메뉴 건너뛰기




Volumn 102, Issue , 2015, Pages 41-48

Jonquailine, a new pretazettine-type alkaloid isolated from Narcissus jonquilla quail, with activity against drug-resistant cancer

Author keywords

Alkaloids; Amaryllidaceae; Antiproliferative effects; Cancer cells; Jonquailine; Narcissus jonquilla quail

Indexed keywords

ANTINEOPLASTIC AGENT; DOXORUBICIN; JONQUAILINE; PACLITAXEL; PODOPHYLLOTOXIN; PRETAZETTINE; UNCLASSIFIED DRUG; VINBLASTINE; ALKALOID; AMARYLLIDACEAE ALKALOID;

EID: 84923328156     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2015.01.009     Document Type: Article
Times cited : (27)

References (56)
  • 1
    • 0034630167 scopus 로고    scopus 로고
    • Induction of apoptosis by cancer chemotherapy
    • S.H. Kaufmann, and W.C. Earnshaw Induction of apoptosis by cancer chemotherapy Exp Cell Res 256 2000 42 49
    • (2000) Exp Cell Res , vol.256 , pp. 42-49
    • Kaufmann, S.H.1    Earnshaw, W.C.2
  • 2
    • 84879584721 scopus 로고    scopus 로고
    • Therapeutic agents triggering nonapoptotic cancer cell death
    • A. Kornienko, V. Mathieu, S. Rastogi, F. Lefranc, and R. Kiss Therapeutic agents triggering nonapoptotic cancer cell death J Med Chem 56 2013 4823 4839
    • (2013) J Med Chem , vol.56 , pp. 4823-4839
    • Kornienko, A.1    Mathieu, V.2    Rastogi, S.3    Lefranc, F.4    Kiss, R.5
  • 5
    • 0037068957 scopus 로고    scopus 로고
    • Long-term survival rates of cancer patients achieved by the end of the 20th century: A period analysis
    • H. Brenner Long-term survival rates of cancer patients achieved by the end of the 20th century: a period analysis Lancet 360 2002 1131 1135
    • (2002) Lancet , vol.360 , pp. 1131-1135
    • Brenner, H.1
  • 6
    • 55949136859 scopus 로고    scopus 로고
    • Anoikis resistance and tumor metastasis
    • C.D. Simpson, K. Anyiwe, and A.D. Schimmer Anoikis resistance and tumor metastasis Cancer Lett 272 2008 177 185
    • (2008) Cancer Lett , vol.272 , pp. 177-185
    • Simpson, C.D.1    Anyiwe, K.2    Schimmer, A.D.3
  • 7
    • 0038179723 scopus 로고    scopus 로고
    • Cost of migration: Invasion of malignant gliomas and implications for treatment
    • A. Giese, R. Bjerkvig, M.E. Berens, and M. Westphal Cost of migration: invasion of malignant gliomas and implications for treatment J Clin Oncol 21 2003 1624 1636
    • (2003) J Clin Oncol , vol.21 , pp. 1624-1636
    • Giese, A.1    Bjerkvig, R.2    Berens, M.E.3    Westphal, M.4
  • 8
    • 77954945991 scopus 로고    scopus 로고
    • Amaryllidaceae alkaloids belonging to different structural subgroups display activity against apoptosis-resistant cancer cells
    • G. Van Goietsenoven, A. Andolfi, B. Lallemand, A. Cimmino, D. Lamoral-Theys, and T. Gras Amaryllidaceae alkaloids belonging to different structural subgroups display activity against apoptosis-resistant cancer cells J Nat Prod 73 2010 1223 1227
    • (2010) J Nat Prod , vol.73 , pp. 1223-1227
    • Van Goietsenoven, G.1    Andolfi, A.2    Lallemand, B.3    Cimmino, A.4    Lamoral-Theys, D.5    Gras, T.6
  • 9
    • 70350068068 scopus 로고    scopus 로고
    • Lycorine, the main phenanthridine Amaryllidaceae alkaloid, exhibits significant antitumor activity in cancer cells that display resistance to proapoptotic stimuli: An investigation of structure-activity relationship and mechanistic insight
    • D. Lamoral-Theys, A. Andolfi, G. Van Goietsenoven, A. Cimmino, B. Le Calvé, and N. Wauthoz Lycorine, the main phenanthridine Amaryllidaceae alkaloid, exhibits significant antitumor activity in cancer cells that display resistance to proapoptotic stimuli: an investigation of structure-activity relationship and mechanistic insight J Med Chem 52 2009 6244 6256
    • (2009) J Med Chem , vol.52 , pp. 6244-6256
    • Lamoral-Theys, D.1    Andolfi, A.2    Van Goietsenoven, G.3    Cimmino, A.4    Le Calvé, B.5    Wauthoz, N.6
  • 10
    • 80655146928 scopus 로고    scopus 로고
    • In search of a cytostatic agent derived from the alkaloid lycorine: Synthesis and growth inhibitory properties of lycorine derivatives
    • N.M. Evdokimov, D. Lamoral-Theys, V. Mathieu, A. Andolfi, S. Pelly, and W.A.L. van Otterlo In search of a cytostatic agent derived from the alkaloid lycorine: synthesis and growth inhibitory properties of lycorine derivatives Bioorg Med Chem 19 2011 7252 7261
    • (2011) Bioorg Med Chem , vol.19 , pp. 7252-7261
    • Evdokimov, N.M.1    Lamoral-Theys, D.2    Mathieu, V.3    Andolfi, A.4    Pelly, S.5    Van Otterlo, W.A.L.6
  • 11
    • 84860253031 scopus 로고    scopus 로고
    • Bulbispermine: A crinine-type Amaryllidaceae alkaloid exhibiting cytostatic activity toward apoptosis-resistant glioma cells
    • G. Luchetti, R. Johnston, V. Mathieu, F. Lefranc, K. Hayden, and A. Andolfi Bulbispermine: a crinine-type Amaryllidaceae alkaloid exhibiting cytostatic activity toward apoptosis-resistant glioma cells ChemMedChem 7 2012 815 822
    • (2012) ChemMedChem , vol.7 , pp. 815-822
    • Luchetti, G.1    Johnston, R.2    Mathieu, V.3    Lefranc, F.4    Hayden, K.5    Andolfi, A.6
  • 12
    • 0034049134 scopus 로고    scopus 로고
    • Effect of 6-aminonicotinamide and other protein synthesis inhibitors on formation of platinum-DNA adducts and cisplatin sensitivity
    • I.I. Budihardjo, S.A. Boerner, S. Eckdahl, P.A. Svingen, R. Rios, and M.M. Ames Effect of 6-aminonicotinamide and other protein synthesis inhibitors on formation of platinum-DNA adducts and cisplatin sensitivity Mol Pharmacol 57 2000 529 583
    • (2000) Mol Pharmacol , vol.57 , pp. 529-583
    • Budihardjo, I.I.1    Boerner, S.A.2    Eckdahl, S.3    Svingen, P.A.4    Rios, R.5    Ames, M.M.6
  • 14
    • 79953743709 scopus 로고    scopus 로고
    • Omacetaxine as an anticancer therapeutic: What is old is new again
    • M. Wetzler, and D. Segal Omacetaxine as an anticancer therapeutic: what is old is new again Curr Pharm Des 17 2011 59 64
    • (2011) Curr Pharm des , vol.17 , pp. 59-64
    • Wetzler, M.1    Segal, D.2
  • 16
    • 0036364467 scopus 로고    scopus 로고
    • Multidrug resistance in cancer: Role of ATP-dependent transporters
    • M.M. Gottesman, T. Fojo, and S.E. Bates Multidrug resistance in cancer: role of ATP-dependent transporters Nat Rev Cancer 2 2002 48 58
    • (2002) Nat Rev Cancer , vol.2 , pp. 48-58
    • Gottesman, M.M.1    Fojo, T.2    Bates, S.E.3
  • 17
    • 84887992978 scopus 로고    scopus 로고
    • Different strategies to overcome multidrug resistance in cancer
    • M. Saraswathy, and S.Q. Gong Different strategies to overcome multidrug resistance in cancer Biotechnol Adv 31 2013 1397 1407
    • (2013) Biotechnol Adv , vol.31 , pp. 1397-1407
    • Saraswathy, M.1    Gong, S.Q.2
  • 18
    • 0033624565 scopus 로고    scopus 로고
    • MDR 1 activation is the predominant resistance mechanism selected by vinblastine in MES-SA cells
    • G.K. Chen, G.E. Duran, A. Mangili, L. Beketic-Oreskovic, and B.I. Sikic MDR 1 activation is the predominant resistance mechanism selected by vinblastine in MES-SA cells Br J Cancer 83 2000 892
    • (2000) Br J Cancer , vol.83 , pp. 892
    • Chen, G.K.1    Duran, G.E.2    Mangili, A.3    Beketic-Oreskovic, L.4    Sikic, B.I.5
  • 19
    • 0036405919 scopus 로고    scopus 로고
    • Overcoming multidrug resistance in taxane chemotherapy
    • R. Geney, M. Ungureanu, D. Li, and I. Ojima Overcoming multidrug resistance in taxane chemotherapy Clin Chem Lab Med 40 2002 918 925
    • (2002) Clin Chem Lab Med , vol.40 , pp. 918-925
    • Geney, R.1    Ungureanu, M.2    Li, D.3    Ojima, I.4
  • 20
    • 84884225721 scopus 로고    scopus 로고
    • Exploring natural product chemistry and biology with multicomponent reactions. 5. Discovery of a novel tubulin-targeting scaffold derived from the rigidin family of marine alkaloids
    • L.V. Frolova, I.V. Magedov, A.E. Romero, M. Karki, I. Otero, and K. Hayden Exploring natural product chemistry and biology with multicomponent reactions. 5. Discovery of a novel tubulin-targeting scaffold derived from the rigidin family of marine alkaloids J Med Chem 56 2013 6886 6900
    • (2013) J Med Chem , vol.56 , pp. 6886-6900
    • Frolova, L.V.1    Magedov, I.V.2    Romero, A.E.3    Karki, M.4    Otero, I.5    Hayden, K.6
  • 21
    • 84858308226 scopus 로고    scopus 로고
    • Natural products as sources of new drugs over the 30 years from 1981 to 2010
    • D.J. Newman, and G.M. Cragg Natural products as sources of new drugs over the 30 years from 1981 to 2010 J Nat Prod 75 2012 311 335
    • (2012) J Nat Prod , vol.75 , pp. 311-335
    • Newman, D.J.1    Cragg, G.M.2
  • 22
    • 33947338579 scopus 로고
    • Plants used against cancer. A survey
    • J.L. Hartwell Plants used against cancer. A survey Lloydia 30 1967 379 436
    • (1967) Lloydia , vol.30 , pp. 379-436
    • Hartwell, J.L.1
  • 23
    • 47249124531 scopus 로고    scopus 로고
    • Chemistry, biology, and medicinal potential of narciclasine and its congeners
    • [and references cited therein]
    • A. Kornienko, and E. Evidente Chemistry, biology, and medicinal potential of narciclasine and its congeners Chem Rev 108 2008 1982 2014 [and references cited therein]
    • (2008) Chem Rev , vol.108 , pp. 1982-2014
    • Kornienko, A.1    Evidente, E.2
  • 24
    • 77957033352 scopus 로고
    • The Amaryllidaceae alkaloids
    • A.R. Brossi, Academic Press New York
    • S.F. Martin The Amaryllidaceae alkaloids A.R. Brossi, The Alkaloids 1987 Academic Press New York 251 376
    • (1987) The Alkaloids , pp. 251-376
    • Martin, S.F.1
  • 25
    • 77956708370 scopus 로고    scopus 로고
    • The Amaryllidaceae alkaloids
    • G.A. Cordell, Academic Press London
    • O. Hoshino The Amaryllidaceae alkaloids G.A. Cordell, The Alkaloids 1998 Academic Press London 323 376
    • (1998) The Alkaloids , pp. 323-376
    • Hoshino, O.1
  • 26
    • 0004279068 scopus 로고
    • R.H.F. Manske, H.L. Holmes, Academic Press New York
    • J.W. Cook, and J.D. Loudon R.H.F. Manske, H.L. Holmes, The Alkaloids 1952 Academic Press New York 331 360
    • (1952) The Alkaloids , pp. 331-360
    • Cook, J.W.1    Loudon, J.D.2
  • 27
    • 0014199791 scopus 로고
    • Narciclasine: An antimitotic substance from Narcissus bulbs
    • G. Ceriotti Narciclasine: an antimitotic substance from Narcissus bulbs Nature 213 1967 595 596
    • (1967) Nature , vol.213 , pp. 595-596
    • Ceriotti, G.1
  • 28
    • 84873993446 scopus 로고    scopus 로고
    • Narciclasine as well as other Amaryllidaceae isocarbostyrils are promising GTP-ase targeting agents against brain cancers
    • G. Van Goietsenoven, V. Mathieu, F. Lefranc, A. Kornienko, A. Evidente, and R. Kiss Narciclasine as well as other Amaryllidaceae isocarbostyrils are promising GTP-ase targeting agents against brain cancers Med Res Rev 33 2013 439 455
    • (2013) Med Res Rev , vol.33 , pp. 439-455
    • Van Goietsenoven, G.1    Mathieu, V.2    Lefranc, F.3    Kornienko, A.4    Evidente, A.5    Kiss, R.6
  • 29
    • 0017258099 scopus 로고
    • Inhibitors of protein synthesis in eukaryotic cells: Comparative effects of some Amaryllidaceae alkaloids
    • A. Jimenez, A. Santos, G. Alonso, and D. Vazquez Inhibitors of protein synthesis in eukaryotic cells: comparative effects of some Amaryllidaceae alkaloids Biochim Biophys Acta 425 1976 342 348
    • (1976) Biochim Biophys Acta , vol.425 , pp. 342-348
    • Jimenez, A.1    Santos, A.2    Alonso, G.3    Vazquez, D.4
  • 30
    • 0016685094 scopus 로고
    • Yeast ribosomal sensitivity and resistance to the Amaryllidaceae alkaloids
    • A. Jimenez, L. Sanchez, and D. Vazquez Yeast ribosomal sensitivity and resistance to the Amaryllidaceae alkaloids FEBS Lett 60 1975 66 70
    • (1975) FEBS Lett , vol.60 , pp. 66-70
    • Jimenez, A.1    Sanchez, L.2    Vazquez, D.3
  • 31
    • 84862082742 scopus 로고    scopus 로고
    • Jacobsen protocols for large-scale epoxidation of cyclic dienyl sulfones: Application to the (+)-pretazettine core
    • [and references cited therein]
    • G.R. Ebrahimian, X.M. du Jourdin, and P.L. Fuchs Jacobsen protocols for large-scale epoxidation of cyclic dienyl sulfones: application to the (+)-pretazettine core Org Lett 14 2012 2630 2633 [and references cited therein]
    • (2012) Org Lett , vol.14 , pp. 2630-2633
    • Ebrahimian, G.R.1    Du Jourdin, X.M.2    Fuchs, P.L.3
  • 33
    • 0018907876 scopus 로고
    • Therapeutic activity of pretazettine on Rauscher leukemia: Comparison with the related Amaryllidaceae alkaloids
    • E. Furusawa, H. Irie, D. Combs, and W.C. Wildman Therapeutic activity of pretazettine on Rauscher leukemia: comparison with the related Amaryllidaceae alkaloids Chemotherapy 26 1980 36 45
    • (1980) Chemotherapy , vol.26 , pp. 36-45
    • Furusawa, E.1    Irie, H.2    Combs, D.3    Wildman, W.C.4
  • 34
    • 0018774753 scopus 로고
    • Therapeutic activity of Pretazettine, a narcissus alkaloid, on spontaneous AKR leukemia
    • E. Furusawa, R.H. Lockwood, S. Furusawa, M.K.M. Lum, and J.Y.B. Lee Therapeutic activity of Pretazettine, a narcissus alkaloid, on spontaneous AKR leukemia Chemotherapy 25 1979 308 315
    • (1979) Chemotherapy , vol.25 , pp. 308-315
    • Furusawa, E.1    Lockwood, R.H.2    Furusawa, S.3    Lum, M.K.M.4    Lee, J.Y.B.5
  • 35
    • 0019439271 scopus 로고
    • Therapeutic activity of pretazettine on Ehrlich ascites carcinoma: Adjuvant effect on standard drugs in ABC regimen
    • E. Furusawa, M.K.M. Lum, and S. Furusawa Therapeutic activity of pretazettine on Ehrlich ascites carcinoma: adjuvant effect on standard drugs in ABC regimen Chemotherapy 27 1981 277 286
    • (1981) Chemotherapy , vol.27 , pp. 277-286
    • Furusawa, E.1    Lum, M.K.M.2    Furusawa, S.3
  • 36
    • 0020565340 scopus 로고
    • Therapeutic activity of pretazettine, standard drugs, and the combinations on intraperitoneally implanted Lewis lung carcinoma in mice
    • E. Furusawa, and L. Sokugawa Therapeutic activity of pretazettine, standard drugs, and the combinations on intraperitoneally implanted Lewis lung carcinoma in mice Chemotherapy 29 1983 294 302
    • (1983) Chemotherapy , vol.29 , pp. 294-302
    • Furusawa, E.1    Sokugawa, L.2
  • 37
    • 33747796587 scopus 로고    scopus 로고
    • Analysis of Amaryllidaceae alkaloids from Narcissus by GC-MS and capillary electrophoresis
    • R. Gotti, J. Fiori, M. Bartolini, and V. Cavrini Analysis of Amaryllidaceae alkaloids from Narcissus by GC-MS and capillary electrophoresis J Pharm Biomed Anal 42 2006 17 24
    • (2006) J Pharm Biomed Anal , vol.42 , pp. 17-24
    • Gotti, R.1    Fiori, J.2    Bartolini, M.3    Cavrini, V.4
  • 39
    • 0141905752 scopus 로고    scopus 로고
    • Alkaloids from Eucharis amazonica (Amaryllidaceae)
    • [and literatures therein cited]
    • F. Cabezas, A. Ramírez, F. Viladomat, C. Codina, and J. Bastida Alkaloids from Eucharis amazonica (Amaryllidaceae) Chem Pharm Bull 51 2003 315 317 [and literatures therein cited]
    • (2003) Chem Pharm Bull , vol.51 , pp. 315-317
    • Cabezas, F.1    Ramírez, A.2    Viladomat, F.3    Codina, C.4    Bastida, J.5
  • 40
    • 0029926723 scopus 로고    scopus 로고
    • Alkaloids from Hippeastrum equestre Herb. - 5. Circular dichroism studies
    • J. Wagner, H.L. Pham, and W. Döpke Alkaloids from Hippeastrum equestre Herb. - 5. Circular dichroism studies Tetrahedron 52 1996 6591 6600
    • (1996) Tetrahedron , vol.52 , pp. 6591-6600
    • Wagner, J.1    Pham, H.L.2    Döpke, W.3
  • 41
    • 0009509818 scopus 로고
    • Mass spectra of Amaryllidaceae alkaloids. Structure of narcissidine
    • T.H. Kinstle, W.C. Wildman, and C.L. Brown Mass spectra of Amaryllidaceae alkaloids. Structure of narcissidine Tetrahedron Lett 39 1966 4659 4666
    • (1966) Tetrahedron Lett , vol.39 , pp. 4659-4666
    • Kinstle, T.H.1    Wildman, W.C.2    Brown, C.L.3
  • 43
    • 84946384873 scopus 로고
    • The toxicity of poisons applied jointly
    • C.I. Bliss The toxicity of poisons applied jointly Ann Appl Biol 26 1939 585 615
    • (1939) Ann Appl Biol , vol.26 , pp. 585-615
    • Bliss, C.I.1
  • 44
    • 0022352607 scopus 로고
    • Multidrug (pleiotropic) resistance in doxorubicin-selected variants of the human sarcoma cell line MES-SA
    • W.G. Harker, and B.I. Sikic Multidrug (pleiotropic) resistance in doxorubicin-selected variants of the human sarcoma cell line MES-SA Cancer Res 45 1985 4091 4096
    • (1985) Cancer Res , vol.45 , pp. 4091-4096
    • Harker, W.G.1    Sikic, B.I.2
  • 48
    • 33747780396 scopus 로고    scopus 로고
    • A general approach to crinine-type Amaryllidaceae alkaloids: Total syntheses of (±)-haemanthidine, (±)-pretazettine, (±)-tazettine and (±)-crinamine
    • F.M. Zhang, Y.Q. Tu, J.D. Liu, X.H. Fan, L. Shi, and X.D. Hu A general approach to crinine-type Amaryllidaceae alkaloids: total syntheses of (±)-haemanthidine, (±)-pretazettine, (±)-tazettine and (±)-crinamine Tetrahedron 62 2006 9446 9455
    • (2006) Tetrahedron , vol.62 , pp. 9446-9455
    • Zhang, F.M.1    Tu, Y.Q.2    Liu, J.D.3    Fan, X.H.4    Shi, L.5    Hu, X.D.6
  • 49
    • 0009520844 scopus 로고
    • Novel alkaloids containing the [2] benzopyrano [3, 4-c] indole nucleus
    • W.C. Wildman, and D.T. Bailey Novel alkaloids containing the [2] benzopyrano [3, 4-c] indole nucleus J Org Chem 33 1968 3749 3753
    • (1968) J Org Chem , vol.33 , pp. 3749-3753
    • Wildman, W.C.1    Bailey, D.T.2
  • 51
    • 0036682304 scopus 로고    scopus 로고
    • Evaluation of the efficiency of chemotherapy in in vivo orthotopic models of human glioma cells with and without 1p19q deletions and in C6 rat orthotopic allografts serving for the evaluation of surgery combined with chemotherapy
    • F. Branle, F. Lefranc, I. Camby, J. Jeuken, A. Geurts-Moespot, and S. Sprenger Evaluation of the efficiency of chemotherapy in in vivo orthotopic models of human glioma cells with and without 1p19q deletions and in C6 rat orthotopic allografts serving for the evaluation of surgery combined with chemotherapy Cancer 95 2002 641 655
    • (2002) Cancer , vol.95 , pp. 641-655
    • Branle, F.1    Lefranc, F.2    Camby, I.3    Jeuken, J.4    Geurts-Moespot, A.5    Sprenger, S.6
  • 52
    • 84867843684 scopus 로고    scopus 로고
    • The apoptosis-resistance in t-AUCB-treated glioblastoma cells depends on activation of Hsp27
    • J. Li, W. Hu, and Q. Lan The apoptosis-resistance in t-AUCB-treated glioblastoma cells depends on activation of Hsp27 J Neurooncol 110 2012 187 194
    • (2012) J Neurooncol , vol.110 , pp. 187-194
    • Li, J.1    Hu, W.2    Lan, Q.3
  • 53
    • 4944242194 scopus 로고    scopus 로고
    • Development of a chemoresistant orthotopic human nonsmall cell lung carcinoma model in nude mice
    • A. Mathieu, M. Remmelink, N. D'Haene, S. Penant, J.F. Gaussin, and R. Van Ginckel Development of a chemoresistant orthotopic human nonsmall cell lung carcinoma model in nude mice Cancer 101 2004 1908 1918
    • (2004) Cancer , vol.101 , pp. 1908-1918
    • Mathieu, A.1    Remmelink, M.2    D'Haene, N.3    Penant, S.4    Gaussin, J.F.5    Van Ginckel, R.6
  • 54
    • 70350080771 scopus 로고    scopus 로고
    • The sodium pump α1 sub-unit: A disease progression-related target for metastatic melanoma treatment
    • V. Mathieu, C. Pirker, E. Martin de Lasalle, M. Vernier, T. Mijatovic, and N. De Neve The sodium pump α1 sub-unit: a disease progression-related target for metastatic melanoma treatment J Cell Mol Med 13 2009 3960 3972
    • (2009) J Cell Mol Med , vol.13 , pp. 3960-3972
    • Mathieu, V.1    Pirker, C.2    Martin De Lasalle, E.3    Vernier, M.4    Mijatovic, T.5    De Neve, N.6
  • 55
    • 84885071106 scopus 로고    scopus 로고
    • In vitro pharmacological and toxicological effects of norterpene peroxides isolated from the Red Sea sponge Diacarnus erythraeanus on normal and cancer cells
    • F. Lefranc, G. Nuzzo, N.A. Hamdy, I. Fakhr, Y. Moreno, and L. Banuls In vitro pharmacological and toxicological effects of norterpene peroxides isolated from the Red Sea sponge Diacarnus erythraeanus on normal and cancer cells J Nat Prod 76 2013 1541 1547
    • (2013) J Nat Prod , vol.76 , pp. 1541-1547
    • Lefranc, F.1    Nuzzo, G.2    Hamdy, N.A.3    Fakhr, I.4    Moreno, Y.5    Banuls, L.6
  • 56
    • 84905896139 scopus 로고    scopus 로고
    • Integrative analysis of two cell lines derived from a non-small-lung cancer patient - A panomics approach
    • O. Mayba, F. Gnad, M. Peyton, F. Zhang, K. Walter, and P. Du Integrative analysis of two cell lines derived from a non-small-lung cancer patient - a panomics approach Pac Symp Biocomput 2014 75 86
    • (2014) Pac Symp Biocomput , pp. 75-86
    • Mayba, O.1    Gnad, F.2    Peyton, M.3    Zhang, F.4    Walter, K.5    Du, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.