ライフサイエンスコーパス: cytoglobin

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1 ectral properties similar to neuroglobin and cytoglobin.

2 dyl ligated globins, such as neuroglobin and cytoglobin.

3 and up to 50-fold higher than neuroglobin or cytoglobin.

4 Fe bonds in paramagnetic, S = 1/2, human met-cytoglobin.

5 paired in mice deficient for skeletal-muscle cytoglobin.

6 e neuroglobins, alpha- and beta-globins, and cytoglobins.

7 The CYGB gene encodes cytoglobin, a member of the globin protein family, which

8 onstrated an age-related increase in only 2 (cytoglobin and GPX-1) of 11 proteins tested.

9 ) are also found in animals (neuroglobin and cytoglobin) and some cyanobacteria, where they are thoug

10 oordinate hemoglobins, human neuroglobin and cytoglobin, and Synechocystis hemoglobin.

11 hemoglobins, including human neuroglobin and cytoglobin, and those from Synechocystis and rice, are c

12 Neuroglobin (Ngb) and Cytoglobin (Cygb) are new members of the globin family a

13 Cytoglobin (Cygb) is a recently discovered cytoplasmic h

14 Cytoglobin (Cygb) is a recently discovered globin expres

15 Cytoglobin (CYGB) is a recently discovered vertebrate gl

16 Cytoglobin (CYGB) is frequently downregulated in many ty

17 nt studies suggest that the mammalian globin cytoglobin (CYGB) regulates nitric oxide (NO) metabolism

18 While cytoglobin (Cygb) was discovered a decade ago, its physi

19 Cytoglobin (Cygb) was investigated for its capacity to f

20 gen-binding molecules, neuroglobin (Ngb) and cytoglobin (Cygb), in mammalian retinas and to determine

21 The expression of neuroglobin (Ngb) and cytoglobin (Cygb), two recently discovered globins with

22 One candidate tumour-suppressor gene is cytoglobin (CYGB), which is contained entirely within th

23 Neuroglobin and cytoglobin display dramatic biphasic time courses for CO

24 n the adult heart and in response to hypoxia cytoglobin expression is markedly up-regulated within th

25 siRNA-mediated depletion of cytoglobin from C2C12 myoblasts increased levels of reac

26 We now show that cytoglobin gene expression in oesophageal biopsies from

27 of the 5' upstream regulatory region of the cytoglobin gene.

28 re located within the upstream region of the cytoglobin gene.

29 unknown but, like hemoglobin, myoglobin, and cytoglobin/histoglobin, it may transport O(2), detoxify

30 our main clades: (i) cyclostome hemoglobin + cytoglobin, (ii) myoglobin + globin E, (iii) globin Y, a

31 muscle were generated to examine the role of cytoglobin in vivo.

32 Cytoglobin is a hemoprotein expressed in response to oxi

33 In the present study, we demonstrate that cytoglobin is a stress-responsive hemoprotein in the hyp

34 In this study, we demonstrate that cytoglobin is up-regulated in activated myogenic progeni

35 ependent transcription factors suggests that cytoglobin may have a functional role in calcium-depende

36 ase in Hba-a2 and Hbb but not neuroglobin or cytoglobin mRNA in transcriptome analyses of nigral dopa

37 ity of NFAT and AP-1 to bind to the putative cytoglobin promoter, especially under hypoxic conditions

38 lobins of cyclostomes are orthologous to the cytoglobin protein of gnathostome vertebrates, a hexacoo

39 Conversely, overexpression of cytoglobin reduced reactive oxygen species levels, caspa

40 Collectively, these data demonstrate that cytoglobin serves an important role in muscle repair and

41 for ligand binding in human neuroglobin and cytoglobin than in the plant hexacoordinate hemoglobins.

42 ism similar to that of human neuroglobin and cytoglobin: the destabilization of one of two heme-ligat

43 and/or AP-1 activities decreases endogenous cytoglobin transcript and protein levels.

44 The cytoglobin transcript level is abundantly expressed in t

45 Thus, the regulation of cytoglobin transcription by calcineurin-dependent transc

46 nstrated that calcineurin activity modulates cytoglobin transcription.

47 Mice in which cytoglobin was knocked out specifically in skeletal musc

48 ular mechanism resulting in the induction of cytoglobin, we undertook a transcriptional analysis of t

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