ライフサイエンスコーパス: outer mitochondrial membrane

1 elle via the TOM complex (translocase of the outer mitochondrial membrane).

2 tial but was absent in mitoplasts lacking an outer mitochondrial membrane.

3 t include the endoplasmic reticulum (ER) and outer mitochondrial membrane.

4 chondria, leading to its accumulation on the outer mitochondrial membrane.

5 ion by increasing Ca(2+) transfer across the outer mitochondrial membrane.

6 that drives the assembly of proteins in the outer mitochondrial membrane.

7 leavage product to the cytosolic face of the outer mitochondrial membrane.

8 l membrane protein or is integrated into the outer mitochondrial membrane.

9 ns (DRPs) must bind specific adaptors on the outer mitochondrial membrane.

10 s 1, 2, and 3), pore-forming proteins in the outer mitochondrial membrane.

11 d demonstrate that it is integrated into the outer mitochondrial membrane.

12 to function as a supportive receptor for the outer mitochondrial membrane.

13 forms the protein-translocating pore in the outer mitochondrial membrane.

14 that is involved in the rearrangement of the outer mitochondrial membrane.

15 an integral membrane protein imbedded in the outer mitochondrial membrane.

16 nsmembrane helices anchor the enzymes to the outer mitochondrial membrane.

17 polyQ domains might associate early with the outer mitochondrial membrane.

18 all molecules and ions across the eukaryotic outer mitochondrial membrane.

19 urified mitochondria and associates with the outer mitochondrial membrane.

20 oapoptotic BCL-2 proteins BAX and BAK at the outer mitochondrial membrane.

21 ied 2Fe-2S-containing protein located in the outer mitochondrial membrane.

22 oltage-dependent anion channel (VDAC) of the outer mitochondrial membrane.

23 s a survival protein that is tethered to the outer mitochondrial membrane.

24 that erastin alters the permeability of the outer mitochondrial membrane.

25 toNEET is an integral protein present in the outer mitochondrial membrane.

26 rst identified Fe-S protein of the mammalian outer mitochondrial membrane.

27 ysiologic exchange of ATP and ADP across the outer mitochondrial membrane.

28 involving Bax's integral insertion into the outer mitochondrial membrane.

29 which assemble into fission complexes on the outer mitochondrial membrane.

30 own to be sufficient for localization to the outer mitochondrial membrane.

31 ltage-dependent anion channel present in the outer mitochondrial membrane.

32 tochondria shows that TARP is located in the outer mitochondrial membrane.

33 promote the timely loss of integrity of the outer mitochondrial membrane.

34 atment, suggesting eNOS association with the outer mitochondrial membrane.

35 ated that huntingtin was associated with the outer mitochondrial membrane.

36 recruitment of the large GTPase Dnm1p to the outer mitochondrial membrane.

37 These proteins localize to the outer mitochondrial membrane.

38 bly an alteration in the permeability of the outer mitochondrial membrane.

39 g some specificity of these channels for the outer mitochondrial membrane.

40 e critical for the passage of MT through the outer mitochondrial membrane.

41 priate conformation and interaction with the outer mitochondrial membrane.

42 nstead, Nrf2 was found to associate with the outer mitochondrial membrane.

43 of dozens of proteins on the surface of the outer mitochondrial membrane.

44 eus, and a third population localizes to the outer mitochondrial membrane.

45 raction of mislocalized TA proteins from the outer mitochondrial membrane.

46 ization of immune regulatory proteins on the outer mitochondrial membrane.

47 me biosynthesis during erythropoiesis at the outer mitochondrial membrane.

48 (VDAC) proteins are major components of the outer mitochondrial membrane.

49 is commitment is the permeabilization of the outer mitochondrial membrane.

50 eins use an alternative pathway to cross the outer mitochondrial membrane.

51 osol, BAK is constitutively localized to the outer mitochondrial membrane.

52 and VDAC1 thus reducing permeability of the outer mitochondrial membrane.

53 rs permeability alterations of the inner and outer mitochondrial membranes.

54 forms at contact sites between the inner and outer mitochondrial membranes.

55 crease in permeability of both the inner and outer mitochondrial membranes.

56 age-dependent anion channel 1 (VDAC1) at the outer mitochondrial membranes.

57 he mitochondrial translocase, translocase of outer mitochondrial membrane 22 (Tom22), steroidogenic a

58 ear factor 4, alpha), TOMM34 (translocase of outer mitochondrial membrane 34) and SRC (SRC proto-onco

59 80 kDa complexes with the translocase of the outer mitochondrial membrane 40 (TOM40) import channel a

60 o studies, 449 participants), translocase of outer mitochondrial membrane 40 gene (one study, 723 par

61 e apolipoprotein E (APOE) and translocase of outer mitochondrial membrane 40 homolog (TOMM40) genotyp

62 ovel BMI associations in loci translocase of outer mitochondrial membrane 40 homolog (yeast) - apolip

63 75650, located in TOMM40 (translocase of the outer mitochondrial membrane 40 homolog)--had a genome-w

64 elated protein 6), and TOM40 (translocase of outer mitochondrial membrane 40), for which antisense ex

65 -2 proteins Bax and Bak can permeabilize the outer mitochondrial membrane and commit cells to apoptos

66 l (VDAC) is the most abundant protein in the outer mitochondrial membrane and constitutes the primary

67 Fis1 in yeast localizes to the outer mitochondrial membrane and facilitates mitochondri

68 EET is a homodimeric protein anchored to the outer mitochondrial membrane and has a C-terminal [2Fe-2

69 , ceramide formation might occur both in the outer mitochondrial membrane and in the mitochondrial ma

70 nal fragment tBid, which translocates to the outer mitochondrial membrane and induces massive cytochr

71 rrier protein that has been recruited to the outer mitochondrial membrane and interacts with the inne

72 that mitochondrial MRP-1 is expressed in the outer mitochondrial membrane and is a client protein of

73 that mitochondrial MRP-1 is expressed in the outer mitochondrial membrane and is a client protein of

74 the flux of metabolites and ions across the outer mitochondrial membrane and is a key player in cell

75 nthesis that is exclusively localized to the outer mitochondrial membrane and is composed of CYB5B, M

76 strate that ABCB6 is uniquely located in the outer mitochondrial membrane and is required for mitocho

77 punctate structures that associate with the outer mitochondrial membrane and mediate mitochondrial d

78 preceded a decrease in the integrity of the outer mitochondrial membrane and respiratory control rat

79 t phospholipase A(2) promotes rupture of the outer mitochondrial membrane and spontaneous release of

80 lls, mitofusin 2 (Mfn2), located on both the outer mitochondrial membrane and the ER surface, has bee

81 VDACs) are the most abundant proteins in the outer mitochondrial membrane and the major transport pat

82 spans from the endoplasmic reticulum to the outer mitochondrial membrane and the matrix.

83 cular weight forms, is localized to both the outer mitochondrial membrane and the plasma membrane, an

84 teins are imported by the translocase of the outer mitochondrial membrane and the presequence translo

85 totic Bcl-2 protein Bax can permeabilize the outer mitochondrial membrane and therefore commit human

86 as the crucial anti-apoptotic protein in the outer mitochondrial membrane, and additionally as a gate

87 mediates release of cytochrome c across the outer mitochondrial membrane, and another, characterized

88 tant for cytosolic Bax to integrate into the outer mitochondrial membrane, and c-Myc is critical for

89 APEX was targeted to the outer mitochondrial membrane, and proximity-labeled prot

90 , differential localization to the inner and outer mitochondrial membranes appears to regulate PINK1

91 localized tail-anchored (TA) proteins of the outer mitochondrial membrane are cleared by a newly iden

92 and mechanisms of their transport across the outer mitochondrial membrane are well recognized.

93 These spherular invaginations of outer mitochondrial membranes are packed with electron-d

94 hat suggest that active BAX inserts into the outer mitochondrial membrane as a monomer and then under

95 ndrial CCP activity because Ccp1 crosses the outer mitochondrial membrane as the heme-free protein.

96 -dependent RNA polymerase interacts with the outer mitochondrial membranes as an integral membrane pr

97 Whereas outer mitochondrial membrane-associated degradation is t

98 stead employs the archaic translocase of the outer mitochondrial membrane (ATOM), a protein that show

99 rotein termed the archaic translocase of the outer mitochondrial membrane (ATOM).

100 , however the precise mechanism by which the outer mitochondrial membrane becomes permeable to these

101 LDH is likely localized inside the outer mitochondrial membrane, but not in the mitochondri

102 increased the content of cardiolipin in the outer mitochondrial membrane, but the distribution of ot

103 e, we report that Bbeta2 is localized to the outer mitochondrial membrane by a novel mechanism, combi

104 e, demonstrating that it associates with the outer mitochondrial membrane by binding a protein partne

105 can directly induce permeabilization of the outer mitochondrial membrane by forming a inhibitory com

106 can directly induce permeabilization of the outer mitochondrial membrane by forming complexes with t

107 n, Drp1 is recruited from the cytosol to the outer mitochondrial membrane by one, or several, integra

108 Localization of MRP-1 to the outer mitochondrial membrane by the chaperone protein HS

109 wild-type cells, where it is detected on the outer mitochondrial membrane by virtue of its sensitivit

110 n of a protein complex that assembles at the outer mitochondrial membrane called the transduceosome.

111 sure of VDAC leads to the opening of another outer mitochondrial membrane channel through which cytoc

112 Dissociation of the outer mitochondrial membrane compartment from that of th

113 e show that exclusive delivery of p53 to the outer mitochondrial membrane confers a significant growt

114 sol and its C-terminal TMD inserted into the outer mitochondrial membrane, consistent with a tail-anc

115 Here, we show that purified rat liver outer mitochondrial membrane contains high amidoxime red

116 ese findings support the hypothesis that the outer mitochondrial membrane contains receptors specific

117 An increase in the permeability of the outer mitochondrial membrane, controlled by BCL-2 family

118 n of His-39, one of the axial ligands in rat outer mitochondrial membrane cytochrome b(5) (OM cyt b(5

119 onformational plasticity in ferric rat liver outer mitochondrial membrane cytochrome b5 (rOM b5) and

120 tochondrial permeability transition, whereas outer mitochondrial membrane damage can occur independen

121 injury during endotoxemia and that inner and outer mitochondrial membrane damage occurs through diffe

122 ay participate in lipopolysaccharide-induced outer mitochondrial membrane damage, but further investi

123 ion of Mcl-1L, which localizes mainly to the outer mitochondrial membrane, decreases significantly in

124 ic mutant stably interacts with Mdv1p on the outer mitochondrial membrane, demonstrating that assembl

125 Rerouting this inhibitor to the outer mitochondrial membrane diminishes its ability to b

126 dria into the cytosol upon disruption of the outer mitochondrial membrane during apoptosis.

127 lin B1 is required for the regulation of the outer mitochondrial membrane dynamics.

128 terparts that face the cytosolic side of the outer mitochondrial membrane/endoplasmic reticulum (ER).

129 carnitine palmitoyltransferase-1 (CPT1), an outer mitochondrial membrane enzyme that controls entry

130 ot detectably cleaved and is retained at the outer mitochondrial membrane, even though it interacts w

131 ndria in association with both the inner and outer mitochondrial membranes facing the intermembrane s

132 ay crystal structure of the first identified outer mitochondrial membrane Fe-S protein, mitoNEET.

133 dases (MAO) A and B are approximately 60-kDa outer mitochondrial membrane flavoenzymes catalyzing the

134 tential independent translocation across the outer mitochondrial membrane followed by heme attachment

135 M7 as essential for stabilizing PINK1 on the outer mitochondrial membrane following mitochondrial dam

136 under the presence of mitochondria, and the outer mitochondrial membrane fraction is sufficient for

137 d 2 that mediate mitochondrial tethering and outer mitochondrial membrane fusion, were interrupted by

138 y regulates Mitofusin, which is required for outer mitochondrial membrane fusion.

139 The outer mitochondrial membrane GTPase mitofusin 2 (Mfn2) i

140 nd fusion machinery via interaction with the outer mitochondrial membrane GTPase proteins Miro1 and M

141 sion requires division of both the inner and outer mitochondrial membranes (IMM and OMM, respectively

142 ports cellular mitochondrial proteins to the outer mitochondrial membrane import receptors, and thus

143 s argue in favor of eNOS localization to the outer mitochondrial membrane in endothelial cells and id

144 late the permeability characteristics of the outer mitochondrial membrane in their nonoligomerized st

145 best-studied alphanodavirus, are located on outer mitochondrial membranes in infected Drosophila mel

146 targets and anchors replication complexes to outer mitochondrial membranes in part via an N-proximal

147 and anchors FHV RNA replication complexes to outer mitochondrial membranes, in part through an N-prox

148 AKAP121, which tethers PKAII to the outer mitochondrial membrane, includes a K homology (KH)

149 on, both of which are known to reside at the outer mitochondrial membrane, increases the mitochondria

150 s deposited onto the cytoplasmic face of the outer mitochondrial membrane, increasing antigenic acces

151 se studies indicate that the permeability of outer mitochondrial membranes influences synaptic transm

152 irus (FHV) RNA replication complexes form on outer mitochondrial membranes inside approximately 50-nm

153 d with respect to their roles in controlling outer mitochondrial membrane integrity and apoptosis.

154 Permeabilization of the outer mitochondrial membrane is an integral step in apop

155 The outer mitochondrial membrane isoform of mammalian cytoch

156 The outer mitochondrial membrane isoform of mammalian cytoch

157 mides can form large, stable channels in the outer mitochondrial membrane, leading to the proposal th

158 o and phosphorylation of Sab by p-JNK on the outer mitochondrial membrane leads to SHP1-dependent and

159 Tim23 tightly associates with both inner and outer mitochondrial membrane-like membranes through a hy

160 mitochondrial membranes in naive cells, the outer mitochondrial membrane loses its integrity; this l

161 ational boost by the MDI-Larp complex on the outer mitochondrial membrane might be essential for mtDN

162 t that the specific lipid composition of the outer mitochondrial membrane might be of crucial relevan

163 somal GPAT) and an NEM-resistant form in the outer mitochondrial membrane (mtGPAT).

164 ssion are mediated by several GTPases in the outer mitochondrial membrane, notably mitofusin-2 (Mfn-2

165 rosomal (Mc) cytochromes b(5) into rat liver outer mitochondrial membrane (OM) cytochrome (cyt) b(5),

166 ed and identified endogenous proteins on the outer mitochondrial membrane (OMM) and endoplasmic retic

167 taVD mutants constitutively localized to the outer mitochondrial membrane (OMM) and fragmented mitoch

168 ontaneous Ca(2+) pacing, Ca(2+) peaks on the outer mitochondrial membrane (OMM) are much greater than

169 active caspase 8 are localized mainly on the outer mitochondrial membrane (OMM) as integral proteins.

170 been studied in their detergent-purified and outer mitochondrial membrane (OMM) bound forms using a s

171 StAR acts exclusively on the outer mitochondrial membrane (OMM) by unknown mechanisms

172 Both proteins were enriched in the IMM-outer mitochondrial membrane (OMM) contact point submito

173 Since the outer mitochondrial membrane (OMM) has been thought to b

174 lular lifespan is contingent upon preserving outer mitochondrial membrane (OMM) integrity, as permeab

175 The outer mitochondrial membrane (OMM) is the last barrier b

176 The outer mitochondrial membrane (OMM) is thought to play a

177 , but not by Bcl-2, implying that changes in outer mitochondrial membrane (OMM) permeability leading

178 However, the mechanism of outer mitochondrial membrane (OMM) permeabilization rema

179 Here, we demonstrate that Miro1, an outer mitochondrial membrane (OMM) protein crucial for t

180 ripheral-type benzodiazepine receptor, is an outer mitochondrial membrane (OMM) protein necessary for

181 Parkin-mediated polyubiquitination of outer mitochondrial membrane (OMM) proteins recruits the

182 ax and Bak spontaneously associated with the outer mitochondrial membrane (OMM) through their respect

183 StAR acts on the outer mitochondrial membrane (OMM) to facilitate movemen

184 a mitochondrial matrix protein, acts on the outer mitochondrial membrane (OMM) to facilitate the mov

185 show that IkappaBalpha also localises to the outer mitochondrial membrane (OMM) to inhibit apoptosis.

186 roapoptotic BCL-2 proteins converge upon the outer mitochondrial membrane (OMM) to promote mitochondr

187 increasing the flow of cholesterol from the outer mitochondrial membrane (OMM) to the inner membrane

188 nels (VDACs) are predominant proteins of the outer mitochondrial membrane (OMM) where they contribute

189 ansferase 1 (CPT1), which is anchored in the outer mitochondrial membrane (OMM), controls the rate-li

190 chondrion-associated membranes (MAMs) to the outer mitochondrial membrane (OMM), where it robustly in

191 oscopy showed that Tom22 is localized at the outer mitochondrial membrane (OMM), while 3betaHSD2 is l

192 Ubiquitin- and proteasome-dependent outer mitochondrial membrane (OMM)-associated degradatio

193 ome system in the regulation and turnover of outer mitochondrial membrane (OMM)-associated proteins.

194 m the ER to mitochondria and clusters at the outer mitochondrial membrane (OMM).

195 inhibit Bax-mediated permeabilization of the outer mitochondrial membrane (OMM).

196 effects in both the mitochondrial matrix and outer mitochondrial membrane (OMM).

197 tosolic and mitochondrial factors across the outer mitochondrial membrane (OMM).

198 and degrades TA proteins mistargeted to the outer mitochondrial membrane (OMM).

199 Because outer-mitochondrial membrane (OMM) constituents insert d

200 KC isoforms that were tethered either to the outer mitochondrial membrane or to the PM.

201 SFV was not significantly different from the outer mitochondrial membrane (P < 0.05).

202 robustly induced by PINK1 expression on the outer mitochondrial membrane, Parkin recruitment to mito

203 Loss of Bax/Bak reduced outer mitochondrial membrane permeability and conductanc

204 n vitro models of lipotoxicity, we show that outer mitochondrial membrane permeability is altered and

205 ell death that is not initiated by increased outer mitochondrial membrane permeability or translocati

206 the BH1,2,3 effector protein Bak, leading to outer mitochondrial membrane permeabilization (OMMP) wit

207 SK3-mediated phosphorylation status controls outer mitochondrial membrane permeabilization in hepatos

208 e as Bax coalescence on the mitochondria and outer mitochondrial membrane permeabilization, and it ma

209 proapoptotic factors and thereby regulating outer mitochondrial membrane permeabilization.

210 regulator) can commit cells to apoptosis via outer mitochondrial membrane permeabilization.

211 e mediated by supramolecular openings in the outer mitochondrial membrane, promoted by BH3/Bax/lipid

212 The tail-anchor of an outer mitochondrial membrane protein also labels autopha

213 6, which is identical to MMM1 and encodes an outer mitochondrial membrane protein essential for maint

214 of mitochondria prior to engulfment, and the outer mitochondrial membrane protein FUNDC1 interacts wi

215 iazepine receptor (PBR), is a crucial 18-kDa outer mitochondrial membrane protein involved in numerou

216 likely by influencing protein levels of the outer mitochondrial membrane protein Miro that anchors m

217 nt of kinesin-1 to mitochondria involves the outer mitochondrial membrane protein mitochondrial Rho G

218 The outer mitochondrial membrane protein mitochondrial Rho G

219 The outer mitochondrial membrane protein mitoNEET was discov

220 pioglitazone led to the discovery of a novel outer mitochondrial membrane protein of unknown function

221 Miro is an outer mitochondrial membrane protein that anchors mitoch

222 MitoNEET is a 2Fe-2S outer mitochondrial membrane protein that was initially

223 MitoNEET is an outer mitochondrial membrane protein that, upon overexpr

224 The outer mitochondrial membrane protein voltage-dependent a

225 gosomes and is sufficient to deliver another outer mitochondrial membrane protein, Fis1, to autophago

226 ong form of B-cell lymphoma-x (Bcl-x(L)), an outer mitochondrial membrane protein, has been proposed

227 Here we show that VAPB interacts with the outer mitochondrial membrane protein, protein tyrosine p

228 we utilized a cell-permeable peptide of the outer mitochondrial membrane protein, Sab (SH3BP5), as a

229 The outer mitochondrial membrane protein, the voltage-depend

230 its recently identified paralog mitoNEET, an outer mitochondrial membrane protein.

231 h is inhibited by yeast Fis1, a pore-forming outer mitochondrial membrane protein.

232 -dependent anion channel (VDAC), an abundant outer mitochondrial membrane protein.

233 Miro; encoded by YAL048C) is a tail-anchored outer mitochondrial membrane protein.

234 Mitofusins (Mfn1 and Mfn2) are outer mitochondrial membrane proteins involved in regula

235 hich is, in turn, known to interact with the outer mitochondrial membrane proteins Miro1/2, linking m

236 Then, Parkin ubiquitinates outer mitochondrial membrane proteins to trigger selecti

237 ligase activity is required to ubiquitinate outer mitochondrial membrane proteins, allowing optineur

238 olarized mitochondria where it ubiquitinates outer mitochondrial membrane proteins, initiating lysoso

239 uses, exerts its activity transiently at the outer mitochondrial membrane rather than at its final re

240 o not regulate PTP activity through TSPO, 3) outer mitochondrial membrane regulation of PTP activity

241 /killer (Bak) undergo oligomerization in the outer mitochondrial membrane resulting in the release of

242 A damage-induced p53/Bcl2 interaction at the outer mitochondrial membrane results in a Bcl2 conformat

243 f these and other signaling molecules to the outer mitochondrial membrane results in the rapid induct

244 otein A recruits FHV RNA specifically to the outer mitochondrial membrane sites of RNA replication co

245 copy imaging method to observe the inner and outer mitochondrial membrane structures and selectively

246 Its localization to the outer mitochondrial membrane suggests an important yet u

247 tes histidine-tagged peptides to a simulated outer mitochondrial membrane surface.

248 MitoNEET (mNT) is an outer mitochondrial membrane target of the thiazolidined

249 mbles into large multimeric complexes on the outer mitochondrial membrane that are visualized as punc

250 ndent proteins take another route across the outer mitochondrial membrane that involves Tom40 in a fo

251 e formation of a multivalent scaffold in the outer mitochondrial membrane that mediates the effect of

252 A and B (MAO-A and MAO-B) are enzymes of the outer mitochondrial membrane that metabolize biogenic am

253 dase A (MAO-A) is an important enzyme on the outer mitochondrial membrane that participates in the ce

254 een Bcl2 and c-Myc in the nucleus and on the outer mitochondrial membrane that significantly enhances

255 el 1 (VDAC-1) is an important protein of the outer mitochondrial membrane that transports energy meta

256 e of four submitochondrial compartments--the outer mitochondrial membrane, the inner mitochondrial me

257 ppress tumor formation by permeabilizing the outer mitochondrial membrane, thereby releasing pro-apop

258 ne protein that forms an aqueous pore in the outer mitochondrial membrane, through which metabolites

259 AKAP1 recruits protein kinase A (PKA) to the outer mitochondrial membrane to phospho-inhibit DRP1.

260 poptosis, Bax-type proteins permeabilize the outer mitochondrial membrane to release intermembrane ap

261 eroidogenesis by moving cholesterol from the outer mitochondrial membrane to the inner mitochondrial

262 litates the movement of cholesterol from the outer mitochondrial membrane to the inner mitochondrial

263 However, an abnormal permeability of outer mitochondrial membranes to cytochrome c was observ

264 Self-interacting BAX proteins permeabilize outer mitochondrial membranes to trigger apoptotic cell

265 Although the translocase of the outer mitochondrial membrane (TOM) complex proteins Tom2

266 a central component of the translocon of the outer mitochondrial membrane (TOM) complex, is essential

267 The preprotein translocase of the outer mitochondrial membrane (TOM) functions as the main

268 rmore, Tim29 contacts the Translocase of the Outer Mitochondrial Membrane, TOM complex, enabling a me

269 ing the interaction of MAM proteins with the outer mitochondrial membrane translocase, Tom22, to acti

270 ropose that 3betaHSD2 associates with IMM or outer mitochondrial membrane translocases facing the int

271 omolecular signaling complex composed of the outer mitochondrial membrane translocator protein (TSPO)

272 s suggests that GSK inhibitors are acting on outer mitochondrial membrane transport.

273 Targeting Rab35 to the outer mitochondrial membrane triggered actin recruitment

274 annels: voltage-dependent anion channel from outer mitochondrial membrane VDAC, bacterial porin OmpC

275 K II) that is overexpressed and bound to the outer mitochondrial membrane via the porin-like protein

276 ter and the mean distance between SR and the outer mitochondrial membrane vs. CD hearts.

277 ix, and formation of vesicles and tubules of outer mitochondrial membrane, was also observed in both

278 StAR acts on the outer mitochondrial membrane where each molecule stimula

279 ependent monooxygenase and is located in the outer mitochondrial membrane where it converts l-kynuren

280 -Ras off of the plasma membrane and onto the outer mitochondrial membrane where it induces cell death

281 punctate structures that are targeted to the outer mitochondrial membrane where they mediate mitochon

282 ia an N-terminal transmembrane domain to the outer mitochondrial membrane, where FHV RNA replication

283 cumulates as a 63-kD full-length form on the outer mitochondrial membrane, where it can recruit Parki

284 mic BAX is activated and translocates to the outer mitochondrial membrane, where it forms an oligomer

285 BNip3 localizes to the outer mitochondrial membrane, where it functions in mito

286 Mammalian Bcl-x(L) protein localizes to the outer mitochondrial membrane, where it inhibits apoptosi

287 ine phosphoprotein (FAST) is tethered to the outer mitochondrial membrane, where it interacts with BC

288 l MRP-1 is glycosylated and localized to the outer mitochondrial membrane, where it is coexpressed wi

289 nserved, ubiquitous protein localized in the outer mitochondrial membrane, where it is thought to pla

290 T-treated BL-3 cells revealed lesions in the outer mitochondrial membrane, which are larger than prev

291 ized by the rapid accumulation of BIM on the outer mitochondrial membrane, which could be functionall

292 monstrate that its apoptotic activity at the outer mitochondrial membrane, which involves conformatio

293 we showed that internalized LKT binds to the outer mitochondrial membrane, which results in the relea

294 ents have thus revealed early changes in the outer mitochondrial membrane, which take place long befo

295 rgeting induced ceramide accumulation on the outer mitochondrial membrane, which then directly bound

296 ia demonstrated that ABCB6 is present in the outer mitochondrial membrane, while back-titration assay

297 ng in dissociation of hexokinase II from the outer mitochondrial membrane with subsequent mitochondri

298 strated that protein A was inserted into the outer mitochondrial membrane with the N terminus in the

299 modimeric iron-sulfur protein located in the outer mitochondrial membrane with unknown function, but

300 state, MondoA:Mlx complexes localize to the outer mitochondrial membrane, yet shuttle between the mi