ライフサイエンスコーパス: mitochondrion

1 logenetic origins (the nucleus, plastid, and mitochondrion).

2 ea and endosomes) and late stationary phase (mitochondrion).

3 endogenous expression of this peptide on the mitochondrion.

4 ion of redox marker genes of the cytosol and mitochondrion.

5 and limited repair mechanisms present in the mitochondrion.

6 in silico role of glycolytic enzymes in the mitochondrion.

7 s across the two membranes that surround the mitochondrion.

8 trated that the SLO3-GFP is localized to the mitochondrion.

9 ondrion of Plasmodium falciparum and a human mitochondrion.

10 oxygen species stress generated by a (proto) mitochondrion.

11 dox homeostasis are intimately linked in the mitochondrion.

12 s of E. coli to anticipate challenges to its mitochondrion.

13 th poorly defined function in the eukaryotic mitochondrion.

14 n T-tubules and ultimately surrounding every mitochondrion.

15 parate pathways, one of which resides in the mitochondrion.

16 ty, and recruits Parkin to the dysfunctional mitochondrion.

17 e lipoylated proteins reside in the parasite mitochondrion.

18 sion and degradation of the damaged daughter mitochondrion.

19 main (TMD) that localizes the protein to the mitochondrion.

20 inkage map spanning all 12 autosomes and the mitochondrion.

21 etic state or to the respective size of each mitochondrion.

22 g c-type cytochrome proteins in the parasite mitochondrion.

23 acid complexes at the inner membrane of the mitochondrion.

24 nsertion/deletion RNA editing process in its mitochondrion.

25 the main ADP/ATP carrier in the trypanosome mitochondrion.

26 F(1)-ATP synthase, for ATP production in the mitochondrion.

27 d in tRNA binding and translocation into the mitochondrion.

28 hat TbCAE is located both in the cytosol and mitochondrion.

29 zation of all but one of the subunits to the mitochondrion.

30 ctive DNA methyltransferases targeted to the mitochondrion.

31 rfamily that is localized exclusively to the mitochondrion.

32 ased oxidative and nitrosative damage to the mitochondrion.

33 three compartments: cytosol, chloroplast and mitochondrion.

34 at the dNTP pool asymmetry arises within the mitochondrion.

35 t on the trapping and extraction of a single mitochondrion.

36 ar circuit initiating and culminating in the mitochondrion.

37 ing ribosome have not been identified in the mitochondrion.

38 or NCX-9 in handling calcium exchange at the mitochondrion.

39 ensive model of Fe/S protein assembly in the mitochondrion.

40 ry increase in oxidative phosphorylation per mitochondrion.

41 PTPMT1 (PTP localized to the Mitochondrion 1) is a member of the protein tyrosine pho

42 ction of the genome revealed an average size mitochondrion (459,678 nt) with relatively little repeti

43 artners--the plastid (a cyanobacterium), the mitochondrion (a proteobacterium), and its host (an arch

44 , we have targeted cytosolic proteins to the mitochondrion, a poly(A) specific 3' exoribonuclease, mt

45 of mutant FUS led to Golgi fragmentation and mitochondrion aggregation.

46 Removal of Miro from the mitochondrion also detaches kinesin from its surface.

47 We investigate the role of the mitochondrion, an organelle highly sensitive to environm

48 The first mitochondrion-anchoring photosensitizer that specificall

49 Here we analyse the mitochondrion and apicoplast genomes of 711 Plasmodium f

50 s are distributed in the nucleus, cytoplasm, mitochondrion and apicoplast.

51 e Drp1, which assembles in a ring around the mitochondrion and appears to constrict both outer and in

52 Fancd2 localizes in the mitochondrion and associates with the nucleoid complex c

53 ionase, whereas its catabolism occurs in the mitochondrion and couples to the energy-yielding electro

54 proteins and transport of vitamin B12 to the mitochondrion and cytoplasm.

55 -1 cells resulted in its accumulation in the mitochondrion and downregulation of functional ATP6 prot

56 p1 mediates fission, and interaction between mitochondrion and endoplasmic reticulum (ER) enhances fi

57 Arabidopsis ETHE1 is localized in the mitochondrion and exhibits sulfur dioxygenase activity.

58 fied TbPSD as type I PS decarboxylase in the mitochondrion and found that it is processed proteolytic

59 has been shown to function primarily at the mitochondrion and is an important regulator of neuronal

60 is located in the intermembrane space of the mitochondrion and is imported via the Mia40 disulfide re

61 se 1, LipL1, has been shown to reside in the mitochondrion and it catalyses the lipoylation of the H-

62 The mitochondrion and its associated proteins are crucial re

63 veal that PtdEtn is produced in the parasite mitochondrion and parasitophorous vacuole by decarboxyla

64 lant species, that MSH1 functions within the mitochondrion and plastid to influence organellar genome

65 e need to transport intermediates out of the mitochondrion and reducing the loss of intermediates to

66 y model the squeezing of the largely tubular mitochondrion and show that proteins and conical lipids

67 namics and inextricably link the fate of the mitochondrion and that of the host eukaryote, as exempli

68 ndosymbionts that gradually evolved into the mitochondrion and the chloroplast.

69 one arm buried in the inner membrane of the mitochondrion and the orthogonal arm protruding about 10

70 hese intimate relationships have yielded the mitochondrion and the plastid (chloroplast) - the ancien

71 lls, mitoNEET receives its clusters from the mitochondrion and transfers them to acceptor proteins in

72 bacterial endosymbiont that gave rise to the mitochondrion and was the source of the mitochondrial ge

73 oteins are regulated by microRNAs inside the mitochondrion and whether subcellular spatial location o

74 subcellular distribution (cytosol, nucleus, mitochondrion, and chloroplast).

75 n cell compartments, favoring the cytoplasm, mitochondrion, and endoplasmic reticulum at the expense

76 OM64, and AtTPR7 reside in the chloroplast, mitochondrion, and endoplasmic reticulum of Arabidopsis

77 sites, including the endoplasmic reticulum, mitochondrion, and nucleus.

78 binding protein within the parasite cytosol, mitochondrion, and plant-like plastid.

79 NA species or editing in the single T. cruzi mitochondrion are linked to differentiation by a yet-unk

80 east and mammalian tumor cells implicate the mitochondrion as a target of artemisinins, and treatment

81 y Ca(2+), which were confirmed in the intact mitochondrion as well as cellular and in vivo systems.

82 presence of lower glycolysis pathways in the mitochondrion, as well as differences between P. tricorn

83 Ribonucleotide reduction within the mitochondrion, as well as outside the organelle, needs t

84 um ATP synthase is localized to the parasite mitochondrion, assembled as a large dimeric complex, and

85 ene encoding apoptosis-inducing factor (AIF) mitochondrion-associated 1.

86 ntial and may in concert with the identified mitochondrion-associated apoptosis inducing factor (AIFM

87 racil auxotrophy by genetically deleting the mitochondrion-associated DHODH of T. gondii (TgDHODH) fa

88 e interface between the mitochondria and the mitochondrion-associated endoplasmic reticulum (ER) memb

89 iral NS3/4A protease cleavage of MAVS on the mitochondrion-associated endoplasmic reticulum (ER) memb

90 ty of 3betaHSD2 and its association with the mitochondrion-associated ER membrane (MAM) and mitochond

91 -mitochondrion interface, referred to as the mitochondrion-associated ER membrane (MAM).

92 68 to 87 of ICP34.5 are required for binding mitochondrion-associated factors.

93 ting protein ICP34.5 interacts with numerous mitochondrion-associated factors.

94 ducing factor (AIF) and AMID (AIF-homologous mitochondrion-associated inducer of death) are flavoprot

95 In addition, MAP1S interacted with mitochondrion-associated leucine-rich PPR-motif containi

96 itochondrial destabilization, generating the mitochondrion-associated ligands that activate the NLRP3

97 ioesterase superfamily member 2 (Them2) is a mitochondrion-associated long-chain fatty acyl coenzyme

98 e physically linked to mitochondria known as mitochondrion-associated membranes (MAM), and to mitocho

99 Mutants in the gene encoding mitochondrion-associated protein LRPPRC were found to be

100 Here, we report that UBE3B is a mitochondrion-associated protein with homologous to the

101 ost cell the tachyzoite maintains its single mitochondrion at its periphery.

102 The nature of the host that acquired the mitochondrion at the eukaryote origin is an important mi

103 few characterized essential pathways of the mitochondrion at this T. brucei life stage.

104 In this study, we developed ER and mitochondrion-based in vitro tombusvirus replication ass

105 subsequent degradation of the dysfunctional mitochondrion before it causes activation of cell death.

106 a new model in which cristae within the same mitochondrion behave as independent bioenergetic units,

107 editing at the cob-908 site is necessary for mitochondrion biogenesis, cell division, and plant growt

108 vidence for Fancd2 as a crucial regulator of mitochondrion biosynthesis, and of a molecular link betw

109 e enzymes were localized to the cytoplasm or mitochondrion, but most were dually localized to both ce

110 The probe is targeted to the matrix of the mitochondrion by an alkyltriphenylphosphonium lipophilic

111 D) quantitative visualization of a mammalian mitochondrion by coherent x-ray diffractive imaging (CXD

112 ge between the endoplasmic reticulum and the mitochondrion, by increasing interaction with a macromol

113 Here, Sig-1Rs regulate ER-mitochondrion Ca(2+) signaling.

114 es are clear: the number of MCU channels per mitochondrion can be calculated, and MCU probability is

115 that different cristae within the individual mitochondrion can have disparate membrane potentials and

116 al for ongoing viability through the female, mitochondrion-carrying line of sexual reproduction in P.

117 s from our and other groups suggest that the mitochondrion-centred hypometabolism is a key feature of

118 in Toxoplasma and the consequences of these mitochondrion changes on parasite physiology.

119 In the pathogenic bloodstream stage, the mitochondrion consumes ATP to maintain an energized stat

120 owth conditions, Vps13 localizes to endosome-mitochondrion contacts and to the nuclear-vacuole juncti

121 er, rather than being degraded by lysosomes, mitochondrion-containing autophagosomes are released fro

122 sible evolutionary sequence giving rise to a mitochondrion-containing eukaryotic cell from an endosym

123 The Plasmodium falciparum mitochondrion contains two enzymes (PfLipL1 and PfLipL2)

124 In the hypoxic mitochondrion, cytochrome c oxidase, which is a major so

125 thesis pathway whose enzymes localize to the mitochondrion, cytosol, or apicoplast, a nonphotosynthet

126 ated the crucial role of plastid-cytosol and mitochondrion-cytosol malate transporters in recycling t

127 n situ spectroscopic real-time monitoring of mitochondrion/cytosol pH gradients.

128 lux distribution for lower glycolysis in the mitochondrion depended on which transporters for TCA cyc

129 Fra-1 deficiency ablated oxidant-induced mitochondrion-dependent apoptosis.

130 sis induced by cellular stressors activating mitochondrion-dependent apoptosis.

131 Whether c-FLIP regulates mitochondrion-dependent apoptotic signals remains unknow

132 However, the functions for mitochondrion-dependent cell death of DCs in immune regu

133 Dendritic cells (DCs) harbor an active mitochondrion-dependent cell death pathway regulated by

134 we observed that cell-cell contact induces a mitochondrion-dependent increase in intracellular calciu

135 al location signal sequence, which undergoes mitochondrion-dependent posttranslational cleavage.

136 ith DKD have significantly reduced levels of mitochondrion-derived metabolites in their urine.

137 one-carbon metabolism, resulting in reduced mitochondrion-derived one-carbon units needed for de nov

138 Increased production of mitochondrion-derived reactive oxygen species (ROS) is c

139 eta but not PDGFRalpha, reduced the level of mitochondrion-derived reactive oxygen species, which are

140 A four-enzyme pathway in the mitochondrion detoxifies H2S by converting it to thiosul

141 In endothelial cells, the mitochondrion-driven reduction in both the cytosolic and

142 mbly factors impinging the biogenesis of the mitochondrion-encoded catalytic core subunit 2 (COX2) re

143 iquely possesses heterologous, nucleus-, and mitochondrion-encoded cytochrome c maturase systems.

144 membrane protein, mediates the insertion of mitochondrion-encoded precursors into the inner mitochon

145 2,2G) base modification in both nucleus- and mitochondrion-encoded tRNAs.

146 , the ribosomal protein Var1, alias uS3m, is mitochondrion-encoded.

147 s in parallel with the endoplasmic reticulum-mitochondrion encounter structure (ERMES).

148 simultaneously with the hosting of the proto-mitochondrion endosymbiont.

149 They have a single large mitochondrion, essential for the parasite survival.

150 ree complementary genes from the nucleus and mitochondrion, establishing a link between genetic drift

151 g active replication in both the nucleus and mitochondrion, even in the absence of exogenous damage.

152 encoded by the maternally inherited parasite mitochondrion, even outcrossing with wild-type strains c

153 ted from healthy components in an individual mitochondrion, followed by mitochondrial fission and deg

154 nduced silencing complex constituents in the mitochondrion for functional mitomiR translational regul

155 r compartments and delivering sterols to the mitochondrion for steroid synthesis.

156 oenzyme shift that diverts pyruvate into the mitochondrion for the final steps of glucose oxidation.

157 The internal structures of a mitochondrion from a mouse embryonic fibroblast cell lin

158 ing axis is critical for effective phagosome-mitochondrion function and bactericidal activity.

159 irulence by protecting the parasites against mitochondrion-generated oxidative stress and by initiati

160 E. coli mutations that stress the C. elegans mitochondrion genetically interact with C. elegans mutat

161 infer that the host that engulfed the proto-mitochondrion had some eukaryote-like complexity, which

162 This strongly suggests that the mitochondrion harbors some Tpx and, another, as yet unid

163 The Ancoracysta mitochondrion has a gene-rich genome with a coding capac

164 , imports about a thousand proteins into the mitochondrion; however, the mitochondrial protein import

165 PCR and sequencing of the D-loop of the mitochondrion identified 32 different haplotypes among 1

166 uld represent a novel direction for numerous mitochondrion-implicated, age-related disorders.

167 Given the vital role of the mitochondrion in metabolic processes, studies of variati

168 The mitochondrion in parasitic protozoans is a clinically pr

169 hanges in the intrinsic functionality of the mitochondrion in skeletal muscle.

170 e energetic boost provided by the colonizing mitochondrion in the eukaryotic lineage.

171 allenges can be delivered to each individual mitochondrion in the nanofluidic system.

172 Cardiolipin, a phospholipid specific to the mitochondrion, interacts with the small electron transfe

173 ecifically at the endoplasmic reticulum (ER)-mitochondrion interface, referred to as the mitochondrio

174 Sig-1Rs mainly reside at the ER-mitochondrion interface.

175 e, we show that this necrosis pathway is not mitochondrion-intrinsic but results from an inter-organe

176 The mitochondrion is a complex organelle that serves essenti

177 ub of cellular metabolism and signaling, the mitochondrion is a crucial organelle whose dysfunction c

178 Finally, the mitochondrion is a platform for innate immunity, contrib

179 As such, the mitochondrion is a potential untapped target for new isc

180 We establish that the mitochondrion is an endogenous substrate of secreted pho

181 The mitochondrion is an organelle originating from an endosy

182 The mitochondrion is arguably the most complex organelle in

183 ed movement of phospholipids to and from the mitochondrion is essential for cellular integrity.

184 w, and the diffusion of O2 from capillary to mitochondrion is impaired.

185 Importantly, the mitochondrion is now a target for therapeutic interventi

186 PtdEtn in the mitochondrion is synthesized by a phosphatidylserine dec

187 In most eukaryotes, the mitochondrion is the main organelle for the formation of

188 r component analysis of variants showed that mitochondrion is the most important organelle for hypoxi

189 onditions, carbohydrate oxidation inside the mitochondrion is the primary energy source for cellular

190 cell and number of mitochondrial genomes per mitochondrion, is an indirect biomarker of mitochondrial

191 Given the oxidizing environment of the mitochondrion, it makes sense that Prx3 would favor disu

192 Fe trafficking away from the cytosol to the mitochondrion, leading to a cytosolic Fe deficiency.

193 mall population (whole device) to the single mitochondrion level (unique well).

194 neous redox signals in neurons at the single mitochondrion level where transients of glutathione oxid

195 oduction and energy metabolism at the single-mitochondrion level.

196 We conclude that Wolbachia may have a mitochondrion-like function in the soma, generating ATP

197 lles, known as hydrogenosomes, mitosomes, or mitochondrion-like organelles, are typically reduced, bo

198 protein (pUL37x1), which is the potent viral mitochondrion-localized inhibitor of apoptosis (vMIA), t

199 -1 was strongly enhanced by depletion of the mitochondrion-localized, GSH-dependent persulfide oxygen

200 n the absence of its apoptotically important mitochondrion-localizing domains.

201 s produced from phosphatidylserine (PS) by a mitochondrion-located PS decarboxylase, Psd1p.

202 The mitochondrion maintains and regulates its proteome with

203 artemisinin resistance and suggest that the mitochondrion may be an important target of inhibition o

204 uttles between the chloroplast, cytosol, and mitochondrion may play a significant role at low light l

205 Ailanthone-induced apoptosis was mitochondrion-mediated and involved the PI3K/AKT signali

206 ce (DeltaPsim) was altered and modulation of mitochondrion-mediated apoptosis regulating genes change

207 Neither receptor- nor mitochondrion-mediated apoptosis signaling was inhibited

208 AITC induced mitochondrion-mediated apoptosis, as shown by cytochrome

209 ed that VDAC1 oligomerization is involved in mitochondrion-mediated apoptosis.

210 -2 protein level, which ultimately triggered mitochondrion-mediated cellular apoptosis.

211 secretion effector of E. chaffeensis blocks mitochondrion-mediated host cell apoptosis.

212 allele, might also lead to the peroxisome-to-mitochondrion mistargeting of AGT, a suggestion that has

213 dox misbalance does not significantly affect mitochondrion morphology or the activity of respiratory

214 m the host cell to the extracellular matrix, mitochondrion morphology radically changes, resulting in

215 Of the human mitochondrion (mt)-encoded tRNAs with A36A37A38, only mt

216 r of Type III cells also exhibit an atypical mitochondrion near the presynaptic vesicle clusters at t

217 of CRMP5 expression at later stages enhanced mitochondrion numbers in cultured neurons, suggesting th

218 The apicoplast and the mitochondrion of Apicomplexa cooperate in providing esse

219 lasma membrane, as designed, and targets the mitochondrion of Leishmania parasites.

220 2 plasmids from bacteria, the apicoplast and mitochondrion of Plasmodium falciparum and a human mitoc

221 The mitochondrion of the parasitic protozoan Trypanosoma bru

222 The mitochondrion of the parasitic protozoan Trypanosoma bru

223 of the thiol redox homeostasis in the single mitochondrion of these parasites has remained largely un

224 FP2-hGrx1 or roGFP2 in either the cytosol or mitochondrion of Trypanosoma brucei.

225 r type I nitroreductase (NTR) located in the mitochondrion of trypanosomatids and, at the same time,

226 ve evolved a function highly specific to the mitochondrion of trypanosomes.

227 Depolarization of an individual mitochondrion or small clusters of mitochondria within c

228 Repeated diagram elements like 'mitochondrion' or 'receptor' are available as a library

229 solic cargo, that is, a protein aggregate, a mitochondrion, or a cytosolic bacterium.

230 les in the phloem, such as plastid, vacuole, mitochondrion, or endoplasmic reticulum, interact with s

231 ge in the fluorescent state of an individual mitochondrion, "oscillation" to refer to a localized cha

232 y identified regions of coupling between the mitochondrion outer membrane and the parasite pellicle,

233 vators of SIRT1 (resveratrol or SRT1720) and mitochondrion oxidation consumption rate and immunoblot

234 lular organelles including cytosol, plastid, mitochondrion, peroxisome and vacuole.

235 by regulating mitochondrial trafficking and mitochondrion-phagosome juxtaposition.

236 hanges in net pro-apoptotic signaling at the mitochondrion ("priming") induced by chemotherapeutic ag

237 These mitochondrion-related disorders in peripheral tissues ca

238 n is a negative transcriptional regulator of mitochondrion-related nuclear genes and genes encoding s

239 myclobutanil, the expression of five of six mitochondrion-related nuclear genes was down-regulated.

240 Predictions of the mitochondrion-related organelle (MRO) proteome reveal an

241 olutionary continuum that includes anaerobic mitochondrion-related organelles (MROs), such as hydroge

242 erobic alternatives to mitochondria known as mitochondrion-related organelles (MROs).

243 in a broad spectrum of reduced and modified mitochondrion-related organelles (MROs).

244 tis ISC system function within its anaerobic mitochondrion-related organelles and can functionally re

245 Proper functioning of the mitochondrion requires the orchestrated assembly of resp

246 cking of CFTR from intracellular vesicles in mitochondrion rich cells to the plasma membrane in the g

247 Mitochondria were stained using a mitochondrion-selective probe in mouse embryonic fibrobl

248 The apicomplexan mitochondrion shows striking differences from common mod

249 We compared axon-myelin-node-mitochondrion-smooth endoplasmic reticulum (SER) interac

250 Previously, we reported that the mitochondrion-specific antioxidant enzyme, manganese-con

251 Moreover, the mitochondrion-specific antioxidant MitoQuinone (MitoQ) r

252 In addition, mitochondrion-specific antioxidants, ubiquinol conjugate

253 s TWINKLE, SSBP1, and TFAM, all of which are mitochondrion-specific DNA effectors and are known to fu

254 antly, both enzymes also associated with the mitochondrion-specific DNA polymerase gamma.

255 glucose or retinas treated with a mixture of mitochondrion-specific fuels.

256 Our results support the hypothesis that the mitochondrion-specific lipid cardiolipin functions as a

257 s (i.e. the BCL2 homology 3 ligand cBID, the mitochondrion-specific lipid cardiolipin, and membrane g

258 ted with the formation of a complex with the mitochondrion-specific phospholipid cardiolipin (CL), le

259 d co-localization of PNKP and NEIL2 with the mitochondrion-specific protein cytochrome c oxidase subu

260 Using Polbeta fragments, mitochondrion-specific protein partners were identified,

261 ed that many Fancd2-interacting proteins are mitochondrion-specific.

262 toxins to mitochondria with tissue, cell, or mitochondrion specificity.

263 glutathione, and the regulation of ROS as a mitochondrion-STAT3-dependent pathway in Ras-transformed

264 e: a majority of axon fragments containing a mitochondrion survive axotomy, whereas those lacking mit

265 d Hep G2 cell lines expressing predominantly mitochondrion-targeted (Mt(++)) CYP2E1 and livers from a

266 emerged as the prototype of a novel class of mitochondrion-targeted agents that deplete cardiolipin a

267 s responsible for MICU1 phosphorylation, and mitochondrion-targeted Akt strongly regulates the mitoch

268 uro-2A cells stably expressing predominantly mitochondrion-targeted CYP2D6 were more sensitive to MPT

269 Recently, we showed that mitochondrion-targeted CYP2E1 augments alcohol-mediated

270 ohol-induced toxicity, which is augmented by mitochondrion-targeted CYP2E1.

271 Here, we demonstrate that mitochondrion-targeted human cytochrome P450 2D6 (CYP2D6

272 FOXO-mediated transcriptional activation of mitochondrion-targeted nuclear genes in concert with red

273 c approach, we characterized the role of the mitochondrion-targeted PPR78 protein in nad5 mature mRNA

274 t of innate immunity and supports the use of mitochondrion-targeted ROS scavengers as potential adjuv

275 Addition of the mitochondrion-targeted ROS-scavenging chemical MitoTEMPO

276 in the parasite, one of which resides in the mitochondrion (TgPEPCKmt), whereas the other protein is

277 Rozella harbors a mitochondrion that contains a very rapidly evolving geno

278 Apicomplexans harbor a mitochondrion that is essential for parasite survival an

279 nt mitochondrial depolarizations in a single mitochondrion that occur in a nonperiodic manner, simula

280 . tricornutum predicts that reactions in the mitochondrion that supply glycerate may support TAG synt

281 flow from the endoplasmic reticulum into the mitochondrion through ryanodine receptors, and the resul

282 thine impairs the ability of the cytosol and mitochondrion to cope with exogenous oxidative stresses,

283 ition to preventing transfer of DNA from the mitochondrion to the nucleus, VPS13 suppresses mitophagy

284 ipate in establishment of signaling cues for mitochondrion-to-nucleus communication.

285 skeletal muscle and liver cells, uptake per mitochondrion varies in magnitude but total uptake per c

286 othelial nitric-oxide synthase (eNOS) to the mitochondrion via a mechanism that requires protein nitr

287 ates from the cell in an autophagosome-bound mitochondrion-virus complex.

288 Thus, although the origin of the mitochondrion was a key event in evolutionary history, t

289 The average mass density of the mitochondrion was about 1.36 g/cm(3).

290 tofluorescence, the metabolic status of each mitochondrion was analyzed following addition of a respi

291 ce between an LD and its nearest neighboring mitochondrion was increased.

292 hese results indicate that the origin of the mitochondrion was not a prerequisite for genome-size exp

293 ipid droplets (LDs) in direct contact with a mitochondrion was reduced, and the average distance betw

294 e its yeast counterpart, is localized to the mitochondrion where it adopts an extremely protease-resi

295 ess involves translocation of viperin to the mitochondrion, where it binds the beta-subunit (HADHB) o

296 r eukaryotes Trypanosoma brucei has a single mitochondrion whose single-unit genome is physically con

297 on and increased translocation of Hk1 to the mitochondrion with corresponding heightened ATP synthase

298 D projection image was captured of a similar mitochondrion with the aid of strongly scattering Au ref

299 cess to "colorize" detailed EM images of the mitochondrion with the position of labeled proteins.

300 of differential centrifugation to enrich for mitochondrion within cell extracts prior to DNA extracti