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

1 cts with the phospholipid cardiolipin in the inner mitochondrial membrane.

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

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

4 en species by modulating the fluidity of the inner mitochondrial membrane.

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

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

7 )-regulatory mechanisms on both sides of the inner mitochondrial membrane.

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

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

10 lacking cleavable transit sequences into the inner mitochondrial membrane.

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

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

13 duction necessitate ion transport across the inner mitochondrial membrane.

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

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

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

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

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

19 at transport specific metabolites across the inner mitochondrial membrane.

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

21 icantly increased cholesterol content in the inner mitochondrial membrane.

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

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

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

25 cost associated with protein crowding in the inner mitochondrial membrane.

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

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

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

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

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

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

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

33 and induced further hyperpolarization of the inner mitochondrial membrane.

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

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

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

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

38 Tim44p can tightly associate with the inner mitochondrial membrane.

39 suing reduction of O(2) by complex IV in the inner mitochondrial membrane.

40 matrix by transporting substrates across the inner mitochondrial membrane.

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

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

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

44 mitochondria and binds to cardiolipin in the inner mitochondrial membrane.

45 and concomitantly pumping protons across the inner mitochondrial membrane.

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

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

48 ollowing translocation of cholesterol to the inner mitochondrial membrane.

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

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

51 mtCLIC associates with the inner mitochondrial membrane.

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

53 isomerase that regulates mPTP opening in the inner mitochondrial membrane.

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

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

56 and release of a proton gradient across the inner mitochondrial membrane.

57 er (AAC) is a major transport protein of the inner mitochondrial membrane.

58 ions and is consistently associated with the inner mitochondrial membrane.

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

60 energize precursor translocation across the inner mitochondrial membrane.

61 steps energize precursor passage across the inner mitochondrial membrane.

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

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

64 cluding critical factors associated with the inner mitochondrial membrane.

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

66 ciate with respiratory supercomplexes of the inner mitochondrial membrane.

67 n electrochemical proton gradient across the inner mitochondrial membrane.

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

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

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

71 rotein that we found was associated with the inner mitochondrial membrane.

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

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

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

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

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

77 ring of the elongating mitoribosome onto the inner-mitochondrial membrane.

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

79 ospholipid trafficking between the outer and inner mitochondrial membranes.

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

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

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

83 1alpha subcomplexes 2 and 3, translocase of inner mitochondrial membrane 50, and valyl-tRNA syntheta

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

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

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

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

88 The inner mitochondrial membrane also contains a large numbe

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

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

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

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

93 significantly prevents maspin binding to the inner mitochondrial membrane and decreases cytochrome c

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

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

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

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

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

99 ous channelrhodopsin-2 fusion protein to the inner mitochondrial membrane and formation of functional

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

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

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

106 rdiolipin (CL), binds to transporters of the inner mitochondrial membrane and plays a central role in

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

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

109 t is dependent on the proton gradient of the inner mitochondrial membrane, and it inhibits the activi

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

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

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

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

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

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

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

117 ds cardiolipin on the concave surface of the inner mitochondrial membrane, before oxidizing the lipid

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

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

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

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

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

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

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

125 rgy to drive proton translocation across the inner mitochondrial membrane by an unresolved mechanism.

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

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

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

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

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

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

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

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

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

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

136 contact sites was modulated by the outer and inner mitochondrial membrane channels, voltage-dependent

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

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

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

140 Inner mitochondrial membrane damage appears to relate to

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

142 Inner mitochondrial membrane density was determined by s

143 Extraocular muscle inner mitochondrial membrane density was similar to that

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

145 Cardiolipin is a phospholipid of the inner mitochondrial membrane essential for the function

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

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

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

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

150 Na(+) interacts with phospholipids, reducing inner mitochondrial membrane fluidity and the mobility o

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

152 Here we record AAC currents directly from inner mitochondrial membranes from various mouse tissues

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

154 In this study we report that MxB is an inner mitochondrial membrane GTPase that plays an import

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

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

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

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

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

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

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

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

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

164 The inner mitochondrial membrane (IMM), consisting of crista

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

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

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

168 mal membrane potential (DeltaPsi) across the inner mitochondrial membrane (IMM).

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

170 Put6 and Put7 are tethered to the inner mitochondrial membrane in a large hetero-oligomeri

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

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

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

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

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

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

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

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

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

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

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

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

183 multi-protein complex whose assembly in the inner mitochondrial membrane is facilitated by the scaff

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

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

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

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

188 ty transition pore, a nonspecific channel in inner mitochondrial membranes, is triggered by an elevat

189 activate a large conductance channel in the inner mitochondrial membrane known as the PTP (permeabil

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

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

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

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

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

195 nd extrusion by cation exchangers across the inner mitochondrial membrane may define the threshold; h

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

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

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

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

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

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

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

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

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

207 The inner mitochondrial membrane plays a crucial role in cel

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

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

210 ng of mitochondria relies on maintaining the inner mitochondrial membrane potential (also known as De

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 Mitochondrial assessment indicated reduced inner mitochondrial membrane potential (DeltaPsim) and m

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

225 The inner mitochondrial membrane protein 3beta-hydroxysteroi

226 itochondrial Ca(2+) uptake is mediated by an inner mitochondrial membrane protein called the mitochon

227 Succinate dehydrogenase (SDH) is an inner mitochondrial membrane protein complex that links

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 RP linked to Fragile-X syndrome elevates the inner mitochondrial membrane proton leak, leading to inc

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

245 ~700-kD multisubunit channel residing in the inner mitochondrial membrane required for mitochondrial

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

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

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

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

250 The ETC is organized into inner mitochondrial membrane supercomplexes that promote

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

252 independently of one another to sites on the inner mitochondrial membrane that are in proximity to co

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

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

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

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

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

258 and tightly controlled Ca(2+) channel of the inner mitochondrial membrane that regulates cellular met

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

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

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

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

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

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

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

266 ific activation of signaling pathways in the inner mitochondrial membrane, thereby modulating its fun

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

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

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

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

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

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

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

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

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

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

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

278 In particular, we identify a network of inner mitochondrial membrane transporters as a hub requi

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

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

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

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

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

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

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

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

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

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

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