ライフサイエンスコーパス: nonapoptotic

1 and cytochrome c loss--whereas others appear nonapoptotic.

2 Rapid nonapoptotic activation of caspase-9 and its downstream

3 However, it also has multiple nonapoptotic activities that are tumorigenic.

4 d with confocal microscopy and determined in nonapoptotic and apoptotic cardiocytes by indirect immun

5 ults in loss of viability, but is apparently nonapoptotic and further differs from cellular death def

6 GP-induced cell death is nonapoptotic and is preceded by downmodulation of cell s

7 staglandin J(2) (15d-PGJ2), induced a novel, nonapoptotic and microtubule-associated protein 1 light

8 This nonapoptotic anti-inflammatory regulation of IL-12 and I

9 equent nuclear fusion by a mechanism that is nonapoptotic, as assessed by multiple criteria.

10 ate that T-oligos stimulate the induction of nonapoptotic autophagic also known as type II programmed

11 Curcumin induced G(2)/M arrest and nonapoptotic autophagic cell death in both cell types.

12 he pathways by which ceramide acts to induce nonapoptotic autophagic cell death in malignant gliomas.

13 as either apoptotic, partially apoptotic, or nonapoptotic based on infected HEp-2 cell morphologies,

14 function that is mediated by IgM binding to nonapoptotic BMDC receptors.

15 phagocytic markers and observe engulfment of nonapoptotic Brn3-labeled RGCs.

16 opulation that is relatively nondividing and nonapoptotic but chemotherapy resistant and chemotactic.

17 is a critical event in caspase-independent, nonapoptotic (but not caspase-dependent, apoptotic) deat

18 Interestingly, physiological nonapoptotic calcium fluxes were capable of activating m

19 highest in the body cells and lowest in the nonapoptotic cap cells, implying that their expression i

20 Compared with nonapoptotic cardiocytes or apoptotic cardiocytes incuba

21 In permeabilized nonapoptotic cardiocytes, Ro and La were predominantly n

22 y immunoprecipitated from apoptotic, but not nonapoptotic cardiocytes.

23 O(2)(.-) levels in nonapoptotic caspase 3-null SCG neurons were lower than

24 ns caspase-dependent cell death, also drives nonapoptotic caspase activation to remodel cells.

25 ochondrial-associated molecular link between nonapoptotic caspase function and autophagy regulation i

26 ce suggests a mitochondrial pathway of local nonapoptotic caspase signaling in mediating spine prunin

27 udies in C. elegans also unearthed conserved nonapoptotic caspase-independent cell death programs tha

28 this set, which acts via a nonmembranolytic, nonapoptotic caspase-independent mechanism, is more effe

29 crophage differentiation is mediated through nonapoptotic, caspase-3-dependent mechanisms.

30 D4(+) T cells, two minor pathways leading to nonapoptotic, caspase-independent AICD were identified,

31 Nonapoptotic, caspase-independent cell death pathways ha

32 ted a striking increase in the percentage of nonapoptotic CD11b+ VLA-4-negative macrophages/monocytes

33 by infiltration of the tumor with activated, nonapoptotic CD8+ effector T lymphocytes on day 7 postth

34 Nevertheless, nonapoptotic cell death and adaptive stress responses ar

35 alternative response closely correlated with nonapoptotic cell death and characterized by proteolysis

36 malignant glioma cells through induction of nonapoptotic cell death and mitochondria hyperpolarizati

37 Small molecules that induce nonapoptotic cell death are of fundamental mechanistic i

38 Ferroptosis is an iron-dependent form of nonapoptotic cell death associated with oxidized polyuns

39 le for the RB tumor suppressor in preventing nonapoptotic cell death by limiting the extent of BNIP3

40 peutics in their ability to induce a form of nonapoptotic cell death called ferroptosis.

41 s is pharmacologically blocked, SAHA-induced nonapoptotic cell death can also be potentiated by autop

42 Methuosis is a form of nonapoptotic cell death characterized by an accumulation

43 grammed necrosis or necroptosis is a form of nonapoptotic cell death driven by the receptor interacti

44 that ferroptosis, an iron-dependent form of nonapoptotic cell death driven by unrestricted lipid per

45 proteolysis is also linked to apoptotic and nonapoptotic cell death following excessive glutamate ex

46 Ferroptosis is a form of nonapoptotic cell death for which key regulators remain

47 of this class, lanperisone, acts by inducing nonapoptotic cell death in a cell cycle- and translation

48 previously been shown that hyperoxia induces nonapoptotic cell death in cultured lung epithelial cell

49 , we first demonstrate that ceramide induces nonapoptotic cell death in malignant glioma cells.

50 e provide molecular inroads to understanding nonapoptotic cell death in metazoan development and dise

51 l trials, can activate a unique mechanism of nonapoptotic cell death in sarcomas and other cancer cel

52 he Rb tumor suppressor in protecting against nonapoptotic cell death in the developing mouse fetal li

53 ollowing vaccination and suggests a role for nonapoptotic cell death in the regulation of CD4 T cell

54 To identify additional factors that regulate nonapoptotic cell death in yeast, a collection of gene k

55 and azole-class antifungal drugs can induce nonapoptotic cell death in yeasts that can be blocked by

56 We observed that cells dying a nonapoptotic cell death induced by adenovirus infection

57 r, about the molecular mechanisms underlying nonapoptotic cell death induced by ceramide.

58 in that was not found following apoptotic or nonapoptotic cell death induced by stimuli other than me

59 anism of tumor necrosis factor (TNF)-induced nonapoptotic cell death is largely unknown, although the

60 olecules serve as valuable tools for probing nonapoptotic cell death mechanisms.

61 Ferroptosis, an iron-dependent form of nonapoptotic cell death mediated by lipid peroxidation,

62 ia, suggesting a hypoxia-induced increase in nonapoptotic cell death of PKCdelta-ECs.

63 his issue, Overholtzer et al. describe a new nonapoptotic cell death pathway termed "entosis" in mamm

64 otein kinase (RIP) 3-mediated necroptosis, a nonapoptotic cell death pathway, is implicated in a vari

65 Here, we provide an overview of nonapoptotic cell death pathways induced by DNA damage a

66 However, nonapoptotic cell death predominated during prolonged hy

67 Ferroptosis is a regulated nonapoptotic cell death process characterized by iron-de

68 that induce the oxidative stress-dependent, nonapoptotic cell death process of ferroptosis.

69 Ferroptosis is a nonapoptotic cell death process that requires cellular i

70 Here we describe a nonapoptotic cell death program in matrix-detached cells

71 aspases) mediate apoptosis, the mediators of nonapoptotic cell death programs are much less well char

72 p53(15)Ant peptide induced rapid, nonapoptotic cell death resembling necrosis in all breas

73 ss responses, such as autophagy, and control nonapoptotic cell death routines, such as regulated necr

74 Ferroptosis is a form of nonapoptotic cell death that involves iron-dependent pho

75 Ferroptosis, a form of iron-dependent, nonapoptotic cell death that is induced by excessive lip

76 Ferroptosis is form of regulated nonapoptotic cell death that is involved in diverse dise

77 tin triggers a unique iron-dependent form of nonapoptotic cell death that we term ferroptosis.

78 gents that induce ferroptosis (iron-mediated nonapoptotic cell death).

79 On the other hand, nonapoptotic cell death, autophagy, has recently attract

80 Ferroptosis, a form of iron-mediated nonapoptotic cell death, has gained considerable attenti

81 anism to mitigate SAHA-induced apoptotic and nonapoptotic cell death, suggesting that targeting autop

82 cellular proliferation and high doses caused nonapoptotic cell death, which was not mediated through

83 etaII spectrin, coinciding with the onset of nonapoptotic cell death.

84 y, which is necessary for both apoptotic and nonapoptotic cell death.

85 in the induction of death receptor-mediated, nonapoptotic cell death.

86 ive JCV infection, which eventually leads to nonapoptotic cell death.

87 yl(OMe)-fluoromethylketone (BAF), a delayed, nonapoptotic cell death.

88 nt feature of ferroptosis, an iron-dependent nonapoptotic cell death.

89 dhesion to ePTFE and Dacron triggers a rapid nonapoptotic cell death.

90 nce EC survival during hypoxia by decreasing nonapoptotic cell death.

91 ve reactive oxygen species (ROS) can promote nonapoptotic cell death.

92 treatment, followed by caspase-independent, nonapoptotic cell death.

93 ferroptosis, a form of regulated, oxidative, nonapoptotic cell death.

94 PARP1 activity and DNA repair and promoting nonapoptotic cell death.

95 Fas-dependent apoptotic and Fas-independent, nonapoptotic cell death.

96 Moreover, when caspase-3 was added to nonapoptotic cell extract, efficient internal cleavage o

97 However, nonapoptotic cell extrusion was increased in Casp3/7(Del

98 endogenous ether lipids act to prevent this nonapoptotic cell fate.

99 optosis, but it is also constitutive on some nonapoptotic cell populations where it plays a role in c

100 This is followed by predominantly nonapoptotic cell-in-cell death of the internalized cell

101 d doxorubicin treatment but not in necrotic (nonapoptotic) cell death.

102 oliferative effects followed by significant, nonapoptotic, cell death within 72 hours occurred in 24

103 Bax is predominantly found in the cytosol of nonapoptotic cells and is commonly thought to translocat

104 cells, including a peak of nonproliferating, nonapoptotic cells at day 14.

105 ative analysis revealed aggresomes in 60% of nonapoptotic cells but only in 10% of apoptotic cells.

106 by approximately 75%, reduced the density of nonapoptotic cells by approximately 70% in residual tumo

107 were determined separately for apoptotic and nonapoptotic cells by flow cytometry.

108 cells were Fas-high-density cells while the nonapoptotic cells expressed a low density of Fas.

109 and CXCL10, which may normally recruit these nonapoptotic cells from the lymph nodes.

110 s had low Bcl-2 and high Bax levels, whereas nonapoptotic cells had high Bcl-2 and low Bax levels.

111 nstitutively targeted to mitochondria but in nonapoptotic cells is constantly translocated back to th

112 uring wound closure promote the extrusion of nonapoptotic cells via mechanically regulated stretch-ac

113 Treatment of surviving nonapoptotic cells with antisense oligonucleotides again

114 bility to discriminate between apoptotic and nonapoptotic cells, an ability restored by exogenous ANX

115 dditional 9-fold reduction of the density of nonapoptotic cells, and an additional 30% increase in th

116 a is found predominantly in the cytoplasm of nonapoptotic cells, and the apoptotic signal that activa

117 When added to nuclei from nonapoptotic cells, cyclophilin C induces 50-kilobase pa

118 ereas apoptotic IL-10(-/-) cells, as well as nonapoptotic cells, favor Th1 induction.

119 lation has been reported to occur at G2-M in nonapoptotic cells, raising the possibility that this an

120 ls of NUC70 expression between apoptotic and nonapoptotic cells, suggesting that activation of NUC70

121 cells induced by photodynamic treatment and nonapoptotic cells, we successfully detected caspase-9 a

122 lved in Bax-dependent O(2)(.-) production in nonapoptotic cells.

123 ocation and confer new functions to cyt c in nonapoptotic cells.

124 s of apoptotic cells but not with lysates of nonapoptotic cells.

125 mitochondrial and cytosolic distribution in nonapoptotic cells.

126 pase-8 can also promote cell migration among nonapoptotic cells; here, we show that caspase-8 can pro

127 fined two distinct groups: those that induce nonapoptotic (Class I) and apoptotic (Class II) parasite

128 tive thymocytes, suggesting the existence of nonapoptotic clonal deletion mechanisms.

129 d these effects in BAECs at much lower (i.e. nonapoptotic) concentrations of C(2)-cer.

130 ivity is restrained and shut down under such nonapoptotic conditions remains unknown.

131 ity of caspase-8 to promote metastasis under nonapoptotic conditions.

132 al targets for autologous NK cells through a nonapoptotic cytotoxic mechanism.

133 y responses of cells dying an apoptotic or a nonapoptotic death as a result of adenoviral infection.

134 also protected cells from ceramide-induced, nonapoptotic death consistent with the idea that severe

135 oinflammatory stimuli, whereas cells dying a nonapoptotic death from infection with E1B 19K-competent

136 cial step for luteolin-induced apoptotic and nonapoptotic death in lung cancer cells.

137 flammatory reactions, but cells that undergo nonapoptotic death in response to such stimuli lack this

138 Nonapoptotic death induced by H2O2 was not prevented by

139 ion of TORC1, which in turn promoted LMP and nonapoptotic death of stressed cells.

140 under pathological conditions, apoptosis and nonapoptotic death paradigms are often interwined, which

141 understand how FAP-alpha is involved in this nonapoptotic death pathway, we performed immunoblotting

142 A related Fas- and caspase-independent, nonapoptotic death process is revealed in wild-type (WT)

143 data indicate that TCR ligation can activate nonapoptotic death programs in WT CD8(+) and CD8(+) T bl

144 totic, involving activation of caspases, but nonapoptotic death responses also have been described.

145 ggering NF-kappaB activation, apoptosis, and nonapoptotic death signals through separate and competin

146 t protein (Q97) undergo a protracted form of nonapoptotic death that is insensitive to Bax deletion o

147 tic death requires caspases; and (4) delayed nonapoptotic death that occurs in the presence of caspas

148 biquitinated proteins; (2) enhanced baseline nonapoptotic death; (3) marked accumulation of autophagi

149 nk between Ca(2+) dysregulation and primary, nonapoptotic degeneration of photoreceptors and a role f

150 Viruses d2-3, d3-4, d4-5, d5-6, and d6-7 are nonapoptotic, demonstrating that ICP27 contains a large

151 us, activation of ferroptosis results in the nonapoptotic destruction of certain cancer cells, wherea

152 Here, we demonstrate that the large-scale nonapoptotic developmental PCD in the Drosophila ovary o

153 can readily be distinguished from cells with nonapoptotic DNA damage.

154 lularly, producing apoptotic cytotoxicity or nonapoptotic effects, respectively.

155 PH oxidase-dependent mechanism of cytolytic, nonapoptotic eosinophil death initiates nuclear chromato

156 y, active NF-kappaB localized exclusively to nonapoptotic epithelial cells both in vivo and in the ma

157 Diverse cell fusions are accompanied by the nonapoptotic exposure of phosphatidylserine at the surfa

158 onversion of naive T cells was mediated by a nonapoptotic Fas signal, resulting in Akt-driven cellula

159 and may therefore be more likely to initiate nonapoptotic Fas signaling due to less RIP1 in the recep

160 In the absence of Fas, the nonapoptotic, Fas-independent pathway could still induce

161 Dying linker cells display nonapoptotic features, including nuclear crenellation, a

162 Ferroptosis, a nonapoptotic form of cell death characterized by iron ac

163 Ferroptosis is a nonapoptotic form of cell death driven by iron-dependent

164 Entosis is a nonapoptotic form of cell death initiated by actomyosin-

165 Necroptosis is a regulated, nonapoptotic form of cell death initiated by receptor-in

166 Ferroptosis is an iron-dependent, oxidative, nonapoptotic form of cell death recently described in an

167 s are known killers, being responsible for a nonapoptotic form of cell death with features similar to

168 reveals that ferroptosis, an iron-dependent, nonapoptotic form of cell death, represents a new regula

169 on injury, we discovered that necroptosis, a nonapoptotic form of cell death, triggers the recruitmen

170 may limit the inflammatory response to this nonapoptotic form of cell death.

171 osis in infected cells but rather leads to a nonapoptotic form of cell death.

172 vive therapy or a mechanism for initiating a nonapoptotic form of programmed cell death remains contr

173 ls has led to the belief that autophagy is a nonapoptotic form of programmed cell death.

174 Ferroptosis is an iron-dependent, nonapoptotic form of regulated cell death triggered by i

175 ts the signaling of the IFN-gamma-activated, nonapoptotic form of TNF receptor superfamily member 6 (

176 During the past three decades, various nonapoptotic forms of cell death have gained increasing

177 Nonapoptotic forms of cell death may facilitate the sele

178 This study investigated the nonapoptotic function and phenotypic expression of activ

179 This finding sheds new light on the CD95 nonapoptotic function and provides a novel mechanism for

180 Casp8 comprises a nonapoptotic function during liver regeneration by balan

181 utes to cell migration and adhesion, a novel nonapoptotic function of an established apoptotic factor

182 This represents a novel nonapoptotic function of caspase-8 acting at the interse

183 The nonapoptotic function of CD95 in gammaherpesvirus-associ

184 ontrol of synaptic vesicle pools, and a new, nonapoptotic function of the BAD-BAX-caspase-3 pathway i

185 ing that caspase-8 possesses an alternative, nonapoptotic function that may contribute to tumor progr

186 of compensatory proliferation in an apparent nonapoptotic function.

187 mediates not only apoptosis but also diverse nonapoptotic functions depending on the tissue and the c

188 The nonapoptotic functions of Fas ligation are incompletely

189 nd absence of Bim to separate apoptotic from nonapoptotic functions of Nur77.

190 from NHEJ deficiency is highly restricted by nonapoptotic functions of p53, such as the G1/S checkpoi

191 d p53-dependent apoptosis but did not impair nonapoptotic functions of p53.

192 it is mainly caspase-8 in its apoptotic and nonapoptotic functions that has been an intense research

193 however, that the protein has numerous other nonapoptotic functions.

194 e of the caspase-8-p85 interaction for these nonapoptotic functions.

195 s, and it inhibits Treg suppression via this nonapoptotic GzmB-mediated mechanism.

196 the mammalian Bcl-2 gene in cis restored the nonapoptotic, immunorepressive cell death activity of vi

197 morphology of cell death changes and becomes nonapoptotic in some cells.

198 sis of both apoptotic (high PS exposure) and nonapoptotic (intermediate PS exposure) activated T cell

199 platelet binding (<5%), which was similar to nonapoptotic iRBCs.

200 Ferroptosis is a nonapoptotic, iron-catalyzed form of regulated necrosis

201 flammatory disorders, histiocytes can engulf nonapoptotic leukocytes and nonsenescent erythrocytes an

202 no nuclear NF-kappaB activity, and LY-ar, a nonapoptotic line with constitutive p50 homodimer activi

203 antitation indicated that there was an early nonapoptotic loss of cortical neurons followed by a prog

204 e to M. avium-infected apoptotic, but not to nonapoptotic M. avium-infected Mphi, suggesting a specif

205 ylated annexin A5 localized in apoptotic and nonapoptotic macrophages.

206 phagy will ultimately induce cell death in a nonapoptotic manner.

207 nists, such as MIA602, kill H295R cells in a nonapoptotic manner.

208 osis, but the neurons still die in a delayed nonapoptotic manner.

209 growth factors did eventually die through a nonapoptotic mechanism associated with loss of DeltaPsi.

210 ses ras-driven skin carcinogenesis through a nonapoptotic mechanism involving ARF and p53.

211 e beta-cell cytotoxicity primarily through a nonapoptotic mechanism linked to a decline in ATP levels

212 of rat beta-cells occurs predominantly by a nonapoptotic mechanism, including the following: 1) A ra

213 at reducing endothelial cell viability via a nonapoptotic mechanism.

214 G(2)-M phase arrest and ultimately died by a nonapoptotic mechanism.

215 , Disruptin inhibits cancer cell growth by a nonapoptotic mechanism.

216 ls vulnerable to weaver die by apoptotic and nonapoptotic mechanisms and indicate that weaver-induced

217 human carcinoma cells by both apoptotic and nonapoptotic mechanisms and potentiates the effects of c

218 inje cells, highlighting a possible role for nonapoptotic mechanisms in the death of these neurons.

219 is and tumor cells engineered to die through nonapoptotic mechanisms, resulting in secretion of eithe

220 e able to kill tumor cells via apoptotic and nonapoptotic mechanisms.

221 Since nonapoptotic membrane blebbing is now recognized as an i

222 cell body, DIP expression induced excessive nonapoptotic membrane blebbing, a physiological process

223 tructures resemble, and may be identical to, nonapoptotic membrane blebs, a feature of the amoeboid f

224 ervention, and lend support to the idea that nonapoptotic modes of cell death may play a crucial role

225 els, the caspase-deficient neurons exhibit a nonapoptotic morphology in which nuclear changes such as

226 a specific interaction between apoptotic and nonapoptotic Mphi.

227 e percentage of apoptotic myocyte nuclei and nonapoptotic myocardial nuclei.

228 The nonapoptotic nature of this cell death is confirmed by n

229 ed polarized intestinal Caco-2 cells undergo nonapoptotic necrotic cell death triggered by inositol 1

230 ich instead induced dramatic accumulation of nonapoptotic necrotic cells.

231 these domains elicits axon degeneration and nonapoptotic neuronal death even in the absence of injur

232 ss exon 1 of mutant huntingtin, showed dark, nonapoptotic neurons and degenerated mitochondria associ

233 at Bax also lies upstream of ROS produced in nonapoptotic neurons and present evidence that caspases

234 Apoptotic and nonapoptotic neurons from Bax-WT/SOD2-null but not Bax-n

235 partially involved in O(2)(.-) production in nonapoptotic neurons, and that other caspases may also b

236 ination by complement-mediated engulfment of nonapoptotic neurons.

237 However, forms of nonapoptotic neutrophil death have also been observed.

238 inflammatory responses to avoid exaggerated nonapoptotic neutrophil death, leading to tissue damage.

239 The results establish that in nonapoptotic neutrophils, G6Pase-beta is essential for n

240 Drosophila ovary is an intriguing example of nonapoptotic, nonautonomous PCD, providing insight on th

241 s in PrP functional activity induce a novel, nonapoptotic, nonautophagic form of neuronal death whose

242 expressing cells had a higher frequency of a nonapoptotic, nonnecrotic type of cell death termed para

243 e also suggests that ASPP2 harbors important nonapoptotic p53-independent functions.

244 asmic reticulum vacuolization that precede a nonapoptotic (paraptotic) cell death.

245 More recently, necroptosis, a parallel, nonapoptotic pathway of cell death, has been described,

246 ay be delayed, and the cells appear to use a nonapoptotic pathway of degeneration.

247 neurons degenerate by a caspase-independent, nonapoptotic pathway that involves autophagy.

248 h can be executed by regulated apoptotic and nonapoptotic pathways, including the iron-dependent proc

249 increase in neural degeneration mediated by nonapoptotic pathways.

250 sociated with apoptosis and also occurred in nonapoptotic patient cells treated with PSC-833.

251 e for NADPH oxidase-derived ROS in mediating nonapoptotic PCD evoked by mAbs in B-cell malignancies.

252 ered Fc regions are type II mAb that trigger nonapoptotic PCD in a range of B-lymphoma cell lines and

253 Here we report that alternative, nonapoptotic pcd induced by the neurokinin-1 receptor (N

254 MEK2, and ERK2 is essential for this form of nonapoptotic pcd, leading to the phosphorylation of the

255 h (pcd) may take the form of apoptosis or of nonapoptotic pcd.

256 ed via arrestin 2, modulates NK(1)R-mediated nonapoptotic pcd.

257 at the rear of the invading cell as well as nonapoptotic plasma membrane (PM) blebbing in this cellu

258 bly overexpressed by fusion to an unrelated, nonapoptotic polypeptide, the N-terminal 37 amino acids

259 tant mice, the accumulation of a sub-G1, but nonapoptotic, population was observed that we believe ma

260 rolling synaptic vesicle pools, and a novel, nonapoptotic, presynaptic function of the BAD-BAX-caspas

261 with DNA damage resulting from a variety of nonapoptotic processes (necrosis, in vitro autolysis, pe

262 anding of the roles of IAPs in apoptotic and nonapoptotic processes and explore the notion that the l

263 ction in apoptosis, but are also crucial for nonapoptotic processes such as NMDA receptor-dependent l

264 with resveratrol's ability to kill cells via nonapoptotic processes, cells transfected to express hig

265 that has led to their implication in several nonapoptotic processes.

266 e caspase and paracaspase families to enable nonapoptotic processes.

267 osis, caspases are also important in several nonapoptotic processes.

268 nto the complex relationship between ROS and nonapoptotic programmed cell death.

269 cal inflammation, contributing to subsequent nonapoptotic renal injury.

270 retinoid, and retinoic acid as well as other nonapoptotic retinoids did not inhibit IKK.

271 opathicity and replication of human CMV by a nonapoptotic, reversible process that requires nuclear f

272 Thus, this study supports a nonapoptotic role for active caspase-3 in cells residing

273 that extracellular GzmB plays an unexpected, nonapoptotic role in regulating Treg suppression and sug

274 apoptosis, recently has been implicated in a nonapoptotic role in the regulation of the cell cycle, c

275 These data highlight a novel nonapoptotic role of caspase-3 and suggest that cleaved

276 Recently, nonapoptotic roles of caspases have been identified, how

277 cent developments have focused on uncovering nonapoptotic roles of caspases ranging from immune regul

278 aspase 8, in particular, also has additional nonapoptotic roles, such as in inflammation.

279 at DIAP2 controls drICE in its apoptotic and nonapoptotic roles.

280 tor inhibited O(2)(.-) in both apoptotic and nonapoptotic SCG neurons.

281 Here, we review the nonapoptotic side of Bcl-2 family, specifically the role

282 ptor complex and also mediate RIP1-dependent nonapoptotic signaling events, thus reducing caspase act

283 Surprisingly, CD95-mediated nonapoptotic signaling induced beta interferon (IFN-beta

284 o emerging as a tumor promoter by activating nonapoptotic signaling pathways.

285 the dual roles of Fas in both apoptotic and nonapoptotic signaling, the aim of the present study was

286 apoptosis but is also capable of triggering nonapoptotic signals.

287 gers apoptosis by driving DU145 cells from a nonapoptotic status (c-FLIP(short)(high), CD95(low), CD9

288 on, KSHV is reactivated predominantly in the nonapoptotic subpopulation of PEL cells.

289 (phosphate-buffered saline)-pretreated mice, nonapoptotic superficial cell death from 2 to 6 hours an

290 Our results identify a role for caspase 3 in nonapoptotic T cells and support that caspase 3-dependen

291 target genes such as BAX and PUMA while the nonapoptotic targets p21 and hMDM2 remain unaffected.

292 mRNA expression was significantly greater in nonapoptotic than in apoptotic T lymphocytes.

293 nges were associated with markedly increased nonapoptotic thyroid cell death, suggesting direct toxic

294 y phosphorylated tyrosine peptides after the nonapoptotic treatments, which we used to distinguish be

295 , by interacting directly with CD28 on live (nonapoptotic) tumor plasma cells, bone marrow mDCs downr

296 Cytokine-primed neutrophils can undergo a nonapoptotic type of cell death using components of the

297 se activity these neurons undergo a distinct nonapoptotic type of degeneration.

298 (+) cells were classified morphologically as nonapoptotic (Type I) or apoptotic (Type II) to verify t

299 Of the nonapoptotic viruses, d4-5 did not produce gC, indicatin

300 of culture with anti-mu, the remaining live, nonapoptotic xid cells were enlarged, viable, and primed