-
1
-
-
0035930133
-
Androgen receptor signaling in androgen-refractory prostate cancer
-
Grossmann ME, Huang H, Tindall DJ. Androgen receptor signaling in androgen-refractory prostate cancer. J Natl Cancer Inst 2001;93: 1687-97.
-
(2001)
J Natl Cancer Inst
, vol.93
, pp. 1687-1697
-
-
Grossmann, M.E.1
Huang, H.2
Tindall, D.J.3
-
2
-
-
0031946389
-
Expression, structure, and function of androgen receptor in advanced prostatic carcinoma
-
Culig Z, Hobisch A, Hittmair A, et al. Expression, structure, and function of androgen receptor in advanced prostatic carcinoma. Prostate 1998;35:63-70.
-
(1998)
Prostate
, vol.35
, pp. 63-70
-
-
Culig, Z.1
Hobisch, A.2
Hittmair, A.3
-
3
-
-
1842612441
-
Molecular determinants of resistance to antiandrogen therapy
-
Chen CD, Welsbie DS, Tran C, et al. Molecular determinants of resistance to antiandrogen therapy. Nat Med 2004; 10:33-9.
-
(2004)
Nat Med
, vol.10
, pp. 33-39
-
-
Chen, C.D.1
Welsbie, D.S.2
Tran, C.3
-
4
-
-
0036170838
-
Disruption of androgen receptor function inhibits proliferation of androgen-refractory prostate cancer cells
-
Zegarra-Moro OL, Schmidt LJ, Huang H, Tindall DJ. Disruption of androgen receptor function inhibits proliferation of androgen-refractory prostate cancer cells. Cancer Res 2002;62:1008-13.
-
(2002)
Cancer Res
, vol.62
, pp. 1008-1013
-
-
Zegarra-Moro, O.L.1
Schmidt, L.J.2
Huang, H.3
Tindall, D.J.4
-
5
-
-
0036494196
-
Functional analysis of 44 mutant androgen receptors from human prostate cancer
-
Shi XB, Ma AH, Xia L, Kung HJ, de Vere White RW. Functional analysis of 44 mutant androgen receptors from human prostate cancer. Cancer Res 2002;62:1496-502.
-
(2002)
Cancer Res
, vol.62
, pp. 1496-1502
-
-
Shi, X.B.1
Ma, A.H.2
Xia, L.3
Kung, H.J.4
de Vere White, R.W.5
-
6
-
-
0035328474
-
Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer
-
Linja MJ, Savinainen KJ, Saramaki OR, Tammela TL, Vessella RL, Visakorpi T. Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer. Cancer Res 2001;61:3550-5.
-
(2001)
Cancer Res
, vol.61
, pp. 3550-3555
-
-
Linja, M.J.1
Savinainen, K.J.2
Saramaki, O.R.3
Tammela, T.L.4
Vessella, R.L.5
Visakorpi, T.6
-
7
-
-
85047697645
-
Inhibition of LNCaP prostate tumor growth in vivo by an antisense oligonucleotide directed against the human androgen receptor
-
Eder IE, Hoffmann J, Rogatsch H, et al. Inhibition of LNCaP prostate tumor growth in vivo by an antisense oligonucleotide directed against the human androgen receptor. Cancer Gene Ther 2002;9:117-25.
-
(2002)
Cancer Gene Ther
, vol.9
, pp. 117-125
-
-
Eder, I.E.1
Hoffmann, J.2
Rogatsch, H.3
-
9
-
-
0036098002
-
Heat shock protein 90 inhibition by 17-allylamino-17-demethoxygeldanamycin: A novel therapeutic approach for treating hormone-refractory prostate cancer
-
Neckers L. Heat shock protein 90 inhibition by 17-allylamino-17-demethoxygeldanamycin: a novel therapeutic approach for treating hormone-refractory prostate cancer. Clin Cancer Res 2002;8:962-6.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 962-966
-
-
Neckers, L.1
-
10
-
-
0037315208
-
Regulation of signaling protein function and trafficking by the hsp90 /hsp7O-based chaperone machinery
-
Pratt WB, Toft DO. Regulation of signaling protein function and trafficking by the hsp90/hsp7O-based chaperone machinery. Exp Biol Mad (Maywood) 2003;228:111-33.
-
(2003)
Exp Biol Mad (Maywood)
, vol.228
, pp. 111-133
-
-
Pratt, W.B.1
Toft, D.O.2
-
11
-
-
0029985050
-
Hsp90 regulates androgen receptor hormone binding affinity in vivo
-
Fang Y, Fliss AE, Robins DM, Caplan AJ. Hsp90 regulates androgen receptor hormone binding affinity in vivo. J Biol Chem 1996;271: 28697-702.
-
(1996)
J Biol Chem
, vol.271
, pp. 28697-28702
-
-
Fang, Y.1
Fliss, A.E.2
Robins, D.M.3
Caplan, A.J.4
-
12
-
-
0142125911
-
Hsp90 as a therapeutic target in prostate cancer
-
Solit DB, Scher HI, Rosen N. Hsp90 as a therapeutic target in prostate cancer. Semin Oncol 2003;30:709-16.
-
(2003)
Semin Oncol
, vol.30
, pp. 709-716
-
-
Solit, D.B.1
Scher, H.I.2
Rosen, N.3
-
14
-
-
0036091221
-
17-Ailylamino-17-demethoxygeldanamycin induces the degradation of androgen receptor and HER-2/neu and inhibits the growth of prostate cancer xenografts
-
Solit DB, Zheng FF, Drobnjak M, at al. 17-Ailylamino-17-demethoxygeldanamycin induces the degradation of androgen receptor and HER-2/neu and inhibits the growth of prostate cancer xenografts. Clin Cancer Res 2002;8:986-93.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 986-993
-
-
Solit, D.B.1
Zheng, F.F.2
Drobnjak, M.3
-
15
-
-
0346995281
-
Combination treatment with 17-N-allylamino-17-demethoxy geldanamycin and acute irradiation produces supra-additive growth suppression in human prostate carcinoma spheroids
-
Enmon R, Yang WH, Ballangrud AM, at al. Combination treatment with 17-N-allylamino-17-demethoxy geldanamycin and acute irradiation produces supra-additive growth suppression in human prostate carcinoma spheroids. Cancer Res 2003;63:8393-9.
-
(2003)
Cancer Res
, vol.63
, pp. 8393-8399
-
-
Enmon, R.1
Yang, W.H.2
Ballangrud, A.M.3
-
16
-
-
0034777916
-
Destabilization of steroid receptors by heat shock protein 90-binding drugs: A ligand-independent approach to hormonal therapy of breast cancer
-
Bagatell R, Khan 0, Paine-Murrieta G, Taylor CW, Akinaga S, Whitesell L. Destabilization of steroid receptors by heat shock protein 90-binding drugs: a ligand-independent approach to hormonal therapy of breast cancer. Clin Cancer Res 2001;7:2076-84.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 2076-2084
-
-
Bagatell, R.1
Khan, O.2
Paine-Murrieta, G.3
Taylor, C.W.4
Akinaga, S.5
Whitesell, L.6
-
17
-
-
0141484615
-
A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
-
Kamal A, Thao L, Sensintaffar J, et al. A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature 2003;425: 407-10.
-
(2003)
Nature
, vol.425
, pp. 407-410
-
-
Kamal, A.1
Thao, L.2
Sensintaffar, J.3
-
18
-
-
0041347519
-
Histone deacetylase inhibitors in cancer therapy: Is transcription the primary target?
-
Johnstone RW, Licht JD. Histone deacetylase inhibitors in cancer therapy: is transcription the primary target? Cancer Cell 2003;4:13-8.
-
(2003)
Cancer Cell
, vol.4
, pp. 13-18
-
-
Johnstone, R.W.1
Licht, J.D.2
-
19
-
-
0035046529
-
Histone deacetylase inhibitors: Development of suberoylanilide hydroxamic acid (SAHA) for the treatment of cancers
-
Richon VM, Zhou X, Rifkind RA, Marks PA. Histone deacetylase inhibitors: development of suberoylanilide hydroxamic acid (SAHA) for the treatment of cancers. Blood Cells Mol Dis 2001;27:260-4.
-
(2001)
Blood Cells Mol Dis
, vol.27
, pp. 260-264
-
-
Richon, V.M.1
Zhou, X.2
Rifkind, R.A.3
Marks, P.A.4
-
20
-
-
85077951985
-
The mechanism of the anti-tumor activity of the histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA)
-
Marks PA. The mechanism of the anti-tumor activity of the histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA). Cell Cycle 2004;3:534-5.
-
(2004)
Cell Cycle
, vol.3
, pp. 534-535
-
-
Marks, P.A.1
-
21
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks P, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 2001;1: 194-202.
-
(2001)
Nat Rev Cancer
, vol.1
, pp. 194-202
-
-
Marks, P.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
22
-
-
0037012344
-
Modulation of p53, ErbB1, ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228
-
Yu X, Guo ZS, Marcu MG, et al. Modulation of p53, ErbB1, ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228. J Natl Cancer Inst 2002;94:504-13.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 504-513
-
-
Yu, X.1
Guo, Z.S.2
Marcu, M.G.3
-
23
-
-
0043016178
-
Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells
-
Nimmanapalli R, Fuino L, Bali P, et al. Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells. Cancer Res 2003;63: 5126-35.
-
(2003)
Cancer Res
, vol.63
, pp. 5126-5135
-
-
Nimmanapalli, R.1
Fuino, L.2
Bali, P.3
-
24
-
-
1642490813
-
Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B
-
Fuino L, Bali P, Wittmann S, at al. Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B. Mol Cancer Ther 2003;2:971 -84.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 971-984
-
-
Fuino, L.1
Bali, P.2
Wittmann, S.3
-
25
-
-
0141953928
-
The discovery of NVP-LA0824: From concept to clinic
-
Remiszewski SW. The discovery of NVP-LA0824: from concept to clinic. Curr Med Chem 2003; 10:2393-402.
-
(2003)
Curr Med Chem
, vol.10
, pp. 2393-2402
-
-
Remiszewski, S.W.1
-
26
-
-
10744229917
-
N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: Discovery of (2E)-N-hydroxy-3-[4-[(2-hydroxyethyl) [2-(1 H-indol-3-yl)ethyl]amino]methyllphenyl]-2-propenamide (NVP-LAQ824)
-
Remiszewski SW, Sambucetti LC, Bair KW, at al. N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: discovery of (2E)-N-hydroxy-3-[4-[(2-hydroxyethyl) [2-(l H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824). J Med Chem 2003;46:4609-24.
-
(2003)
J Med Chem
, vol.46
, pp. 4609-4624
-
-
Remiszewski, S.W.1
Sambucetti, L.C.2
Bair, K.W.3
-
27
-
-
9144225360
-
Selective growth inhibition of tumor cells by a novel histone deacetylase inhibitor, NVP-LAQ824
-
Atadja P, Gao L, Kwon P, et al. Selective growth inhibition of tumor cells by a novel histone deacetylase inhibitor, NVP-LAQ824. Cancer Res 2004;64:689-95.
-
(2004)
Cancer Res
, vol.64
, pp. 689-695
-
-
Atadja, P.1
Gao, L.2
Kwon, P.3
-
28
-
-
0141593496
-
NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma
-
Catley L, Weisberg E, Tai YT, at al. NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma. Blood 2003;102:2615-22.
-
(2003)
Blood
, vol.102
, pp. 2615-2622
-
-
Catley, L.1
Weisberg, E.2
Tai, Y.T.3
-
29
-
-
3142676436
-
Overriding imatinib resistance with a novel ABL kinase inhibitor
-
Shah NP, Tran C, Lee FY, Chen P, Norris D, Sawyers CL. Overriding imatinib resistance with a novel ABL kinase inhibitor. Science 2004;305: 399-401.
-
(2004)
Science
, vol.305
, pp. 399-401
-
-
Shah, N.P.1
Tran, C.2
Lee, F.Y.3
Chen, P.4
Norris, D.5
Sawyers, C.L.6
-
30
-
-
5144231866
-
SRCircumventing imatinib resistance
-
Deininger MW, Druker BJ. SRCircumventing imatinib resistance. Cancer Cell 2004;6:108-10.
-
(2004)
Cancer Cell
, vol.6
, pp. 108-110
-
-
Deininger, M.W.1
Druker, B.J.2
-
31
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
Butler LM, Agus DB, Scher HI, at al. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res 2000;60:5165-70.
-
(2000)
Cancer Res
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
-
32
-
-
0028321891
-
Derivation of androgen-independent human LNCaP prostatic cancer cell sublines: Role of bone stromal cells
-
Wu HC, Hsieh JT, Gleave ME, Brown NM, Pathak S, Chung LW. Derivation of androgen-independent human LNCaP prostatic cancer cell sublines: role of bone stromal cells. Int J Cancer 1994;57:406-12.
-
(1994)
Int J Cancer
, vol.57
, pp. 406-412
-
-
Wu, H.C.1
Hsieh, J.T.2
Gleave, M.E.3
Brown, N.M.4
Pathak, S.5
Chung, L.W.6
-
33
-
-
0028272478
-
Androgen-independent cancer progression and bone metastasis in the LNCaP model of human prostate cancer
-
Thalmann GN, Anezinis PE, Chang SM, at al. Androgen-independent cancer progression and bone metastasis in the LNCaP model of human prostate cancer. Cancer Res 1994;54:2577-81.
-
(1994)
Cancer Res
, vol.54
, pp. 2577-2581
-
-
Thalmann, G.N.1
Anezinis, P.E.2
Chang, S.M.3
-
34
-
-
16944366096
-
Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice
-
Klein KA, Reiter RE, Redula J, at al. Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice. Nat Mad 1997;3:402-8.
-
(1997)
Nat Mad
, vol.3
, pp. 402-408
-
-
Klein, K.A.1
Reiter, R.E.2
Redula, J.3
-
35
-
-
0038561224
-
Androgen stimulates matrix metalloproteinase-2 expression in human prostate cancer
-
Liao X, Thrasher JB, Pelling J, Holzbeierlein J, Sang QX, Li B. Androgen stimulates matrix metalloproteinase-2 expression in human prostate cancer. Endocrinology 2003; 144:1656-63.
-
(2003)
Endocrinology
, vol.144
, pp. 1656-1663
-
-
Liao, X.1
Thrasher, J.B.2
Pelling, J.3
Holzbeierlein, J.4
Sang, Q.X.5
Li, B.6
-
36
-
-
0032486476
-
Role of tyrosine kinase activity of epidermal growth factor receptor in the lysophosphatidic acid-stimulated mitogen-activated protein kinase pathway
-
Cunnick JM, Dorsey JF, Standley T, et al. Role of tyrosine kinase activity of epidermal growth factor receptor in the lysophosphatidic acid-stimulated mitogen-activated protein kinase pathway. J Biol Chem 1998; 273:14468-75.
-
(1998)
J Biol Chem
, vol.273
, pp. 14468-14475
-
-
Cunnick, J.M.1
Dorsey, J.F.2
Standley, T.3
-
37
-
-
1542289021
-
Roles of Gab1 and SHP2 in paxillin tyrosine dephosphorylation and Src activation in response to epidermal growth factor
-
Ren Y, Meng S, Mai L, Zhao ZJ, Jove R, Wu J. Roles of Gab1 and SHP2 in paxillin tyrosine dephosphorylation and Src activation in response to epidermal growth factor. J Biol Chem 2004;279:8497-505.
-
(2004)
J Biol Chem
, vol.279
, pp. 8497-8505
-
-
Ren, Y.1
Meng, S.2
Mai, L.3
Zhao, Z.J.4
Jove, R.5
Wu, J.6
-
38
-
-
0034095603
-
The pyrido[2,3-d]pyrimidine derivative PD180970 inhibits p210Bcr-Abl tyrosine kinase and induces apoptosis of K562 leukemic cells
-
Dorsey JF, Jove R, Kraker AJ, Wu J. The pyrido[2,3-d]pyrimidine derivative PD180970 inhibits p210Bcr-Abl tyrosine kinase and induces apoptosis of K562 leukemic cells. Cancer Res 2000;60: 3127-31.
-
(2000)
Cancer Res
, vol.60
, pp. 3127-3131
-
-
Dorsey, J.F.1
Jove, R.2
Kraker, A.J.3
Wu, J.4
-
39
-
-
0028170951
-
Rapid deactivation of MAP kinase in PC12 cells occurs independently of induction of phosphatase MKP-1
-
Wu J, Lau LF, Sturgill TW. Rapid deactivation of MAP kinase in PC12 cells occurs independently of induction of phosphatase MKP-1. FEES Lett 1994;353:9-12.
-
(1994)
FEES Lett
, vol.353
, pp. 9-12
-
-
Wu, J.1
Lau, L.F.2
Sturgill, T.W.3
-
40
-
-
0036479127
-
Molecular cloning and characterization of a novel histone deacetylase HDAC10
-
Guardiola AR, Yao TP. Molecular cloning and characterization of a novel histone deacetylase HDAC10. J Biol Chem 2002;277:3350-6.
-
(2002)
J Biol Chem
, vol.277
, pp. 3350-3356
-
-
Guardiola, A.R.1
Yao, T.P.2
-
41
-
-
0242637385
-
Acetylation of androgen receptor enhances coactivator binding and promotes prostate cancer cell growth
-
Fu M, Rao M, Wang C, et al. Acetylation of androgen receptor enhances coactivator binding and promotes prostate cancer cell growth. Mol Cell Biol 2003;23:8563-75.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 8563-8575
-
-
Fu, M.1
Rao, M.2
Wang, C.3
-
42
-
-
0037112372
-
Characterization of a novel androgen receptor mutation in a relapsed CWR22 prostate cancer xenograft and cell line
-
Tepper CG, Boucher DL, Ryan PE, et al. Characterization of a novel androgen receptor mutation in a relapsed CWR22 prostate cancer xenograft and cell line. Cancer Res 2002;62:6606-14.
-
(2002)
Cancer Res
, vol.62
, pp. 6606-6614
-
-
Tepper, C.G.1
Boucher, D.L.2
Ryan, P.E.3
-
43
-
-
0033930522
-
Inhibition of LncaP prostate cancer cells by means of androgen receptor antisense oligonucleotides
-
Eder IE, Culig Z, Ramoner R, et al. Inhibition of LncaP prostate cancer cells by means of androgen receptor antisense oligonucleotides. Cancer Gene Ther 2000;7:997-1007.
-
(2000)
Cancer Gene Ther
, vol.7
, pp. 997-1007
-
-
Eder, I.E.1
Culig, Z.2
Ramoner, R.3
-
44
-
-
3142706069
-
Androgen receptor level controlled by a suppressor complex lost in an androgen-independent prostate cancer cell line
-
Wang LG, Ossowski L, Ferrari AC. Androgen receptor level controlled by a suppressor complex lost in an androgen-independent prostate cancer cell line. Oncogene 2004;23:5175-84.
-
(2004)
Oncogene
, vol.23
, pp. 5175-5184
-
-
Wang, L.G.1
Ossowski, L.2
Ferrari, A.C.3
-
45
-
-
0034614108
-
Her-2-neu expression and progression toward androgen independence in human prostate cancer
-
Signoretti S, Montironi R, Manola J, et al. Her-2-neu expression and progression toward androgen independence in human prostate cancer. J Natl Cancer Inst 2000;92:1918-25.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1918-1925
-
-
Signoretti, S.1
Montironi, R.2
Manola, J.3
-
46
-
-
0037339753
-
Human epidermal receptor-2 expression in prostate cancer
-
Calvo BF, Levine AM, Marcos M, et al. Human epidermal receptor-2 expression in prostate cancer. Clin Cancer Res 2003;9:1087-97.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 1087-1097
-
-
Calvo, B.F.1
Levine, A.M.2
Marcos, M.3
-
47
-
-
0034671668
-
HER-2/neu promotes androgen-independent survival and growth of prostate cancer cells through the Akt pathway
-
Wen Y, Hu MC, Makino K, et al. HER-2/neu promotes androgen-independent survival and growth of prostate cancer cells through the Akt pathway. Cancer Res 2000;60:6841-5.
-
(2000)
Cancer Res
, vol.60
, pp. 6841-6845
-
-
Wen, Y.1
Hu, M.C.2
Makino, K.3
-
48
-
-
0033022342
-
A mechanism for hormone-independent prostate cancer through modulation of androgen receptor signaling by the HER-2/neu tyrosine kinase
-
Craft N, Shostak Y, Carey M, Sawyers CL. A mechanism for hormone-independent prostate cancer through modulation of androgen receptor signaling by the HER-2/neu tyrosine kinase. Nat Mad 1999;5: 280-5.
-
(1999)
Nat Mad
, vol.5
, pp. 280-285
-
-
Craft, N.1
Shostak, Y.2
Carey, M.3
Sawyers, C.L.4
-
49
-
-
7944234374
-
HER2/neu kinase-dependent modulation of androgen receptor function through effects on DNA binding and stability
-
Mellinghoff IK, Vivanco I, Kwon A, Tran C, Wongvipat J, Sawyers CL. HER2/ neu kinase-dependent modulation of androgen receptor function through effects on DNA binding and stability. Cancer Cell 2004;6:517-27.
-
(2004)
Cancer Cell
, vol.6
, pp. 517-527
-
-
Mellinghoff, I.K.1
Vivanco, I.2
Kwon, A.3
Tran, C.4
Wongvipat, J.5
Sawyers, C.L.6
-
50
-
-
4344602002
-
The biology and clinical relevance of the PTEN tumor suppressor pathway
-
Sansal I, Sellers WR. The biology and clinical relevance of the PTEN tumor suppressor pathway. J Clin Oncol 2004;22:2954-63.
-
(2004)
J Clin Oncol
, vol.22
, pp. 2954-2963
-
-
Sansal, I.1
Sellers, W.R.2
|