-
1
-
-
2642532810
-
Emerging treatments in acute myeloid leukaemia
-
1:CAS:528:DC%2BD2cXkt1Ggt7o%3D 10.1517/14728214.9.1.55 15155136
-
J Kell, et al. 2004 Emerging treatments in acute myeloid leukaemia Expert Opin Emerg Drugs 9 55 71 1:CAS:528:DC%2BD2cXkt1Ggt7o%3D 10.1517/14728214.9.1.55 15155136
-
(2004)
Expert Opin Emerg Drugs
, vol.9
, pp. 55-71
-
-
Kell, J.1
-
2
-
-
61549135160
-
Emerging treatment strategies for acute myeloid leukemia (AML) in the elderly
-
1:CAS:528:DC%2BD1MXivVWhsr8%3D 10.1016/j.ctrv.2008.09.001 18951721
-
A Kuendgen U Germing 2009 Emerging treatment strategies for acute myeloid leukemia (AML) in the elderly Cancer Treat Rev 35 97 120 1:CAS:528: DC%2BD1MXivVWhsr8%3D 10.1016/j.ctrv.2008.09.001 18951721
-
(2009)
Cancer Treat Rev
, vol.35
, pp. 97-120
-
-
Kuendgen, A.1
Germing, U.2
-
3
-
-
33750020532
-
The incidence and outcome of myeloid malignancies in 2112 adult patients in southeast England
-
17018393
-
KJ Phekoo MA Richards H Moller SA Schey 2006 The incidence and outcome of myeloid malignancies in 2112 adult patients in southeast England Haematologica 91 1400 1404 17018393
-
(2006)
Haematologica
, vol.91
, pp. 1400-1404
-
-
Phekoo, K.J.1
Richards, M.A.2
Moller, H.3
Schey, S.A.4
-
4
-
-
0014347896
-
Arabinosyl cytosine: A useful agent in the treatment of acute leukemia in adults
-
1:STN:280:DyaF1M%2FhtFKnsg%3D%3D 4879053
-
RR Ellison JF Holland M Weil, et al. 1968 Arabinosyl cytosine: a useful agent in the treatment of acute leukemia in adults Blood 32 507 523 1:STN:280:DyaF1M%2FhtFKnsg%3D%3D 4879053
-
(1968)
Blood
, vol.32
, pp. 507-523
-
-
Ellison, R.R.1
Holland, J.F.2
Weil, M.3
-
5
-
-
0014675775
-
Daunorubicin in the treatment of acute myelocytic leukaemia
-
1:STN:280:DyaF1M7gvV2mtg%3D%3D 10.1016/S0140-6736(69)91296-3 4179349
-
M Boiron M Weil C Jacquillat, et al. 1969 Daunorubicin in the treatment of acute myelocytic leukaemia Lancet 1 330 333 1:STN:280:DyaF1M7gvV2mtg%3D%3D 10.1016/S0140-6736(69)91296-3 4179349
-
(1969)
Lancet
, vol.1
, pp. 330-333
-
-
Boiron, M.1
Weil, M.2
Jacquillat, C.3
-
6
-
-
73249135797
-
Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics
-
10.1186/1756-8722-2-23 19490647
-
TK Gregory D Wald Y Chen JM Vermaat Y Xiong W Tse 2009 Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics J Hematol Oncol 2 23 10.1186/1756-8722-2-23 19490647
-
(2009)
J Hematol Oncol
, vol.2
, pp. 23
-
-
Gregory, T.K.1
Wald, D.2
Chen, Y.3
Vermaat, J.M.4
Xiong, Y.5
Tse, W.6
-
7
-
-
33847789058
-
Synthesis of furopyrazole analogs of 1-benzyl-3-(5-hydroxymethyl-2-furyl) indazole (YC-1) as novel anti-leukemia agents
-
1:CAS:528:DC%2BD2sXmtVeitQ%3D%3D 10.1016/j.bmc.2006.12.001 17189698
-
LC Chou LJ Huang JS Yang FY Lee CM Teng SC Kuo 2007 Synthesis of furopyrazole analogs of 1-benzyl-3-(5-hydroxymethyl-2-furyl)indazole (YC-1) as novel anti-leukemia agents Bioorg Med Chem 15 1732 1740 1:CAS:528: DC%2BD2sXmtVeitQ%3D%3D 10.1016/j.bmc.2006.12.001 17189698
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 1732-1740
-
-
Chou, L.C.1
Huang, L.J.2
Yang, J.S.3
Lee, F.Y.4
Teng, C.M.5
Kuo, S.C.6
-
8
-
-
35349005731
-
Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors
-
1:CAS:528:DC%2BD2sXht1ams7zP 10.1016/j.steroids.2007.08.004 17884122
-
VM Moreira TS Vasaitis VC Njar JA Salvador 2007 Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors Steroids 72 939 948 1:CAS:528:DC%2BD2sXht1ams7zP 10.1016/j.steroids.2007.08.004 17884122
-
(2007)
Steroids
, vol.72
, pp. 939-948
-
-
Moreira, V.M.1
Vasaitis, T.S.2
Njar, V.C.3
Salvador, J.A.4
-
9
-
-
34347219022
-
Syntheses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase B/Akt inhibitors with reduced hypotension
-
1:CAS:528:DC%2BD2sXlslGgsrs%3D 10.1021/jm0701019 17523610
-
GD Zhu VB Gandhi J Gong S Thomas, et al. 2007 Syntheses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase B/Akt inhibitors with reduced hypotension J Med Chem 50 2990 3003 1:CAS:528:DC%2BD2sXlslGgsrs%3D 10.1021/jm0701019 17523610
-
(2007)
J Med Chem
, vol.50
, pp. 2990-3003
-
-
Zhu, G.D.1
Gandhi, V.B.2
Gong, J.3
Thomas, S.4
-
10
-
-
33750529730
-
3-(Indol-2-yl) indazoles as Chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6
-
1:CAS:528:DC%2BD28XhtF2jsrbO 10.1016/j.bmcl.2006.08.118 16978863
-
ME Fraley JT Steen EJ Brnardic, et al. 2006 3-(Indol-2-yl) indazoles as Chek1 kinase inhibitors: optimization of potency and selectivity via substitution at C6 Bioorg Med Chem Lett 16 6049 6053 1:CAS:528: DC%2BD28XhtF2jsrbO 10.1016/j.bmcl.2006.08.118 16978863
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 6049-6053
-
-
Fraley, M.E.1
Steen, J.T.2
Brnardic, E.J.3
-
11
-
-
33845868779
-
MZ3 induces apoptosis in human leukemia cells
-
1:CAS:528:DC%2BD28XhtlCksb%2FF 10.1007/s00280-006-0294-6 16900371
-
L Fang Q He Y Hu B Yang 2007 MZ3 induces apoptosis in human leukemia cells Cancer Chemother Pharmacol 59 397 405 1:CAS:528:DC%2BD28XhtlCksb%2FF 10.1007/s00280-006-0294-6 16900371
-
(2007)
Cancer Chemother Pharmacol
, vol.59
, pp. 397-405
-
-
Fang, L.1
He, Q.2
Hu, Y.3
Yang, B.4
-
12
-
-
33847400139
-
R16, a novel amonafide analogue, induces apoptosis and G2-M arrest via poisoning topoisomerase II
-
1:CAS:528:DC%2BD2sXhvVWku7k%3D 10.1158/1535-7163.MCT-06-0584 17308047
-
H Zhu M Huang F Yang Y Chen ZH Miao XH Qian, et al. 2007 R16, a novel amonafide analogue, induces apoptosis and G2-M arrest via poisoning topoisomerase II Mol Cancer Ther 6 484 495 1:CAS:528:DC%2BD2sXhvVWku7k%3D 10.1158/1535-7163.MCT-06-0584 17308047
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 484-495
-
-
Zhu, H.1
Huang, M.2
Yang, F.3
Chen, Y.4
Miao, Z.H.5
Qian, X.H.6
-
13
-
-
17644416399
-
Tirapazamine cytotoxicity for neuroblastoma is p53 dependent
-
1:CAS:528:DC%2BD2MXivFKisb8%3D 10.1158/1078-0432.CCR-04-2382 15814660
-
B Yang CP Reynolds 2005 Tirapazamine cytotoxicity for neuroblastoma is p53 dependent Clin Cancer Res 11 2774 2780 1:CAS:528:DC%2BD2MXivFKisb8%3D 10.1158/1078-0432.CCR-04-2382 15814660
-
(2005)
Clin Cancer Res
, vol.11
, pp. 2774-2780
-
-
Yang, B.1
Reynolds, C.P.2
-
14
-
-
53749099768
-
CPT21, a novel compound with anti-proliferative effect against gastric cancer cell SGC7901
-
1:CAS:528:DC%2BD1cXht1amsrrF 10.1007/s10637-008-9120-9
-
B Zhang Y Luo Q Weng Q He W Lu B Yang 2008 CPT21, a novel compound with anti-proliferative effect against gastric cancer cell SGC7901 Investig New Drugs 26 517 524 1:CAS:528:DC%2BD1cXht1amsrrF 10.1007/s10637-008-9120-9
-
(2008)
Investig New Drugs
, vol.26
, pp. 517-524
-
-
Zhang, B.1
Luo, Y.2
Weng, Q.3
He, Q.4
Lu, W.5
Yang, B.6
-
15
-
-
0037115761
-
Oxidation-triggered c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein (MAP) kinase pathways for apoptosis in human leukaemic cells stimulated by epigallocatechin-3-gallate (EGCG): A distinct pathway from those of chemically induced and receptor-mediated apoptosis
-
1:CAS:528:DC%2BD38Xptlykt70%3D 10.1042/BJ20020101 12206715
-
K Saeki N Kobayashi Y Inazawa, et al. 2002 Oxidation-triggered c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein (MAP) kinase pathways for apoptosis in human leukaemic cells stimulated by epigallocatechin-3-gallate (EGCG): a distinct pathway from those of chemically induced and receptor-mediated apoptosis Biochem J 368 705 720 1:CAS:528:DC%2BD38Xptlykt70%3D 10.1042/BJ20020101 12206715
-
(2002)
Biochem J
, vol.368
, pp. 705-720
-
-
Saeki, K.1
Kobayashi, N.2
Inazawa, Y.3
-
16
-
-
0034765627
-
Apoptosis and the response to anticancer therapy
-
1:CAS:528:DC%2BD3MXos1Oqs7w%3D 10.1097/00001622-200111000-00007 11673685
-
BM Mow AL Blajeski J Chandra SH Kaufmann 2001 Apoptosis and the response to anticancer therapy Curr Opin Oncol 13 453 462 1:CAS:528:DC%2BD3MXos1Oqs7w%3D 10.1097/00001622-200111000-00007 11673685
-
(2001)
Curr Opin Oncol
, vol.13
, pp. 453-462
-
-
Mow, B.M.1
Blajeski, A.L.2
Chandra, J.3
Kaufmann, S.H.4
-
17
-
-
0034641932
-
From bench to clinic with apoptosis-based therapeutic agents
-
1:CAS:528:DC%2BD3cXnsFWrtr8%3D 10.1038/35037747 11048733
-
DW Nicholson 2000 From bench to clinic with apoptosis-based therapeutic agents Nature 407 810 816 1:CAS:528:DC%2BD3cXnsFWrtr8%3D 10.1038/35037747 11048733
-
(2000)
Nature
, vol.407
, pp. 810-816
-
-
Nicholson, D.W.1
-
18
-
-
62549108186
-
Inhibitor of apoptosis proteins in hematological malignancies
-
1:CAS:528:DC%2BD1MXivVKhu7o%3D 10.1038/leu.2008.329 19039324
-
S Fulda, et al. 2009 Inhibitor of apoptosis proteins in hematological malignancies Leukemia 23 467 476 1:CAS:528:DC%2BD1MXivVKhu7o%3D 10.1038/leu.2008.329 19039324
-
(2009)
Leukemia
, vol.23
, pp. 467-476
-
-
Fulda, S.1
-
19
-
-
0037868272
-
Apoptosis induced by topoisomerase inhibitors
-
1:CAS:528:DC%2BD3sXks1Giu7g%3D 10.2174/1568011033482378 12769773
-
O Sordet QA Khan KW Kohn Y Pommier 2003 Apoptosis induced by topoisomerase inhibitors Curr Med Chem Anticancer Agents 3 271 290 1:CAS:528:DC%2BD3sXks1Giu7g%3D 10.2174/1568011033482378 12769773
-
(2003)
Curr Med Chem Anticancer Agents
, vol.3
, pp. 271-290
-
-
Sordet, O.1
Khan, Q.A.2
Kohn, K.W.3
Pommier, Y.4
-
20
-
-
0034708169
-
Differential role of caspase-8 and Bid activation during radiation- and CD95-induced apoptosis
-
1:CAS:528:DC%2BD3cXitFeqtLk%3D 10.1038/sj.onc.1203401 10713706
-
C Belka J Rudner S Wesselborg A Stepczynska P Marini 2000 Differential role of caspase-8 and Bid activation during radiation- and CD95-induced apoptosis Oncogene 19 1181 1190 1:CAS:528:DC%2BD3cXitFeqtLk%3D 10.1038/sj.onc.1203401 10713706
-
(2000)
Oncogene
, vol.19
, pp. 1181-1190
-
-
Belka, C.1
Rudner, J.2
Wesselborg, S.3
Stepczynska, A.4
Marini, P.5
-
21
-
-
49849090421
-
Emodin azide methyl anthraquinone derivative triggers mitochondrial-dependent cell apoptosis involving in caspase-8-mediated Bid cleavage
-
1:CAS:528:DC%2BD1cXnsVSkur0%3D 10.1158/1535-7163.MCT-07-2362 18566240
-
Y Yan X Su Y Liang J Zhang C Shi Y Lu 2008 Emodin azide methyl anthraquinone derivative triggers mitochondrial-dependent cell apoptosis involving in caspase-8-mediated Bid cleavage Mol Cancer Ther 7 1688 1697 1:CAS:528:DC%2BD1cXnsVSkur0%3D 10.1158/1535-7163.MCT-07-2362 18566240
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 1688-1697
-
-
Yan, Y.1
Su, X.2
Liang, Y.3
Zhang, J.4
Shi, C.5
Lu, Y.6
-
22
-
-
15144345497
-
Pro-caspase-3 is a major physiologic target of caspase-8
-
1:CAS:528:DyaK1cXntVShtr0%3D 10.1074/jbc.273.42.27084 9765224
-
HR Stennicke JM Jürgensmeier H Shin, et al. 1998 Pro-caspase-3 is a major physiologic target of caspase-8 J Biol Chem 273 27084 27090 1:CAS:528:DyaK1cXntVShtr0%3D 10.1074/jbc.273.42.27084 9765224
-
(1998)
J Biol Chem
, vol.273
, pp. 27084-27090
-
-
Stennicke, H.R.1
Jürgensmeier, J.M.2
Shin, H.3
-
23
-
-
0033647484
-
Caspase-8 in apoptosis: The beginning of "the end"?
-
1:CAS:528:DC%2BD3cXoslWks7c%3D 11185963
-
M Kruidering GI Evan 2000 Caspase-8 in apoptosis: the beginning of "the end"? IUBMB Life 50 85 90 1:CAS:528:DC%2BD3cXoslWks7c%3D 11185963
-
(2000)
IUBMB Life
, vol.50
, pp. 85-90
-
-
Kruidering, M.1
Evan, G.I.2
-
24
-
-
33644657517
-
Bid, a BH3-only multi-functional molecule, is at the cross road of life and death
-
1:CAS:528:DC%2BD28XhvF2nurs%3D 10.1016/j.gene.2005.10.038 16446060
-
XM Yin 2006 Bid, a BH3-only multi-functional molecule, is at the cross road of life and death Gene 369 7 19 1:CAS:528:DC%2BD28XhvF2nurs%3D 10.1016/j.gene.2005.10.038 16446060
-
(2006)
Gene
, vol.369
, pp. 7-19
-
-
Yin, X.M.1
-
25
-
-
0033525591
-
Solution structure of Bid, an intracellular amplifier of apoptotic signaling
-
1:CAS:528:DyaK1MXitVChsro%3D 10.1016/S0092-8674(00)80572-3 10089877
-
JJ Chou H Li GS Salvesen J Yuan G Wagner 1999 Solution structure of Bid, an intracellular amplifier of apoptotic signaling Cell 96 615 624 1:CAS:528:DyaK1MXitVChsro%3D 10.1016/S0092-8674(00)80572-3 10089877
-
(1999)
Cell
, vol.96
, pp. 615-624
-
-
Chou, J.J.1
Li, H.2
Salvesen, G.S.3
Yuan, J.4
Wagner, G.5
-
26
-
-
17844362452
-
Bid acts on the permeability transition pore complex to induce apoptosis
-
1:CAS:528:DC%2BD3MXnsleiug%3D%3D 10.1038/sj.onc.1204030 11175349
-
N Zamzami, et al. 2000 Bid acts on the permeability transition pore complex to induce apoptosis Oncogene 19 6342 6350 1:CAS:528: DC%2BD3MXnsleiug%3D%3D 10.1038/sj.onc.1204030 11175349
-
(2000)
Oncogene
, vol.19
, pp. 6342-6350
-
-
Zamzami, N.1
-
27
-
-
0042324618
-
Bid activates multiple mitochondrial apoptotic mechanisms in primary hepatocytes after death receptor engagement
-
1:CAS:528:DC%2BD3sXnvVSiu7s%3D 10.1016/S0016-5085(03)01066-7 12949730
-
Y Zhao WX Ding T Qian S Watkins JJ Lemasters XM Yin 2003 Bid activates multiple mitochondrial apoptotic mechanisms in primary hepatocytes after death receptor engagement Gastroenterology 125 854 867 1:CAS:528:DC%2BD3sXnvVSiu7s%3D 10.1016/S0016-5085(03)01066-7 12949730
-
(2003)
Gastroenterology
, vol.125
, pp. 854-867
-
-
Zhao, Y.1
Ding, W.X.2
Qian, T.3
Watkins, S.4
Lemasters, J.J.5
Yin, X.M.6
-
28
-
-
0037016814
-
Caspase activation in equine influenza virus induced apoptotic cell death
-
1:CAS:528:DC%2BD3MXpt1ansrc%3D 10.1016/S0378-1135(01)00468-0 11750143
-
C Lin RE Holland Jr JC Donofrio MH McCoy LR Tudor TM Chambers 2002 Caspase activation in equine influenza virus induced apoptotic cell death Vet Microbiol 84 357 365 1:CAS:528:DC%2BD3MXpt1ansrc%3D 10.1016/S0378-1135(01)00468- 0 11750143
-
(2002)
Vet Microbiol
, vol.84
, pp. 357-365
-
-
Lin, C.1
Holland Jr., R.E.2
Donofrio, J.C.3
McCoy, M.H.4
Tudor, L.R.5
Chambers, T.M.6
-
29
-
-
39049092700
-
Effect of proteasome inhibitors on proliferation and apoptosis of human cutaneous melanoma-derived cell lines
-
1:CAS:528:DC%2BD1cXktFelu7s%3D 10.1111/j.1365-2133.2007.08390.x 18205878
-
A Sorolla A Yeramian X Dolcet AM Pérez de Santos D Llobet, et al. 2008 Effect of proteasome inhibitors on proliferation and apoptosis of human cutaneous melanoma-derived cell lines Br J Dermatol 158 496 504 1:CAS:528:DC%2BD1cXktFelu7s%3D 10.1111/j.1365-2133.2007.08390.x 18205878
-
(2008)
Br J Dermatol
, vol.158
, pp. 496-504
-
-
Sorolla, A.1
Yeramian, A.2
Dolcet, X.3
Santos De Pérez, A.M.4
Llobet, D.5
|