ライフサイエンスコーパス: cytochrome oxidase

1 mation of the Cu(A) center on the aa(3)-type cytochrome oxidase.

2 This tendency is substantially suppressed by cytochrome oxidase.

3 per metallation of the Cu(A) site in Cox2 of cytochrome oxidase.

4 electrostatically near CuA in subunit II of cytochrome oxidase.

5 ts I and II in the assembly of mitochondrial cytochrome oxidase.

6 c content, and the rate of oxidation through cytochrome oxidase.

7 t and a diminished rate of oxidation through cytochrome oxidase.

8 competing with O(2) for its binding site on cytochrome oxidase.

9 effect of mutations in the catalytic core of cytochrome oxidase.

10 inhibit the essential mitochondrial enzyme, cytochrome oxidase.

11 ear CuA binding region of N(2)O reductase or cytochrome oxidase.

12 talysts are comparable to those reported for cytochrome oxidase.

13 eased the activities of citrate synthase and cytochrome oxidase.

14 H dehydrogenase, alternative complex III and cytochrome oxidase.

15 of the high-resolution crystal structures of cytochrome oxidases.

16 group of all eukaryotic and some prokaryotic cytochrome oxidases.

17 ic properties of the ferryl intermediates in cytochrome oxidases.

18 gulated the cba genes, encoding one of three cytochrome oxidases.

19 ns revealed by analysis of the mitochondrial cytochrome oxidase 1 (CO1) gene.

20 dehydrogenase 1 (ND1) by 11-fold, P < 0.005; cytochrome oxidase 1 (COX1) by 4-fold, P < 0.001; and AT

21 ignificantly decreased immunoreactivities of cytochrome oxidase 1 and cytochrome b were found in HD p

22 o of the candidate glycoproteins identified (cytochrome oxidase 2 (COX2) and NADH:ubiquinone oxidored

23 ), photoreceptors (L-M opsin, rhodopsin, and cytochrome oxidase 2), and the outer limiting membrane (

24 chondrial electron transport chain activity (cytochrome oxidase 4.1/4.2 in complex IV).

25 been reported to modulate the expression of cytochrome oxidase, a marker for metabolic activity, in

26 on by covalent modification of mitochondrial cytochrome oxidase, a phenomenon of pathological relevan

27 l ATP production and/or citrate synthase and cytochrome oxidase activities in the cerebrum, hypothala

28 Hypoxia inhibited cytochrome oxidase activity (depolarised m) with a P50 o

29 mal adult animals by staining flatmounts for cytochrome oxidase activity after enucleation of one eye

30 Abeta levels, hydrogen peroxide production, cytochrome oxidase activity and carbonyl proteins in Tg2

31 al bioenergetics, characterized by decreased cytochrome oxidase activity and defective calcium handli

32 of reduced membrane potential due to loss of cytochrome oxidase activity because Cox2p C-tail export

33 Cytochrome oxidase activity correlated negatively with i

34 Mitochondrial citrate synthase and cytochrome oxidase activity decreased slightly with the

35 e on forced swim behavior and regional brain cytochrome oxidase activity in congenitally helpless rat

36 otein restores respiratory growth and normal cytochrome oxidase activity in cox17Delta cells.

37 eins failed to restore respiratory growth or cytochrome oxidase activity in sco1Delta cells.

38 ADH (P50 = 0.3 mm Hg), electron transport or cytochrome oxidase activity in sympathetic neurons.

39 -dose methylene blue increases mitochondrial cytochrome oxidase activity in the brain and improves me

40 ess of separation group, females had greater cytochrome oxidase activity in the habenula and ventral

41 tegmental area, and subiculum, but increased cytochrome oxidase activity in the lateral frontal corte

42 is revealed that maternal separation reduced cytochrome oxidase activity in the medial prefrontal cor

43 Early handling reduced cytochrome oxidase activity in the posterior parietal co

44 PBM did not alter cytochrome oxidase activity in the retina or in cultured

45 rease in hydrogen peroxide and a decrease in cytochrome oxidase activity were found in young Tg2576 m

46 The effects of hypoxia upon cytochrome oxidase activity were investigated using rote

47 e sex-dependent effects of early handling on cytochrome oxidase activity were limited to the medial p

48 Nissl staining, cytochrome oxidase activity, and neurofilament SMI32 imm

49 athway is not always directly linked to Cbb3 cytochrome oxidase activity, at least with respect to cb

50 s of the flattened cortex were processed for cytochrome oxidase activity, Nissl substance, or myelin.

51 to higher H(2) O(2) sensitivity and reduced cytochrome oxidase activity.

52 f photosynthetic proficiency and respiratory cytochrome oxidase activity.

53 pression coincide with a marked reduction in cytochrome oxidase activity.

54 ote cell survival in vitro by stimulation of cytochrome oxidase activity.

55 -xylose, hydrolysis of urea, and the lack of cytochrome oxidase activity.

56 tial increase (150-300%) in the steady-state cytochrome oxidase activity.

57 ssembled 104 complete body maps, revealed by cytochrome-oxidase activity in layer 4 of 8 rodent and 1

58 The rate of oxidation through cytochrome oxidase also was improved in rotenone-treated

59 nuclei and reduced mitochondrial density and cytochrome oxidase and citrate synthase activities relat

60 Photosynthetic organisms need copper for cytochrome oxidase and for plastocyanin in the fundament

61 he complexity surrounding copper delivery to cytochrome oxidase and highlight additional roles for so

62 assessed at postnatal (P days) 4 and 6 using cytochrome oxidase and Nissl staining.

63 Whole-brain cytochrome oxidase and superoxide dismutase activities w

64 seal and sea lion pups for Nissl substance, cytochrome oxidase, and vesicular glutamate transporters

65 Using stains for Nissl, cytochrome oxidase, and vesicular glutamate transporters

66 that intermediates of the catalytic cycle of cytochrome oxidase are dynamically modulated with metabo

67 rogenase, ubiquinone-cytochrome c reductase, cytochrome oxidase, as well as ATP synthase and UCP3.

68 In particular, P2 silencing caused defective cytochrome oxidase assembly and function.

69 of human SURF1, which when mutated causes a cytochrome oxidase assembly defect.

70 deliver it in a distinct state competent for cytochrome oxidase assembly.

71 unctional Cox4 proteins that fail to lead to cytochrome oxidase assembly.

72 regulating Cox1p synthesis by the status of cytochrome oxidase assembly.

73 is with insertion into the inner membrane or cytochrome oxidase assembly.

74 on of dioxygen to water by the fully reduced cytochrome oxidase at pH 6.2, 7.5, and 8.5 in the visibl

75 stituted with an active proton-translocating cytochrome oxidase, ATP synthesis readily occurred at th

76 s also prevented the emergence of the normal cytochrome oxidase barrel pattern in forepaw and hindpaw

77 PCu(A)C and YcnJ, where they play a role in cytochrome oxidase biogenesis and copper transport, resp

78 ells are located in color-activated regions (cytochrome oxidase blobs and bridges) of primary visual

79 Color domains were tightly colocalized with cytochrome oxidase blobs in V1 and with thin stripes in

80 ay in layer 4Cbeta, and the K pathway in the cytochrome oxidase blobs of layer 2/3.

81 eurons are located preferentially underneath cytochrome oxidase blobs, indicating that MT-projecting

82 ing in the gene encoding the Cox1 subunit of cytochrome oxidase but contain wild-type levels of the b

83 Cytochrome oxidase catalyzes the reduction of O2 to wate

84 the properties of one of the cell's terminal cytochrome oxidases, causing an increase in superoxide p

85 y intermediate, which weakly associates with cytochrome oxidase (CcO) in a respiratory supercomplex.

86 Cytochrome oxidase (CcOX), the terminal oxidase of the e

87 zing behavioral experience effects on neural cytochrome oxidase (CO) activity is well recognized, the

88 ransneuronal transporters and examination of cytochrome oxidase (CO) activity patterns after monocula

89 input nucleus HVc showed sharp increases in cytochrome oxidase (CO) activity relative to surrounding

90 osest evolutionary relative of humans, using cytochrome oxidase (CO) and acetylcholinesterase (AChE)

91 Alternate sections were processed for cytochrome oxidase (CO) and CTB-Au, or dipped for autora

92 Metabolic labeling with cytochrome oxidase (CO) and electrophysiological mapping

93 s of layer IV, and K cells send axons to the cytochrome oxidase (CO) blobs of layer III and to layer

94 elationships between orientation domains and cytochrome oxidase (CO) blobs or interblobs, CO blobs te

95 ominance columns, orientation pinwheels, and cytochrome oxidase (CO) blobs.

96 in the primary visual cortex was labeled by cytochrome oxidase (CO) histochemistry analysis or [(3)H

97 PO (TPOr, TPOi, and TPOc) were examined with cytochrome oxidase (CO) histochemistry and neurofilament

98 We used cytochrome oxidase (CO) histochemistry in conjunction wi

99 Here we used cytochrome oxidase (CO) histochemistry to demonstrate th

100 l serotonin transporter, in conjunction with cytochrome oxidase (CO) histochemistry, to investigate t

101 divisions of the IC were identified based on cytochrome oxidase (CO) histochemistry.

102 ch are evident in histological variations of cytochrome oxidase (CO) levels.

103 Cytochrome oxidase (CO) reveals two compartments in V1 (

104 ationship between orientation preference and cytochrome oxidase (CO) staining patterns.

105 mary (striate) visual cortex, the pattern of cytochrome oxidase (CO) staining was examined in four ma

106 , patterns of labeled cells, and patterns of cytochrome oxidase (CO) staining.

107 lumns (ODCs) of the primary visual cortex by cytochrome oxidase (CO) staining.

108 d 4B send segregated projections to distinct cytochrome oxidase (CO) stripes in area V2: neurons in C

109 Flat-mounts were processed for cytochrome oxidase (CO) to reveal metabolic activity in

110 re for lower jaw skin surface was developed, cytochrome oxidase (CO) was used to label flattened-cut

111 The caudal (C) nucleus, distinct in cytochrome oxidase (CO), acetylcholinesterase (AChE), an

112 NADPH-d), glutamic acid decarboxylase (GAD), cytochrome oxidase (CO), and calretinin (CR).

113 ion, Pc, stains moderately dark for AChE and cytochrome oxidase (CO), and very light for Cat-301.

114 y cortex in the rat and by layers IIIa/b and Cytochrome Oxidase (CO)-blobs boundaries in the human pr

115 It has been controversial whether the cytochrome oxidase (CO)-dense blobs in primate primary v

116 corticostriatal neurons with respect to the cytochrome oxidase (CO)-labeled barrels in SI.

117 terblob compartments, were revealed by using cytochrome oxidase (CO).

118 to flattened cortical sections processed for cytochrome oxidase (CO).

119 ue that was stained for Nissl or reacted for cytochrome oxidase (CO).

120 Two mitochondrial markers (cytochrome oxidase COI and 16S rDNA) were employed for s

121 distributed indiscriminately with respect to cytochrome oxidase compartment in layer 4B, revealing a

122 sed a transient and potent surge in isolated cytochrome oxidase (complex IV) activity, with rapid rec

123 The yeast bc1 complex (complex III) and cytochrome oxidase (complex IV) are mosaics of core subu

124 he mitochondrial gene COX1, for subunit 1 of cytochrome oxidase, contains multiple exons and introns.

125 on fragment length polymorphisms (RFLPs) and cytochrome oxidase (cox 1/2) sequence typing was perform

126 Previous studies of yeast cytochrome oxidase (COX) biogenesis identified Cox1p, on

127 Mitochondrial cytochrome oxidase (COX) catalyzes the last step in the

128 e used the nuclear-encoded components of the cytochrome oxidase (COX) complex of the trypanosome resp

129 e involvement of Oxa1 in the assembly of the cytochrome oxidase (COX) complex, where it facilitates t

130 igh's syndrome, a neuropathy associated with cytochrome oxidase (COX) deficiency.

131 rial protein required for full expression of cytochrome oxidase (COX) in Saccharomyces cerevisiae.

132 aled that SphK2 is complexed with NCDase and cytochrome oxidase (COX) subunit 1 in mitochondria and t

133 t organizational state of the cytochrome bc1-cytochrome oxidase (COX) supercomplex.

134 Yeast cytochrome oxidase (COX) was previously inferred to asse

135 x1p, one of the three core subunits of yeast cytochrome oxidase (COX), was previously shown to associ

136 mitochondrial genes, cytochrome b (cob) and cytochrome oxidase (cox1), for multiple populations of s

137 rther impaired tissue oxygenation (decreased cytochrome oxidase CuA redox state and increased deoxyhe

138 Cytochrome oxidase (CYO) and acetylcholinesterase (AChE)

139 induction of steady-state protein levels of cytochrome oxidase, cytochrome c, and adenine nucleotide

140 We studied the time course of changes of cytochrome oxidase (CytOx) blob spatial density and blob

141 formation processing and its relation to the cytochrome oxidase (CytOx) modules in visual area V2, we

142 We studied the tangential distribution of cytochrome oxidase (CytOx)-rich patches (blobs) in the s

143 ant has high expression of aox2, whereas the cytochrome oxidase-defective NCS6 mutant predominantly e

144 pling mechanism in humans might underlie the cytochrome oxidase deficiency that causes a form of Leig

145 argely but not completely focused within the cytochrome oxidase dense cell clusters.

146 here was also a close correspondence between cytochrome oxidase density and VGluT2-ir puncta distribu

147 ovudine-induced mitochondrial DNA depletion, cytochrome oxidase depletion, and mitochondrial prolifer

148 t a temperature-sensitive mutation affecting cytochrome oxidase, driving decreases in the abundance o

149 al findings from the present study examining cytochrome oxidase expression replicated previous findin

150 onto brain sections stained with myelin and cytochrome oxidase for architectonic analysis.

151 O increases the apparent K(m) of endothelial cytochrome oxidase for O(2), allowing the endothelium to

152 ons based on these patterns include separate cytochrome oxidases for aerobic growth and oxygen scaven

153 Brain sections processed for cytochrome oxidase from the same cases provided architec

154 enter located in subunit 2 of the ba(3)-type cytochrome oxidase from Thermus thermophilus.

155 D3 and a mitochondrial DNA fragment flanking cytochrome oxidase gene subunit II - the intergenic spac

156 Low Ka/Ks ratios of apocytochrome b and cytochrome oxidase genes support their utility as marker

157 Recent studies on cytochrome oxidase have indicated that the putative "per

158 gional metabolic activity using quantitative cytochrome oxidase histochemistry as in our previous stu

159 Cytochrome oxidase histochemistry reveals large-scale co

160 and non-helpless strains were compared using cytochrome oxidase histochemistry, an endogenous marker

161 ptide abundance, succinate dehydrogenase and cytochrome oxidase histochemistry, and electron microsco

162 rains of preweanling Holtzman rat pups using cytochrome oxidase histochemistry, which reflects long-t

163 ss rats were investigated using quantitative cytochrome oxidase histochemistry.

164 prachiasmatic nucleus (SCN) were assessed by cytochrome oxidase histochemistry.

165 n color tuning, orientation selectivity, and cytochrome oxidase histology.

166 ue relies on sequencing of the mitochondrial cytochrome oxidase I (COI) 'barcode' gene, which remains

167 ity trade data and mitochondrial DNA (mtDNA) cytochrome oxidase I (COI) and cytochrome b (Cyt b) gene

168 To date, two mitochondrial gene markers, Cytochrome Oxidase I (COI) and Cytochrome b oxidase (COB

169 aused by respiratory chain defects, notably, cytochrome oxidase I (COI) deficiency.

170 genetic analyses of a 920 bp fragment of the cytochrome oxidase I (COI) gene revealed a well-supporte

171 rs were designed, based on the mitochondrial cytochrome oxidase I (COI) gene.

172 obe which amplifies a 276 bp fragment of the cytochrome oxidase I (COI) mitochondrial DNA region.

173 Cytochrome oxidase I (COI) mitochondrial DNA sequences w

174 Sequence data from mitochondrial cytochrome oxidase I (COI) revealed that neither species

175 , the NADH dehydrogenase subunit 1 (ND1) and cytochrome oxidase I (COI)).

176 from the mitochondrial cytochrome b (cyt b), cytochrome oxidase I (COI), and 12s rRNA gene.

177 ally validated barcoding gene, mitochondrial cytochrome oxidase I (COI).

178 exhibited 98-100% partial mitochondrial DNA Cytochrome Oxidase I (mtCOI) gene identity with the B. t

179 es of four genetic loci (16S rDNA, 28S rDNA, Cytochrome oxidase I and Cytochrome b).

180 cid changes found in ATP6, cytochrome b, and cytochrome oxidase I appeared to be functionally signifi

181 diversity, and large-scale mitochondrial DNA cytochrome oxidase I barcoding has exposed many potentia

182 pacer, mitochondrial large-subunit rDNA, and cytochrome oxidase I DNA) from all 11 recognized taxa.

183 We sequenced a portion of the cytochrome oxidase I gene for 432 gnathiids, collected f

184 etic markers: a portion of the mitochondrial cytochrome oxidase I gene, nine polymorphic nuclear micr

185 on a single locus, the barcode region in the cytochrome oxidase I mitochondrial gene, and analyzed re

186 urve or constraint by gene flow, we analyzed cytochrome oxidase I mtDNA sequences, which revealed fou

187 icularly variable in the temperate zone, and cytochrome oxidase I was notably more variable in the tr

188 ture of P. coloradensis using mitochondrial (cytochrome oxidase I) and nuclear (elongation factor 1 a

189 bomoylphosphate synthase) and mitochondrial (cytochrome oxidase I) genes representing 216 individuals

190 morphological identifications, DNA barcodes (cytochrome oxidase I) revealed significant cryptic speci

191 fic primers were designed from cytochrome b, cytochrome oxidase I, and 16S rRNA genes to generate PCR

192 oci include mitochondrial barcode sequences- Cytochrome oxidase I, NADH2, 16S rRNA and 12S rRNA- and

193 ll subunit rDNA (nSSU-rDNA) or mitochondrial cytochrome oxidase I].

194 has an RNase III motif, specifically cleave cytochrome oxidase II (COII) pre-mRNA insertion editing

195 TFB2M mRNA and mitochondrial transcripts for cytochrome oxidase II (COXII) and cytochrome b.

196 Here, we analyse the cytochrome oxidase II mitochondrial gene of 250 Sabethes

197 e identify COII(G177S), a mtDNA hypomorph of cytochrome oxidase II, which specifically impairs male f

198 with this mitochondrial regulation, NOS and cytochrome oxidase immunoreactivity demonstrated mitocho

199 hat the membrane biogenesis of subunit II of cytochrome oxidase in bacteria and mitochondria have con

200 The abundant concentration of cytochrome oxidase in patches or blobs of primate striat

201 ylcarnitine (AcCN) increases the activity of cytochrome oxidase in the aged heart.

202 acrophages inhibits heme-containing terminal cytochrome oxidases, inactivates iron/sulfur proteins, a

203 tation with exogenous cytochrome c overcomes cytochrome oxidase inhibition and improves cardiac funct

204 We hypothesized that cytochrome oxidase inhibition coupled with reduced subst

205 rvational study aimed to overcome myocardial cytochrome oxidase inhibition with excess cytochrome c a

206 Consistent with cytochrome oxidase involvement, the glycolytic effect wa

207 tions processed for Nissl substance, myelin, cytochrome oxidase, ionic zinc, neurofilaments, and vesi

208 Overall, these findings indicate that cytochrome oxidase is a metabolic target of caffeine and

209 In the septic heart, cytochrome oxidase is competitively inhibited.

210 oint for protons going into the K-channel of cytochrome oxidase is the surface-exposed glutamic acid

211 Maturation of cytochrome oxidases is a complex process requiring assem

212 -encoded subunit of the mitochondrial enzyme cytochrome oxidase, is up-regulated in the striatum of m

213 nic mice resulted in enhanced Pgc-1alpha and cytochrome oxidase IV protein expression in fast-twitch

214 creased threonine phosphorylation of COX IV (cytochrome oxidase IV), increased mitochondrial membrane

215 ine), restored heme c content, and increased cytochrome oxidase kinetic activity.

216 lutamate transporter-2, which suggested that cytochrome-oxidase maps closely mirror thalamic innervat

217 which is synthesized in mss51 mutants and in cytochrome oxidase mutants in which Cox1p translation is

218 ture; and 3) the overexpression of Cox15p in cytochrome oxidase mutants that accumulate heme O leads

219 by binding the metal centres of enzymes and cytochrome oxidase, necessitating a release mechanism fo

220 s, and three galagos that were processed for cytochrome oxidase, Nissl bodies, or the vesicular gluta

221 rkably changed in histological appearance in cytochrome oxidase, Nissl, and Wisteria floribunda agglu

222 the gracile nuclei in sections processed for cytochrome oxidase or stained for cell bodies (Nissl sta

223 sections processed for cell bodies (Nissl), cytochrome oxidase, or myelin.

224 ) xenobiotic metabolism, bioenergetics (e.g. cytochrome oxidase), osmotic balance (e.g. Na(+)/K(+) AT

225 during the reduction of dioxygen to water by cytochrome oxidase (P(R)) is a pH-dependent mixture of c

226 are just two main streams, originating from cytochrome oxidase patches and interpatches, that projec

227 One hypothesis is that the projection from cytochrome oxidase patches to thin stripes is responsibl

228 ns from both the inner and outer surfaces of cytochrome oxidase, perhaps accounting for the long-obse

229 Here we show that cytochrome oxidase pretreated with a low concentration o

230 siological maps of body representations with cytochrome oxidase-reacted cortical sections we were abl

231 cally, we examined the myeloarchitecture and cytochrome oxidase reactivity for several well-identifie

232 rate constant of 20,000 s-1 with the bovine cytochrome oxidase, regardless of whether the enzyme had

233 opper donors to the Cu(B) and Cu(A) sites of cytochrome oxidase, respectively, whereas Cox17 is belie

234 mitochondrial respiratory chain, Complex IV (cytochrome oxidase) retains all partially reduced interm

235 educed Thermus thermophilus ba(3) (Tt ba(3)) cytochrome oxidase revealed that O(2) binding was slowed

236 ds are principally found in layer 4C and the cytochrome oxidase-rich blobs in layer 2/3.

237 nactivation of ccoN, part of the cbb(3)-type cytochrome oxidase shown to regulate the kinase activity

238 Thus, in the absence of subunit III cytochrome oxidase shows greater flexibility in terms of

239 biotically essential, Cu(A)-free cbb(3)-type cytochrome oxidase specifically in endosymbiotic bactero

240 s traversed through a complete complement of cytochrome-oxidase stained clusters (called barrelettes)

241 Analysis of cytochrome-oxidase-stained somatosensory whisker-associa

242 induces a learning-specific expansion of the cytochrome oxidase staining expression for conditioned b

243 inals, TUNEL-labeled photoreceptors, loss of cytochrome oxidase staining in photoreceptors, neurite o

244 Cytochrome oxidase staining in V2 reveals a repeating pa

245 s a normal structural appearance viewed with cytochrome oxidase staining.

246 e compared with underlying neuroanatomy with cytochrome oxidase staining.

247 histological techniques including myelin and cytochrome oxidase staining.

248 omical organization, initially defined using cytochrome-oxidase staining of post-mortem tissue.

249 al penis and clitoris input maps revealed by cytochrome-oxidase-staining of cortical layer 4.

250 In macaque visual cortex, different cytochrome oxidase stripes of area V2 receive segregated

251 logical, and tracing studies suggest that V2 cytochrome oxidase stripes participate in functionally d

252 omatic modulation, which are located in thin cytochrome oxidase stripes.

253 led the existence of a group I intron in the cytochrome oxidase subunit 1 (cox1) gene in 13 of 41 gen

254 nnoprotein [MP1], and a gene fragment of the cytochrome oxidase subunit 1 gene [COX1] of the P. marne

255 r two mitochondrial DNA-encoded genes, cox1 (cytochrome oxidase subunit 1) and cob (apocytochrome b).

256 sion of the mitochondrially encoded proteins Cytochrome oxidase subunit 1, Apocytochrome b, and ATP s

257 sted that the NCS6 mitochondrial mutation, a cytochrome oxidase subunit 2 (cox2) deletion, is associa

258 transcription factor A of the mitochondria, cytochrome oxidase subunit 4 isoform 1, cAMP-response el

259 o the cytochrome c promoter and NRF-2 to the cytochrome oxidase subunit 4 promoter increased in respo

260 We detected the mitochondrial DNA cytochrome oxidase subunit I (COI) barcodes for Triboliu

261 Focusing on the cytochrome oxidase subunit I (COI) gene, we found that 1

262 and mismatch distribution with mitochondrial cytochrome oxidase subunit I (COI) sequences.

263 barcoding region of the mitochondrial gene, cytochrome oxidase subunit I (COI), is highly variable a

264 nd the use of CCG as an initiation codon for cytochrome oxidase subunit I (COI); these represent the

265 the studied species using the mitochondrial cytochrome oxidase subunit I gene (COXI) as molecular ma

266 al transcribed spacer of rRNA, mitochondrial cytochrome oxidase subunit I genes and the cytochrome ox

267 e stability and translation of mitochondrial cytochrome oxidase subunit I mRNA.

268 De novo synthesis of the apocytochrome b and cytochrome oxidase subunit I proteins was no longer dete

269 , lower VDAC and the mitochondrially encoded cytochrome oxidase subunit I relative to actin; in corte

270 Mitochondrial (mt) sequences from cytochrome oxidase subunit I to the subunit II gene (COI

271 An exception from this process is the cytochrome oxidase subunit II (COII) mRNA, which encodes

272 logenies of SFV polymerase and mitochondrial cytochrome oxidase subunit II from African and Asian mon

273 poly(A,U,G) or an in vitro transcript of the cytochrome oxidase subunit II gene as mRNA.

274 l cytochrome oxidase subunit I genes and the cytochrome oxidase subunit II-16S rRNA intergeneric frag

275 ocyclic form of T. brucei and functions as a cytochrome oxidase subunit II-specific k-RNA-editing acc

276 uding those encoding the bovine orthologs of cytochrome oxidase subunit III, IL-1 receptor type I, an

277 etion of cardiolipin synthase, the levels of cytochrome oxidase subunit IV and cytochrome c1, reflect

278 . brucei impairs the mitochondrial import of cytochrome oxidase subunit IV, an N-terminal signal-cont

279 he anti-TbTim17 antibody inhibited import of cytochrome oxidase subunit IV, indicating a direct invol

280 mutation, tenured (tend), in a gene encoding cytochrome oxidase subunit Va.

281 s were defective in C-to-U editing events in cytochrome oxidase subunit2 and NADH dehydrogenase subun

282 Pases that are expressed in association with cytochrome oxidase subunits.

283 a and heme c levels and reduced activity of cytochrome oxidase, suggesting a defect between protopor

284 dues each induced stabilization of the bc(1):cytochrome oxidase supercomplex in a Bcs1-dependent mann

285 enotype, including defects in the aa(3)-type cytochrome oxidase, symbiotic nitrogen fixation, and ano

286 ntibodies to rod opsin, S and M cone opsins, cytochrome oxidase, synaptophysin, glial fibrillary acid

287 in the electron transport chain proximal to cytochrome oxidase that contribute to the ischemic damag

288 is a clear involvement with the assembly of cytochrome oxidases that contain the Cu(A) center in sub

289 chnique was used to form the pulsed state of cytochrome oxidase (the "OH" state) from several sources

290 abnormalities in the function of complex IV (cytochrome oxidase), the final electron acceptor in this

291 The first step in the catalytic cycle of cytochrome oxidase, the one-electron reduction of the fu

292 Maternal separation reduced prefrontal cytochrome oxidase to a greater degree in female pups th

293 ectron transfer by targeting haem-containing cytochrome oxidases under microaerobic conditions to mai

294 Cytochrome oxidase uses electrons donated by its substra

295 n of cellular respiration by knockout of the cytochrome oxidases was sufficient to attenuate bacteric

296 In sections processed for cytochrome oxidase, we found star-like segmentation cons

297 myelin, acetylcholinesterase, calbindin, or cytochrome oxidase, we identified three PI chemoarchitec

298 lattened sections of neocortex processed for cytochrome oxidase were used to determine the topography

299 I contained genes, such as that for the aa3 cytochrome oxidase, whose expression levels increased af

300 y the Cu(A) and intramembrane Cu(B) sites of cytochrome oxidase, within the trans-Golgi network to su