of initiator caspase-9 and executioner caspase-3.
33 are cleaved by caspases, most of them by the executioner caspase-3.
34  of cytochrome c and Smac, and activation of executioner caspase-3.
35 me c, and subsequently the processing of the executioner caspase-3.
36 for an analogous intermediate of the related executioner caspase-3.
37                                We identified executioner caspase-6 as a transcriptional target of p53
38  initiator caspases 1 and 8 but not from the executioner caspase-6.
39 nd pattern of GrB-mediated activation of the executioner caspase-7 in vitro and in vivo.
40            We report here that the apoptotic executioner caspase-7 was activated in the splenocytes o
41 e a caspase cascade involving the downstream executioners caspase-3, -6, and -7.
42 s and their applications to directly monitor executioner (caspase-3 and -7) and initiator (caspase-8
43                        Caspase-3 is the key "executioner" caspase, catalyzing the hydrolysis of a mul
44 ns, we have designed an infrared fluorogenic executioner-caspase reporter, which reveals spatiotempor
45           Here, we test directly the role of executioner caspases (caspase-3, -6, and -7) in fiber ce
46 hways converge to activate common downstream executioner caspases (caspase-3, -6, and -7), resulting
47                                Activities of executioner caspases (e.g., cas-6 and -3) became elevate
48 eolytic cleavage of apical caspases 8 and 2, executioner caspases 3 and 6, Bid cleavage, and release
49 MP also showed robust and fast activation of executioner caspases and apoptosis, the colorectal cance
50 hondrial factors necessary for activation of executioner caspases and apoptosis.
51 at displays attributes of both initiator and executioner caspases and includes a caspase recruitment
52 ngly suggest that Fas-mediated activation of executioner caspases and induction of apoptosis do not d
53 shion leading to activation of caspase-9 and executioner caspases and, surprisingly, activation of th
54 udy demonstrates the efficiency by which the executioner caspases are activated in vivo.
55  in many metazoans, translational control of executioner caspases by RBPs might be a strategy used wi
56  caspase 8 arose during evolution to trigger executioner caspases directly, circumventing viral suppr
57                                Activation of executioner caspases during receptor-mediated apoptosis
58 orted here will enable direct control of the executioner caspases in apoptosis and in cellular differ
59 imaging to observe tangles and activation of executioner caspases in living tau transgenic mice (Tg45
60 eful in assessing the role of inhibiting the executioner caspases in minimizing tissue damage in dise
61                        We tested the role of executioner caspases in organelle degradation by examini
62  the peptide linker by caspase-3, one of the executioner caspases involved in apoptosis, results in a
63 ose further processing is mediated by mature executioner caspases rather than initiator caspases.
64  that cleavage of Bid to tBid is mediated by executioner caspases suggests that a self-amplifying fee
65 s (KCs) activating the signaling kinases and executioner caspases that damage KCs, causing their shri
66 rt half-life may inhibit the activity of the executioner caspases toward specific substrates.
67                                              Executioner caspases were activated in detached pancreat
68                    Transcripts for all three executioner caspases were identified in lens fiber cells
69 m activation of caspase-8 but not of distal, executioner caspases, and does not lead to apoptosis.
70 stricts the infection-mediated activation of executioner caspases, and inhibits virus propagation.
71 ssing, caspase-8 can be cleaved by activated executioner caspases, and reports of whether this cleava
72 ds have nanomolar potency for inhibiting the executioner caspases, caspase-3 and caspase-7, and have
73 aying a nanomolar potency for inhibiting the executioner caspases, caspase-3 and caspase-7, were iden
74 hway downstream of FLICE but upstream of the executioner caspases, caspase-3, -6, and -7.
75      Baculovirus p35, a suicide substrate of executioner caspases, is not cleaved by purified Dredd i
76 r of apoptosis protein (XIAP) suppression of executioner caspases, respectively.
77 aspase p10 subunit for initiator but not for executioner caspases, so that any free p20 formed by dea
78                             Upon exposure to executioner caspases, TcapQ(647) was specifically cleave
79  demolition during apoptosis is completed by executioner caspases, that selectively cleave more than
80                      We find that unlike the executioner caspases, which are readily activated by int
81 is autoproteolysis, which directly activates executioner caspases-3 and -7, is unknown for the apical
82 ase specificity with the prototype apoptotic executioner caspases-3 and -7, suggesting that caspase-2
83 h regulates the initiator caspase-9, and the executioner caspases-3 and -7.
84 han a proteasome inhibitor at mobilizing the executioner caspases-3 and -7.
85 ded initiator caspases-8 and -10, as well as executioner caspases-3, -6, and -7.
86 on of caspase-8, consequently activating the executioner caspases-3, -6, and -7.
87 937 cells that was preceded by activation of executioner caspases.
88  membrane permeabilization and activation of executioner caspases.
89 se of caspase-8 into the cytoplasm to engage executioner caspases.
90 f imaging, despite the presence of activated executioner caspases.
91 n contributes substantially to inhibition of executioner caspases.
92 te that tau is cleaved at D421 (DeltaTau) by executioner caspases.
93                                Caspase-8, an executioner enzyme in the death receptor pathway, was sh
94 tion of apical caspases 8 and 9 and also the executioner enzyme, caspase 3, whereas infection alone h
95 ed that Y-linked genes Zfy1 and Zfy2 act as 'executioners' for this checkpoint, and that wrongful exp
96 ormation from Texas and Virginia showed that executioners had no anaesthesia training, drugs were adm
97                 Since the aggression used by executioners is proactive, the execution paradox is solv
98 sible commitment to positive feedback in the executioner module.
99                    Caspase-3 is an essential executioner of apoptosis responsible for regulating many
100                          Caspase-3 is a main executioner of apoptotic cell death.
101                   Importantly, release of an executioner of caspase-independent apoptosis, apoptosis-
102                     The C5b-9 complex is the executioner of CDC.
103  which leads to activation of caspase-3, the executioner of cell death.
104 phosphorylation and aggregation of MLKL, the executioner of necroptosis.
105                         SARM1 is the central executioner of the axonal degeneration pathway that culm
106 ein 1 (SARM1) is an evolutionarily conserved executioner of this degeneration cascade, also known as
107                                          The executioners of apoptosis are caspase family proteases.
108 ve overlapping but nonredundant roles as the executioners of apoptosis in humans.
109                        Caspases are critical executioners of apoptosis, and living cells prevent thei
110 ptotic proteins, including caspases, the key executioners of apoptosis, and review the nonlethal func
111 ce caspases-3 and -6 are the most downstream executioners of apoptosis, the constitutively active ver
112 s) can bind to and inhibit caspases, the key executioners of apoptosis.
113 tensively studied as critical initiators and executioners of cell death pathways.
114 ccrued to impugn the presenilins (PS) as the executioners of intramembranous processing of APP.
115                                Caspases, the executioners of programmed cell death, are normally synt
116  on caspases and their putative role as sole executioners of programmed cell death.
117 d Arl6ip5, Tnfrsf10b, Traf2, and Ubc are key executioners of this program.
118 activates caspase-9 and then caspase-3, the "executioner" of the cell.
119                    Caspase-3 carries out the executioner phase of apoptosis, however under special ci
120 ator caspases-8 and -10 directly process the executioner pro-caspase-3 with activation rates (kcat/Km
121  stimulate procaspase activity, showing that executioner procaspase conformational equilibrium can be
122 Mechanistically, B-PAC-1 treatment activated executioner procaspases and not other Zn-dependent enzym
123  including B-PAC-1 (L14R8), convert inactive executioner procaspases to their active cleaved forms by
124 tions demonstrated that direct activation of executioner procaspases via B-PAC-1 treatment bypasses a
125 ted caspase-3 has properties of a cell death executioner protease.
126  of the antiapoptotic protein Bcl-2 and the "executioner" protease caspase-3 in sepsis-induced gut ce
127 ibitor 2A (Spi2A), an inhibitor of lysosomal executioner proteases dependent on transcription factor
128 apoptotic proteins such as the mitochondrial executioner protein BAX.
129 totic Bcl-2-associated X protein (BAX) is an executioner protein of the BCL-2 family that represents
130  induced by different stimuli share a common executioner proteolysis cascade, including caspase-3 and
131 caspases 6 and 7, other important downstream executioners, remained unchanged.
132 r understanding of IRE1alpha as a cell-death executioner, showing that upon ER stress, IRE1alpha degr
133 In plant systems, the identities of the main executioners that orchestrate cell death remain elusive.
134 strates for the cysteine protease cell death executioners, the caspases.
135  PCD through the induction of the cell death executioner VPE.
136 ay into three modules (initiator, amplifier, executioner), we use computer simulation and bifurcation
137 tivation of caspases, called the "cell death executioners." We examined Survivin (n = 116) and XIAP (

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