ライフサイエンスコーパス: cytochrome c oxidase

1 is also utilized in other enzymes, including cytochrome c oxidase.

2 (2+) centres of soluble guanylate cyclase or cytochrome c oxidase.

3 m by association of the bc1 complex with the cytochrome c oxidase.

4 e a biosynthesis and/or transfer to maturing cytochrome c oxidase.

5 ation by potently inhibiting the heme-copper cytochrome c oxidase.

6 tner of Cox17 in transferring copper ions to cytochrome c oxidase.

7 by the binuclear heme a3/CuB active site of cytochrome c oxidase.

8 talation of the Cu(B) center of subunit 1 of cytochrome c oxidase.

9 a toxin at high concentrations and inhibits cytochrome c oxidase.

10 ansfer in the IMS and thus for biogenesis of cytochrome c oxidase.

11 p372 as the location of this site in the ba3 cytochrome c oxidase.

12 preformed stores and reduced deactivation by cytochrome c oxidase.

13 on, if any, of reduced deactivation of NO by cytochrome c oxidase.

14 A recent example is provided by studies of cytochrome c oxidase.

15 itochondrial matrix for eventual assembly of cytochrome c oxidase.

16 plays an important role in the formation of cytochrome c oxidase.

17 within different MRC components upstream of cytochrome c oxidase.

18 tory activity caused by diminished levels of cytochrome c oxidase.

19 ancer because of its action on mitochondrial cytochrome c oxidase.

20 rget, COX2 mRNA, which encodes subunit II of cytochrome c oxidase.

21 enosine triphosphate (ATP) and a decrease in cytochrome c oxidase.

22 a more specific defect of respiratory chain cytochrome-c oxidase.

23 tion into California using the mitochondrial cytochrome c oxidase 1 (CO1) gene.

24 enase, pyruvate kinase, creatine kinase, and cytochrome c oxidase activities, and increased myoglobin

25 othesised a mechanistic relationship between cytochrome c oxidase activity and Cox7a1 protein levels

26 ction by measuring H2O2, lipid peroxidation, cytochrome c oxidase activity and mitochondrial ATP.

27 Loss of Blp decreases cytochrome c oxidase activity and uncouples oxidative ph

28 Cytochrome c oxidase activity assays verified this findi

29 tein, have approximately 50-70% reduction in cytochrome c oxidase activity in all tissues yet a parad

30 Methylene blue increased cytochrome c oxidase activity in the presence of hydroge

31 s occur in mild hypoxia, where mitochondrial cytochrome c oxidase activity is unimpaired, suggesting

32 synthase activity was lower (P < 0.0001) and cytochrome c oxidase activity per Mt unit was higher (P

33 Cytochrome c oxidase activity was measured using a cytoc

34 Cytochrome c oxidase activity was significantly reduced

35 lls, for example, mitochondrial respiration, cytochrome c oxidase activity, and ATP production.

36 l density, mDNA/nDNA ratio), and functional (cytochrome c oxidase activity, ATP synthesis rate) marke

37 Total cytochrome c content, cytochrome c oxidase activity, citrate synthase activity

38 ned AMP-dependent kinase activation improved cytochrome c oxidase activity, rescued the motor phenoty

39 ator of mitochondrial bioenergetics enhanced cytochrome c oxidase activity, reversed oxidative stress

40 Cytochrome c oxidase activity, uncoupling protein 1 expr

41 he respiratory chain by up-regulation of the cytochrome c oxidase activity.

42 and I, respectively, and consequently lacked cytochrome c oxidase activity.

43 ostasis protein influential in mitochondrial cytochrome c oxidase activity.

44 associated with a selective 65% reduction of cytochrome c oxidase activity.

45 itochondrial respiratory chain complex IV or cytochrome c oxidase activity.

46 biopsies, cocoa improved mitochondrial COX (cytochrome c oxidase) activity (P=0.013), increased capi

47 ansport chain complexes) markers and COX IV (cytochrome C oxidase) activity in myocardium from patien

48 enzyme, is well expressed in neurons rich in cytochrome c oxidase, an important enzyme of the energy-

49 We measured the oxidation state of cytochrome c oxidase, an intracellular measure of metabo

50 o terminal respiratory oxidases, an aa3-type cytochrome c oxidase and a cytochrome bd-type menaquinol

51 tected the activity of mitochondrial enzymes cytochrome c oxidase and aconitase in differentiating NS

52 tected the activity of mitochondrial enzymes cytochrome c oxidase and aconitase.

53 ytochrome c in the mammalian brain regulates cytochrome c oxidase and caspase-3 activity.

54 e bc1 complex in the absence of a functional cytochrome c oxidase and identify a supercomplex indepen

55 nd exhibited comparatively lower activity of cytochrome c oxidase and increased glucose uptake.

56 degradation of hypohemylated Cox1 subunit of cytochrome c oxidase and is active in cytochrome c oxida

57 pression of ATP synthase's catalytic domain, cytochrome c oxidase and its tyrosine phosphorylation, m

58 Methylene blue's ability to increase cytochrome c oxidase and protect RGCs against these noxi

59 y of the copper-binding mitochondrial enzyme cytochrome c oxidase and reduced ATP levels, despite enh

60 al fragment of Rcf2 associate with monomeric cytochrome c oxidase and respiratory chain supercomplexe

61 tochondrial fragmentation and a reduction of cytochrome c oxidase and succinate dehydrogenase activit

62 Activities of cytochrome c oxidase and succinate reductase were increa

63 are structurally unrelated to mitochondrial cytochrome c oxidases and are therefore a prime target f

64 pressions of mediators of energy metabolism (cytochrome c oxidase) and mediators of neuronal activity

65 Cox17, a protein involved in the assembly of cytochrome c oxidase, and the MICOS complex.

66 respiratory electron chain dependent on the cytochrome c oxidase, and this uncoupling induces the al

67 ease of the transcript abundance/activity of cytochrome-c-oxidase, and slower phycocyanin degradation

68 ated MT-CO2, the mtDNA-encoded subunit II of cytochrome c oxidase; and (3) reduced spare respiratory

69 llary-to-fiber ratio ( approximately 78.8%), cytochrome-c oxidase ( approximately 35%), and activity

70 biochemical deconvolution cascade suggested cytochrome c oxidase as the potential target of IPE clas

71 rome c oxidase activity was measured using a cytochrome c oxidase assay kit to monitor the health of

72 The mitochondrial cytochrome c oxidase assembles in the inner membrane fro

73 The requirement for Cox20 in cytochrome c oxidase assembly and respiratory growth is

74 Our analyses show that Oms1 participates in cytochrome c oxidase assembly by stabilizing newly synth

75 present in the promoter of the mitochondrial cytochrome c oxidase assembly gene (SCO2), which is crit

76 dicate that KLF6-dependent regulation of the cytochrome c oxidase assembly gene is critical for maint

77 Here we isolate a cytochrome c oxidase assembly intermediate in preparator

78 ets, iron-sulfur cluster scaffold (ISCU) and cytochrome c oxidase assembly protein (COX10), decreased

79 iron-sulfur assembly proteins)1/2 and COX10 (cytochrome c oxidase assembly protein-10), indicating en

80 he matrix side into the inner membrane while Cytochrome c oxidase assembly protein18 (Cox18/Oxa2) is

81 Cytochrome c oxidase assembly requires the synthesis of

82 chain 3 (LC3) associated with mitochondrial (cytochrome c oxidase), autophagosome (p62), and autolyso

83 The reaction of oxidized bovine cytochrome c oxidase (bCcO) with hydrogen peroxide (H(2)

84 the COX1 mRNA is coupled to the assembly of cytochrome c oxidase by a mechanism that involves Mss51.

85 tion (oxygenated hemoglobin) and metabolism (cytochrome c oxidase) by 15% +/- 6.7% and 49% +/- 18%, r

86 Here, we identify the proposed cbb (3)-type cytochrome c oxidase (cbb (3)-Cox) assembly factor CcoG

87 latus, Cu-detoxification and Cu delivery for cytochrome c oxidase (cbb(3) -Cox) assembly depend on tw

88 pper importer CcoA, required for cbb(3)-type cytochrome c oxidase (cbb(3)-Cox) biogenesis, revealed a

89 y, we analyzed Cu delivery to the cbb3 -type cytochrome c oxidase (cbb3 -Cox) of Rhodobacter capsulat

90 Clones deficient in cytochrome c oxidase (CCO(-)) were identified by histoch

91 res in the reduction of dioxygen to water by cytochrome c oxidase (CcO) are particularly important to

92 Cytochrome c oxidase (CcO) catalyzes the reduction of di

93 Cytochrome c oxidase (CcO) catalyzes the reduction of ox

94 functional mimic of the mitochondrial enzyme cytochrome c oxidase (CcO) has been a long-term goal of

95 13-subunit integral membrane protein bovine cytochrome c oxidase (CcO) have been studied by differen

96 on of the electron transport chain component cytochrome c oxidase (CcO) in cancer progression.

97 Cytochrome c oxidase (CcO) is a transmembrane protein th

98 The synthesis of the heme a cofactor used in cytochrome c oxidase (CcO) is dependent on the sequentia

99 Cytochrome c Oxidase (CcO) is known to catalyze the redu

100 Cytochrome c oxidase (CcO) is the last electron acceptor

101 The enzyme cytochrome c oxidase (CcO) or complex IV (EC 1.9.3.1) is

102 tional analyses have shown that bovine heart cytochrome c oxidase (CcO) pumps protons electrostatical

103 Cytochrome c oxidase (CcO) reduces dioxygen to water and

104 Cytochrome c oxidase (CcO) reduces oxygen to water and u

105 Proton pumping A-type cytochrome c oxidase (CcO) terminates the respiratory ch

106 Cytochrome c oxidase (CcO) uses the energy released by r

107 malfunction of multiple proteins, including cytochrome c oxidase (CcO), and Cu/Zn superoxide dismuta

108 Cytochrome c oxidase (CcO), the terminal enzyme in the e

109 T is assumed to rely on photon absorption by cytochrome c oxidase (CCO), the terminal enzyme in the m

110 Biogenesis of cytochrome c oxidase (CcO), the terminal enzyme of the m

111 o hemoglobin and by inhibiting mitochondrial cytochrome c oxidase (CcO), thereby decreasing oxygen de

112 A key enzyme in aerobic metabolism is cytochrome c oxidase (CcO), which catalyzes the reductio

113 gen that we consume, reducing it to water by cytochrome c oxidase (CcO).

114 by knockdown (KD) of subunits IVi1 or Vb of cytochrome c oxidase (CcO).

115 ivities of succinate dehydrogenase (SDH) and cytochrome c oxidase (CCO).

116 ctor of the mitochondrial respiratory enzyme cytochrome c oxidase (CcO).

117 The largest subgroup contains the cytochrome c oxidases (CcO), which reduce molecular oxyg

118 etics based on the activity of mitochondrial Cytochrome-C Oxidase (CCO).

119 phism fingerprinting of the protein-encoding cytochrome c oxidase ccoN gene.

120 Cytochrome c oxidases (CcOs) are the terminal enzymes in

121 nalysis revealed R25 to be the subunit II of cytochrome c oxidase (CCOX), an essential constituent of

122 presses mitochondrial function by inhibiting cytochrome-c oxidase (CcOX; complex IV).

123 In Saccharomyces cerevisiae, cytochrome c oxidase (CIV) forms SCs of varying stoichio

124 dendritic mitochondria and histochemistry of cytochrome c oxidase (CO) activity were examined in pre-

125 otein synthesis but rather have a problem in cytochrome c oxidase complex (COX) assembly.

126 tein p27 (Ldp27) is a component of an active cytochrome c oxidase complex in Leishmania donovani and

127 Deficiencies of cytochrome c oxidase complex IV, which reduces O2 in mit

128 x1, Cox2, and Cox3, comprise the core of the cytochrome c oxidase complex.

129 Hydrogen sulphide (H2S) blocks the cytochrome-c oxidase complex (COX), predicting the evolu

130 tide (reduced) dehydrogenase (complex I) and cytochrome c oxidase (complex IV) activity levels (immun

131 The formation of the mature cytochrome c oxidase (complex IV) involves the associati

132 particular the cytochrome bc1 (complex III)-cytochrome c oxidase (complex IV) supercomplex (termed I

133 We describe human COX6B2, a component of cytochrome c oxidase (complex IV).

134 Cytochrome c oxidase (complex IV, CIV) is known in mamma

135 bly and/or modulation of the activity of the cytochrome c oxidase (complex IV, CIV).

136 he terminal enzyme of the respiratory chain, cytochrome c oxidase, consists of a hydrophobic reaction

137 Cytochrome c oxidase contributes to the transmembrane pr

138 ression of key mitochondrial genes including cytochrome C oxidase copper chaperone (COX17) and ATP Sy

139 ociated with electron and proton transfer in cytochrome c oxidase could, in principle, be used to dis

140 present study, we found that the decrease in cytochrome c oxidase (COX) activity was ascribable to a

141 alized respiratory terminal oxidases (RTOs), cytochrome c oxidase (Cox) and cytochrome bd quinol oxid

142 ant decrease in the level of fully assembled cytochrome c oxidase (COX) and in its activity, suggesti

143 l oxidases: the thylakoid membrane-localized cytochrome c oxidase (COX) and quinol oxidase (Cyd) and

144 , suggesting an involvement in the CRC, with cytochrome c oxidase (COX) as a relevant protein complex

145 itochondrial protein with essential roles in cytochrome c oxidase (COX) assembly and the regulation o

146 dentify an interaction between EGFL9 and the cytochrome c oxidase (COX) assembly factor COA3.

147 frequently associated with cardiomyopathy is cytochrome c oxidase (COX) deficiency caused by mutation

148 Cytochrome c oxidase (COX) deficiency is a frequent bioc

149 Accordingly, CO increased cytochrome c oxidase (COX) enzymatic specific activity a

150 llar cristae was associated with the gain of cytochrome c oxidase (COX) function, and the COX subunit

151 oxidase subunit 4 isoform 1 (Cox4i1) impair cytochrome C oxidase (COX) function, the multimeric enzy

152 -2-HG-mediated inhibition of the activity of cytochrome c oxidase (COX) in the mitochondrial electron

153 rone COX19 participates in the biogenesis of cytochrome c oxidase (COX) in yeast and humans.

154 Cytochrome c oxidase (COX) is the terminal enzyme of the

155 Cytochrome c oxidase (COX) is the terminal enzyme of the

156 Cytochrome c oxidase (COX) or complex IV of the mitochon

157 ng cox10 gene encoding an assembly factor of cytochrome c oxidase (COX) specifically in mouse ECs, pr

158 of this pathway involves phosphorylation of cytochrome c oxidase (COX) subunit 4-isoform 1 (COX4i1),

159 Cytochrome c oxidase (COX) was initially purified more t

160 it shuttles electrons from bc(1) complex to cytochrome c oxidase (COX), and as a trigger of type II

161 Cytochrome c oxidase (COX), the last enzyme of the respi

162 Copper is required for the activity of cytochrome c oxidase (COX), the terminal electron-accept

163 Cytochrome c oxidase (COX), the terminal enzyme of the m

164 sed mitochondrial iron loading and levels of cytochrome c oxidase (COX), which led to mitochondrial d

165 isorders from a range of 'large' and 'small' cytochrome c oxidase (COX)-deficient regions in skeletal

166 Ragged-red and cytochrome c oxidase (COX)-negative fibers, together wit

167 mtDNA was analyzed from cytochrome c oxidase (COX)-positive and COX-negative are

168 add two copper ions to the catalytic core of cytochrome c oxidase (COX).

169 tes to fail in the assembly of mitochondrial cytochrome c oxidase (COX).

170 Mitochondrial Complex IV [cytochrome c oxidase (COX)] deficiency is one of the mos

171 chondrial transcription factor A (T-fam) and cytochrome c oxidase (COX, complex IV).

172 Isolated cytochrome-c oxidase (COX) deficiency is one of the most

173 ults of histochemical analysis revealed that cytochrome-c oxidase (COX) deficiency was more evident i

174 mitochondrial respiratory chain complex IV (cytochrome c oxidase, COX).

175 I (NADH dehydrogenase, NDU) and complex IV (cytochrome-c-oxidase, COX) of the mitochondrial electron

176 The cytochrome c oxidase Cox2 has been purified from native

177 We focused on subunit II of cytochrome c oxidase (Cox2) to study which modifications

178 Cytochrome c oxidases (Coxs) are the basic energy transd

179 In cytochrome c oxidase (CytcO) reduction of O(2) to water

180 ol-cytochrome c reductase; cyt. bc1) and IV (cytochrome c oxidase; CytcO).

181 th MICOS disassembly, abnormal cristae, mild cytochrome c oxidase defect, and sensitivity to glucose

182 der characterized with neurodegeneration and cytochrome c oxidase deficiency.

183 Muscle studies showed global cytochrome-c oxidase deficiency in all patients tested a

184 ndividuals with mitochondrial complex IV (or cytochrome c oxidase) deficiency have mutations in the b

185 Oxidative histochemistry showed cytochrome c oxidase-deficient fibres in skeletal and ca

186 colemmal accumulation of mitochondria and/or cytochrome c oxidase-deficient fibres.

187 d inhibition are significantly attenuated in cytochrome c oxidase-deficient mice.

188 nit of cytochrome c oxidase and is active in cytochrome c oxidase-deficient mitochondria.

189 ions in individual muscle fibres with 20% of cytochrome c oxidase-deficient myofibres accumulating tw

190 Laser capture microdissection of cytochrome-c oxidase-deficient fibers revealed mitochond

191 tant lines impaired in the expression of the CYTOCHROME C OXIDASE DEFICIENT1 (COD1) gene, which encod

192 In the absence of high-affinity cytochrome c oxidases, deletion of mhr no longer caused

193 ble reduction of oxygen to bound peroxide at cytochrome c oxidase determining the net flux.

194 Fluorophore-labeled cytochrome c oxidase displayed a similar increase when r

195 Cytochrome c oxidase dysfunction enhances phagocytic fun

196 cluding impaired energy generation caused by cytochrome c oxidase dysfunction in the mitochondria.

197 osensor based on the bacterial expression of cytochrome c oxidase for the selective detection of clin

198 trochemical modulation has been performed on cytochrome c oxidase from Rhodobacter sphaeroides.

199 Proton transfer in cytochrome c oxidase from the cellular inside to the bin

200 The ba3-type cytochrome c oxidase from Thermus thermophilus is a memb

201 an 844 base pair region of the mitochondrial Cytochrome c oxidase gene, present at approximately 1 pp

202 elevated expression of several mitochondrial cytochrome C oxidase genes, suggesting increased aerobic

203 ulated with the Anr-controlled high-affinity cytochrome c oxidase genes.

204 of proton translocation in these cbb(3)-type cytochrome c oxidases has remained controversial.

205 chondrial proliferation and total absence of cytochrome- c oxidase histochemical stain.

206 argeting short (127-314 bp) fragments of the cytochrome c oxidase I (CO1) DNA barcode region were dev

207 ochondrial DNA control region (mtDNA CR) and cytochrome c oxidase I (COI) gene from five populations

208 Here, metabarcoding of cytochrome c oxidase I (COI) region of mitochondrial DNA

209 uce DNA barcodes from the mitochondrial gene cytochrome c oxidase I (COI).

210 in expression of the mitochondrially encoded cytochrome C oxidase I (MTCO1), complex I activity, and

211 , extracted DNA and sequenced mitochondrial (cytochrome c oxidase I [mtCOI]) and nuclear (small subun

212 techniques based on two mitochondrial genes (cytochrome c oxidase I and 16S rRNA) we prove the existe

213 seq flowcell to obtain 658 base pairs of the cytochrome c oxidase I DNA barcode in 1,010 specimens fr

214 is of sequence analysis of the mitochondrial cytochrome c oxidase I gene.

215 e, including genes encoding cytochrome b and cytochrome c oxidase I.

216 nd decreased levels of mitochondrial complex cytochrome c oxidase I/IV and lower ATP levels.

217 the available structures of ba(3)- and aa(3)-cytochrome c oxidases identifies possible active pathway

218 atomistic molecular dynamics simulations of cytochrome c oxidase in an explicit membrane-solvent env

219 binding of Na(+) and Ca(2+)cations to bovine cytochrome c oxidase in its fully oxidized and partially

220 Cytochrome c oxidase in the inner membrane of mitochondr

221 tochondrial function that directly activates cytochrome c oxidase in the mitochondria and functions i

222 e a is an essential cofactor for function of cytochrome c oxidase in the mitochondrial electron trans

223 Deletion of subunit Va of cytochrome c oxidase, inhibition of F(1)F(0) adenosine t

224 enzymes (P-450s, peroxidases, catalases, and cytochrome c oxidase) involved in biological respiration

225 on function (Q) of the redox center CuA from cytochrome c oxidase is attained by tuning the accessibi

226 on of the protonation rate at the surface of cytochrome c oxidase is found when the lipid area surrou

227 rmore, a reaction step that in the wild-type cytochrome c oxidase is linked to simultaneous proton up

228 The heme(a3)/Cu(B) active site of cytochrome c oxidase is responsible for cellular nitrite

229 The O-->E intermediate of cytochrome c oxidase is the first redox state in its cat

230 Cytochrome c oxidase is the last respiratory complex of

231 ted copper to the mitochondria and increased cytochrome c oxidase levels in the brain.

232 te (Cu(A)) on subunit II (CoxB) of bacterial cytochrome c oxidase lie on the periplasmic side of the

233 This approach identified cytochrome c oxidase (LmCOX) subunit IV as a LACK-depend

234 ession of mitochondrial-encoded subunit 1 of cytochrome c oxidase (MTCO1), a subunit of respiratory c

235 mtDNA depletion and cytochrome c oxidase-negative cells were found ex vivo i

236 Muscle biopsies showed cytochrome c oxidase-negative fibers and mtDNA multiple

237 atients, muscle biopsy showed ragged-red and cytochrome c oxidase-negative fibres with combined respi

238 nce of ragged-red fibers, however, scattered cytochrome c oxidase-negative staining and electron dens

239 ies of specific membrane proteins, including cytochrome c oxidase, NhaA Na(+)/H(+) exchanger, ClC-7 H

240 Cytochrome c oxidases of facultative members of the comm

241 plex I (NADH:quinone oxidoreductase) and IV (cytochrome c oxidase) of this patient.

242 In cytochrome c oxidase, one such pathway starts near a con

243 ong with a correlation between the number of cytochrome c oxidase operons and heterotrophic or diazot

244 Defects in mitochondrial cytochrome c oxidase or respiratory chain complex IV (CI

245 his prediction measuring oxidation states of cytochrome c oxidase (oxCCO), an intracellular marker of

246 the oxidation state of mitochondrial enzyme cytochrome-c-oxidase (oxCCO) have the potential to yield

247 impressive results, a model of mitochondrial cytochrome c oxidase polypeptide I was obtained with a T

248 uptake in the Asn-139-Thr/Asp-132-Asn mutant cytochrome c oxidase, proton pumping was impaired, which

249 Cytochrome c oxidase reduces O(2) to H(2)O, a reaction c

250 e to Zn(2+) addition, which in the wild-type cytochrome c oxidase slows the reaction, indicating that

251 We assembled individual mitochondrial cytochrome c oxidase subunit 1 (COI) sequences (n = 866)

252 unravel the use of the mitochondrial marker cytochrome c oxidase subunit 1 (coxI) as barcode for Lon

253 mitochondrial fraction indicates binding of cytochrome c oxidase subunit 1 (mt-COX1) mRNA from the m

254 in a stretch of 22 identical amino acids in cytochrome c oxidase subunit 1 and NADH dehydrogenase su

255 e KRIPP1 knockdown, A/U-tailed mRNA encoding cytochrome c oxidase subunit 1 declined concomitantly wi

256 nal assays, CB9032258 restored mitochondrial cytochrome c oxidase subunit 1 levels and rescued impair

257 The region of the mitochondrial cytochrome c oxidase subunit 1 used as the animal barcod

258 EIL2 with the mitochondrion-specific protein cytochrome c oxidase subunit 2 (MT-CO2).

259 TPR domain of OXA2b directly interacts with cytochrome c oxidase subunit 2, aiding in efficient memb

260 h the mitochondrial genes MT-CO2 and MT-CO3 (cytochrome c oxidase subunit 3); importantly, both enzym

261 voltage-dependent anion channel (VDAC), and cytochrome c oxidase subunit 4 (COX IV).

262 he assembly of nuclear-encoded subunits like cytochrome c oxidase subunit 4 (Cox4) into the mature co

263 ow that the mitochondrial complex IV subunit cytochrome C oxidase subunit 4 (Cox4i1) is a direct TAp7

264 Specifically, decreased levels of cytochrome C oxidase subunit 4 isoform 1 (Cox4i1) impair

265 was to analyze the function of lung-specific cytochrome c oxidase subunit 4 isoform 2 (COX4i2) in vit

266 Complex III's Rieske Fe-S center and COX4i2 [cytochrome c oxidase subunit 4 isoform 2] in Complex IV)

267 Two DNA barcode regions, namely cytochrome c oxidase subunit I (COI) and cytochrome b (c

268 in fragments of the mitochondrial (mt) genes cytochrome c oxidase subunit I (COI) and Cytochrome b as

269 Drosophila, mt:CoI(T300I), which affects the cytochrome c oxidase subunit I (CoI) locus.

270 S and of the main alternatively used marker [Cytochrome c oxidase subunit I (COI) mtDNA] belonging to

271 A 450 base pairs (bp) segment of cytochrome c oxidase subunit I (COI) was amplified and s

272 sed on a single mitochondrial locus, such as cytochrome c oxidase subunit I (COI).

273 equence of the "DNA barcoding" region of the cytochrome c oxidase subunit I (COI).

274 in the mtDNA [NADH dehydrogenase 6 (ND6) and cytochrome c oxidase subunit I (COI)] or nuclear DNA [ad

275 rtial sequence for the mitochondrial-encoded cytochrome c oxidase subunit I (Cox 1) gene in the cell

276 chondrial transcription factor-1 (Tfam), and cytochrome c oxidase subunit I (Cox-1) was determined by

277 translation-competent, long poly(AU)-tailed cytochrome c oxidase subunit I and edited apocytochrome

278 tures) over a 6-mo period were identified by cytochrome c oxidase subunit I barcoding (>2-mm mobile o

279 preferential inhibition of synthesis of the cytochrome c oxidase subunit I over apocytochrome b were

280 For the second objective, mitochondrial cytochrome c oxidase subunit I sequences of 16 individua

281 Here we used eDNA metabarcoding of COI (cytochrome c oxidase subunit I) and 18S (nuclear small s

282 Pyrosequencing of genetic marker, COI (cytochrome c oxidase subunit I) and subsequent sequence

283 ted, and the norE product is a member of the cytochrome c oxidase subunit III family.

284 The cytochrome c oxidase subunit isoform Cox7a1 is highly ab

285 EPAS1, and the nuclear-encoded mitochondrial cytochrome c oxidase subunit, COX4I2, in glomus cell sen

286 ons: Cox6a2, which codes for an isoform of a cytochrome c oxidase subunit.

287 ption-factor-A (TFAM), mitochondrial-protein-cytochrome-C-oxidase subunit-2 (COX2), sirtuin-1 (SIRT1)

288 ntially affected, with near normal levels of cytochrome c oxidase subunit2 and Nad7 but little Nad6 p

289 ichiometric imbalance between mitochondrial (cytochrome c oxidase subunits 1 and 2) and nuclear (succ

290 pecies, respiratory dysfunction, and loss of cytochrome c oxidase subunits and activity.

291 and genes coding for NADH dehydrogenase and cytochrome c oxidase subunits.

292 vity of the mitochondrial respiratory chain (cytochrome c-oxidase/succinate dehydrogenase [COX/SDH]-r

293 ith a subpopulation of the cytochrome bc (1)-cytochrome c oxidase supercomplex and have been proposed

294 Conditional deletion of cytochrome c oxidase, the terminal enzyme in the respira

295 t the unusual sensitivity of skeletal muscle cytochrome c oxidase to sulfide poisoning in ethylmaloni

296 nstant approximately 65 mus in the wild-type cytochrome c oxidase) was impaired in the Asp372Ile vari

297 gly, yeast, mouse liver, and isolated bovine cytochrome c oxidase were directly inhibited by the drug

298 , whereas mice deficient in the synthesis of cytochrome c oxidase, which have reduced COX, were prote

299 In the hypoxic mitochondrion, cytochrome c oxidase, which is a major source of NO, als

300 cbb3-type cytochrome c oxidases, which catalyze the terminal step