-
1
-
-
0025077481
-
Redox regulation of fos and jun DNA-binding activity in vitro
-
Abate C, Patel L, Rauscher FJ 3rd, and Curran T (1990) Redox regulation of fos and jun DNA-binding activity in vitro. Science 249:1157-1161.
-
(1990)
Science
, vol.249
, pp. 1157-1161
-
-
Abate, C.1
Patel, L.2
Rauscher III, F.J.3
Curran, T.4
-
2
-
-
33751178410
-
The thioredoxin system in cancer
-
DOI 10.1016/j.semcancer.2006.10.009, PII S1044579X06001027
-
Arnér ES and Holmgren A (2006) The thioredoxin system in cancer. Semin Cancer Biol 16:420-426. (Pubitemid 44780139)
-
(2006)
Seminars in Cancer Biology
, vol.16
, Issue.6
, pp. 420-426
-
-
Arner, E.S.J.1
Holmgren, A.2
-
3
-
-
0035425182
-
Thioredoxin peroxidase-1 (peroxiredoxin-1) is increased in thioredoxin-1 transfected cells and results in enhanced protection against apoptosis caused by hydrogen peroxide but not by other agents including dexamethasone, etoposide, and doxorubicin
-
DOI 10.1006/abbi.2001.2435
-
Berggren MI, Husbeck B, Samulitis B, Baker AF, Gallegos A, and Powis G (2001) Thioredoxin peroxidase-1 (peroxiredoxin-1) is increased in thioredoxin-1 transfected cells and results in enhanced protection against apoptosis caused by hydrogen peroxide but not by other agents including dexamethasone, etoposide, and doxorubicin. Arch Biochem Biophys 392:103-109. (Pubitemid 32725020)
-
(2001)
Archives of Biochemistry and Biophysics
, vol.392
, Issue.1
, pp. 103-109
-
-
Berggren, M.I.1
Husbeck, B.2
Samulitis, B.3
Baker, A.F.4
Gallegos, A.5
Powis, G.6
-
4
-
-
31044455445
-
Redox modifications of protein-thiols: Emerging roles in cell signaling
-
DOI 10.1016/j.bcp.2005.10.044, PII S0006295205007173
-
Biswas S, Chida AS, and Rahman I (2006) Redox modifications of protein-thiols: emerging roles in cell signaling. Biochem Pharmacol 71:551-564. (Pubitemid 43121989)
-
(2006)
Biochemical Pharmacology
, vol.71
, Issue.5
, pp. 551-564
-
-
Biswas, S.1
Chida, A.S.2
Rahman, I.3
-
5
-
-
33845357331
-
Thioredoxin reductase is required for the inactivation of tumor suppressor p53 and for apoptosis induced by endogenous electrophiles
-
DOI 10.1093/carcin/bgl111
-
Cassidy PB, Edes K, Nelson CC, Parsawar K, Fitzpatrick FA, and Moos PJ (2006) Thioredoxin reductase is required for the inactivation of tumor suppressor p53 and for apoptosis induced by endogenous electrophiles. Carcinogenesis 27:2538-2549. (Pubitemid 44884113)
-
(2006)
Carcinogenesis
, vol.27
, Issue.12
, pp. 2538-2549
-
-
Cassidy, P.B.1
Edes, K.2
Nelson, C.C.3
Parsawar, K.4
Fitzpatrick, F.A.5
Moos, P.J.6
-
6
-
-
63649115838
-
Crystal structure and catalysis of the selenoprotein thioredoxin reductase 1
-
Cheng Q, Sandalova T, Lindqvist Y, and Arnér ES (2009) Crystal structure and catalysis of the selenoprotein thioredoxin reductase 1. J Biol Chem 284:3998-4008.
-
(2009)
J Biol Chem
, vol.284
, pp. 3998-4008
-
-
Cheng, Q.1
Sandalova, T.2
Lindqvist, Y.3
Arnér, E.S.4
-
7
-
-
44949114211
-
Thioredoxin reductase inhibition by antitumor quinols: A quinol pharmacophore effect correlating to antiproliferative activity
-
DOI 10.1096/fj.07-101477
-
Chew EH, Lu J, Bradshaw TD, and Holmgren A (2008) Thioredoxin reductase inhibition by antitumor quinols: a quinol pharmacophore effect correlating to antiproliferative activity. FASEB J 22:2072-2083. (Pubitemid 351811483)
-
(2008)
FASEB Journal
, vol.22
, Issue.6
, pp. 2072-2083
-
-
Chew, E.-H.1
Lu, J.2
Bradshaw, T.D.3
Holmgren, A.4
-
8
-
-
36148970403
-
Synthesis and evaluation of 3-aryloxymethyl-1,2-dimethylindole-4,7-diones as mechanism-based inhibitors of NAD(P)H:quinone oxidoreductase 1 (NQO1) activity
-
DOI 10.1021/jm070396q
-
Colucci MA, Reigan P, Siegel D, Chilloux A, Ross D, and Moody CJ (2007) Synthesis and evaluation of 3-aryloxymethyl-1,2-dimethylindole-4,7-diones as mechanism-based inhibitors of NAD(P)H:quinone oxidoreductase 1 (NQO1) activity. J Med Chem 50:5780-5789. (Pubitemid 350106033)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.23
, pp. 5780-5789
-
-
Colucci, M.A.1
Reigan, P.2
Siegel, D.3
Chilloux, A.4
Ross, D.5
Moody, C.J.6
-
9
-
-
0024421652
-
Human transcription factor IIIC (TFIIIC). Purification, polypeptide structure, and the involvement of thiol groups in specific DNA binding
-
Cromlish JA and Roeder RG (1989) Human transcription factor IIIC (TFIIIC). Purification, polypeptide structure, and the involvement of thiol groups in specific DNA binding. J Biol Chem 264:18100-18109. (Pubitemid 19279280)
-
(1989)
Journal of Biological Chemistry
, vol.264
, Issue.30
, pp. 18100-18109
-
-
Cromlish, J.A.1
Roeder, R.G.2
-
10
-
-
0035968287
-
Novel role for JNK as a stress-activated Bcl2 kinase
-
Deng X, Xiao L, Lang W, Gao F, Ruvolo P, and May WS Jr (2001) Novel role for JNK as a stress-activated Bcl2 kinase. J Biol Chem 276:23681-23688.
-
(2001)
J Biol Chem
, vol.276
, pp. 23681-23688
-
-
Deng, X.1
Xiao, L.2
Lang, W.3
Gao, F.4
Ruvolo, P.5
May Jr., W.S.6
-
11
-
-
21644477778
-
Thioredoxin reductase is irreversibly modified by curcumin: A novel molecular mechanism for its anticancer activity
-
DOI 10.1074/jbc.M414645200
-
Fang J, Lu J, and Holmgren A (2005) Thioredoxin reductase is irreversibly modified by curcumin: a novel molecular mechanism for its anticancer activity. J Biol Chem 280:25284-25290. (Pubitemid 40934623)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.26
, pp. 25284-25290
-
-
Fang, J.1
Lu, J.2
Holmgren, A.3
-
12
-
-
78650364895
-
ASK1-P38 pathway is important for anoikis induced by microtubule- targeting aryl chloroethylureas
-
Fortin J, Patenaude A, Deschesnes RG, Côté MF, Petitclerc E, and C-Gaudreault R (2010) ASK1-P38 pathway is important for anoikis induced by microtubule-targeting aryl chloroethylureas. J Pharm Pharm Sci 13:175-190.
-
(2010)
J Pharm Pharm Sci
, vol.13
, pp. 175-190
-
-
Fortin, J.1
Patenaude, A.2
Deschesnes, R.G.3
Côté, M.F.4
Petitclerc, E.A.C.-G.R.5
-
13
-
-
0026773434
-
Identification of novel reduced pyridinium derivatives as synthetic co-factors for the enzyme DT diaphorase (NAD(P)H dehydrogenase (quinone), EC 1.6.99.2)
-
Friedlos F, Jarman M, Davies LC, Boland MP, and Knox RJ (1992) Identification of novel reduced pyridinium derivatives as synthetic co-factors for the enzyme DT diaphorase (NAD(P)H dehydrogenase (quinone), EC 1.6.99.2). Biochem Pharmacol 44:25-31.
-
(1992)
Biochem Pharmacol
, vol.44
, pp. 25-31
-
-
Friedlos, F.1
Jarman, M.2
Davies, L.C.3
Boland, M.P.4
Knox, R.J.5
-
14
-
-
0021078605
-
Evidence that the endogenous heat-stable glucocorticoid receptor-activating factor is thioredoxin
-
Grippo JF, Tienrungroj W, Dahmer MK, Housley PR, and Pratt WB (1983) Evidence that the endogenous heat-stable glucocorticoid receptor-activating factor is thioredoxin. J Biol Chem 258:13658-13664. (Pubitemid 14212006)
-
(1983)
Journal of Biological Chemistry
, vol.258
, Issue.22
, pp. 13658-13664
-
-
Grippo, J.F.1
Tienrungroj, W.2
Dahmer, M.K.3
-
15
-
-
0032493647
-
Human placenta thioredoxin reductase. Isolation of the selenoenzyme, steady state kinetics, and inhibition by therapeutic gold compounds
-
DOI 10.1074/jbc.273.32.20096
-
Gromer S, Arscott LD, Williams CH Jr, Schirmer RH, and Becker K (1998) Human placenta thioredoxin reductase. Isolation of the selenoenzyme, steady state kinetics, and inhibition by therapeutic gold compounds. J Biol Chem 273:20096-20101. (Pubitemid 28377564)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.32
, pp. 20096-20101
-
-
Gromer, S.1
Arscott, L.D.2
Williams Jr., C.H.3
Schirmeri, R.H.4
Becker, K.5
-
16
-
-
0030873554
-
The 58 kDa mouse selenoprotein is a BCNU-sensitive thioredoxin reductase
-
DOI 10.1016/S0014-5793(97)00816-8, PII S0014579397008168
-
Gromer S, Schirmer RH, and Becker K (1997) The 58 kDa mouse selenoprotein is a BCNU-sensitive thioredoxin reductase. FEBS Lett 412:318-320. (Pubitemid 27321274)
-
(1997)
FEBS Letters
, vol.412
, Issue.2
, pp. 318-320
-
-
Gromer, S.1
Schirmer, R.H.2
Becker, K.3
-
17
-
-
71349086917
-
PIM1 phosphorylates and negatively regulates ASK1-mediated apoptosis
-
Gu JJ, Wang Z, Reeves R, and Magnuson NS (2009) PIM1 phosphorylates and negatively regulates ASK1-mediated apoptosis. Oncogene 28:4261-4271.
-
(2009)
Oncogene
, vol.28
, pp. 4261-4271
-
-
Gu, J.J.1
Wang, Z.2
Reeves, R.3
Magnuson, N.S.4
-
18
-
-
14444281569
-
Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways
-
DOI 10.1126/science.275.5296.90
-
Ichijo H, Nishida E, Irie K, ten Dijke P, Saitoh M, Moriguchi T, Takagi M, Matsumoto K, Miyazono K, and Gotoh Y (1997) Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways. Science 275:90-94. (Pubitemid 27020316)
-
(1997)
Science
, vol.275
, Issue.5296
, pp. 90-94
-
-
Ichijo, H.1
Nishida, E.2
Irie, K.3
Ten, D.P.4
Saitoh, M.5
Moriguchi, T.6
Takagi, M.7
Matsumoto, K.8
Miyazono, K.9
Gotoh, Y.10
-
19
-
-
55149107716
-
Radical-free biology of oxidative stress
-
Jones DP (2008) Radical-free biology of oxidative stress. Am J Physiol Cell Physiol 295:C849-C868.
-
(2008)
Am J Physiol Cell Physiol
, vol.295
-
-
Jones, D.P.1
-
20
-
-
0035133227
-
Akt phosphorylates and negatively regulates apoptosis signal-regulating kinase 1
-
DOI 10.1128/MCB.21.3.893-901.2001
-
Kim AH, Khursigara G, Sun X, Franke TF, and Chao MV (2001) Akt phosphorylates and negatively regulates apoptosis signal-regulating kinase 1. Mol Cell Biol 21: 893-901. (Pubitemid 32104737)
-
(2001)
Molecular and Cellular Biology
, vol.21
, Issue.3
, pp. 893-901
-
-
Kim, A.H.1
Khursigara, G.2
Sun, X.3
Franke, T.F.4
Chao, M.V.5
-
21
-
-
78651146370
-
Enzymatic synthesis of deoxyribonucleotides. IV. Isolation and characterization of thioredoxin, the hydrogen donor from Escherichia coli b
-
Laurent TC, Moore EC, and Reichard P (1964) Enzymatic synthesis of deoxyribonucleotides. IV. Isolation and characterization of thioredoxin, the hydrogen donor from Escherichia coli b. J Biol Chem 239:3436-3444.
-
(1964)
J Biol Chem
, vol.239
, pp. 3436-3444
-
-
Laurent, T.C.1
Moore, E.C.2
Reichard, P.3
-
22
-
-
30344473340
-
Seizure-induced changes in mitochondrial redox status
-
Liang LP and PatelM(2006) Seizure-induced changes in mitochondrial redox status. Free Radic Biol Med 40:316-322.
-
(2006)
Free Radic Biol Med
, vol.40
, pp. 316-322
-
-
Liang, L.P.1
Patel, M.2
-
25
-
-
0026715172
-
Thioredoxin regulates the DNA binding activity of NF-kappa B by reduction of a disulphide bond involving cysteine 62
-
Matthews JR, Wakasugi N, Virelizier JL, Yodoi J, and Hay RT (1992) Thioredoxin regulates the DNA binding activity of NF-kappa B by reduction of a disulphide bond involving cysteine 62. Nucleic Acids Res 20:3821-3830.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 3821-3830
-
-
Matthews, J.R.1
Wakasugi, N.2
Virelizier, J.L.3
Yodoi, J.4
Hay, R.T.5
-
26
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 65:55-63.
-
(1983)
J Immunol Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
-
27
-
-
0032080238
-
Mammalian thioredoxin reductase is irreversibly inhibited by dinitrohalobenzenes by alkylation of both the redox active selenocysteine and its neighboring cysteine residue
-
DOI 10.1074/jbc.273.18.10835
-
Nordberg J, Zhong L, Holmgren A, and Arnér ES (1998) Mammalian thioredoxin reductase is irreversibly inhibited by dinitrohalobenzenes by alkylation of both the redox active selenocysteine and its neighboring cysteine residue. J Biol Chem 273:10835-10842. (Pubitemid 28204917)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.18
, pp. 10835-10842
-
-
Nordberg, J.1
Zhong, L.2
Holmgren, A.3
Arner, E.S.J.4
-
28
-
-
0035577760
-
2-terminal kinase/p38 mitogen-activated protein kinases
-
Ortiz MA, Lopez-Hernandez FJ, Bayon Y, Pfahl M, and Piedrafita FJ (2001) Retinoid-related molecules induce cytochrome c release and apoptosis through activation of c-Jun NH(2)-terminal kinase/p38 mitogen-activated protein kinases. Cancer Res 61:8504-8512. (Pubitemid 33131132)
-
(2001)
Cancer Research
, vol.61
, Issue.23
, pp. 8504-8512
-
-
Ortiz, M.A.1
Lopez-Hernandez, F.J.2
Bayon, Y.3
Pfahl, M.4
Piedrafita, F.J.5
-
29
-
-
0023547926
-
Metabolism and reactions of quinoid anticancer agents
-
Powis G (1987) Metabolism and reactions of quinoid anticancer agents. Pharmacol Ther 35:57-162.
-
(1987)
Pharmacol Ther
, vol.35
, pp. 57-162
-
-
Powis, G.1
-
30
-
-
33645466124
-
Molecular pharmacology and antitumor activity of palmarumycin-based inhibitors of thioredoxin reductase
-
Powis G, Wipf P, Lynch SM, Birmingham A, and Kirkpatrick DL (2006) Molecular pharmacology and antitumor activity of palmarumycin-based inhibitors of thioredoxin reductase. Mol Cancer Ther 5:630-636.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 630-636
-
-
Powis, G.1
Wipf, P.2
Lynch, S.M.3
Birmingham, A.4
Kirkpatrick, D.L.5
-
31
-
-
0031584269
-
The crystal structure of seleno-glutathione peroxidase from human plasma at 2.9 A resolution
-
DOI 10.1006/jmbi.1997.1005
-
Ren B, Huang W, Akesson B, and Ladenstein R (1997) The crystal structure of seleno-glutathione peroxidase from human plasma at 2.9 A resolution. J Mol Biol 268:869-885. (Pubitemid 27229170)
-
(1997)
Journal of Molecular Biology
, vol.268
, Issue.5
, pp. 869-885
-
-
Ren, B.1
Huang, W.2
Akesson, B.3
Ladenstein, R.4
-
32
-
-
0032080283
-
Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1
-
DOI 10.1093/emboj/17.9.2596
-
Saitoh M, Nishitoh H, Fujii M, Takeda K, Tobiume K, Sawada Y, Kawabata M, Miyazono K, and Ichijo H (1998) Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1. EMBO J 17:2596-2606. (Pubitemid 28221195)
-
(1998)
EMBO Journal
, vol.17
, Issue.9
, pp. 2596-2606
-
-
Saitoh, M.1
Nishitoh, H.2
Fujii, M.3
Takeda, K.4
Tobiume, K.5
Sawada, Y.6
Kawabata, M.7
Miyazono, K.8
Ichijo, H.9
-
33
-
-
0035859927
-
Three-dimensional structure of a mammalian thioredoxin reductase: Implications for mechanism and evolution of a selenocysteine-dependent enzyme
-
DOI 10.1073/pnas.171178698
-
Sandalova T, Zhong L, Lindqvist Y, Holmgren A, and Schneider G (2001) Three-dimensional structure of a mammalian thioredoxin reductase: implications for mechanism and evolution of a selenocysteine-dependent enzyme. Proc Natl Acad Sci USA 98:9533-9538. (Pubitemid 32769338)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.17
, pp. 9533-9538
-
-
Sandalova, T.1
Zhong, L.2
Lindqvist, Y.3
Holmgren, A.4
Schneider, G.5
-
34
-
-
0014428865
-
Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent
-
Sedlak J and Lindsay RH (1968) Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem 25:192-205.
-
(1968)
Anal Biochem
, vol.25
, pp. 192-205
-
-
Sedlak, J.1
Lindsay, R.H.2
-
35
-
-
54249105017
-
The thioredoxin system mediates redox-induced cell death in human colon cancer cells: Implications for the mechanism of action of anticancer agents
-
Sun Y and Rigas B (2008) The thioredoxin system mediates redox-induced cell death in human colon cancer cells: implications for the mechanism of action of anticancer agents. Cancer Res 68:8269-8277.
-
(2008)
Cancer Res
, vol.68
, pp. 8269-8277
-
-
Sun, Y.1
Rigas, B.2
-
36
-
-
0033544915
-
Thioredoxin-dependent redox regulation of p53-mediated p21 activation
-
Ueno M, Masutani H, Arai RJ, Yamauchi A, Hirota K, Sakai T, Inamoto T, Yamaoka Y, Yodoi J, and Nikaido T (1999) Thioredoxin-dependent redox regulation of p53-mediated p21 activation. J Biol Chem 274:35809-35815. (Pubitemid 129512885)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.50
, pp. 35809-35815
-
-
Ueno, M.1
Masutani, H.2
Arai, R.J.3
Yamauchi, A.4
Hirota, K.5
Sakai, T.6
Inamoto, T.7
Yamaoka, Y.8
Yodoi, J.9
Nikaido, T.10
-
37
-
-
33751181030
-
On the potential of thioredoxin reductase inhibitors for cancer therapy
-
DOI 10.1016/j.semcancer.2006.09.004, PII S1044579X06000927
-
Urig S and Becker K (2006) On the potential of thioredoxin reductase inhibitors for cancer therapy. Semin Cancer Biol 16:452-465. (Pubitemid 44780136)
-
(2006)
Seminars in Cancer Biology
, vol.16
, Issue.6
, pp. 452-465
-
-
Urig, S.1
Becker, K.2
-
38
-
-
33845914554
-
Cyclophosphamide as a potent inhibitor of tumor thioredoxin reductase in vivo
-
DOI 10.1016/j.taap.2006.10.029, PII S0041008X06004091
-
Wang X, Zhang J, and Xu T (2007) Cyclophosphamide as a potent inhibitor of tumor thioredoxin reductase in vivo. Toxicol Appl Pharmacol 218:88-95. (Pubitemid 46026846)
-
(2007)
Toxicology and Applied Pharmacology
, vol.218
, Issue.1
, pp. 88-95
-
-
Wang, X.1
Zhang, J.2
Xu, T.3
-
39
-
-
2942700238
-
Natural product based inhibitors of the thioredoxin-thioredoxin reductase system
-
Wipf P, Lynch SM, Birmingham A, Tamayo G, Jiménez A, Campos N, and Powis G (2004) Natural product based inhibitors of the thioredoxin-thioredoxin reductase system. Org Biomol Chem 2:1651-1658.
-
(2004)
Org Biomol Chem
, vol.2
, pp. 1651-1658
-
-
Wipf, P.1
Lynch, S.M.2
Birmingham, A.3
Tamayo, G.4
Jiménez, A.5
Campos, N.6
Powis, G.7
-
40
-
-
23444435104
-
Inhibition of thioredoxin reductase but not of glutathione reductase by the major classes of alkylating and platinum-containing anticancer compounds
-
Witte AB, Anestål K, Jerremalm E, Ehrsson H, and Arnér ES (2005) Inhibition of thioredoxin reductase but not of glutathione reductase by the major classes of alkylating and platinum-containing anticancer compounds. Free Radic Biol Med 39:696-703.
-
(2005)
Free Radic Biol Med
, vol.39
, pp. 696-703
-
-
Witte, A.B.1
Anestål, K.2
Jerremalm, E.3
Ehrsson, H.4
Arnér, E.S.5
-
41
-
-
57349135857
-
Dissecting the role of multiple reductases in bioactivation and cytotoxicity of the antitumor agent 2,5-diaziridinyl-3-(hydroxymethyl)-6-methyl- 1,4-benzoquinone (RH1)
-
Yan C, Kepa JK, Siegel D, Stratford IJ, and Ross D (2008) Dissecting the role of multiple reductases in bioactivation and cytotoxicity of the antitumor agent 2,5-diaziridinyl-3-(hydroxymethyl)-6-methyl-1,4-benzoquinone (RH1). Mol Pharmacol 74:1657-1665.
-
(2008)
Mol Pharmacol
, vol.74
, pp. 1657-1665
-
-
Yan, C.1
Kepa, J.K.2
Siegel, D.3
Stratford, I.J.4
Ross, D.5
-
42
-
-
67649847825
-
Potent activity of indolequinones against human pancreatic cancer: Identification of thioredoxin reductase as a potential target
-
Yan C, Shieh B, Reigan P, Zhang Z, Colucci MA, Chilloux A, Newsome JJ, Siegel D, Chan D, Moody CJ, et al. (2009) Potent activity of indolequinones against human pancreatic cancer: identification of thioredoxin reductase as a potential target. Mol Pharmacol 76:163-172.
-
(2009)
Mol Pharmacol
, vol.76
, pp. 163-172
-
-
Yan, C.1
Shieh, B.2
Reigan, P.3
Zhang, Z.4
Colucci, M.A.5
Chilloux, A.6
Newsome, J.J.7
Siegel, D.8
Chan, D.9
Moody, C.J.10
-
43
-
-
77952687350
-
ASK1-JNK signaling cascade mediates Ad-ST13-induced apoptosis in colorectal HCT116 cells
-
Yang M, Yu M, Guan D, Gu J, Cao X, Wang W, Zheng S, Xu Y, Shen Z, and Liu X (2010) ASK1-JNK signaling cascade mediates Ad-ST13-induced apoptosis in colorectal HCT116 cells. J Cell Biochem 110:581-588.
-
(2010)
J Cell Biochem
, vol.110
, pp. 581-588
-
-
Yang, M.1
Yu, M.2
Guan, D.3
Gu, J.4
Cao, X.5
Wang, W.6
Zheng, S.7
Xu, Y.8
Shen, Z.9
Liu, X.10
-
44
-
-
0034714334
-
P38 mitogen-activated protein kinase mediates bid cleavage, mitochondrial dysfunction, and caspase-3 activation during apoptosis induced by singlet oxygen but not by hydrogen peroxide
-
Zhuang S, Demirs JT, and Kochevar IE (2000) p38 mitogen-activated protein kinase mediates bid cleavage, mitochondrial dysfunction, and caspase-3 activation during apoptosis induced by singlet oxygen but not by hydrogen peroxide. J Biol Chem 275:25939-25948.
-
(2000)
J Biol Chem
, vol.275
, pp. 25939-25948
-
-
Zhuang, S.1
Demirs, J.T.2
Kochevar, I.E.3
|