-
1
-
-
67650385302
-
-
American Cancer Society, American Cancer Society, Atlanta
-
Cancer facts and figures 2009 2009, American Cancer Society, American Cancer Society, Atlanta.
-
(2009)
Cancer facts and figures 2009
-
-
-
2
-
-
0032949187
-
Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits the growth of PC-82 human prostate cancer in nude mice
-
Koppán M., Nagy A., Schally A.V., Plonowski A., Halmos G., Arencibia J.M., et al. Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits the growth of PC-82 human prostate cancer in nude mice. The Prostate 1999, 38:151-158.
-
(1999)
The Prostate
, vol.38
, pp. 151-158
-
-
Koppán, M.1
Nagy, A.2
Schally, A.V.3
Plonowski, A.4
Halmos, G.5
Arencibia, J.M.6
-
3
-
-
0030471103
-
Prostate cancer treatment strategies based on tumor-specific biological principles: future directions
-
Carducci M., DeWeese T., Nelson W., Simons J., Sinibaldi V., Eisenberger M. Prostate cancer treatment strategies based on tumor-specific biological principles: future directions. Semin Oncol 1996, 23:56-62.
-
(1996)
Semin Oncol
, vol.23
, pp. 56-62
-
-
Carducci, M.1
DeWeese, T.2
Nelson, W.3
Simons, J.4
Sinibaldi, V.5
Eisenberger, M.6
-
4
-
-
0033104343
-
Gastrin-releasing peptide receptors in the human prostate: relation to neoplastic transformation
-
Markwalder R., Reubi J.C. Gastrin-releasing peptide receptors in the human prostate: relation to neoplastic transformation. Cancer Res 1999, 59:1152-1159.
-
(1999)
Cancer Res
, vol.59
, pp. 1152-1159
-
-
Markwalder, R.1
Reubi, J.C.2
-
5
-
-
0033953894
-
Presence of receptors for bombesin/gastrin-releasing peptide and mRNA for three receptor subtypes in human prostate cancers
-
Sun B., Halmos G., Schally A.V., Wang X., Martinez M. Presence of receptors for bombesin/gastrin-releasing peptide and mRNA for three receptor subtypes in human prostate cancers. The Prostate 2000, 42:295-303.
-
(2000)
The Prostate
, vol.42
, pp. 295-303
-
-
Sun, B.1
Halmos, G.2
Schally, A.V.3
Wang, X.4
Martinez, M.5
-
7
-
-
0034534349
-
Bombesin receptors in distinct tissue compartments of human pancreatic diseases
-
Fleischmann A., Läderach U., Friess H., Buechler M., Reubi J. Bombesin receptors in distinct tissue compartments of human pancreatic diseases. Lab Invest 2000, 80:1807-1817.
-
(2000)
Lab Invest
, vol.80
, pp. 1807-1817
-
-
Fleischmann, A.1
Läderach, U.2
Friess, H.3
Buechler, M.4
Reubi, J.5
-
10
-
-
33846120590
-
Copper chelation chemistry and its role in copper radiopharmaceuticals
-
Wadas T.J., Wong E., Weisman G.R., Anderson C.J. Copper chelation chemistry and its role in copper radiopharmaceuticals. Curr Pharm Des 2007, 13:3-16.
-
(2007)
Curr Pharm Des
, vol.13
, pp. 3-16
-
-
Wadas, T.J.1
Wong, E.2
Weisman, G.R.3
Anderson, C.J.4
-
11
-
-
67651151216
-
True radiotracers: Cu-64 targeting vectors based upon bombesin peptide
-
Hoffman T.J., Smith C.J. True radiotracers: Cu-64 targeting vectors based upon bombesin peptide. Nucl Med Biol 2009, 36:579-585.
-
(2009)
Nucl Med Biol
, vol.36
, pp. 579-585
-
-
Hoffman, T.J.1
Smith, C.J.2
-
13
-
-
0001579481
-
Radiometal-labeled agents (non-technetium) for diagnostic imaging
-
Anderson C.J., Welch M.J. Radiometal-labeled agents (non-technetium) for diagnostic imaging. Chem Rev 1999, 99:2219-2234.
-
(1999)
Chem Rev
, vol.99
, pp. 2219-2234
-
-
Anderson, C.J.1
Welch, M.J.2
-
14
-
-
0030292909
-
Copper radionuclides and radiopharmaceuticals in nuclear medicine
-
Blower P.J., Lewis J.S., Zweit J. Copper radionuclides and radiopharmaceuticals in nuclear medicine. Nucl Med Biol 1996, 23:957-980.
-
(1996)
Nucl Med Biol
, vol.23
, pp. 957-980
-
-
Blower, P.J.1
Lewis, J.S.2
Zweit, J.3
-
15
-
-
1542328068
-
Comparative in vivo stability of copper-64-labeled cross-bridged and conventional tetraazamacrocyclic complexes
-
Boswell C.A., Sun X., Niu W., Weisman G.R., Wong E.H., Rheingold A.L., et al. Comparative in vivo stability of copper-64-labeled cross-bridged and conventional tetraazamacrocyclic complexes. J Med Chem 2004, 47:1465-1474.
-
(2004)
J Med Chem
, vol.47
, pp. 1465-1474
-
-
Boswell, C.A.1
Sun, X.2
Niu, W.3
Weisman, G.R.4
Wong, E.H.5
Rheingold, A.L.6
-
16
-
-
0031853012
-
The in vivo behavior of copper-64-labeled azamacrocyclic complexes
-
Jones-Wilson T.M., Deal K.A., Anderson C.J., McCarthy D.W., Kovacs Z., Motekaitis R.J., et al. The in vivo behavior of copper-64-labeled azamacrocyclic complexes. Nucl Med Biol 1998, 25:523-530.
-
(1998)
Nucl Med Biol
, vol.25
, pp. 523-530
-
-
Jones-Wilson, T.M.1
Deal, K.A.2
Anderson, C.J.3
McCarthy, D.W.4
Kovacs, Z.5
Motekaitis, R.J.6
-
17
-
-
0037122750
-
Radiolabeling and in vivo behavior of copper-64-labeled cross-bridged cyclam ligands
-
Sun X., Wuest M., Weisman G.R., Wong E.H., Reed D.P., Boswell C.A., et al. Radiolabeling and in vivo behavior of copper-64-labeled cross-bridged cyclam ligands. J Med Chem 2002, 45:469-477.
-
(2002)
J Med Chem
, vol.45
, pp. 469-477
-
-
Sun, X.1
Wuest, M.2
Weisman, G.R.3
Wong, E.H.4
Reed, D.P.5
Boswell, C.A.6
-
18
-
-
0034741572
-
Synthesis of a new cage ligand, SarAr, and its complexation with selected transition metal ions for potential use in radioimaging
-
Bartolo N.M.D., Sargeson A.M., Donlevy T.M., Smith S.V. Synthesis of a new cage ligand, SarAr, and its complexation with selected transition metal ions for potential use in radioimaging. J Chem Soc, Dalton Trans 2001, 2303-2309.
-
(2001)
J Chem Soc, Dalton Trans
, pp. 2303-2309
-
-
Bartolo, N.M.D.1
Sargeson, A.M.2
Donlevy, T.M.3
Smith, S.V.4
-
19
-
-
41149175119
-
64Cu-labeling, and bioconjugation of a new bis(2-pyridylmethyl) derivative of 1,4,7-triazacyclononane
-
64Cu-labeling, and bioconjugation of a new bis(2-pyridylmethyl) derivative of 1,4,7-triazacyclononane. Bioconjugate Chem 2008, 19:719-730.
-
(2008)
Bioconjugate Chem
, vol.19
, pp. 719-730
-
-
Gasser, G.1
Tjioe, L.2
Graham, B.3
Belousoff, M.J.4
Juran, S.5
Walther, M.6
-
20
-
-
0025976881
-
Kinetics of the isotopic exchange between copper(II) and copper(II) 1,4,7-triazacyclononane-N,N',N' triacetate
-
Pippin C.G.K.K., Mirzadeh S., Gansow O.A. Kinetics of the isotopic exchange between copper(II) and copper(II) 1,4,7-triazacyclononane-N,N',N' triacetate. J Labelled Compd Radiopharm 1991, 30:221.
-
(1991)
J Labelled Compd Radiopharm
, vol.30
, pp. 221
-
-
Pippin, C.G.K.K.1
Mirzadeh, S.2
Gansow, O.A.3
-
21
-
-
77952504766
-
Capturing copper for molecular imaging and therapy
-
Research Signpost, Kerala, India, X. Chen (Ed.)
-
Meares C.F. Capturing copper for molecular imaging and therapy. Recent Advances of Bioconjugation Chemistry in Molecular Imaging 2008, 227-241. Research Signpost, Kerala, India. X. Chen (Ed.).
-
(2008)
Recent Advances of Bioconjugation Chemistry in Molecular Imaging
, pp. 227-241
-
-
Meares, C.F.1
-
22
-
-
0015861774
-
i) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
i) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 1973, 22:3099-3108.
-
(1973)
Biochem Pharmacol
, vol.22
, pp. 3099-3108
-
-
Yung-Chi, C.1
Prusoff, W.H.2
-
23
-
-
33646050623
-
64Cu-labeled bombesin analogs in a mouse model of human prostate adenocarcinoma
-
64Cu-labeled bombesin analogs in a mouse model of human prostate adenocarcinoma. Nucl Med Biol 2006, 33:371-380.
-
(2006)
Nucl Med Biol
, vol.33
, pp. 371-380
-
-
Yang, Y.S.1
Zhang, X.2
Xiong, Z.3
Chen, X.4
-
24
-
-
33746771019
-
Imaging pancreatic cancer with a peptide-nanoparticle conjugate targeted to normal pancreas
-
Montet X., Weissleder R., Josephson L. Imaging pancreatic cancer with a peptide-nanoparticle conjugate targeted to normal pancreas. Bioconjugate Chem 2006, 17:905-911.
-
(2006)
Bioconjugate Chem
, vol.17
, pp. 905-911
-
-
Montet, X.1
Weissleder, R.2
Josephson, L.3
-
25
-
-
25044449670
-
Crystallographic and thermodynamic study of metal ion size selectivity in the ligand 1,4,7-triazacyclononane-N,N',N'-triacetate
-
Van der Merwe M.J., Boeyens J.C.A., Hancock R.D. Crystallographic and thermodynamic study of metal ion size selectivity in the ligand 1,4,7-triazacyclononane-N,N',N'-triacetate. Inorg Chem 1985, 24:1208-1213.
-
(1985)
Inorg Chem
, vol.24
, pp. 1208-1213
-
-
Van der Merwe, M.J.1
Boeyens, J.C.A.2
Hancock, R.D.3
-
26
-
-
0037945450
-
111In-labeled bombesin analogs as potential radiopharmaceuticals for specific targeting of gastrin-releasing peptide receptors expressed on human prostate cancer cells
-
111In-labeled bombesin analogs as potential radiopharmaceuticals for specific targeting of gastrin-releasing peptide receptors expressed on human prostate cancer cells. J Nucl Med 2003, 44:823-831.
-
(2003)
J Nucl Med
, vol.44
, pp. 823-831
-
-
Hoffman, T.J.1
Gali, H.2
Smith, C.J.3
Sieckman, G.L.4
Hayes, D.L.5
Owen, N.K.6
-
27
-
-
12244301557
-
2: an in vitro/in vivo structure-activity relationship study where X= 0-, 3-, 5-, 8-, and 11-carbon tethering moieties
-
2: an in vitro/in vivo structure-activity relationship study where X= 0-, 3-, 5-, 8-, and 11-carbon tethering moieties. Bioconjugate Chem 2002, 14:93-102.
-
(2002)
Bioconjugate Chem
, vol.14
, pp. 93-102
-
-
Smith, C.J.1
Gali, H.2
Sieckman, G.L.3
Higginbotham, C.4
Volkert, W.A.5
Hoffman, T.J.6
-
31
-
-
20244376908
-
Progress and promise of FDG-PET imaging for cancer patient management and oncologic drug development
-
Kelloff G.J., Hoffman J.M., Johnson B., Scher H.I., Siegel B.A., Cheng E.Y., et al. Progress and promise of FDG-PET imaging for cancer patient management and oncologic drug development. Clin Cancer Res 2005, 11:2785-2808.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 2785-2808
-
-
Kelloff, G.J.1
Hoffman, J.M.2
Johnson, B.3
Scher, H.I.4
Siegel, B.A.5
Cheng, E.Y.6
-
33
-
-
0032993484
-
Fluorine-18-fluorodeoxyglucose positron emission tomography is useless for the detection of local recurrence after radical prostatectomy
-
Hofer C., Laubenbacher C., Block T., Breul J., Hartung R., Schwaiger M. Fluorine-18-fluorodeoxyglucose positron emission tomography is useless for the detection of local recurrence after radical prostatectomy. Eur Urol 1999, 36:31-35.
-
(1999)
Eur Urol
, vol.36
, pp. 31-35
-
-
Hofer, C.1
Laubenbacher, C.2
Block, T.3
Breul, J.4
Hartung, R.5
Schwaiger, M.6
-
35
-
-
38949198118
-
Bombesin receptor antagonists may be preferable to agonists for tumor targeting
-
Cescato R., Maina T., Nock B., Nikolopoulou A., Charalambidis D., Piccand V., et al. Bombesin receptor antagonists may be preferable to agonists for tumor targeting. J Nucl Med 2008, 49:318-326.
-
(2008)
J Nucl Med
, vol.49
, pp. 318-326
-
-
Cescato, R.1
Maina, T.2
Nock, B.3
Nikolopoulou, A.4
Charalambidis, D.5
Piccand, V.6
-
36
-
-
77956996650
-
64Cu-NO2A-bombesin antagonist and agonist ligands
-
[submitted]
-
64Cu-NO2A-bombesin antagonist and agonist ligands. Nucl Med Biol 2010, [submitted].
-
(2010)
Nucl Med Biol
-
-
Smith, C.J.1
|