ライフサイエンスコーパス: heat-shock protein 60

1 ssion of glial fibrillary acidic protein and heat shock protein 60.

2 ial virus fusion (F) protein, and chlamydial heat shock protein 60.

3 rferon and interleukin-10 in the efficacy of heat shock protein 60.

4 a component of human peripheral nerve axon, heat shock protein 60.

5 entical, to an intracellular stress protein, heat shock protein 60.

6 N)-gamma, CXCL9, Perforin 1, Granzyme B, and heat shock protein 60.

7 ns, translation elongation factor-1alpha and heat-shock protein 60.

8 (30)); MSH2 (MutShomolog 2) and HSP60 (heat-shock protein 60)(24); ULBP4 (UL16-binding protein

9 ccupying the surface presented LAP receptor, heat shock protein 60 and ameliorates the Lm-induced int

10 upregulating the cell surface expression of heat shock protein 60 and heat shock protein 90, as well

11 ss-reacted with a peptide derived from mouse heat shock protein 60 and recognized stressed macrophage

12 cturally unrelated TLR4 agonists, chlamydial heat shock protein 60 and RSV F protein, with the double

13 d protein response (reduced concentration of heat shock proteins 60 and 70).

14 autoantigens glutamic acid decarboxylase 65, heat shock protein 60, and tyrosine phosphatase (IL-5, I

15 ns (glutamic acid decarboxylase 65, insulin, heat shock protein 60, and tyrosine phosphatase).

16 se to the atherosclerosis-associated antigen heat shock protein-60, and a change in T-dependent isoty

17 d (N), but lacking elongation factor-1alpha, heat-shock protein 60, and guanylyltransferase.

18 ion induced autoantibodies against dsDNA and heat shock protein 60 as well as antibody accumulation i

19 acid dehydrogenase (psi LDH) from mouse, and heat shock protein 60 chaperonin (psi HSP60) from Chines

20 entary body (EB) and 3 genotypically variant heat shock protein 60 (CHSP60) antigens using peripheral

21 Chlamydial heat shock protein 60 (cHSP60) has been implicated in th

22 Antibodies to chlamydial heat shock protein 60 (cHSP60) have been associated with

23 and ELISA antibody to recombinant chlamydial heat-shock protein 60 (Chsp60) determined.

24 esponse (mtUPR) as measured by expression of heat shock protein 60, Clp protease, and Lon peptidase 1

25 Heat shock protein 60 derived from Chlamydia pneumoniae

26 we report the isolation and sequencing of a heat shock protein 60-derived peptide (GMKFDRGYI) from Q

27 n protein (LAP) with the host cell receptor (heat shock protein 60) disrupts the epithelial barrier,

28 L-17A, GM-CSF, and CCL2 in response to human heat shock protein 60, easily discriminated the early RA

29 interleukin-10-deficient mice immunized with heat shock protein 60 failed to confer protection in T-c

30 0735 altered cortical expression of multiple heat shock protein 60 forms along with neurofilaments an

31 Immunization of mice with heat shock protein 60 from Histoplasma capsulatum or a p

32 amined TCR usage to a protective fragment of heat shock protein 60 from the fungus, Histoplasma capsu

33 responding to the protective domain (F3) of heat-shock protein 60 from Histoplasma capsulatum.

34 70 (DmaK from Escherichia coli) but not with heat shock protein 60 (GroEL) or heat shock protein 10 (

35 Heat shock proteins 60 (GroEL) are highly expressed esse

36 rix metalloproteinase-9 and upregulated C1q, heat shock protein 60, heat shock protein 70, CCR2, and

37 interacted with MHC class I-presenting human heat shock protein 60 (hHSP60) inducing cytotoxicity.

38 alovirus (HCMV), Chlamydia pneumoniae, human heat-shock protein 60 (hHSP60), or oxidized LDL (ox-LDL)

39 Chlamydiae produce large amounts of heat shock protein 60 (HSP 60) during chronic, persisten

40 tion of major outer membrane protein (MOMP), heat shock protein 60 (Hsp-60/GroEL), and proteins with

41 Both chlamydial and human heat shock protein 60s (HSP 60), which colocalize in hum

42 Heat shock protein 60 (HSP60) and HSP70 (DnaK) are two m

43 e established a positive association of anti-heat shock protein 60 (HSP60) autoantibodies and the pre

44 Here, we show that the molecular chaperone heat shock protein 60 (Hsp60) directly associates with c

45 Vaccination with heat shock protein 60 (Hsp60) from Histoplasma capsulatu

46 cence studies showed increased expression of heat shock protein 60 (Hsp60) in influenza virus- but no

47 The stress protein heat shock protein 60 (Hsp60) induces secretion of proin

48 Heat shock protein 60 (Hsp60) is a chaperone localizing

49 The human mitochondrial heat shock protein 60 (hsp60) is a tetradecameric chaper

50 Heat shock protein 60 (hsp60) is constitutively expresse

51 t mice that had been immunized with purified heat shock protein 60 (Hsp60) isolated from Francisella

52 eptide-1 ring complex (TRiC) is a eukaryotic heat shock protein 60 (hsp60) molecule that has been sho

53 is showed that this antigenic fraction was a heat shock protein 60 (HSP60) of Strongyloides sp. The s

54 inhibition of the main chaperone of UPR(mt) heat shock protein 60 (HSP60) reduced neuroendocrine pro

55 Heat shock protein 60 (Hsp60), a eukaryotic mitochondria

56 h to identify binding partners and show that heat shock protein 60 (HSP60), a molecular chaperone loc

57 a suitable model for its eukaryotic homolog, heat shock protein 60 (Hsp60), due to the high number of

58 78 kDa glucose-regulated protein precursor, heat shock protein 60 (HSP60), HSP70, and HSP27 were als

59 receptor gamma coactivator 1 alpha (PGC1a), heat shock protein 60 (Hsp60), interleukin 6 (IL-6) expr

60 sional antigens, including oxidized LDLs and heat shock protein 60 (HSP60), may promote lesion develo

61 t database search identified this protein as heat shock protein 60 (Hsp60).

62 ngle 60-kDa protein, which was identified as heat shock protein 60 (hsp60).

63 identified by N-terminal microsequencing as heat shock protein 60 (Hsp60).

64 t (immunoblot) analysis to be the chlamydial heat shock protein 60 (hsp60).

65 F-kappaB) signaling activation by binding to heat shock protein 60 (HSP60).

66 show that the 2 key components of the UPRmt, heat shock protein 60 (HSP60, a mitochondrial chaperonin

67 al administration of a modulatory APL of the heat-shock protein 60 (Hsp60) 180-188 T cell epitope, al

68 Here, we show that heat-shock protein 60 (hsp60) is required for blastema f

69 ceraldehyde-3-phosate dehydrogenase (G3PDH), heat-shock protein 60 (HSP60), DNA-dependent RNA polymer

70 nous ligands (cellular fibronectin [cFN] and heat shock protein 60 [HSP60]) in patients with and with

71 In primary placental fibroblasts, chlamydial heat shock protein 60-induced apoptosis was caspase depe

72 this study, we show that in vitro chlamydial heat shock protein 60 induces apoptosis in primary human

73 Mitochondrial chaperonin Heat Shock Protein 60 kDa (Hsp60) oversees the correct f

74 synthesis was associated with an increase in heat shock protein 60 levels, which may be an additional

75 Anti-heat shock protein 60 mAb had no protective effect.

76 s study, we demonstrate that M. tuberculosis heat shock protein 60 (Mtbhsp60, Cpn60.1, and Rv3417c) i

77 suggested for E. histolytica genes encoding heat shock protein 60, nicotinamide nucleotide transhydr

78 this study, we found that the GroEL protein (heat shock protein 60) of Mycoplasma gallisepticum could

79 ison as the major outer membrane protein and heat shock protein 60 paradigm.

80 A Qa-1-restricted CTL clone recognizes this heat shock protein 60 peptide, further verifying that it

81 Neutralizing antiserum to heat shock protein 60 produced neuronal cell death that

82 hat commercially available recombinant human heat shock protein 60 (rhHSP60) could induce tumor necro

83 Immunization with recombinant heat shock protein 60 (rHsp60) from Histoplasma capsulat

84 Recombinant urease (rURE) and recombinant heat shock protein 60 (rHSP60) of C. immitis were expres

85 2B11, that has been described as targeting a heat shock protein 60 (RiHSP60).

86 The levels of serum S. japonicum heat shock protein 60 (SjHSP60)-specific IgG and its sub

87 lear cells (PBMCs) stimulated with chlamydia heat-shock protein 60 strongly correlated with protectio

88 r chlamydial major outer membrane protein or heat shock protein 60, suggesting that CPAF is both prod

89 NOD mice and the lack of anti-GAD65 and anti-heat shock protein 60 T cell responses in these mice.

90 Heat shock protein 60 was the only antigen shown to indu

91 mononuclear cells in response to chlamydial heat-shock protein 60 was associated with low risk of in

92 P. aeruginosa GroEL, a homolog of heat shock protein 60, was identified as one of the fact