ライフサイエンスコーパス: mitochondrion

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

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

3 th poorly defined function in the eukaryotic mitochondrion.

4 n T-tubules and ultimately surrounding every mitochondrion.

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

6 ty, and recruits Parkin to the dysfunctional mitochondrion.

7 e lipoylated proteins reside in the parasite mitochondrion.

8 sion and degradation of the damaged daughter mitochondrion.

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

10 inkage map spanning all 12 autosomes and the mitochondrion.

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

12 acid complexes at the inner membrane of the mitochondrion.

13 nsertion/deletion RNA editing process in its mitochondrion.

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

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

16 d in tRNA binding and translocation into the mitochondrion.

17 ry increase in oxidative phosphorylation per mitochondrion.

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

19 ctive DNA methyltransferases targeted to the mitochondrion.

20 rfamily that is localized exclusively to the mitochondrion.

21 ased oxidative and nitrosative damage to the mitochondrion.

22 at the dNTP pool asymmetry arises within the mitochondrion.

23 r genes whose products are imported into the mitochondrion.

24 lyadenylation facilitates translation in the mitochondrion.

25 ane potential, as a GrB substrate within the mitochondrion.

26 ignalling, TgMSH-1 localizes to the parasite mitochondrion.

27 al termination and ribosome recycling in the mitochondrion.

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

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

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

31 and limited repair mechanisms present in the mitochondrion.

32 in silico role of glycolytic enzymes in the mitochondrion.

33 s across the two membranes that surround the mitochondrion.

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

35 ondrion of Plasmodium falciparum and a human mitochondrion.

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

37 dox homeostasis are intimately linked in the mitochondrion.

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

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

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

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

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

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

44 orms a productive signaling complex with the mitochondrion-anchored MAVS protein, resulting in nuclea

45 The first mitochondrion-anchoring photosensitizer that specificall

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

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

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

49 taining import substrates are taken into the mitochondrion and are used as templates for damage drive

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

51 etabolite analysis to define the role of the mitochondrion and cellular heme in the chemical and mole

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

53 -1 cells resulted in its accumulation in the mitochondrion and downregulation of functional ATP6 prot

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

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

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

57 ryotes, the traditional relationship between mitochondrion and host has been subverted in E. cuniculi

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

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

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

61 In plants, where the mitochondrion and plastid must share a considerable port

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

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

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

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

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

67 first to demonstrate GrB activity within the mitochondrion and to identify Hax-1 cleavage as a novel

68 ation, translocates to the nucleus or to the mitochondrion and triggers two complementary antiviral r

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

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

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

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

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

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

75 rotein localization to the nucleus, cytosol, mitochondrion, and/or chloroplast.

76 es of orthologous proteins representing both mitochondrion- and plastid-encoded proteomes across stre

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

78 other organisms where isoforms occur in the mitochondrion as well.

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

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

81 cal flow was used in combination with single mitochondrion assay of mitochondrial thiol redox status

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

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

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

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

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

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

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

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

90 intracellular ATP content, and expression of mitochondrion-associated genes were decreased by overexp

91 ntracellular ATP content, and transcripts of mitochondrion-associated genes were prevented by blockad

92 NA and levels of transcripts and proteins of mitochondrion-associated genes, increased ectopic fat ac

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

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

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

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

97 m the endoplasmic reticulum (ER) through the mitochondrion-associated membrane compartment to the mit

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

99 fected cells, UL37 proteins traffic into the mitochondrion-associated membranes (MAM), the site of co

100 from the endoplasmic reticulum (ER) through mitochondrion-associated membranes (MAMs) to the outer m

101 acts between the two organelles, provided by mitochondrion-associated membranes (MAMs).

102 cal changes in mitochondria, myofibrils, and mitochondrion-associated membranes in skeletal and cardi

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

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

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

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

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

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

109 lidation of protein function predictions for mitochondrion biogenesis in Saccharomyces cerevisiae.

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

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

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

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

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

115 oid cells, ferrous iron is imported into the mitochondrion by mitoferrin-1 (Mfrn1).

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

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

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

119 Thus, our results indicate that the mitochondrion can use AMP and ROS at sublethal concentra

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

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

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

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

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

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

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

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

128 distributed between three compartments: the mitochondrion, cytosol, and apicoplast, a plastid acquir

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

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

131 Moreover, hypoxia failed to activate AMPK in mitochondrion-deficient rho(0)-A549 cells, suggesting th

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

133 ts as a positive feedback loop involving the mitochondrion-dependent activation of caspases, independ

134 Inhibition of the mitochondrion-dependent apoptosis signaling cascade is a

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

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

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

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

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

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

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

142 lin caused oxidative stress, and blockade of mitochondrion-derived oxidative stress by overexpression

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

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

145 eated T cells correlated with an increase in mitochondrion-derived superoxide.

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

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

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

149 itiates with synthesis and maturation of the mitochondrion-encoded Cox1 subunit prior to the addition

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

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

152 2,2G) base modification in both nucleus- and mitochondrion-encoded tRNAs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 The mitochondrion is a complex organelle that serves essenti

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

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

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

177 The mitochondrion is an organelle originating from an endosy

178 The mitochondrion is arguably the most complex organelle in

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

180 Although the mitochondrion is known for its bioenergetic function, th

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

182 PtdEtn in the mitochondrion is synthesized by a phosphatidylserine dec

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

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

185 in quality control of matrix proteins of the mitochondrion is well characterized and until recently t

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

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

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

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

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

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

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

193 n UL37 exon 1 (pUL37x1), also known as viral mitochondrion-localized inhibitor of apoptosis (vMIA), s

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

195 -1 was strongly enhanced by depletion of the mitochondrion-localized, GSH-dependent persulfide oxygen

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

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

198 The mitochondrion maintains and regulates its proteome with

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

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

201 previously showed that MVC infection induces mitochondrion-mediated apoptosis and G(2)/M-phase arrest

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

203 lts demonstrate that MVC infection induces a mitochondrion-mediated apoptosis that is dependent on th

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

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

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

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

208 consumption (V(O2)) was first assessed in a mitochondrion model, and then in the integrated cardiac

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

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

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

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

213 at the release of cytochrome c from a single mitochondrion occurs in a single step.

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

215 insertion/deletion RNA editing in the single mitochondrion of kinetoplastids, an ancient lineage of e

216 2 plasmids from bacteria, the apicoplast and mitochondrion of Plasmodium falciparum and a human mitoc

217 The mitochondrion of the parasitic protozoan Trypanosoma bru

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

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

220 which more than one genome type occurs in a mitochondrion or chloroplast.

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

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

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

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

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

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

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

228 by regulating mitochondrial trafficking and mitochondrion-phagosome juxtaposition.

229 lary electrophoresis separation after single-mitochondrion photolysis.

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

231 It has been shown that DNA repair in the mitochondrion proceeds through both short- and long-patc

232 tion and suggest a free radical-sensitive ER-mitochondrion-Rac1.GTP pathway in the regulation of dend

233 How the mitochondrion regulates phospholipid levels and maintain

234 These mitochondrion-related disorders in peripheral tissues ca

235 of mtDNA, ATP production, and expression of mitochondrion-related genes was largely prevented by inh

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

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

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

239 No examples of examined eukaryotes lacking a mitochondrion-related organelle exist, implying that the

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

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

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

243 strategy to label the acidic contents of the mitochondrion relies on the use of the membrane-permeabl

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

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

246 of kinesin and dynein motors according to a mitochondrion's programmed direction of transport.

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

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

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

250 In addition, mitochondrion-specific antioxidants, ubiquinol conjugate

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

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

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

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

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

256 fic anionic phospholipids, in particular the mitochondrion-specific phospholipid cardiolipin.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 ris(4-methoxyphenyl)phosphonium) is a better mitochondrion-targeting molecule than TPP and 3mTPP (tri

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

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

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

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

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

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

280 nction, thereby influencing the fate of each mitochondrion, to be either destined for a subsequent fu

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

282 The discovery of mitochondrion-type genes in organisms thought to lack mi

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

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

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

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

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

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

289 is well characterized and until recently the mitochondrion was considered a 'ubiquitination-free' org

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

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

292 that the endosymbiont that gave rise to the mitochondrion was present in the first eukaryote.

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

296 has evolved an energy metabolism involving a mitochondrion with an unusual genome.

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

298 th efficient trafficking of (18)F-FTO to the mitochondrion with subsequent metabolism to protein-boun

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

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