ライフサイエンスコーパス: manganese superoxide dismutase

1 mitochondrial targeting sequence (MTS) from manganese superoxide dismutase.

2 -1 signaling, thereby inducing expression of manganese superoxide dismutase.

3 1, catalase, Cu/Zn superoxide dismutase, and manganese superoxide dismutase.

4 stimates of the metal binding affinities for manganese superoxide dismutase.

5 an adenoviral vector containing the cDNA for manganese superoxide dismutase.

6 y transfection with an expression vector for manganese superoxide dismutase.

7 tem and is specific to cells totally lacking manganese superoxide dismutase.

8 sphorylation, by uncoupling protein-1 and by manganese superoxide dismutase.

9 with no difference in protein expression of manganese superoxide dismutase.

10 s downstream anti-oxidant genes catalase and manganese superoxide dismutase.

11 nse of the cell against superoxide radicals, manganese superoxide dismutase.

12 idative stress response enzymes catalase and manganese superoxide dismutase.

13 n of the anti-apoptotic factors Survivin and manganese superoxide dismutase.

14 the mitochondrial localization sequence from manganese-superoxide dismutase.

15 Manganese superoxide dismutase 2 (SOD2) is a critical co

16 Expressions of the antioxidants catalase and manganese superoxide dismutase-2 (SOD2) and the autophag

17 The mitochondrial antioxidant manganese superoxide dismutase-2 (Sod2) might protect ag

18 arkers of mitochondrial dysfunction, such as manganese superoxide dismutase (9-fold), and reduced rat

19 In addition, manganese superoxide dismutase, a major mitochondrial an

20 Apolipoprotein E(-/-) mice deficient in manganese superoxide dismutase, a mitochondrial antioxid

21 of transcription 3-mediated upregulation of manganese superoxide dismutase, a primary mitochondrial

22 hione reductase, glutathione peroxidase, and manganese superoxide dismutase activities were slightly

23 onylation in the myocardium despite elevated manganese superoxide dismutase activity during endotoxem

24 oups had hippocampal reduced glutathione and manganese superoxide dismutase activity levels comparabl

25 Hippocampal manganese superoxide dismutase activity was significantl

26 ria to inhibit mROS by rapidly up-regulating manganese superoxide dismutase activity.

27 Knock-out (KO) mice containing 50% manganese-superoxide dismutase activity (SOD2-KO) and tr

28 in, glutathione-S-transferases, and possibly manganese superoxide dismutase, affect ascorbate levels

29 theta-1 [T-1], and pi-1 [P-1: Ile-105Val]), manganese superoxide dismutase (Ala-9Val), and catalase

30 cytochrome c, subunit IV of complex IV, and manganese superoxide dismutase, all encoded in the nucle

31 Adenoviral overexpression of manganese superoxide dismutase also failed to prevent th

32 vels of c-IAP1, c-IAP2, and Bcl-2 as well as manganese superoxide dismutase and c-Jun NH2-terminal ki

33 cies (peroxides) and to the induction of the manganese superoxide dismutase and catalase activities b

34 ulation of FOXO3a targets antioxidant enzyme manganese superoxide dismutase and catalase.

35 endothelial cells has identified two genes, manganese superoxide dismutase and cyclooxygenase-2, tha

36 synthase (eNOS) and the antioxidant enzymes manganese superoxide dismutase and cytochrome c oxidase.

37 ation and (2) the effect of gene transfer of manganese superoxide dismutase and endothelial nitric ox

38 d upregulated the expression and activity of manganese superoxide dismutase and glutathione levels, s

39 e there is an up-regulation of mitochondrial manganese superoxide dismutase and glutathione peroxidas

40 as well as induction of antioxidant enzymes manganese superoxide dismutase and heme oxygenase 1 in i

41 lternative oxidase, dynamin related protein, manganese superoxide dismutase and Lon protease, respect

42 Overexpression of manganese superoxide dismutase and mitochondrial-targete

43 h down-regulation of GR and up-regulation of manganese superoxide dismutase and reduced glutathione l

44 e in mediating Sirt1-induced upregulation of manganese superoxide dismutase and suppression of oxidat

45 Leptin induces the production of manganese superoxide dismutase and the anti-apoptotic pr

46 Among them, only up-regulation of manganese superoxide dismutase and the cyclin-dependent

47 performed to differentiate polymorphisms for manganese superoxide dismutase and three classes of glut

48 in a concentration-dependent manner by both manganese-superoxide dismutase and cytochrome c proteins

49 expression of either uncoupling protein 1 or manganese superoxide dismutase, and azaserine, an inhibi

50 utathione system (e.g. ascorbate peroxidase, manganese superoxide dismutase, and dehydroascorbate red

51 As much as 40% of the total Mn(II) was in manganese superoxide dismutase, and it is this protein a

52 thione synthetase genes, increased levels of manganese superoxide dismutase, and NADPH oxidase-comple

53 RNA expression of the glucose 6-phosphatase, manganese superoxide dismutase, and sterol carrier prote

54 iron can outcompete manganese for binding to manganese superoxide dismutase, and through Fenton chemi

55 ression of catalase, glutathione peroxidase, manganese superoxide dismutase, and VDUP1, a protein tha

56 by vitamin E treatment or transfection with manganese superoxide dismutase, and was further increase

57 ondrial topoisomerase I, peroxiredoxin 3 and manganese superoxide dismutase--are elevated in A-T cell

58 In addition, inactivation of manganese superoxide dismutase by peroxynitrite may repr

59 id leader peptide of a new human recombinant manganese superoxide dismutase can enter cells and carry

60 ng enzymes copper/zinc superoxide dismutase, manganese superoxide dismutase, catalase, and glutathion

61 ioxidant enzyme profiles, including those of manganese superoxide dismutase, catalase, and GPx.

62 Manganese superoxide dismutase, catalase, and tocopherol

63 Because mitochondrial manganese superoxide dismutase catalyzes conversion of s

64 e utility of this methodology in examining a manganese superoxide dismutase cDNA fragment which we de

65 PLP animals expressed increased (P<0.01) manganese superoxide-dismutase, copper-zinc superoxide-d

66 Copper/zinc superoxide dismutase, manganese superoxide dismutase (corrected or not correct

67 neutron diffraction of two redox-controlled manganese superoxide dismutase crystals reveal the all-a

68 total superoxide dismutase and mitochondrial manganese superoxide dismutase (cytochrome c reduction m

69 oxic environment increases the resistance of manganese superoxide dismutase-deficient astrocytes to s

70 ty, and MC fibronectin accumulation, whereas manganese superoxide dismutase depletion increases mitoc

71 composed of 215 amino acids, and has an iron/manganese superoxide dismutase domain.

72 vascular cell adhesion molecule-1 (VCAM-1), manganese superoxide dismutase, endothelial-specific mol

73 e dismutase (cytochrome c reduction method), manganese superoxide dismutase expression (Western blot)

74 Manganese superoxide dismutase expression increased with

75 tablish a novel nutrient-sensing pathway for manganese superoxide dismutase expression mediated throu

76 ns with 8Br-cGMP also activated catalase and manganese superoxide dismutase expression, indicating th

77 nd a non-significant trend towards decreased manganese superoxide dismutase expression.

78 Manganese superoxide dismutase from the extremely thermo

79 d region and have mapped the position of the manganese superoxide dismutase gene (SOD2).

80 talloproteinase 1, ferritin light chain, and manganese superoxide dismutase genes were identified as

81 ntified: tropomyosin, heat shock protein 27, manganese superoxide dismutase, glutathione S-transferas

82 n of E-selectin, ICAM-1, VCAM-1, IL-6, IL-8, manganese superoxide dismutase, HLA-DR, and CD86.

83 e replacement Tyr 34 --> Phe (Y34F) in human manganese superoxide dismutase (hMnSOD) and crystallized

84 parent full-length cDNA sequences coding for manganese superoxide dismutase (HvMnSOD) and extracellul

85 genes, the proapoptotic Bim and antioxidant manganese superoxide dismutase in MC.

86 dothelial growth factor, p21(WAF1/CIP1), and manganese superoxide dismutase in MCF7 breast cancer cel

87 fic biological oxidants on recombinant human manganese superoxide dismutase in vitro have been evalua

88 conserved residue in the active site of the manganese superoxide dismutases in organisms from bacter

89 umarase, upstream of the sodA gene, encoding manganese superoxide dismutase, in Pseudomonas aeruginos

90 Manganese superoxide dismutase increased 3-fold with IFN

91 dependent absorption) for anion complexes of manganese superoxide dismutase indicating a change in co

92 ese results, a mechanism for metal uptake by manganese superoxide dismutase involving reorientation o

93 Manganese superoxide dismutase is a nuclear encoded prim

94 demonstrated that the mitochondrial protein manganese superoxide dismutase is inactivated, tyrosine

95 ssion of both Cu/Zn superoxide dismutase and manganese superoxide dismutase, leading to increased oxi

96 ncoding the mitochondrial antioxidant enzyme manganese superoxide dismutase, led to the identificatio

97 rotein locus (chromosome 16) (P=.01) and the manganese superoxide dismutase locus (chromosome 6) (P=.

98 diation (MCF+FIR cells) or overexpression of manganese superoxide dismutase (MCF+SOD cells) demonstra

99 g mitochondrial-targeted MPG using the human manganese superoxide dismutase mitochondrial-targeting s

100 ochondrial adaptive or stress proteins (e.g. manganese superoxide dismutase, mitochondrial KATP chann

101 opper/zinc superoxide dismutase (Cu/Zn SOD), manganese superoxide dismutase (Mn SOD), catalase, and g

102 Expression of the antioxidant enzymes manganese superoxide dismutase (Mn-SOD) and copper-zinc

103 Increased manganese superoxide dismutase (Mn-SOD) and decreased ca

104 ential role of the mitochondrial antioxidant manganese superoxide dismutase (Mn-SOD) as a potential e

105 adjacent subunits in the homotetramer human manganese superoxide dismutase (Mn-SOD) form a hydrogen

106 Manganese superoxide dismutase (Mn-SOD) immunoreactivity

107 enes c-inhibitor of apoptosis 2 (c-IAP2) and manganese superoxide dismutase (Mn-SOD) in breast cancer

108 Overexpression of manganese superoxide dismutase (Mn-SOD) in human breast

109 Manganese superoxide dismutase (Mn-SOD) is a primary ant

110 Manganese superoxide dismutase (Mn-SOD) is an enzyme tha

111 The mitochondrial antioxidant enzyme manganese superoxide dismutase (Mn-SOD) is crucial in ma

112 Manganese superoxide dismutase (Mn-SOD) is one of many g

113 Mitochondrial manganese superoxide dismutase (Mn-SOD) is the primary c

114 The mitochondrial antioxidant manganese superoxide dismutase (Mn-SOD) plays a critical

115 in, albumin, total antioxidant status (TAS), manganese superoxide dismutase (Mn-SOD), aconitase, glut

116 n the level of the mitochondrial antioxidant manganese superoxide dismutase (Mn-SOD).

117 k-out gene (Sod2 -/+) encoding mitochondrial manganese superoxide dismutase (Mn-SOD).

118 sed levels of catalase/peroxidase (KatG) and manganese superoxide dismutase (Mn-SOD).

119 ncides with loss of the mitochondrial enzyme manganese superoxide dismutase (Mn-SOD).

120 Manganese superoxide dismutase (Mn-SOD; SOD2), a primary

121 r if the polyamine-deficient cells contain a manganese-superoxide dismutase (Mn-SOD) plasmid.

122 the six-coordinate azide adduct of oxidized manganese superoxide dismutase (Mn3+ SOD) that is formed

123 Mutagenesis of Escherichia coli manganese superoxide dismutase (MnSD) demonstrates invol

124 es, which expressed a range of mitochondrial manganese superoxide dismutase (MnSOD) activities, with

125 n part, this derived from TAM downregulating manganese superoxide dismutase (MnSOD) activity by causi

126 A 50% decrease in manganese superoxide dismutase (MnSOD) activity was obse

127 The antioxidant enzyme manganese superoxide dismutase (MnSOD) also modulates th

128 re not well understood, reports suggest that manganese superoxide dismutase (MnSOD) and calpain may b

129 oxo3a-dependent), antioxidant-encoding genes manganese superoxide dismutase (MnSOD) and catalase (Cat

130 dentified the p53-dependent up-regulation of manganese superoxide dismutase (MnSOD) and glutathione p

131 DNA despite eight- and fourfold increases in manganese superoxide dismutase (MnSOD) and mitochondrial

132 ve oxygen species, in part, by deacetylating manganese superoxide dismutase (MnSOD) and mitochondrial

133 mitochondrial targeting sequence (MTS) from manganese superoxide dismutase (MnSOD) and placed them u

134 phosphorylated eNOS (p-eNOS) (ser 1177), and manganese superoxide dismutase (MnSOD) and reduced serum

135 totic role via the induction of target genes manganese superoxide dismutase (MnSOD) and/or calbindin.

136 complex on the promoters of the catalase and manganese superoxide dismutase (MnSOD) antioxidant genes

137 +)-induced dephosphorylation was observed in manganese superoxide dismutase (MnSOD) as well as the pr

138 In other cell types, increasing manganese superoxide dismutase (MnSOD) can increase intr

139 We hypothesized that manganese superoxide dismutase (MnSOD) could mediate MMP

140 Manganese superoxide dismutase (MnSOD) cycles between th

141 ency of the mitochondrial antioxidant enzyme manganese superoxide dismutase (MnSOD) exacerbated amylo

142 /CS-like individuals, 74 (20%) had increased manganese superoxide dismutase (MnSOD) expression, a man

143 -dependent genes heme oxygenase-1 (Ho-1) and manganese superoxide dismutase (Mnsod) following DHB pre

144 Glutamine 143 in human manganese superoxide dismutase (MnSOD) forms a hydrogen

145 Manganese superoxide dismutase (MnSOD) from different sp

146 Manganese superoxide dismutase (MnSOD) functions as a tu

147 Bacterial lipopolysaccharide can induce manganese superoxide dismutase (MnSOD) gene expression i

148 luating the tumor suppressor activity of the manganese superoxide dismutase (MnSOD) gene on establish

149 Trx induces manganese superoxide dismutase (MnSOD) gene transcriptio

150 n, concentration-dependent p53 effect on the manganese superoxide dismutase (MnSOD) gene was investig

151 e induction of antioxidant and antiapoptotic manganese superoxide dismutase (MnSOD) gene.

152 The redox potential of human manganese superoxide dismutase (MnSOD) has been difficul

153 Manganese superoxide dismutase (MnSOD) has been found to

154 Manganese superoxide dismutase (MnSOD) has been previous

155 Manganese superoxide dismutase (MnSOD) has been shown to

156 Manganese superoxide dismutase (MnSOD) has been shown to

157 ncoupling protein-1 (UCP1) HVJ-liposomes, or manganese superoxide dismutase (MnSOD) HVJ-liposomes com

158 estigates the role of the antioxidant enzyme manganese superoxide dismutase (MnSOD) in androgen-indep

159 Here we report that decreased expression of manganese superoxide dismutase (MnSOD) in EPCs contribut

160 Decreased expression of manganese superoxide dismutase (MnSOD) in IPAH-ECs paral

161 Overexpression of functional human manganese superoxide dismutase (MnSOD) in lung alveolar

162 related with a higher level of expression of manganese superoxide dismutase (MnSOD) in the latter cel

163 ased expression of the NF-kappaB target gene manganese superoxide dismutase (MnSOD) in the pulmonary

164 Human manganese superoxide dismutase (MnSOD) is a crucial oxid

165 Human manganese superoxide dismutase (MnSOD) is a homotetramer

166 Human manganese superoxide dismutase (MnSOD) is a homotetramer

167 Manganese superoxide dismutase (MnSOD) is a mitochondria

168 Manganese superoxide dismutase (MnSOD) is a nuclear enco

169 Manganese superoxide dismutase (MnSOD) is a nuclear enco

170 Manganese superoxide dismutase (MnSOD) is a primary anti

171 Manganese superoxide dismutase (MnSOD) is a superoxide a

172 Manganese superoxide dismutase (MnSOD) is an antioxidant

173 Manganese superoxide dismutase (MnSOD) is an important a

174 he disproportionation of superoxide by human manganese superoxide dismutase (MnSOD) is characterized

175 Human manganese superoxide dismutase (MnSOD) is characterized

176 alysis of the interfaces between subunits in manganese superoxide dismutase (MnSOD) is currently unde

177 rial analysis of gene expression (SAGE) that manganese superoxide dismutase (MnSOD) is enriched in th

178 Histidine 30 in human manganese superoxide dismutase (MnSOD) is located at a s

179 Manganese superoxide dismutase (MnSOD) is rapidly induce

180 Manganese superoxide dismutase (MnSOD) is reduced in a v

181 group: liver pathology, lipid peroxidation, manganese superoxide dismutase (MnSOD) levels, copper-zi

182 ersed by free radical scavengers such as the manganese superoxide dismutase (MnSOD) mimetic TBAP and

183 The antioxidant enzyme manganese superoxide dismutase (MnSOD) modulates the cel

184 o induce transcriptional activation of human manganese superoxide dismutase (MnSOD) mRNA in human lun

185 Transcriptional activation of human manganese superoxide dismutase (MnSOD) mRNA induced by a

186 5) but there was no change in mRNA levels of manganese superoxide dismutase (MnSOD) or glutamate cyst

187 Manganese superoxide dismutase (MnSOD) plays a critical

188 has a reduced ability to activate the human manganese superoxide dismutase (MnSOD) promoter in A293

189 m Sed females exhibited significantly higher manganese superoxide dismutase (MnSOD) protein expressio

190 r laboratories showed that overexpression of manganese superoxide dismutase (MnSOD) reduced tumor inc

191 This study investigates the hypothesis that manganese superoxide dismutase (MnSOD) regulates cellula

192 regimen of cutaneous gene therapy of eNOS or manganese superoxide dismutase (MnSOD) restored such hea

193 binds to the 3' untranslated region (UTR) of manganese superoxide dismutase (MnSOD) RNA has been desc

194 ined region in the 3' untranslated region of manganese superoxide dismutase (MnSOD) RNA; both the MnS

195 ratories demonstrated that overexpression of manganese superoxide dismutase (MnSOD) suppressed both t

196 ion of the mitochondrial antioxidant protein manganese superoxide dismutase (MnSOD) to the heart to p

197 ss was assessed using aconitase activity and manganese superoxide dismutase (MnSOD) transcript levels

198 ribozyme that targets the protective enzyme manganese superoxide dismutase (MnSOD) was expressed in

199 e depletion of superoxide catalyzed by human manganese superoxide dismutase (MnSOD) was observed spec

200 AC5 Tg hearts, whereas protein expression of manganese superoxide dismutase (MnSOD) was reduced by 38

201 month-old mice showed that protein levels of manganese superoxide dismutase (MnSOD) were unchanged in

202 ation of Tumour protein 53 (p53)(Lys382) and Manganese superoxide dismutase (MnSOD)(Lys122) were also

203 e lines expressing increased levels of human manganese superoxide dismutase (MnSOD), a mitochondrial

204 Manganese superoxide dismutase (MnSOD), a mitochondrial

205 Manganese superoxide dismutase (MnSOD), a tumor necrosis

206 We tested the hypothesis that manganese superoxide dismutase (MnSOD), an antioxidant e

207 ppaB-dependent anti-apoptotic genes A20, A1, manganese superoxide dismutase (MnSOD), and cellular inh

208 chondrial levels of the anti-oxidant enzyme, manganese superoxide dismutase (MnSOD), are dramatically

209 tified sod2, encoding the antioxidant enzyme manganese superoxide dismutase (MnSOD), as a RelA target

210 We transferred an antioxidant gene, manganese superoxide dismutase (MnSOD), by adenoviral in

211 dants (enzymatic), including the polymorphic manganese superoxide dismutase (MnSOD), can act to reduc

212 teracts with the primary antioxidant enzyme, manganese superoxide dismutase (MnSOD), consistent with

213 and enzyme activity gels were performed for manganese superoxide dismutase (MnSOD), copper/zinc, cat

214 side chain of Gln143, a conserved residue in manganese superoxide dismutase (MnSOD), forms a hydrogen

215 One component of this system, manganese superoxide dismutase (MnSOD), has also been sh

216 the cytokine-inducible cytoprotective genes manganese superoxide dismutase (MnSOD), interleukin-6 (I

217 These loci contain the genes for manganese superoxide dismutase (MnSOD), on chromosome 6q

218 up of NF-kappaB-related proteins [i.e., p65, manganese superoxide dismutase (MnSOD), phosphorylated e

219 The mitochondria-localized manganese superoxide dismutase (MnSOD), serves a key cyt

220 In Escherichia coli manganese superoxide dismutase (MnSOD), the absolutely c

221 ncrease the activity, but not the levels, of manganese superoxide dismutase (MnSOD), the mitochondria

222 polymorphism [valine (V) --> alanine (A)] of manganese superoxide dismutase (MnSOD), the primary anti

223 Overexpression of manganese superoxide dismutase (MnSOD), when combined wi

224 on of either uncoupling protein-1 (UCP-1) or manganese superoxide dismutase (MnSOD), which decrease h

225 Two polymorphic variants of manganese superoxide dismutase (MnSOD), with either Ile

226 ydrophobic side of the active site cavity of manganese superoxide dismutase (MnSOD), with its indole

227 ease was partially reversed by expression of manganese superoxide dismutase (MnSOD).

228 mice with an adipocyte-selective deletion of manganese superoxide dismutase (MnSOD).

229 maturation of every metalloenzyme, including manganese superoxide dismutase (MnSOD).

230 ole of an active-site residue Tyr34 in human manganese superoxide dismutase (MnSOD).

231 -f subunit of mitochondrial ATP synthase and manganese superoxide dismutase (MnSOD).

232 he anti-apoptotic genes A1, A20, c-IAP2, and manganese superoxide dismutase (MnSOD).

233 cies in the mitochondrial antioxidant enzyme manganese superoxide dismutase (MnSOD).

234 duction with uncoupling protein-1 (UCP-1) or manganese superoxide dismutase (MnSOD).

235 the sixth ligand bound to the active site of manganese superoxide dismutase (MnSOD).

236 overexpress the human form of mitochondrial manganese superoxide dismutase (MnSOD).

237 ic mice that overexpress human mitochondrial manganese superoxide dismutase (MnSOD).

238 reased acetylation and decreased activity of manganese superoxide dismutase (MnSOD).

239 product of the SOD2 gene, the homotetrameric manganese superoxide dismutase (MnSOD).

240 ctly induces the expression of p27(kip1) and manganese superoxide dismutase (MnSOD).

241 and downregulates the ROS-scavenging protein manganese superoxide dismutase (MnSOD); the alpha(1)-AR-

242 ncreased mitochondrial antioxidant defenses [manganese superoxide dismutase (MnSOD)P< 0.05; copper/zi

243 Manganese superoxide dismutase (MnSOD/SOD2) is a mitocho

244 Manganese superoxide-dismutase (MnSOD), copper-zinc supe

245 cal neurons with normal or reduced levels of manganese-superoxide dismutase (MnSOD) activity.

246 from Pseudomonas putida (Pp), sodA, encoding manganese-superoxide dismutase (MnSOD) and, sodB, iron-s

247 Manganese-superoxide dismutase (MnSOD) is one of the maj

248 the present study, we show that VEGF induces manganese-superoxide dismutase (MnSOD) mRNA and protein

249 We recently reported that wild-type (WT) manganese superoxide dismutases (MnSODs) from Saccharomy

250 No upregulation of endogenous manganese superoxide dismutase mRNA expression was obser

251 proteins play roles in antioxidant defense (manganese superoxide dismutase), neuronal communication

252 etic mice by either transgenic expression of manganese superoxide dismutase or by administration of a

253 e scavenger, TEMPOL, or by overexpression of manganese superoxide dismutase or catalase.

254 Ex vivo gene transfer of manganese superoxide dismutase or endothelial nitric oxi

255 Transgenic mice overexpressing mitochondrial manganese superoxide dismutase or extracellular superoxi

256 As a cofactor for manganese superoxide dismutase or through formation of n

257 hereas there was no change in c-IAP2 levels, manganese superoxide dismutase, or c-Jun NH2-terminal ki

258 Manganese superoxide dismutase overexpression also prote

259 Dismutation of mROS by manganese superoxide dismutase overexpression and a cell

260 are elevated in the retina in diabetes, and manganese superoxide dismutase overexpression prevents t

261 erived oxidative stress by overexpression of manganese-superoxide dismutase prevented insulin resista

262 Overexpression of mitochondrial manganese superoxide dismutase prevents the stimulatory

263 ransient transfection with catalase (but not manganese-superoxide dismutase) produced a decrease in G

264 Total manganese superoxide dismutase protein was increased in

265 Overexpression of manganese superoxide dismutase reduced the levels of int

266 Manganese superoxide dismutase removes superoxide radica

267 the overture to elevated gene expression of manganese superoxide dismutase reported earlier.

268 Mice that overexpress manganese superoxide dismutase showed significantly smal

269 The ubiquitous iron/manganese superoxide dismutase (SOD) family exemplifies

270 copper-zinc superoxide dismutase (CuZnSOD), manganese superoxide dismutase (SOD), catalase T, or met

271 is mediated by the mitochondrial antioxidant manganese superoxide dismutase (SOD).

272 expression array analysis revealed increased manganese superoxide dismutase (SOD-2) expression in the

273 significant elevations in the expression of manganese superoxide dismutase (Sod2) are associated wit

274 In this study, we identified mitochondrial manganese superoxide dismutase (SOD2) as one of the key

275 Manganese superoxide dismutase (SOD2) converts superoxid

276 cytes deficient in the mitochondrial form of manganese superoxide dismutase (SOD2) do not survive in

277 interaction between plasma selenium and the manganese superoxide dismutase (SOD2) gene and incident

278 Manganese superoxide dismutase (SOD2) is a primary defen

279 f mitochondrial derived H2O2, as a result of manganese superoxide dismutase (Sod2) overexpression, le

280 a mechanism whereby Saccharomyces cerevisiae manganese superoxide dismutase (SOD2) preferentially bin

281 transgenic mice with a partial depletion of manganese superoxide dismutase (SOD2) would affect the d

282 copper, zinc superoxide dismutase (SOD1), or manganese superoxide dismutase (SOD2), and against marke

283 Because manganese superoxide dismutase (SOD2), localized in mito

284 e surges in detached cells by regulating the manganese superoxide dismutase (SOD2).

285 ic increase in the ROS detoxification enzyme manganese superoxide dismutase (Sod2, also known as MnSo

286 Manganese-superoxide dismutase (Sod2) removes mitochondr

287 ntH in order to make wild-type levels of its manganese superoxide dismutase SodA.

288 ion within the natural diversity of the iron/manganese superoxide dismutase (SodFM) family of reactiv

289 of 27- and 70-kD stress proteins as well as manganese superoxide dismutase, suggesting that TNF-alph

290 he nigrostriatal system by overexpression of manganese superoxide dismutase supports a role for mitoc

291 amino acid sequencing techniques identified manganese superoxide dismutase, the major antioxidant en

292 pression of prosurvival molecules, including manganese superoxide dismutase, thioredoxin-1, and Bcl-x

293 The binding affinity of bacterial manganese superoxide dismutase to nonsequence-specific D

294 Exposure of recombinant human manganese superoxide dismutase to peroxynitrite resulted

295 quence, TGACGTCT, which we identified as the manganese superoxide dismutase TPA-responsive element, M

296 e anti-apoptotic genes for Bcl-2, Bcl-x, and manganese superoxide dismutase was observed in PEDF-trea

297 In particular, the SOD2 promoter, encoding manganese superoxide dismutase, was activated less stron

298 Y193) of the nine total tyrosine residues in manganese superoxide dismutase were nitrated by peroxyni

299 oxidation was demonstrated by overexpressing manganese superoxide dismutase, which improved HRas palm

300 we examined whether overexpression of SOD2, manganese superoxide dismutase, would prevent the hypoxi