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Volumn 7, Issue , 2008, Pages

Farnesyl transferase inhibitors induce extended remissions in transgenic mice with mature B cell lymphomas

Author keywords

[No Author keywords available]

Indexed keywords

2 [[2 [[2 [(2 AMINO 3 MERCAPTOPROPYL)AMINO] 3 METHYLPENTYL]OXY] 1 OXO 3 PHENYLPROPYL]AMINO] 4 (METHYLSULFONYL)BUTANOIC ACID ISOPROPYL ESTER; LONAFARNIB; MYC PROTEIN; PROTEIN FARNESYLTRANSFERASE INHIBITOR; DRUG DERIVATIVE; ENZYME INHIBITOR; FARNESYL TRANS TRANSFERASE; METHIONINE; PIPERIDINE DERIVATIVE; PYRIDINE DERIVATIVE;

EID: 44949153485     PISSN: None     EISSN: 14764598     Source Type: Journal    
DOI: 10.1186/1476-4598-7-39     Document Type: Article
Times cited : (6)

References (54)
  • 1
    • 0030749458 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors and cancer treatment: Targeting simply Ras?
    • 9294018
    • Cox AD Der CJ Farnesyltransferase inhibitors and cancer treatment: targeting simply Ras? Biochim Biophys Acta 1997, 1333(1):F51-71 9294018
    • (1997) Biochim Biophys Acta , vol.1333 , Issue.1
    • Cox, A.D.1    Der, C.J.2
  • 2
    • 0028835253 scopus 로고
    • A peptidomimetic inhibitor of farnesyl: Protein transferase blocks the anchorage-dependent and -independent growth of human tumor cell lines
    • 7585592
    • Sepp-Lorenzino L Ma Z Rands E Kohl NE Gibbs JB Oliff A Rosen N A peptidomimetic inhibitor of farnesyl: protein transferase blocks the anchorage-dependent and -independent growth of human tumor cell lines Cancer Res 1995, 55(22):5302-5309 7585592
    • (1995) Cancer Res , vol.55 , Issue.22 , pp. 5302-5309
    • Sepp-Lorenzino, L.1    Ma, Z.2    Rands, E.3    Kohl, N.E.4    Gibbs, J.B.5    Oliff, A.6    Rosen, N.7
  • 3
    • 0033539952 scopus 로고    scopus 로고
    • Growth inhibition of astrocytoma cells by farnesyl transferase inhibitors is mediated by a combination of anti-proliferative, pro-apoptotic and anti-angiogenic effects
    • 10.1038/sj.onc.1203105 10602510
    • Feldkamp MM Lau N Guha A Growth inhibition of astrocytoma cells by farnesyl transferase inhibitors is mediated by a combination of anti-proliferative, pro-apoptotic and anti-angiogenic effects Oncogene 1999, 18(52):7514-7526 10.1038/sj.onc.1203105 10602510
    • (1999) Oncogene , vol.18 , Issue.52 , pp. 7514-7526
    • Feldkamp, M.M.1    Lau, N.2    Guha, A.3
  • 4
    • 0036599583 scopus 로고    scopus 로고
    • Reversion of RhoC GTPase-induced inflammatory breast cancer phenotype by treatment with a farnesyl transferase inhibitor
    • 12479217
    • van Golen KL Bao L DiVito MM Wu Z Prendergast GC Merajver SD Reversion of RhoC GTPase-induced inflammatory breast cancer phenotype by treatment with a farnesyl transferase inhibitor Mol Cancer Ther 2002, 1(8):575-583 12479217
    • (2002) Mol Cancer Ther , vol.1 , Issue.8 , pp. 575-583
    • van Golen, K.L.1    Bao, L.2    DiVito, M.M.3    Wu, Z.4    Prendergast, G.C.5    Merajver, S.D.6
  • 5
    • 0033934641 scopus 로고    scopus 로고
    • A peptidomimetic inhibitor of ras functionality markedly suppresses growth of human prostate tumor xenografts in mice. Prospects for long-term clinical utility
    • 10.1007/s002800000126 10912583
    • Sirotnak FM Sepp-Lorenzino L Kohl NE Rosen N Scher HI A peptidomimetic inhibitor of ras functionality markedly suppresses growth of human prostate tumor xenografts in mice. Prospects for long-term clinical utility Cancer Chemother Pharmacol 2000, 46(1):79-83 10.1007/ s002800000126 10912583
    • (2000) Cancer Chemother Pharmacol , vol.46 , Issue.1 , pp. 79-83
    • Sirotnak, F.M.1    Sepp-Lorenzino, L.2    Kohl, N.E.3    Rosen, N.4    Scher, H.I.5
  • 8
    • 0032521211 scopus 로고    scopus 로고
    • Antitumor effect of a farnesyl protein transferase inhibitor in mammary and lymphoid tumors overexpressing N-ras in transgenic mice
    • 9515813
    • Mangues R Corral T Kohl NE Symmans WF Lu S Malumbres M Gibbs JB Oliff A Pellicer A Antitumor effect of a farnesyl protein transferase inhibitor in mammary and lymphoid tumors overexpressing N-ras in transgenic mice Cancer Res 1998, 58(6):1253-1259 9515813
    • (1998) Cancer Res , vol.58 , Issue.6 , pp. 1253-1259
    • Mangues, R.1    Corral, T.2    Kohl, N.E.3    Symmans, W.F.4    Lu, S.5    Malumbres, M.6    Gibbs, J.B.7    Oliff, A.8    Pellicer, A.9
  • 9
    • 0033214846 scopus 로고    scopus 로고
    • In vitro and in vivo effects of a farnesyltransferase inhibitor on Nf1-deficient hematopoietic cells
    • 10498620
    • Mahgoub N Taylor BR Gratiot M Kohl NE Gibbs JB Jacks T Shannon KM In vitro and in vivo effects of a farnesyltransferase inhibitor on Nf1-deficient hematopoietic cells Blood 1999, 94(7):2469-2476 10498620
    • (1999) Blood , vol.94 , Issue.7 , pp. 2469-2476
    • Mahgoub, N.1    Taylor, B.R.2    Gratiot, M.3    Kohl, N.E.4    Gibbs, J.B.5    Jacks, T.6    Shannon, K.M.7
  • 10
    • 0032900619 scopus 로고    scopus 로고
    • Treatment with farnesyl-protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) alpha and TGF alpha/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis
    • 9918200
    • Norgaard P Law B Joseph H Page DL Shyr Y Mays D Pietenpol JA Kohl NE Oliff A Coffey RJ Jr. Poulsen HS Moses HL Treatment with farnesyl-protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) alpha and TGF alpha/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis Clin Cancer Res 1999, 5(1):35-42 9918200
    • (1999) Clin Cancer Res , vol.5 , Issue.1 , pp. 35-42
    • Norgaard, P.1    Law, B.2    Joseph, H.3    Page, D.L.4    Shyr, Y.5    Mays, D.6    Pietenpol, J.A.7    Kohl, N.E.8    Oliff, A.9    Coffey Jr., R.J.10    Poulsen, H.S.11    Moses, H.L.12
  • 15
    • 0035990832 scopus 로고    scopus 로고
    • A phase II trial of farnesyl protein transferase inhibitor SCH 66336, given by twice-daily oral administration, in patients with metastatic colorectal cancer refractory to 5-fluorouracil and irinotecan
    • 10.1093/annonc/mdf173 12176785
    • Sharma S Kemeny N Kelsen DP Ilson D O'Reilly E Zaknoen S Baum C Statkevich P Hollywood E Zhu Y Saltz LB A phase II trial of farnesyl protein transferase inhibitor SCH 66336, given by twice-daily oral administration, in patients with metastatic colorectal cancer refractory to 5-fluorouracil and irinotecan Ann Oncol 2002, 13(7):1067-1071 10.1093/ annonc/mdf173 12176785
    • (2002) Ann Oncol , vol.13 , Issue.7 , pp. 1067-1071
    • Sharma, S.1    Kemeny, N.2    Kelsen, D.P.3    Ilson, D.4    O'Reilly, E.5    Zaknoen, S.6    Baum, C.7    Statkevich, P.8    Hollywood, E.9    Zhu, Y.10    Saltz, L.B.11
  • 16
    • 0034232138 scopus 로고    scopus 로고
    • Inhibition of cell growth in human glioblastoma cell lines by farnesyltransferase inhibitor SCH66336
    • 1920495 10.1215/15228517-2-3-151
    • Glass TL Liu TJ Yung WK Inhibition of cell growth in human glioblastoma cell lines by farnesyltransferase inhibitor SCH66336 Neuro-oncol 2000, 2(3):151-158 1920495 11302335 10.1215/15228517-2-3-151
    • (2000) Neuro-oncol , vol.2 , Issue.3 , pp. 151-158
    • Glass, T.L.1    Liu, T.J.2    Yung, W.K.3
  • 17
    • 0035282901 scopus 로고    scopus 로고
    • Activity of the farnesyl protein transferase inhibitor SCH66336 against BCR/ABL-induced murine leukemia and primary cells from patients with chronic myeloid leukemia
    • 10.1182/blood.V97.5.1404 11222387
    • Peters DG Hoover RR Gerlach MJ Koh EY Zhang H Choe K Kirschmeier P Bishop WR Daley GQ Activity of the farnesyl protein transferase inhibitor SCH66336 against BCR/ABL-induced murine leukemia and primary cells from patients with chronic myeloid leukemia Blood 2001, 97(5):1404-1412 10.1182/blood.V97.5.1404 11222387
    • (2001) Blood , vol.97 , Issue.5 , pp. 1404-1412
    • Peters, D.G.1    Hoover, R.R.2    Gerlach, M.J.3    Koh, E.Y.4    Zhang, H.5    Choe, K.6    Kirschmeier, P.7    Bishop, W.R.8    Daley, G.Q.9
  • 18
    • 0034826412 scopus 로고    scopus 로고
    • Farnesyl protein transferase inhibition: A novel approach to anti-tumor therapy. The discovery and development of SCH 66336
    • 11562275
    • Ganguly AK Doll RJ Girijavallabhan VM Farnesyl protein transferase inhibition: A novel approach to anti-tumor therapy. The discovery and development of SCH 66336 Curr Med Chem 2001, 8(12):1419-1436 11562275
    • (2001) Curr Med Chem , vol.8 , Issue.12 , pp. 1419-1436
    • Ganguly, A.K.1    Doll, R.J.2    Girijavallabhan, V.M.3
  • 19
    • 0034993869 scopus 로고    scopus 로고
    • Orally bioavailable farnesyltransferase inhibitors as anticancer agents in transgenic and xenograft models
    • 11400347
    • Liu M Bishop WR Nielsen LL Bryant MS Kirschmeier P Orally bioavailable farnesyltransferase inhibitors as anticancer agents in transgenic and xenograft models Methods Enzymol 2001, 333:306-318 11400347
    • (2001) Methods Enzymol , vol.333 , pp. 306-318
    • Liu, M.1    Bishop, W.R.2    Nielsen, L.L.3    Bryant, M.S.4    Kirschmeier, P.5
  • 21
    • 0035282735 scopus 로고    scopus 로고
    • Treatment of Bcr/Abl-positive acute lymphoblastic leukemia in P190 transgenic mice with the farnesyl transferase inhibitor SCH66336
    • 10.1182/blood.V97.5.1399 11222386
    • Reichert A Heisterkamp N Daley GQ Groffen J Treatment of Bcr/ Abl-positive acute lymphoblastic leukemia in P190 transgenic mice with the farnesyl transferase inhibitor SCH66336 Blood 2001, 97(5):1399-1403 10.1182/blood.V97.5.1399 11222386
    • (2001) Blood , vol.97 , Issue.5 , pp. 1399-1403
    • Reichert, A.1    Heisterkamp, N.2    Daley, G.Q.3    Groffen, J.4
  • 22
    • 0141842714 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors: An overview of the results of preclinical and clinical investigations
    • 14522880
    • Brunner TB Hahn SM Gupta AK Muschel RJ McKenna WG Bernhard EJ Farnesyltransferase inhibitors: An overview of the results of preclinical and clinical investigations Cancer Res 2003, 63(18):5656-5668 14522880
    • (2003) Cancer Res , vol.63 , Issue.18 , pp. 5656-5668
    • Brunner, T.B.1    Hahn, S.M.2    Gupta, A.K.3    Muschel, R.J.4    McKenna, W.G.5    Bernhard, E.J.6
  • 23
    • 34249979529 scopus 로고    scopus 로고
    • Farnesyltransferase inihibitors in hematologic malignancies
    • 10.1016/j.blre.2006.12.001 17293017
    • Harousseau JL Farnesyltransferase inihibitors in hematologic malignancies Blood Rev 2007, 21(4):173-182 10.1016/j.blre.2006.12.001 17293017
    • (2007) Blood Rev , vol.21 , Issue.4 , pp. 173-182
    • Harousseau, J.L.1
  • 24
    • 27744475074 scopus 로고    scopus 로고
    • In vitro profiling of the sensitivity of pediatric leukemia cells to tipifarnib: Identification of T-cell ALL and FAB M5 AML as the most sensitive subsets
    • 10.1182/blood-2005-04-1640 16051737
    • Goemans BF Zwaan CM Harlow A Loonen AH Gibson BE Hahlen K Reinhardt D Creutzig U Heinrich MC Kaspers GJ In vitro profiling of the sensitivity of pediatric leukemia cells to tipifarnib: Identification of T-cell ALL and FAB M5 AML as the most sensitive subsets Blood 2005, 106(10):3532-3537 10.1182/blood-2005-04-1640 16051737
    • (2005) Blood , vol.106 , Issue.10 , pp. 3532-3537
    • Goemans, B.F.1    Zwaan, C.M.2    Harlow, A.3    Loonen, A.H.4    Gibson, B.E.5    Hahlen, K.6    Reinhardt, D.7    Creutzig, U.8    Heinrich, M.C.9    Kaspers, G.J.10
  • 25
    • 0032477263 scopus 로고    scopus 로고
    • Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell differentiation
    • 10.1016/S0192-0561(98)00064-2 9848396
    • Koh WS Yoon SY Kwon BM Jeong TC Nam KS Han MY Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell differentiation Int J Immunopharmacol 1998, 20(11):643-660 10.1016/S0192-0561(98)00064-2 9848396
    • (1998) Int J Immunopharmacol , vol.20 , Issue.11 , pp. 643-660
    • Koh, W.S.1    Yoon, S.Y.2    Kwon, B.M.3    Jeong, T.C.4    Nam, K.S.5    Han, M.Y.6
  • 26
    • 0037388883 scopus 로고    scopus 로고
    • Farnesyltransferase inhibition: A novel method of immunomodulation
    • 10.1016/S1567-5769(02)00278-3 12689653
    • Si MS Ji P Tromberg BJ Lee M Kwok J Ng SC Imagawa DK Farnesyltransferase inhibition: A novel method of immunomodulation Int Immunopharmacol 2003, 3(4):475-483 10.1016/S1567-5769(02)00278-3 12689653
    • (2003) Int Immunopharmacol , vol.3 , Issue.4 , pp. 475-483
    • Si, M.S.1    Ji, P.2    Tromberg, B.J.3    Lee, M.4    Kwok, J.5    Ng, S.C.6    Imagawa, D.K.7
  • 27
    • 8644285459 scopus 로고    scopus 로고
    • Inhibition of lymphocyte activation and function by the prenylation inhibitor L-778,123
    • 10.1023/B:DRUG.0000047102.26698.08 15528977
    • Si MS Reitz BA Borie DC Inhibition of lymphocyte activation and function by the prenylation inhibitor L-778,123 Invest New Drugs 2005, 23(1):21-29 10.1023/B:DRUG.0000047102.26698.08 15528977
    • (2005) Invest New Drugs , vol.23 , Issue.1 , pp. 21-29
    • Si, M.S.1    Reitz, B.A.2    Borie, D.C.3
  • 28
    • 33646354412 scopus 로고    scopus 로고
    • Statin therapy and autoimmune disease: From protein prenylation to immunomodulation
    • 10.1038/nri1839 16639429
    • Greenwood J Steinman L Zamvil SS Statin therapy and autoimmune disease: from protein prenylation to immunomodulation Nat Rev Immunol 2006, 6(5):358-370 10.1038/nri1839 16639429
    • (2006) Nat Rev Immunol , vol.6 , Issue.5 , pp. 358-370
    • Greenwood, J.1    Steinman, L.2    Zamvil, S.S.3
  • 29
    • 15244351967 scopus 로고    scopus 로고
    • The protooncogene MYC can break B cell tolerance
    • 552974 10.1073/pnas.0409832102
    • Refaeli Y Field KA Turner BC Trumpp A Bishop JM The protooncogene MYC can break B cell tolerance Proc Natl Acad Sci U S A 2005, 102(11):4097-4102 552974 15753301 10.1073/pnas.0409832102
    • (2005) Proc Natl Acad Sci U S A , vol.102 , Issue.11 , pp. 4097-4102
    • Refaeli, Y.1    Field, K.A.2    Turner, B.C.3    Trumpp, A.4    Bishop, J.M.5
  • 33
    • 14944339170 scopus 로고    scopus 로고
    • Deregulated expression of the Myc cellular oncogene drives development of mouse "Burkitt-like" lymphomas from naive B cells
    • 10.1182/blood-2004-07-2573 15522957
    • Zhu D Qi CF Morse HC 3rd Janz S Stevenson FK Deregulated expression of the Myc cellular oncogene drives development of mouse "Burkitt-like" lymphomas from naive B cells Blood 2005, 105(5):2135-2137 10.1182/blood-2004-07-2573 15522957
    • (2005) Blood , vol.105 , Issue.5 , pp. 2135-2137
    • Zhu, D.1    Qi, C.F.2    Morse III, H.C.3    Janz, S.4    Stevenson, F.K.5
  • 34
    • 16844385104 scopus 로고    scopus 로고
    • Regulatory elements in the immunoglobulin heavy chain gene 3′-enhancers induce c-myc deregulation and lymphomagenesis in murine B cells
    • 10.1074/jbc.M412446200 15687498
    • Wang J Boxer LM Regulatory elements in the immunoglobulin heavy chain gene 3′-enhancers induce c-myc deregulation and lymphomagenesis in murine B cells J Biol Chem 2005, 280(13):12766-12773 10.1074/ jbc.M412446200 15687498
    • (2005) J Biol Chem , vol.280 , Issue.13 , pp. 12766-12773
    • Wang, J.1    Boxer, L.M.2
  • 35
    • 16844381831 scopus 로고    scopus 로고
    • Mechanisms of B-cell lymphoma pathogenesis
    • 10.1038/nrc1589 15803153
    • Kuppers R Mechanisms of B-cell lymphoma pathogenesis Nat Rev Cancer 2005, 5(4):251-262 10.1038/nrc1589 15803153
    • (2005) Nat Rev Cancer , vol.5 , Issue.4 , pp. 251-262
    • Kuppers, R.1
  • 36
    • 0036675208 scopus 로고    scopus 로고
    • Burkitt's and Burkitt-like lymphoma
    • 10.1007/s11864-002-0029-9 12074766
    • Evens AM Gordon LI Burkitt's and Burkitt-like lymphoma Curr Treat Options Oncol 2002, 3(4):291-305 10.1007/s11864-002-0029-9 12074766
    • (2002) Curr Treat Options Oncol , vol.3 , Issue.4 , pp. 291-305
    • Evens, A.M.1    Gordon, L.I.2
  • 37
    • 4944233187 scopus 로고    scopus 로고
    • Tumour lysis syndrome: New therapeutic strategies and classification
    • 10.1111/j.1365-2141.2004.05094.x 15384972
    • Cairo MS Bishop M Tumour lysis syndrome: New therapeutic strategies and classification Br J Haematol 2004, 127(1):3-11 10.1111/ j.1365-2141.2004.05094.x 15384972
    • (2004) Br J Haematol , vol.127 , Issue.1 , pp. 3-11
    • Cairo, M.S.1    Bishop, M.2
  • 39
    • 0035993192 scopus 로고    scopus 로고
    • Farnesyl transferase inhibitors as anticancer agents
    • 10.1016/S0959-8049(02)00166-1 12175684
    • Haluska P Dy GK Adjei AA Farnesyl transferase inhibitors as anticancer agents Eur J Cancer 2002, 38(13):1685-1700 10.1016/S0959-8049(02)00166-1 12175684
    • (2002) Eur J Cancer , vol.38 , Issue.13 , pp. 1685-1700
    • Haluska, P.1    Dy, G.K.2    Adjei, A.A.3
  • 40
    • 0032541625 scopus 로고    scopus 로고
    • Non-Ras targets of farnesyltransferase inhibitors: Focus on Rho
    • (Reviews) 10.1038/sj.onc.1202175 9779989
    • Lebowitz PF Prendergast GC Non-Ras targets of farnesyltransferase inhibitors: Focus on Rho Oncogene 1998, 17(11 Reviews):1439-1445 10.1038/ sj.onc.1202175 9779989
    • (1998) Oncogene , vol.17 , Issue.11 , pp. 1439-1445
    • Lebowitz, P.F.1    Prendergast, G.C.2
  • 41
    • 0034730625 scopus 로고    scopus 로고
    • Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules
    • 10.1074/jbc.M003469200 10852915
    • Ashar HR James L Gray K Carr D Black S Armstrong L Bishop WR Kirschmeier P Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules J Biol Chem 2000, 275(39):30451-30457 10.1074/jbc.M003469200 10852915
    • (2000) J Biol Chem , vol.275 , Issue.39 , pp. 30451-30457
    • Ashar, H.R.1    James, L.2    Gray, K.3    Carr, D.4    Black, S.5    Armstrong, L.6    Bishop, W.R.7    Kirschmeier, P.8
  • 42
    • 0034777538 scopus 로고    scopus 로고
    • Protein farnesylation in mammalian cells: Effects of farnesyltransferase inhibitors on cancer cells
    • 10.1007/PL00000802 11706990
    • Tamanoi F Gau CL Jiang C Edamatsu H Kato-Stankiewicz J Protein farnesylation in mammalian cells: Effects of farnesyltransferase inhibitors on cancer cells Cell Mol Life Sci 2001, 58(11):1636-1649 10.1007/PL00000802 11706990
    • (2001) Cell Mol Life Sci , vol.58 , Issue.11 , pp. 1636-1649
    • Tamanoi, F.1    Gau, C.L.2    Jiang, C.3    Edamatsu, H.4    Kato-Stankiewicz, J.5
  • 43
    • 34548842466 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors inhibit T-cell cytokine production at the posttranscriptional level
    • 10.1182/blood-2006-06-031088 17545504
    • Marks RE Ho AW Robbel C Kuna T Berk S Gajewski TF Farnesyltransferase inhibitors inhibit T-cell cytokine production at the posttranscriptional level Blood 2007, 110(6):1982-1988 10.1182/blood-2006-06-031088 17545504
    • (2007) Blood , vol.110 , Issue.6 , pp. 1982-1988
    • Marks, R.E.1    Ho, A.W.2    Robbel, C.3    Kuna, T.4    Berk, S.5    Gajewski, T.F.6
  • 46
    • 0011782475 scopus 로고
    • Analysis of RAS oncogene mutations in human lymphoid malignancies
    • 282720 3057505 10.1073/pnas.85.23.9268
    • Neri A Knowles DM Greco A McCormick F Dalla-Favera R Analysis of RAS oncogene mutations in human lymphoid malignancies Proc Natl Acad Sci U S A 1988, 85(23):9268-9272 282720 3057505 10.1073/pnas.85.23.9268
    • (1988) Proc Natl Acad Sci U S A , vol.85 , Issue.23 , pp. 9268-9272
    • Neri, A.1    Knowles, D.M.2    Greco, A.3    McCormick, F.4    Dalla-Favera, R.5
  • 49
    • 0025813213 scopus 로고
    • Autoantibody activity of immunoglobulins isolated from B-cell follicular lymphomas
    • 1859876
    • Dighiero G Hart S Lim A Borche L Levy R Miller RA Autoantibody activity of immunoglobulins isolated from B-cell follicular lymphomas Blood 1991, 78(3):581-585 1859876
    • (1991) Blood , vol.78 , Issue.3 , pp. 581-585
    • Dighiero, G.1    Hart, S.2    Lim, A.3    Borche, L.4    Levy, R.5    Miller, R.A.6
  • 51
    • 0025863138 scopus 로고
    • Effective treatment of small-noncleaved-cell lymphoma with high-intensity, brief-duration chemotherapy
    • 1709685
    • McMaster ML Greer JP Greco FA Johnson DH Wolff SN Hainsworth JD Effective treatment of small-noncleaved-cell lymphoma with high-intensity, brief-duration chemotherapy J Clin Oncol 1991, 9(6):941-946 1709685
    • (1991) J Clin Oncol , vol.9 , Issue.6 , pp. 941-946
    • McMaster, M.L.1    Greer, J.P.2    Greco, F.A.3    Johnson, D.H.4    Wolff, S.N.5    Hainsworth, J.D.6
  • 52
    • 38349165920 scopus 로고    scopus 로고
    • The efficacy of rituximab in high-grade pediatric B-cell lymphoma/ leukemia: A review of available evidence
    • 10.1097/MOP.0b013e3282f424b0 18197034
    • Attias D Weitzman S The efficacy of rituximab in high-grade pediatric B-cell lymphoma/leukemia: A review of available evidence Curr Opin Pediatr 2008, 20(1):17-22 10.1097/MOP.0b013e3282f424b0 18197034
    • (2008) Curr Opin Pediatr , vol.20 , Issue.1 , pp. 17-22
    • Attias, D.1    Weitzman, S.2
  • 53
    • 0022380768 scopus 로고
    • The c-myc oncogene driven by immunoglobulin enhancers induces lymphoid malignancy in transgenic mice
    • 10.1038/318533a0 3906410
    • Adams JM Harris AW Pinkert CA Corcoran LM Alexander WS Cory S Palmiter RD Brinster RL The c-myc oncogene driven by immunoglobulin enhancers induces lymphoid malignancy in transgenic mice Nature 1985, 318(6046);533-538 10.1038/318533a0 3906410
    • (1985) Nature , vol.318 , Issue.6046 , pp. 533-538
    • Adams, J.M.1    Harris, A.W.2    Pinkert, C.A.3    Corcoran, L.M.4    Alexander, W.S.5    Cory, S.6    Palmiter, R.D.7    Brinster, R.L.8
  • 54
    • 0025948793 scopus 로고
    • Elimination from peripheral lymphoid tissues of self-reactive B lymphocytes recognizing membrane-bound antigens
    • 10.1038/353765a0 1944535
    • Hartley SB Crosbie J Brink R Kantor AB Basten A Goodnow CC Elimination from peripheral lymphoid tissues of self-reactive B lymphocytes recognizing membrane-bound antigens Nature 1991, 353(6346):765-769 10.1038/353765a0 1944535
    • (1991) Nature , vol.353 , Issue.6346 , pp. 765-769
    • Hartley, S.B.1    Crosbie, J.2    Brink, R.3    Kantor, A.B.4    Basten, A.5    Goodnow, C.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.