메뉴 건너뛰기




Volumn 52, Issue 20, 2009, Pages 6474-6483

Structure mechanism insights and the role of nitric oxide donation guide the development of oxadiazole-2-oxides as therapeutic agents against schistosomiasis

Author keywords

[No Author keywords available]

Indexed keywords

ANTISCHISTOSOMAL AGENT; GLUTATHIONE REDUCTASE; NITRIC OXIDE; OXADIAZOLE 2 OXIDE DERIVATIVE; THIOREDOXIN GLUTATHIONE REDUCTASE; UNCLASSIFIED DRUG;

EID: 70350059120     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm901021k     Document Type: Article
Times cited : (73)

References (64)
  • 2
    • 33745436655 scopus 로고    scopus 로고
    • Schistosomiasis and water resources development: Systematic review, meta-analysis, and estimates of people at risk
    • Steinmann, P.; Keiser, J.; Bos, R.; Tanner, M.; Utzinger, J. Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect. Dis. 2006, 6, 411-425.
    • (2006) Lancet Infect. Dis. , vol.6 , pp. 411-425
    • Steinmann, P.1    Keiser, J.2    Bos, R.3    Tanner, M.4    Utzinger, J.5
  • 3
    • 0037847426 scopus 로고    scopus 로고
    • Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa
    • DOI 10.1016/S0001-706X(03)00029-9
    • van der Werf, M. J.; de Vlas, S. J.; Brooker, S.; Looman, C. W.; Nagelkerke, N. J.; Habbema, J. D.; Engels, D. Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa. Acta Trop. 2003, 86, 125-139. (Pubitemid 36561364)
    • (2003) Acta Tropica , vol.86 , Issue.2-3 , pp. 125-139
    • Van Der Werf, M.J.1    De Vlas, S.J.2    Brooker, S.3    Looman, C.W.N.4    Nagelkerke, N.J.D.5    Habbema, J.D.F.6    Engels, D.7
  • 4
    • 40349085389 scopus 로고    scopus 로고
    • The unacknowledged impact of chromic schistosomiasis
    • King, C. H.; Dangerfield-Cha, M. The unacknowledged impact of chromic schistosomiasis. Chronic Illness 2008, 4, 65-79.
    • (2008) Chronic Illness , vol.4 , pp. 65-79
    • King, C.H.1    Dangerfield-Cha, M.2
  • 5
    • 0017622884 scopus 로고
    • Praziquantel, a new broad spectrum antischistosomal agent
    • Gonnert, R.; Andrews, P. Praziquantel, a new broad spectrum antischistosomal agent. Z. Parasitenk. 1977, 52, 129-150.
    • (1977) Z. Parasitenk. , vol.52 , pp. 129-150
    • Gonnert, R.1    Andrews, P.2
  • 7
    • 33750508142 scopus 로고    scopus 로고
    • Schistosomiasis: Challenges for control, treatment and drug resistance
    • Fenwick, A.; Webster, J. P. Schistosomiasis: challenges for control, treatment and drug resistance. Curr. Opin. Infect. Dis. 2006, 19, 577-582.
    • (2006) Curr. Opin. Infect. Dis. , vol.19 , pp. 577-582
    • Fenwick, A.1    Webster, J.P.2
  • 8
    • 21644469993 scopus 로고    scopus 로고
    • 2+ channels targets of Praziquantel action?
    • 2+ channels targets of Praziquantel action? Int. J. Parasitol. 2004, 35, 1-9.
    • (2004) Int. J. Parasitol. , vol.35 , pp. 1-9
    • Greenberg, R.M.1
  • 10
    • 57049129327 scopus 로고    scopus 로고
    • Praziquantel: Mechanisms of action, resistance and new derivatives for schistosomiasis
    • Doenhoff, M. J.; Cioli, D.; Utzinger, J. Praziquantel: mechanisms of action, resistance and new derivatives for schistosomiasis. Curr. Opin. Infect. Dis. 2008, 21, 659-667.
    • (2008) Curr. Opin. Infect. Dis. , vol.21 , pp. 659-667
    • Doenhoff, M.J.1    Cioli, D.2    Utzinger, J.3
  • 11
  • 12
    • 33845428642 scopus 로고    scopus 로고
    • Thioredoxin and related molecules - from biology to health and disease
    • Lillig, C. H.; Holmgren, A. Thioredoxin and related molecules - from biology to health and disease. Antioxid. Redox Signaling 2007, 9, 25-47.
    • (2007) Antioxid. Redox Signaling , vol.9 , pp. 25-47
    • Lillig, C.H.1    Holmgren, A.2
  • 13
    • 0036710531 scopus 로고    scopus 로고
    • Molecular and enzymatic characterisation of Schistosoma mansoni thioredoxin
    • Alger, H. M.; Sayed, A. A.; Stadecker, M. J.; Williams, D. L. Molecular and enzymatic characterisation of Schistosoma mansoni thioredoxin. Int. J. Parasitol. 2002, 32, 1285-1292.
    • (2002) Int. J. Parasitol. , vol.32 , pp. 1285-1292
    • Alger, H.M.1    Sayed, A.A.2    Stadecker, M.J.3    Williams, D.L.4
  • 14
    • 47349121027 scopus 로고    scopus 로고
    • Glutathione reductase and thioredoxin reductase at the crossroad: The structure of Schistosoma mansoni thioredoxin glutathione reductase
    • DOI 10.1002/prot.21986
    • Angelucci, F.; Miele, A. E.; Boumis, G.; Dimastrogiovanni, D.; Brunori, M.; Bellelli, A. Glutathione reductase and thioredoxin reductase at the crossroad: the structure of Schistosoma mansoni thioredoxin glutathione reductase. Proteins 2008, 72, 936-945. (Pubitemid 352000871)
    • (2008) Proteins: Structure, Function and Genetics , vol.72 , Issue.3 , pp. 936-945
    • Angelucci, F.1    Miele, A.E.2    Boumis, G.3    Dimastrogiovanni, D.4    Brunori, M.5    Bellelli, A.6
  • 15
    • 34347264532 scopus 로고    scopus 로고
    • Thioredoxin glutathione reductase from Schistosoma mansoni: An essential parasite enzyme and a key drug target
    • DOI 10.1371/journal.pmed.0040206
    • Kuntz, A. N.; Davioud-Charvet, E.; Sayed, A. A.; Califf, L. L.; Dessolin, J.; Arnér, E. S.; Williams, D. L. Thioredoxin glutathione reductase from Schistosoma mansoni: an essential parasite enzyme and a key drug target. PLoS Med. 2007, 4, e206. (Pubitemid 46998624)
    • (2007) PLoS Medicine , vol.4 , Issue.6 , pp. 1071-1086
    • Kuntz, A.N.1    Davioud-Charvet, E.2    Sayed, A.A.3    Califf, L.L.4    Dessolin, J.5    Arner, E.S.J.6    Williams, D.L.7
  • 19
    • 33746789921 scopus 로고    scopus 로고
    • Quantitative high-throughput screening: A titration-based approach that efficiently identifies biological activities in large chemical libraries
    • Inglese, J.; Auld, D. S.; Jadhav, A.; Johnson, R. L.; Simeonov, A.; Yasgar, A.; Zheng, W.; Austin, C. P. Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries. Proc. Natl. Acad. Sci. U.S.A. 2006, 103, 11473-11478.
    • (2006) Proc. Natl. Acad. Sci. U.S.A. , vol.103 , pp. 11473-11478
    • Inglese, J.1    Auld, D.S.2    Jadhav, A.3    Johnson, R.L.4    Simeonov, A.5    Yasgar, A.6    Zheng, W.7    Austin, C.P.8
  • 20
  • 21
    • 33750531864 scopus 로고    scopus 로고
    • Innovative lead discovery strategies for tropical diseases
    • DOI 10.1038/nrd2144, PII NRD2144
    • Nwaka, S.; Hudson, A. Innovative lead discovery strategies for tropical diseases. Nature Rev. Drug Discovery 2006, 5, 941-955. (Pubitemid 44660607)
    • (2006) Nature Reviews Drug Discovery , vol.5 , Issue.11 , pp. 941-955
    • Nwaka, S.1    Hudson, A.2
  • 23
    • 84889770501 scopus 로고    scopus 로고
    • The NO-releasing heterocycles
    • Wang, G., Cai, T. B., Taniguchi, N., Eds.;Wiley-VCH: Weinheim, Germany
    • Gasco, A.; Schoenafinger, K. The NO-releasing heterocycles. In Nitric Oxide Nonors;Wang, G., Cai, T. B., Taniguchi, N., Eds.;Wiley-VCH: Weinheim, Germany, 2005.
    • (2005) Nitric Oxide Nonors
    • Gasco, A.1    Schoenafinger, K.2
  • 24
    • 38849162730 scopus 로고    scopus 로고
    • The nitrate-nitrite-nitric oxide pathway in physiology and therapeutics
    • Lundberg, J. O.; Weitzberg, E.; Gladwin, M. T. The nitrate-nitrite-nitric oxide pathway in physiology and therapeutics. Nature Rev. Drug Discovery 2008, 7, 156-167.
    • (2008) Nature Rev. Drug Discovery , vol.7 , pp. 156-167
    • Lundberg, J.O.1    Weitzberg, E.2    Gladwin, M.T.3
  • 27
    • 0028604328 scopus 로고
    • Furoxans as nitric oxide donors. 4-Phenyl-3-furoxan-carbonitrile: Thiol-mediated nitric oxide release and biological evaluation
    • Medana, C.; Ermondi, G.; Fruttero, R.; Di Stilo, A.; Ferretti, C.; Gasco, A. Furoxans as nitric oxide donors. 4-Phenyl-3-furoxan-carbonitrile: thiol-mediated nitric oxide release and biological evaluation. J. Med. Chem. 1994, 37, 4412-4416.
    • (1994) J. Med. Chem. , vol.37 , pp. 4412-4416
    • Medana, C.1    Ermondi, G.2    Fruttero, R.3    Di Stilo, A.4    Ferretti, C.5    Gasco, A.6
  • 29
    • 33745073063 scopus 로고    scopus 로고
    • Mechanism of action of novel NO-releasing furoxan derivatives of aspirin in human platelets
    • Turnbull, C. M.; Cena, C.; Fruttero, R.; Gasco, A.; Rossi, A. G.; Megson, I. L. Mechanism of action of novel NO-releasing furoxan derivatives of aspirin in human platelets. Br. J. Pharmacol. 2006, 148, 517-526.
    • (2006) Br. J. Pharmacol. , vol.148 , pp. 517-526
    • Turnbull, C.M.1    Cena, C.2    Fruttero, R.3    Gasco, A.4    Rossi, A.G.5    Megson, I.L.6
  • 31
    • 0034929425 scopus 로고    scopus 로고
    • Nitric oxide in parasitic infections
    • Brunet, L. R. Nitric oxide in parasitic infections. Int. Immunopharmacol. 2001, 1, 1457-1467.
    • (2001) Int. Immunopharmacol. , vol.1 , pp. 1457-1467
    • Brunet, L.R.1
  • 33
    • 33646233193 scopus 로고    scopus 로고
    • Nitric oxide: An antiparasitic molecule of invertebrates
    • Rivero, A. Nitric oxide: an antiparasitic molecule of invertebrates. Trends Parasitol. 2006, 22, 219-225.
    • (2006) Trends Parasitol. , vol.22 , pp. 219-225
    • Rivero, A.1
  • 34
    • 0024821351 scopus 로고
    • Macrophage cytotoxicity against schistosomula of Schistosoma mansoni involves arginine-dependent production of reactive nitrogen intermediates
    • James, S. L.; Glaven, J. Macrophage cytotoxicity against schistosomula of Schistosoma mansoni involves arginine-dependent production of reactive nitrogen intermediates. J. Immunol. 1989, 143, 4208-4212. (Pubitemid 20012616)
    • (1989) Journal of Immunology , vol.143 , Issue.12 , pp. 4208-4212
    • James, S.L.1    Glaven, J.2
  • 36
    • 34548511303 scopus 로고    scopus 로고
    • Tumor Necrosis Factor (TNF) Receptor-1 (TNFp55) Signal Transduction and Macrophage-Derived Soluble TNF are Crucial for Nitric Oxide-Mediated Trypansosoma congolense Parasite Killing
    • Magez, S.; Radwanska, M.; Drennan, M.; Fick, L.; Baral, T. N.; Allie, N.; Jacobs, M.; Nedospasov, S.; Brombacher, F.; Ryffel, B.; De Baetselier, P. Tumor Necrosis Factor (TNF) Receptor-1 (TNFp55) Signal Transduction and Macrophage-Derived Soluble TNF are Crucial for Nitric Oxide-Mediated Trypansosoma congolense Parasite Killing. J. Infect. Dis. 2007, 196, 954-962.
    • (2007) J. Infect. Dis. , vol.196 , pp. 954-962
    • Magez, S.1    Radwanska, M.2    Drennan, M.3    Fick, L.4    Baral, T.N.5    Allie, N.6    Jacobs, M.7    Nedospasov, S.8    Brombacher, F.9    Ryffel, B.10    De Baetselier, P.11
  • 37
    • 34548251838 scopus 로고    scopus 로고
    • Leishmania donovani: Inhibition of phagosomal maturation is rescued by nitric oxide in macrophages
    • Winberg, M. E.; Rasmusson, B.; Sundqvist, T. Leishmania donovani: inhibition of phagosomal maturation is rescued by nitric oxide in macrophages. Exp. Parasitol. 2007, 117, 165-170.
    • (2007) Exp. Parasitol. , vol.117 , pp. 165-170
    • Winberg, M.E.1    Rasmusson, B.2    Sundqvist, T.3
  • 40
    • 52949090075 scopus 로고    scopus 로고
    • Benznidazole and Chagas disease: Can an old drug be the answer to an old problem?
    • Mady, C.; Ianni, B. M.; de Souza, J. L., Jr. Benznidazole and Chagas disease: can an old drug be the answer to an old problem? Expert Opin. Investig. Drugs 2008, 17, 1427-1433.
    • (2008) Expert Opin. Investig. Drugs , vol.17 , pp. 1427-1433
    • Mady, C.1    Ianni, B.M.2    De Souza Jr., J.L.3
  • 43
    • 0027403233 scopus 로고
    • Antagonistic action of imidazolineoxyl N-oxides against endothelium- Derived relaxing factor/NO through a radical reaction
    • DOI 10.1021/bi00054a013
    • Akaike, T.; Yoshida, M.; Miyamoto, Y.; Sato, K.; Kohno, M.; Sasamoto, K.; Miyazaki, K.; Ueda, S.; Maeda, H. Antagonistic action of imidazolineoxyl N-Oxides against endothelium-derived relaxing factor/NO through a radical reaction. Biochemistry 1993, 32, 827-832. (Pubitemid 23059363)
    • (1993) Biochemistry , vol.32 , Issue.3 , pp. 827-832
    • Akaike, T.1    Yoshida, M.2    Miyamoto, Y.3    Sato, K.4    Kohno, M.5    Sasamoto, K.6    Miyazaki, K.7    Ueda, S.8    Maeda, H.9
  • 44
    • 60649115274 scopus 로고    scopus 로고
    • Synthesis of oxadiazole-2-oxide analogues as potential antischistosomal agents
    • Rai, G.; Thomas, C. J.; Leister, W.; Maloney, D. J. Synthesis of oxadiazole-2-oxide analogues as potential antischistosomal agents. Tetrahedron Lett. 2009, 50, 1710-1713.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1710-1713
    • Rai, G.1    Thomas, C.J.2    Leister, W.3    Maloney, D.J.4
  • 45
    • 0026632865 scopus 로고
    • Effect of nitric oxide production on the redox modulatory site of the NMDA receptor-channel complex
    • Lei, S. Z.; Pan, Z. H.; Aggarwal, S. K.; Chen, H. S.; Hartman, J.; Sucher, N. J.; Lipton, S. A. Effect of nitric oxide production on the redox modulatory site of the NMDA receptor-channel complex. Neuron 1992, 8, 1087-1099.
    • (1992) Neuron , vol.8 , pp. 1087-1099
    • Lei, S.Z.1    Pan, Z.H.2    Aggarwal, S.K.3    Chen, H.S.4    Hartman, J.5    Sucher, N.J.6    Lipton, S.A.7
  • 49
    • 0033026199 scopus 로고    scopus 로고
    • An antiviral mechanism of nitric oxide: Inhibition of a viral protease
    • DOI 10.1016/S1074-7613(00)80003-5
    • Saura, M.; Zaragoza, C.; McMillian, A.; Quick, R. A.; Hohenadl, C.; Lowenstein, J. M.; Lowenstein, C. J. An antiviral mechanism of nitric oxide: Inhibition of a viral protease. Immunity 1999, 10, 21-28. (Pubitemid 29077380)
    • (1999) Immunity , vol.10 , Issue.1 , pp. 21-28
    • Saura, M.1    Zaragoza, C.2    McMillan, A.3    Quick, R.A.4    Hohenadl, C.5    Lowenstein, J.M.6    Lowenstein, C.J.7
  • 50
    • 0033822494 scopus 로고    scopus 로고
    • S-Nitrosothiols as novel, reversible inhibitors of human rhinovirus 3C protease
    • Xian, M.; Wang, Q. M.; Chen, X.; Wang, K.; Wang, P. G. S-Nitrosothiols as novel, reversible inhibitors of human rhinovirus 3C protease. Bioorg. Med. Chem. Lett. 2000, 10, 2097-2100.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 2097-2100
    • Xian, M.1    Wang, Q.M.2    Chen, X.3    Wang, K.4    Wang, P.G.5
  • 51
    • 0035849715 scopus 로고    scopus 로고
    • The biotin switch method for the detection of S-nitrosylated proteins
    • Jaffrey, S. R.; Snyder, S. H. The biotin switch method for the detection of S-nitrosylated proteins. Sci. STKE 2001, 86, pl1.
    • (2001) Sci. STKE , vol.86
    • Jaffrey, S.R.1    Snyder, S.H.2
  • 52
    • 0036918081 scopus 로고    scopus 로고
    • Nitrosopeptide Mapping: A Novel Methodology Reverses S-nitrosylation of Dexras1 on a Single Cysteine Residue
    • Jaffrey, S. R.; Fang, M.; Snyder, S. H. Nitrosopeptide Mapping: A Novel Methodology Reverses S-nitrosylation of Dexras1 on a Single Cysteine Residue. Chem. Biol. 2002, 9, 1329-1335.
    • (2002) Chem. Biol. , vol.9 , pp. 1329-1335
    • Jaffrey, S.R.1    Fang, M.2    Snyder, S.H.3
  • 54
    • 33846640469 scopus 로고    scopus 로고
    • A generally applicable method for assessing the electrophilicity and reactivity of diverse nitrile-containing compounds
    • Oballa, R. M.; Truchon, J.-F.; Bayly, C. I.; Chauret, N.; Day, S.; Crane, S.; Berthelette, C. A generally applicable method for assessing the electrophilicity and reactivity of diverse nitrile-containing compounds. Bioorg. Med. Chem. Lett. 2007, 17, 998-1002.
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 998-1002
    • Oballa, R.M.1    Truchon, J.-F.2    Bayly, C.I.3    Chauret, N.4    Day, S.5    Crane, S.6    Berthelette, C.7
  • 55
    • 33947295086 scopus 로고
    • Homogeneous Chemiluminescent Measurement of Nitric Oxide with Ozone
    • Fontijn, A.; Sabadell, A. J.; Ronco, R. J. Homogeneous Chemiluminescent Measurement of Nitric Oxide with Ozone. Anal. Chem. 1970, 42, 575-579.
    • (1970) Anal. Chem. , vol.42 , pp. 575-579
    • Fontijn, A.1    Sabadell, A.J.2    Ronco, R.J.3
  • 57
    • 2942546160 scopus 로고    scopus 로고
    • The prokaryotic selenoproteome
    • Kryukov, G. V.; Gladyschev, V. N. The prokaryotic selenoproteome. EMBO Rep. 2004, 5, 538-543.
    • (2004) EMBO Rep. , vol.5 , pp. 538-543
    • Kryukov, G.V.1    Gladyschev, V.N.2
  • 58
    • 0000373477 scopus 로고
    • The acid strength of the SH group in cysteine and related compounds
    • Benesch, R. E.; Benesch, R. The acid strength of the SH group in cysteine and related compounds. J. Am. Chem. Soc. 1955, 77, 5877-5881.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 5877-5881
    • Benesch, R.E.1    Benesch, R.2
  • 59
    • 0014143854 scopus 로고
    • Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs
    • Huber, R. E.; Criddle, R. S. Comparison of the chemical properties of selenocysteine and selenocystine with their sulfur analogs. Arch. Biochem. Biophys. 1967, 122, 164-173.
    • (1967) Arch. Biochem. Biophys. , vol.122 , pp. 164-173
    • Huber, R.E.1    Criddle, R.S.2
  • 60
    • 27144469008 scopus 로고    scopus 로고
    • Selenocysteine in proteins;properties and biotechnological use
    • Johansson, L.; Gafvelin, G.; Arnér, E. S. J. Selenocysteine in proteins;properties and biotechnological use. Biochem. Biophys. Acta. 2005, 1726, 1-13.
    • (2005) Biochem. Biophys. Acta. , vol.1726 , pp. 1-13
    • Johansson, L.1    Gafvelin, G.2    Arnér, E.S.J.3
  • 61
    • 68949206430 scopus 로고    scopus 로고
    • Low Exchangeability of Selenocysteine, the 21st Amino Acid, in Vertebrate Proteins
    • Castellano, S.; André;s, A. M.; Bosch, E.; Bayes, M.; Guigó, R.; Clark, A. G. Low Exchangeability of Selenocysteine, the 21st Amino Acid, in Vertebrate Proteins. Mol. Biol. Evol. 2009, 26, 2031-2040.
    • (2009) Mol. Biol. Evol. , vol.26 , pp. 2031-2040
    • Castellano, S.1    Andrés, A.M.2    Bosch, E.3    Bayes, M.4    Guigó, R.5    Clark, A.G.6
  • 62
    • 52449114832 scopus 로고    scopus 로고
    • Mitochondria-Targeted Chemotherapeutics: The Rational Design of Gold(I) N-Heterocyclic Carbene Complexes that are Selectively Toxic to Cancer Cells and Target Protein Selenols in Preference to Thiols
    • Hickey, J. L.; Ruhayel, R. A.; Barnard, P. J.; Baker, M. V.; Berners-Price, S. J.; Filipovska, A. Mitochondria-Targeted Chemotherapeutics: The Rational Design of Gold(I) N-Heterocyclic Carbene Complexes that are Selectively Toxic to Cancer Cells and Target Protein Selenols in Preference to Thiols. J. Am. Chem. Soc. 2008, 130, 12570-12571.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 12570-12571
    • Hickey, J.L.1    Ruhayel, R.A.2    Barnard, P.J.3    Baker, M.V.4    Berners-Price, S.J.5    Filipovska, A.6
  • 63
    • 44849125526 scopus 로고    scopus 로고
    • Cell Death by SecTRAPs: Thioredoxin Reductase as a Prooxidant Killer of Cells
    • Anestål, K.; Prast-Nielsen, S.; Cenas, N.; Arnér, E. S. J. Cell Death by SecTRAPs: Thioredoxin Reductase as a Prooxidant Killer of Cells. PLoS One 2008, 3, e1846.
    • (2008) PLoS One , vol.3
    • Anestål, K.1    Prast-Nielsen, S.2    Cenas, N.3    Arnér, E.S.J.4
  • 64
    • 0032502720 scopus 로고    scopus 로고
    • Rat and calf thioredoxin reductase are homologous to glutathione reductase with a carboxyl-terminal elongation containing a conserved catalytically active penultimate selenocysteine residue
    • Zhong, L.; Arnér, E. S. J.; Ljung, J.; Aslund, F.; Holmgren, A. Rat and calf thioredoxin reductase are homologous to glutathione reductase with a carboxyl-terminal elongation containing a conserved catalytically active penultimate selenocysteine residue. J. Biol. Chem. 1998, 273, 8581-8591.
    • (1998) J. Biol. Chem. , vol.273 , pp. 8581-8591
    • Zhong, L.1    Arnér, E.S.J.2    Ljung, J.3    Aslund, F.4    Holmgren, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.