ライフサイエンスコーパス: Mn-superoxide dismutase

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1 n-evolving complex of photosystem II and the Mn superoxide dismutase.

2 iocarbamate, as well as to overexpression of Mn-superoxide dismutase.

3 s largely dependent on MSD1, a mitochondrial Mn-superoxide dismutase.

4 rted to hydrogen peroxide though activity of Mn-superoxide dismutase.

5 There were also age-related reductions in Mn superoxide dismutase activities and carbonic anhydras

6 These proteins include Mn superoxide dismutase and neurofilament light subunit

7 the unfolding enthalpy and DeltaC(p) for apo-Mn superoxide dismutase and the observed T(m) values for

8 rosine and 4-HNE, as well as lower levels of Mn-superoxide dismutase and catalase expression.

9 is also required for enhanced expression of Mn-superoxide dismutase and resistance to paraquat, but

10 species (ROS) generation, downregulation of Mn-superoxide dismutase and XIAP, and c-Jun N-terminal k

11 ynthase, cyclooxygenase-2, aldose reductase, Mn superoxide dismutase, and probably other cardioprotec

12 ioxidant enzymes Cu/Zn-superoxide dismutase, Mn-superoxide dismutase, and catalase were significantly

13 Likewise, the transfection of cells with Mn-superoxide dismutase blocked the NF-kappaB activation

14 stern blots showed no difference in Cu/Zn or Mn superoxide dismutase, endothelial NO synthase, or ind

15 ompensatory evolutionary branching in the Fe/Mn superoxide dismutase enzyme, providing a Paleoprotero

16 These processes are inhibited by Mn-superoxide dismutase, establishing the generation of

17 Mn-Superoxide dismutase expression was increased 13-fold

18 ve sites of Escherichia coli Fe-substituted (Mn)superoxide dismutase [Fe-sub-(Mn)SOD] and Fe-SOD to e

19 +) complexes, not antioxidant enzymes (e.g., Mn superoxide dismutase), govern IR survival.

20 ue glutamine 143 near the manganese of human Mn superoxide dismutase (hMnSOD), a homotetramer of 22 k

21 ion of intercellular adhesion molecule 1 and Mn superoxide dismutase messenger RNA, and by analysis o

22 enced by decreased O2- production, increased Mn superoxide dismutase (Mn-SOD) activity, increased cal

23 lizing the oxygen-sensitive Escherichia coli Mn-superoxide dismutase (Mn-SOD) promoter, we have devel

24 Assay of Mn superoxide dismutase (MnSOD) indicates loss of activi

25 C7120 encodes for a membrane-targeted 30 kDa Mn-superoxide dismutase (MnSOD) and a cytosolic FeSOD.

26 tein cyclin D1 and the ROS scavenging enzyme Mn-superoxide dismutase (MnSOD).

27 d the 25-kD MAC protein showed homology with Mn-superoxide dismutase of MAC and Mycobacterium leprae.

28 proteins and of the activity of secreted Fe/Mn-superoxide dismutase, particularly in M. smegmatis.

29 n increased superoxide release and levels of Mn superoxide dismutase protein were significantly eleva

30 brane potential and the antioxidant protein, Mn superoxide dismutase (SOD).

31 -activated protein kinase (MAPK), manganese (Mn) superoxide dismutase (SOD), copper-zinc (CuZn) SOD,

32 The gene expression of mitochondrial Mn-superoxide dismutase (SOD), but not of cytosolic Cu,Z

33 nzymes related to oxidative injury (CuZn and Mn superoxide dismutases [SOD], catalase, and glutathion

34 tion factor FOXO3, an important regulator of Mn-superoxide dismutase (SOD2) expression, a tumor suppr

35 e two antioxidant enzymes catalase (CAT) and Mn-superoxide dismutase (SOD2) in four treatment groups

36 Erythrocyte Mn-superoxide dismutase was also reduced at 6 (0.154 vs.

37 d concentration of the anti-oxidative enzyme Mn-superoxide dismutase were observed in C3KO muscles.

38 Additionally, overexpression of Mn-superoxide dismutase, which can mitigate iron-derived

39 hat is comparable to the value of 50 muM for Mn-superoxide dismutase, which catalyzes a similar react

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