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

1 te to form an ~150-kilodalton complex in the inner mitochondrial membrane.

2 oes not depend on proper localization to the inner mitochondrial membrane.

3 at transport specific metabolites across the inner mitochondrial membrane.

4 ed shuttle of ATP-Mg(2+) and P(i) across the inner mitochondrial membrane.

5 icantly increased cholesterol content in the inner mitochondrial membrane.

6 ansfer of charged small molecules across the inner mitochondrial membrane.

7 lex (presequence translocase) located in the inner mitochondrial membrane.

8 d to the translocation of protons across the inner mitochondrial membrane.

9 the respiratory chain and is located in the inner mitochondrial membrane.

10 e mitochondrial fusion of both the outer and inner mitochondrial membrane.

11 mitochondrial origin and are embedded in the inner mitochondrial membrane.

12 G', suggesting a mode of insertion into the inner mitochondrial membrane.

13 he movement of cholesterol from the outer to inner mitochondrial membrane.

14 e lipophilic electron carrier located in the inner mitochondrial membrane.

15 e), thereby shuttling nucleotides across the inner mitochondrial membrane.

16 orter, a Ca(2+)-selective ion channel in the inner mitochondrial membrane.

17 to the negatively charged environment of the inner mitochondrial membrane.

18 e oxidoreductase, an integral protein of the inner mitochondrial membrane.

19 none, and four protons are pumped across the inner mitochondrial membrane.

20 orm in the matrix weakly associated with the inner mitochondrial membrane.

21 F-QO) is a 4Fe4S flavoprotein located in the inner mitochondrial membrane.

22 Tim44p can tightly associate with the inner mitochondrial membrane.

23 matrix by transporting substrates across the inner mitochondrial membrane.

24 ation, and DeltaPsi and K+ fluxes across the inner mitochondrial membrane.

25 of the multisubunit protein complexes in the inner mitochondrial membrane.

26 cluding critical factors associated with the inner mitochondrial membrane.

27 can release superoxide to both sides of the inner mitochondrial membrane.

28 nsport precursor proteins into or across the inner mitochondrial membrane.

29 and concomitantly pumping protons across the inner mitochondrial membrane.

30 is too strongly charged to readily cross the inner mitochondrial membrane.

31 otides, possibly from the matrix side of the inner mitochondrial membrane.

32 ciate with respiratory supercomplexes of the inner mitochondrial membrane.

33 ollowing translocation of cholesterol to the inner mitochondrial membrane.

34 ein that localizes to the matrix side of the inner mitochondrial membrane.

35 d cardiolipin (CL) is primarily found in the inner mitochondrial membrane.

36 n electrochemical proton gradient across the inner mitochondrial membrane.

37 mtCLIC associates with the inner mitochondrial membrane.

38 e NADH dehydrogenase is loosely bound to the inner mitochondrial membrane.

39 using ADP/ATP carriers (AAC) located in the inner mitochondrial membrane.

40 e dehydrogenase complex (PDC) located in the inner mitochondrial membrane.

41 metal-dependent protease associated with the inner mitochondrial membrane.

42 he flux of cholesterol from the outer to the inner mitochondrial membrane.

43 se that is located on the matrix side of the inner mitochondrial membrane.

44 tochrome c release and depolarization of the inner mitochondrial membrane.

45 otential of NADH to drive protons across the inner mitochondrial membrane.

46 respiratory enzyme complexes residing in the inner mitochondrial membrane.

47 rofound reduction in binding of sMtCK to the inner mitochondrial membrane.

48 subunits to link this enzyme directly to the inner mitochondrial membrane.

49 of cholesterol to cytochrome P450scc on the inner mitochondrial membrane.

50 iratory chain complexes I, III and IV in the inner mitochondrial membrane.

51 s dissipating the proton gradient across the inner mitochondrial membrane.

52 ting a possible mode of interaction with the inner mitochondrial membrane.

53 ion protein is localized specifically in the inner mitochondrial membrane.

54 that likely affects its mobility within the inner mitochondrial membrane.

55 pcmAAT chimera is found associated with the inner mitochondrial membrane.

56 a carotenoid cleavage enzyme located in the inner mitochondrial membrane.

57 We demonstrate that MSL1 localises to the inner mitochondrial membrane.

58 f the mitochondrial respiratory chain in the inner mitochondrial membrane.

59 energize precursor translocation across the inner mitochondrial membrane.

60 coupling protein 1 (UCP1) located within the inner mitochondrial membrane.

61 ult from futile leak conductance through the inner mitochondrial membrane.

62 steps energize precursor passage across the inner mitochondrial membrane.

63 stitute for its homologue Mrs2p in the yeast inner mitochondrial membrane.

64 ia confirmed the localization of BCO2 to the inner mitochondrial membrane.

65 ines, that human BCO2 is associated with the inner mitochondrial membrane.

66 in brain mitochondria and is targeted to the inner mitochondrial membrane.

67 nel called the uniporter that resides in the inner mitochondrial membrane.

68 phore and TPP ensure partitioning within the inner mitochondrial membrane.

69 pids, mainly cardiolipin, and in vivo to the inner mitochondrial membrane.

70 mitochondrial-localized STAT3 resides in the inner mitochondrial membrane.

71 lacking cleavable transit sequences into the inner mitochondrial membrane.

72 accomplish the transfer of Ca(2+) across the inner mitochondrial membrane.

73 istae by interacting with cardiolipin on the inner mitochondrial membrane.

74 duction necessitate ion transport across the inner mitochondrial membrane.

75 llowing rapid Ca(2+) accumulation across the inner mitochondrial membrane.

76 of mitochondrion-encoded precursors into the inner mitochondrial membrane.

77 ospholipid trafficking between the outer and inner mitochondrial membranes.

78 machines called translocons on the outer and inner mitochondrial membranes.

79 einaceous structure that spans the outer and inner mitochondrial membranes.

80 ed during translocation across the outer and inner mitochondrial membranes.

81 m NADH in the matrix to ubiquinone-10 in the inner mitochondrial membranes.

82 enzyme was located on the matrix side of the inner mitochondrial membranes.

83 rion and appears to constrict both outer and inner mitochondrial membranes.

84 tochondrial TOM40 and the translocase of the inner mitochondrial membrane 23 (TIM23) import channel T

85 1alpha subcomplexes 2 and 3, translocase of inner mitochondrial membrane 50, and valyl-tRNA syntheta

86 Mature AS seemed to translocate across the inner mitochondrial membrane a second time to finally re

87 ction reaction for proton pumping across the inner-mitochondrial membrane, a process that results in

88 present an atomic model of a substrate-bound inner mitochondrial membrane AAA+ quality control protea

89 respiratory chain, pumps protons across the inner mitochondrial membrane against an opposing electro

90 The inner mitochondrial membrane also contains a large numbe

91 s compete for the proton gradient across the inner mitochondrial membrane, an efficient mechanism is

92 ted with persistent hyperpolarization of the inner mitochondrial membrane and a modest increase in ca

93 VLCAD associates with the inner mitochondrial membrane and catalyzes the initial s

94 ontinuous futile cycles of Ca(2+) across the inner mitochondrial membrane and consequent massive ener

95 ast, [Dmt1,atnDap4]DALDA was retained in the inner mitochondrial membrane and did not induce mitochon

96 at an extranuclear pool of BMI1 localizes to inner mitochondrial membrane and directly regulates mito

97 Uncoupling proteins (UCPs) occur in the inner mitochondrial membrane and dissipate the proton gr

98 ely associated with the interior face of the inner mitochondrial membrane and distinct in its propert

99 suggested that Stoml2 is associated with the inner mitochondrial membrane and faces the intermembrane

100 dynamin-related protein associated with the inner mitochondrial membrane and functions in mitochondr

101 rved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in

102 The OPA3 protein is enriched in the inner mitochondrial membrane and has mitochondrial targe

103 y acid beta-oxidation systems located in the inner mitochondrial membrane and in the mitochondrial ma

104 show that SRT2 resides predominantly at the inner mitochondrial membrane and interacts with a small

105 from the outer mitochondrial membrane to the inner mitochondrial membrane and is a critical regulator

106 otic cells, CL is found predominantly in the inner mitochondrial membrane and is generally thought to

107 sistent with this, Rbd1p is localized in the inner mitochondrial membrane and mutant cells have disru

108 -Phe-NH2 (SS-31), previously shown to target inner mitochondrial membrane and prevent oxidative damag

109 s; one associated with the inner face of the inner mitochondrial membrane and the other in the matrix

110 bound to the inner and outer aspects of the inner mitochondrial membrane and, as a result, were accu

111 for octamer formation, binding of sMtCK with inner mitochondrial membrane, and coupling of sMtCK to o

112 cytochrome c outflow, depolarization of the inner mitochondrial membrane, and DNA fragmentation were

113 cated that Cx43 was located primarily on the inner mitochondrial membrane, and mtCx43 protein level w

114 long-chain-specific enzymes are bound to the inner mitochondrial membrane, and some enzymes are expre

115 omolecular complex on the matrix face of the inner mitochondrial membrane, and this complex is requir

116 otide transport across the outer but not the inner mitochondrial membrane, and we found that GSK inhi

117 lecules that govern Ca2+ movement across the inner mitochondrial membrane are unknown.

118 Human ferrochelatase is a homodimeric, inner mitochondrial membrane-associated enzyme that poss

119 ted by the pumping of protons out across the inner mitochondrial membrane at the mitochondrial comple

120 O2*- alone evoked CCR without damage of the inner mitochondrial membrane barrier, as mitochondrial m

121 At the onset of this process, the inner mitochondrial membrane becomes depolarized and per

122 n of the electrochemical gradient across the inner mitochondrial membrane blocked Ca2+ uptake and pac

123 chrome c oxidase subunit polypeptides to the inner mitochondrial membrane but instead functions after

124 ciated with altered lipid composition of the inner mitochondrial membrane, but a putative secondary i

125 of cardiolipin, the main phospholipid of the inner mitochondrial membrane, but a secondary impairment

126 dent targeting of the Pink1 precursor to the inner mitochondrial membrane, but it is dispensable for

127 OPA1 is essential for the fusion of the inner mitochondrial membranes, but its mechanism of acti

128 the cardioprotective signal from cytosol to inner mitochondrial membrane by a pathway that includes

129 from the outer mitochondrial membrane to the inner mitochondrial membrane by an unclear process that

130 osis, the peroxidation of cardiolipin at the inner mitochondrial membrane by cytochrome c requires an

131 back loop regulates protein synthesis at the inner mitochondrial membrane by directly monitoring the

132 nsfer chain, translocates protons across the inner mitochondrial membrane by harnessing the free ener

133 Selective transport of pyruvate across the inner mitochondrial membrane by the mitochondrial pyruva

134 issipation of the proton gradient across the inner mitochondrial membrane by treatment with an uncoup

135 el from which the observed morphology of the inner mitochondrial membrane can be inferred as minimizi

136 ermeabilization, and unchanged expression of inner mitochondrial membrane cardiolipin.

137 affected by uncoupling protein-2 (UCP2), an inner mitochondrial membrane carrier that senses and neg

138 ADP/ATP carriers in the inner mitochondrial membrane catalyze the exchange of cy

139 xidase (POX), a flavoenzyme localized at the inner mitochondrial membrane, catalyzes the first step o

140 failed deoxynucleotide transport across the inner mitochondrial membrane causes MCPHA.

141 ome c oxidase (CcO) pumps protons across the inner mitochondrial membrane, contributing to the genera

142 nd IV in the electron-transport chain in the inner mitochondrial membrane) couple the redox reactions

143 djacent mitochondria exhibit coordination of inner mitochondrial membrane cristae at inter-mitochondr

144 st that modulation of a complex V-associated inner mitochondrial membrane current is metabolically im

145 Inner mitochondrial membrane damage appears to relate to

146 atory control, reflecting protection against inner mitochondrial membrane damage.

147 Inner mitochondrial membrane density was determined by s

148 Extraocular muscle inner mitochondrial membrane density was similar to that

149 ect the association of cytochrome c with the inner mitochondrial membrane, directly influencing the p

150 the influence of Ca(2+) movement across the inner mitochondrial membrane during both subcellular and

151 cholesterol transport from the outer to the inner mitochondrial membrane during steroid biosynthesis

152 own the electrochemical potential across the inner mitochondrial membrane, establishing an NADPH/NADP

153 we show that Mmm1p spans both the outer and inner mitochondrial membranes, exposing its N terminus t

154 sting that the increased permeability of the inner mitochondrial membrane facilitates the loss of thi

155 where it is peripherally associated with the inner mitochondrial membrane facing the mitochondrial ma

156 on with latent binding sites on the outer or inner mitochondrial membranes, followed by an increase i

157 es are essential for fusion of the outer and inner mitochondrial membranes, Fzo1 (yeast)/Mfn1/Mfn2 (m

158 Selective K(+) transport in the inner mitochondrial membrane has been attributed to at l

159 oxoglutarate (OGC) carriers localized to the inner mitochondrial membrane have been established as GS

160 oxidative stress, precipitate opening of an inner mitochondrial membrane, high-conductance channel:

161 of cytochrome c (cyt c) remains bound to the inner mitochondrial membrane (IMM) at physiological ioni

162 hesized in the cytosol, is imported into the inner mitochondrial membrane (IMM) by translocases.

163 culum (SR) ryanodine receptors (RyR2) to the inner mitochondrial membrane (IMM) Ca(2+) uniporter (mtC

164 The relationship of the inner mitochondrial membrane (IMM) cristae structure and

165 Mitochondria maintain tight regulation of inner mitochondrial membrane (IMM) permeability to susta

166 CFAs), UCP1 increases the conductance of the inner mitochondrial membrane (IMM) to make BAT mitochond

167 tion of cytochrome c from cardiolipin on the inner mitochondrial membrane (IMM), and cytochrome c may

168 SOD1 mice had a reduced association with the inner mitochondrial membrane (IMM).

169 on IP(3)-driven Ca(2+) transport through the inner mitochondrial membrane (IMM).

170 l carrier super family that localizes to the inner mitochondrial membrane (IMM).

171 Because AQP8 is expressed in hepatocyte inner mitochondrial membranes (IMMs), we studied whether

172 peptides have been shown to move across the inner mitochondrial membrane in a manner suggesting an i

173 he movement of cholesterol from the outer to inner mitochondrial membrane in adrenal and gonadal cell

174 nificant fraction of PB1-F2 localizes to the inner mitochondrial membrane in influenza A virus-infect

175 ggers the disorganization of the cristae and inner mitochondrial membrane in several cancer cells and

176 ranslocate cholesterol from the outer to the inner mitochondrial membrane in steroidogenic cells, the

177 he transfer of cholesterol from the outer to inner mitochondrial membrane in vitro.

178 We have also localized Pet100p to the inner mitochondrial membrane in wild type cells, where i

179 nesis of multimeric protein complexes of the inner mitochondrial membrane in yeast requires a number

180 revealed that zeaxanthin accumulates in the inner mitochondrial membrane; in contrast, beta-carotene

181 rial electron transport via perturbations in inner mitochondrial membrane integrity.

182 Cox25 is an inner mitochondrial membrane intrinsic protein with a hy

183 protein 2, UCP2, is a member of a family of inner mitochondrial membrane ion carriers involved in a

184 The transfer of Ca(2+) across the inner mitochondrial membrane is an important physiologic

185 uence by the electrical potential across the inner mitochondrial membrane is calculated on the basis

186 tight regulation of proton transport in the inner mitochondrial membrane is crucial for physiologica

187 In particular, the inner mitochondrial membrane is generally impermeable to

188 -binding cassette transporter located in the inner mitochondrial membrane is involved in iron-sulfur

189 ngs suggest that cholesterol delivery to the inner mitochondrial membrane is the predominant rate-det

190 th the translocase on the matrix side of the inner mitochondrial membrane, is critical for protein tr

191 ning of permeability transition pores in the inner mitochondrial membrane, leading to matrix swelling

192 n X-100 disrupted the plasma, acrosomal, and inner mitochondrial membranes, leaving axonemes intact.

193 d penetrates lipid structures containing the inner mitochondrial membrane lipid cardiolipin (CL), lea

194 -F2 that is necessary and sufficient for its inner mitochondrial membrane localization, as determined

195 Although the influx of Ca(2+) across the inner mitochondrial membrane maintains metabolic functio

196 dylserine to phosphatidylethanolamine in the inner mitochondrial membrane, must undergo an autocataly

197 They are also located in the inner mitochondrial membrane near the ROS-producing site

198 tions in the electron transport chain in the inner mitochondrial membrane of eukaryotes and the plasm

199 s with distinct functional properties to the inner mitochondrial membrane of intact cells.

200 prevent lipid chain autoxidation, within the inner mitochondrial membrane of live cells.

201 ce that SK2 channels are also located in the inner mitochondrial membrane of neuronal mitochondria.

202 ydrogenase, found in bacterial membranes and inner mitochondrial membranes of animal cells, couples t

203 at Coq5p is peripherally associated with the inner mitochondrial membrane on the matrix side.

204 meability transition, a large channel in the inner mitochondrial membrane opens, leading to the loss

205 ociated with either the interior face of the inner mitochondrial membrane or with the mitochondrial m

206 eins in repair complexes associated with the inner mitochondrial membrane, perhaps providing a novel

207 rome c oxidase (COX) complex, present in the inner mitochondrial membrane, placed the p27 protein in

208 The inner mitochondrial membrane plays a crucial role in cel

209 tal mitochondrial dehydrogenase activity and inner mitochondrial membrane polarization were all signi

210 dria exhibit modest hyperpolarization of the inner mitochondrial membrane potential (> or =22% versus

211 d a concentration-dependant reduction in the inner mitochondrial membrane potential (DeltaPsi(m)), as

212 ve oxygen species (ROS) at clamped levels of inner mitochondrial membrane potential (DeltaPsi), enabl

213 Ca(2+) overload is thought to dissipate the inner mitochondrial membrane potential (DeltaPsim) and e

214 bcl-X(s) expression causes loss of the inner mitochondrial membrane potential (deltapsim) but d

215 the mitochondria using depolarization of the inner mitochondrial membrane potential (DeltaPsim), the

216 in the presence of glucose, showed a higher inner mitochondrial membrane potential and ATP:ADP ratio

217 Furthermore, dissipation of the inner mitochondrial membrane potential and enhanced prod

218 tic ATP into the mitochondria to generate an inner mitochondrial membrane potential through the F(1)F

219 tured neurons revealed large fluctuations in inner mitochondrial membrane potential when Bcl-x(L) was

220 (ATP synthesis, dehydrogenase activity, and inner mitochondrial membrane potential), and protected t

221 glucose, decreased lipid oxidation, reduced inner mitochondrial membrane potential, and mitochondria

222 by this sequence resulted in the loss of the inner mitochondrial membrane potential, leading to cell

223 dative stress challenge, Pim-1 preserves the inner mitochondrial membrane potential.

224 etic relationship between oxygen use and the inner mitochondrial membrane potential.

225 from mitochondria and the alterations in the inner mitochondrial membrane potential.

226 dylserine decarboxylase Psd1, located in the inner mitochondrial membrane, promotes mitochondrial PE

227 The inner mitochondrial membrane protein 3beta-hydroxysteroi

228 pecies metabolism and a close homolog of the inner mitochondrial membrane protein Mpv17.

229 recessive disease caused by mutations in the inner mitochondrial membrane protein MPV17.

230 of mitochondrial fusion via knockdown of the inner mitochondrial membrane protein Opa1 had no effect

231 of this phenotype is a point mutation in an inner mitochondrial membrane protein required for transp

232 We determined that TMEM14C, an inner mitochondrial membrane protein that is enriched in

233 leotide transporter 1 gene (ANT1) encodes an inner mitochondrial membrane protein that transports ATP

234 cytochrome c reductase core protein 2 or the inner mitochondrial membrane protein, ADP/ATP translocas

235 Bcl-2, an inner mitochondrial membrane protein, inhibits apoptotic

236 Here, we identify the inner mitochondrial membrane protein, prohibitin 2 (PHB2

237 adenine nucleotide translocase 2 (ANT2), an inner mitochondrial membrane protein, which leads to the

238 n, is a multi-subunit, bigenomically encoded inner mitochondrial membrane protein.

239 pearl (Blp) is a highly conserved, essential inner-mitochondrial membrane protein.

240 y implicated in quality control of misfolded inner mitochondrial membrane proteins and in regulatory

241 olipin synthase was shown to colocalize with inner mitochondrial membrane proteins and to be part of

242 In eukaryotes, two inner mitochondrial membrane proteins, heme O synthase (

243 he proteins that transport copper across the inner mitochondrial membrane remain unknown.

244 by increasing the proton permeability of the inner mitochondrial membrane, simulations with the combi

245 An ATP-Mg(2+/)P(i) inner mitochondrial membrane solute transporter (SLC25A2

246 the same time undergo progressive changes in inner mitochondrial membrane structure (swelling and los

247 p53 protein was detected in an inner mitochondrial membrane subfraction containing comp

248 ression of UCP-2 or UCP-3 can depolarize the inner mitochondrial membrane, suppression of UCP-2 mRNA

249 rine decarboxylase, which is embedded in the inner mitochondrial membrane, synthesizes phosphatidylet

250 cent data demonstrate that components of the inner mitochondrial membrane that are unmasked upon oute

251 CPs) are a family of proteins located in the inner mitochondrial membrane that can dissociate oxidati

252 ial pyruvate carrier (MPC), a complex in the inner mitochondrial membrane that consists of two essent

253 knowledge about the ion transporters in the inner mitochondrial membrane that contribute to control

254 in, an anionic phospholipid expressed on the inner mitochondrial membrane that is required for crista

255 tes remains unknown, several proteins of the inner mitochondrial membrane, that are likely to accompl

256 ments--the outer mitochondrial membrane, the inner mitochondrial membrane, the intramembraneous space

257 The import of cholesterol to the inner mitochondrial membrane, the rate-limiting step in

258 d as essential for cholesterol import to the inner mitochondrial membrane, the rate-limiting step in

259 ovement of cholesterol from the outer to the inner mitochondrial membrane, the site of cholesterol si

260 A sudden increase in permeability of the inner mitochondrial membrane, the so-called mitochondria

261 acids, nucleotides, and cofactors across the inner mitochondrial membrane, thereby connecting cytosol

262 lates, nucleotides, and coenzymes across the inner mitochondrial membrane, thereby connecting cytosol

263 ondria can lead to the depolarization of the inner mitochondrial membrane, thereby sensitizing impair

264 is driven by a membrane potential across the inner mitochondrial membrane; this potential is generate

265 +) stimulates metabolite transfer across the inner mitochondrial membrane through activation of Ca(2+

266 Bax could then enter and permeabilize the inner mitochondrial membrane through the same hole.

267 and ATP by an antiport mechanism across the inner mitochondrial membrane, thus playing an essential

268 The presequence translocase of the inner mitochondrial membrane (TIM23) translocates prepro

269 movement of cholesterol from the OMM to the inner mitochondrial membrane to be converted to pregneno

270 ompanied by an increased permeability of the inner mitochondrial membrane to matrix-entrapped calcein

271 Bcl-x(L) reduces futile ion flux across the inner mitochondrial membrane to prevent a wasteful drain

272 nstitutes a hetero-oligomeric complex on the inner mitochondrial membranes to maintain crista structu

273 res a 470-bp common promoter region with the inner mitochondrial membrane translocase 23 (TIM23).

274 helical transmembrane region of the SLC25A40 inner mitochondrial membrane transport protein.

275 Furthermore, we establish that the inner mitochondrial membrane transporter, pyrimidine nuc

276 Sequence homology of this protein with the inner mitochondrial membrane transporters suggested a do

277 Uncoupling proteins (UCP) are inner mitochondrial membrane transporters which dissipat

278 IRT5 is targeted to protein complexes on the inner mitochondrial membrane via affinity for cardiolipi

279 he movement of cholesterol from the outer to inner mitochondrial membrane via an unknown mechanism.

280 idative phosphorylation machinery within the inner mitochondrial membrane was >90%.

281 using direct patch-clamp recording from the inner mitochondrial membrane, we compare mitochondrial c

282 By patch-clamping the inner mitochondrial membrane, we identified a previously

283 Changes in the permeability of the inner mitochondrial membrane were evaluated by monitorin

284 he single-channel level, recordings from the inner mitochondrial membrane were obtained by a patch-cl

285 a protein that transports cholesterol to the inner mitochondrial membrane) were markedly increased in

286 gative curvature of the invaginations of the inner mitochondrial membrane where cytochrome c resides.

287 eriments reveal that SKIP is enriched at the inner mitochondrial membrane where it associates with a

288 increase the delivery of cholesterol to the inner mitochondrial membrane where P450scc resides.

289 ling of transcription and translation at the inner mitochondrial membrane, where assembly of the oxid

290 CYP27 is located in the inner mitochondrial membrane, where cholesterol content

291 1)F(0)-ATP synthase enzyme is located in the inner mitochondrial membrane, where it forms dimeric com

292 spholipid cardiolipin (CL) is located in the inner mitochondrial membrane, where it maintains mitocho

293 he full-length enzyme is associated with the inner mitochondrial membrane, where ubiquinone (CoQ) ser

294 ovement of cholesterol from the outer to the inner mitochondrial membranes, where it is metabolized i

295 lear dynamin-related GTPase, targeted to the inner mitochondrial membrane, which plays a role in mito

296 s mediated by direct permeabilization of the inner mitochondrial membrane, which results in the rapid

297 ort of the Cox2 N-terminal domain across the inner mitochondrial membrane, while Cox18 is known to be

298 t a splicing variant of AtGLR3.5 targets the inner mitochondrial membrane, while the other variant lo

299 g, we identified a ryanodine receptor in the inner mitochondrial membrane with a molecular mass of ap

300 olated mitoplasts suggest insertion into the inner mitochondrial membrane with the C and N termini fa