-
1
-
-
38349054953
-
Novel therapies targeting the apoptosis pathway for the treatment of acute myeloid leukemia
-
Schimmer A.D. Novel therapies targeting the apoptosis pathway for the treatment of acute myeloid leukemia. Curr. Treat. Options Oncol. 8 (2007) 277-286
-
(2007)
Curr. Treat. Options Oncol.
, vol.8
, pp. 277-286
-
-
Schimmer, A.D.1
-
2
-
-
0023752982
-
Use of all-trans retinoic acid in the treatment of acute promyelocytic leukemia
-
Huang M.E., Ye Y.C., Chen S.R., Chai J.R., Lu J.X., Zhoa L., Gu L.J., and Wang Z.Y. Use of all-trans retinoic acid in the treatment of acute promyelocytic leukemia. Blood 72 (1988) 567-572
-
(1988)
Blood
, vol.72
, pp. 567-572
-
-
Huang, M.E.1
Ye, Y.C.2
Chen, S.R.3
Chai, J.R.4
Lu, J.X.5
Zhoa, L.6
Gu, L.J.7
Wang, Z.Y.8
-
3
-
-
33846621955
-
Small molecule tyrosine kinase inhibitors in the treatment of solid tumors: an update of recent developments
-
Steeghs N., Nortier J.W., and Gelderblom H. Small molecule tyrosine kinase inhibitors in the treatment of solid tumors: an update of recent developments. Ann. Surg. Oncol. 14 (2007) 942-953
-
(2007)
Ann. Surg. Oncol.
, vol.14
, pp. 942-953
-
-
Steeghs, N.1
Nortier, J.W.2
Gelderblom, H.3
-
4
-
-
60749136424
-
Targeted drugs in chronic myeloid leukemia
-
Gora-Tybor J., and Robak T. Targeted drugs in chronic myeloid leukemia. Curr. Med. Chem. 15 (2008) 3036-3051
-
(2008)
Curr. Med. Chem.
, vol.15
, pp. 3036-3051
-
-
Gora-Tybor, J.1
Robak, T.2
-
5
-
-
38349062330
-
Exploiting signal transduction pathways in acute myelogenous leukemia
-
Perl A.E., and Carroll M. Exploiting signal transduction pathways in acute myelogenous leukemia. Curr. Treat. Options Oncol. 8 (2007) 265-276
-
(2007)
Curr. Treat. Options Oncol.
, vol.8
, pp. 265-276
-
-
Perl, A.E.1
Carroll, M.2
-
6
-
-
54249090796
-
Significant cytotoxic activity in vitro of the EGFR tyrosine kinase inhibitor gefitinib in acute myeloblastic leukaemia
-
Lindhagen E., Eriksson A., Wickström M., Danielsson K., Grundmark B., Henriksson R., Nygren P., Aleskog A., Larsson R., and Höglund M. Significant cytotoxic activity in vitro of the EGFR tyrosine kinase inhibitor gefitinib in acute myeloblastic leukaemia. Eur. J. Haematol. 81 (2008) 344-353
-
(2008)
Eur. J. Haematol.
, vol.81
, pp. 344-353
-
-
Lindhagen, E.1
Eriksson, A.2
Wickström, M.3
Danielsson, K.4
Grundmark, B.5
Henriksson, R.6
Nygren, P.7
Aleskog, A.8
Larsson, R.9
Höglund, M.10
-
7
-
-
27144443376
-
Gefitinib induces myeloid differentiation of acute myeloid leukemia
-
Stegmaier K., Corsello S.M., Ross K.N., Wong J.S., Deangelo D.J., and Golub T.R. Gefitinib induces myeloid differentiation of acute myeloid leukemia. Blood 106 (2005) 2841-2848
-
(2005)
Blood
, vol.106
, pp. 2841-2848
-
-
Stegmaier, K.1
Corsello, S.M.2
Ross, K.N.3
Wong, J.S.4
Deangelo, D.J.5
Golub, T.R.6
-
8
-
-
34547582880
-
Molecular mechanisms of ZD1839 (Iressa)-induced apoptosis in human leukemic U937 cells
-
Moon D.O., Kim M.O., Lee J.D., Choi Y.H., Lee M.K., and Kim G.Y. Molecular mechanisms of ZD1839 (Iressa)-induced apoptosis in human leukemic U937 cells. Acta Pharmacol. Sin. 28 (2007) 1205-1214
-
(2007)
Acta Pharmacol. Sin.
, vol.28
, pp. 1205-1214
-
-
Moon, D.O.1
Kim, M.O.2
Lee, J.D.3
Choi, Y.H.4
Lee, M.K.5
Kim, G.Y.6
-
9
-
-
41349111281
-
Erlotinib exhibits antineoplastic off-target effects in AML and MDS: a preclinical study
-
Boehrer S., Ades L., Braun T., Galluzzi L., Grosjean J., Fabre C., Le Roux G., Gardin C., Martin A., de Botton S., Fenaux P., and Kroemer G. Erlotinib exhibits antineoplastic off-target effects in AML and MDS: a preclinical study. Blood 111 (2008) 2170-2180
-
(2008)
Blood
, vol.111
, pp. 2170-2180
-
-
Boehrer, S.1
Ades, L.2
Braun, T.3
Galluzzi, L.4
Grosjean, J.5
Fabre, C.6
Le Roux, G.7
Gardin, C.8
Martin, A.9
de Botton, S.10
Fenaux, P.11
Kroemer, G.12
-
10
-
-
0033587022
-
Tyrosine kinase inhibitors. 15. 4-(Phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor
-
Smaill J.B., Palmer B.D., Rewcastle G.W., Denny W.A., McNamara D.J., Dobrusin E.M., Bridges A.J., Zhou H., Showalter H.D., Winters R.T., Leopold W.R., Fry D.W., Nelson J.M., Slintak V., Elliot W.L., Roberts B.J., Vincent P.W., and Patmore S.J. Tyrosine kinase inhibitors. 15. 4-(Phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor. J. Med. Chem. 42 (1999) 1803-1815
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1803-1815
-
-
Smaill, J.B.1
Palmer, B.D.2
Rewcastle, G.W.3
Denny, W.A.4
McNamara, D.J.5
Dobrusin, E.M.6
Bridges, A.J.7
Zhou, H.8
Showalter, H.D.9
Winters, R.T.10
Leopold, W.R.11
Fry, D.W.12
Nelson, J.M.13
Slintak, V.14
Elliot, W.L.15
Roberts, B.J.16
Vincent, P.W.17
Patmore, S.J.18
-
12
-
-
0026600990
-
Characterization of a U-937 subline which can be induced to differentiate in serum-free medium
-
Öberg F., Hult N., Bjare U., Ivhed I., Kivi S., Bergh J., Larsson L.G., Sundstrom C., and Nilsson K. Characterization of a U-937 subline which can be induced to differentiate in serum-free medium. Int. J. Cancer 50 (1992) 153-160
-
(1992)
Int. J. Cancer
, vol.50
, pp. 153-160
-
-
Öberg, F.1
Hult, N.2
Bjare, U.3
Ivhed, I.4
Kivi, S.5
Bergh, J.6
Larsson, L.G.7
Sundstrom, C.8
Nilsson, K.9
-
13
-
-
67849099218
-
ErbB receptor tyrosine kinases contribute to proliferation of malignant melanoma cells: inhibition by gefitinib (ZD1839)
-
Djerf E.A., Trinks C., Abdiu A., Thunell L.K., Hallbeck A.L., and Walz T.M. ErbB receptor tyrosine kinases contribute to proliferation of malignant melanoma cells: inhibition by gefitinib (ZD1839). Melanoma Res. 19 (2009) 156-166
-
(2009)
Melanoma Res.
, vol.19
, pp. 156-166
-
-
Djerf, E.A.1
Trinks, C.2
Abdiu, A.3
Thunell, L.K.4
Hallbeck, A.L.5
Walz, T.M.6
-
14
-
-
0020530724
-
A detergent-trypsin method for the preparation of nuclei for flow cytometric DNA analysis
-
Vindelov L.L., Christensen I.J., and Nissen N.I. A detergent-trypsin method for the preparation of nuclei for flow cytometric DNA analysis. Cytometry 3 (1983) 323-327
-
(1983)
Cytometry
, vol.3
, pp. 323-327
-
-
Vindelov, L.L.1
Christensen, I.J.2
Nissen, N.I.3
-
15
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
16
-
-
1442332300
-
An inhibitor of the EGF receptor family blocks myeloma cell growth factor activity of HB-EGF and potentiates dexamethasone or anti-IL-6 antibody-induced apoptosis
-
Mahtouk K., Jourdan M., De Vos J., Hertogh C., Fiol G., Jourdan E., Rossi J.F., and Klein B. An inhibitor of the EGF receptor family blocks myeloma cell growth factor activity of HB-EGF and potentiates dexamethasone or anti-IL-6 antibody-induced apoptosis. Blood 103 (2004) 1829-1837
-
(2004)
Blood
, vol.103
, pp. 1829-1837
-
-
Mahtouk, K.1
Jourdan, M.2
De Vos, J.3
Hertogh, C.4
Fiol, G.5
Jourdan, E.6
Rossi, J.F.7
Klein, B.8
-
17
-
-
0035476803
-
The tyrosine kinase inhibitor ZD1839 ("Iressa") inhibits HER2-driven signaling and suppresses the growth of HER2-overexpressing tumor cells
-
Moasser M.M., Basso A., Averbuch S.D., and Rosen N. The tyrosine kinase inhibitor ZD1839 ("Iressa") inhibits HER2-driven signaling and suppresses the growth of HER2-overexpressing tumor cells. Cancer Res. 61 (2001) 7184-7188
-
(2001)
Cancer Res.
, vol.61
, pp. 7184-7188
-
-
Moasser, M.M.1
Basso, A.2
Averbuch, S.D.3
Rosen, N.4
-
18
-
-
0033106398
-
Heparin-binding epidermal growth factor-like growth factor/diphtheria toxin receptor expression by acute myeloid leukemia cells
-
Vinante F., Rigo A., Papini E., Cassatella M.A., and Pizzolo G. Heparin-binding epidermal growth factor-like growth factor/diphtheria toxin receptor expression by acute myeloid leukemia cells. Blood 93 (1999) 1715-1723
-
(1999)
Blood
, vol.93
, pp. 1715-1723
-
-
Vinante, F.1
Rigo, A.2
Papini, E.3
Cassatella, M.A.4
Pizzolo, G.5
-
19
-
-
0033594546
-
Characterization of a naturally occurring ErbB4 isoform that does not bind or activate phosphatidyl inositol 3-kinase
-
Elenius K., Choi C.J., Paul S., Santiestevan E., Nishi E., and Klagsbrun M. Characterization of a naturally occurring ErbB4 isoform that does not bind or activate phosphatidyl inositol 3-kinase. Oncogene 18 (1999) 2607-2615
-
(1999)
Oncogene
, vol.18
, pp. 2607-2615
-
-
Elenius, K.1
Choi, C.J.2
Paul, S.3
Santiestevan, E.4
Nishi, E.5
Klagsbrun, M.6
-
20
-
-
30044432092
-
Proteolytic cleavage and phosphorylation of a tumor-associated ErbB4 isoform promote ligand-independent survival and cancer cell growth
-
Maatta J.A., Sundvall M., Junttila T.T., Peri L., Laine V.J., Isola J., Egeblad M., and Elenius K. Proteolytic cleavage and phosphorylation of a tumor-associated ErbB4 isoform promote ligand-independent survival and cancer cell growth. Mol. Biol. Cell 17 (2006) 67-79
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 67-79
-
-
Maatta, J.A.1
Sundvall, M.2
Junttila, T.T.3
Peri, L.4
Laine, V.J.5
Isola, J.6
Egeblad, M.7
Elenius, K.8
-
21
-
-
0031562676
-
Heregulin degradation in the absence of rapid receptor-mediated internalization
-
Baulida J., and Carpenter G. Heregulin degradation in the absence of rapid receptor-mediated internalization. Exp. Cell Res. 232 (1997) 167-172
-
(1997)
Exp. Cell Res.
, vol.232
, pp. 167-172
-
-
Baulida, J.1
Carpenter, G.2
-
22
-
-
0037224231
-
Identification of ErbB-2 kinase domain motifs required for geldanamycin-induced degradation
-
Tikhomirov O., and Carpenter G. Identification of ErbB-2 kinase domain motifs required for geldanamycin-induced degradation. Cancer Res. 63 (2003) 39-43
-
(2003)
Cancer Res.
, vol.63
, pp. 39-43
-
-
Tikhomirov, O.1
Carpenter, G.2
|