-
1
-
-
0024491628
-
Localisation of endocrine-related tumours with radioiodinated analogue of somatostatin
-
2563413 1:STN:280:DyaL1M7is1KitQ%3D%3D 10.1016/S0140-6736(89)91258-0
-
Krenning EP, Bakker WH, Breeman WA, Koper JW, Kooij PP, Ausema L, et al. Localisation of endocrine-related tumours with radioiodinated analogue of somatostatin. Lancet 1989;1:242-4.
-
(1989)
Lancet
, vol.1
, pp. 242-244
-
-
Krenning, E.P.1
Bakker, W.H.2
Breeman, W.A.3
Koper, J.W.4
Kooij, P.P.5
Ausema, L.6
-
2
-
-
0042854927
-
Peptide receptors as molecular targets for cancer diagnosis and therapy
-
12920149 1:CAS:528:DC%2BD3sXntlKjtbs%3D 10.1210/er.2002-0007
-
Reubi JC. Peptide receptors as molecular targets for cancer diagnosis and therapy. Endocr Rev 2003;24:389-427.
-
(2003)
Endocr Rev
, vol.24
, pp. 389-427
-
-
Reubi, J.C.1
-
3
-
-
0038579396
-
[99mTc]Demobesin 1, a novel potent bombesin analogue for GRP receptor-targeted tumour imaging
-
12552343 1:CAS:528:DC%2BD3sXms1CntA%3D%3D 10.1007/s00259-002-1040-x
-
Nock B, Nikolopoulou A, Chiotellis E, Loudos G, Maintas D, Reubi JC, et al. [99mTc]Demobesin 1, a novel potent bombesin analogue for GRP receptor-targeted tumour imaging. Eur J Nucl Med Mol Imaging 2003;30:247-58.
-
(2003)
Eur J Nucl Med Mol Imaging
, vol.30
, pp. 247-258
-
-
Nock, B.1
Nikolopoulou, A.2
Chiotellis, E.3
Loudos, G.4
Maintas, D.5
Reubi, J.C.6
-
4
-
-
12144279487
-
Potent bombesin-like peptides for GRP-receptor targeting of tumors with 99mTc: A preclinical study
-
15634004 1:CAS:528:DC%2BD2cXhtVCqsr7P 10.1021/jm049437y
-
Nock BA, Nikolopoulou A, Galanis A, Cordopatis P, Waser B, Reubi JC, et al. Potent bombesin-like peptides for GRP-receptor targeting of tumors with 99mTc: a preclinical study. J Med Chem 2005;48:100-10.
-
(2005)
J Med Chem
, vol.48
, pp. 100-110
-
-
Nock, B.A.1
Nikolopoulou, A.2
Galanis, A.3
Cordopatis, P.4
Waser, B.5
Reubi, J.C.6
-
5
-
-
76449099768
-
Tetraamine-derived bifunctional chelators for technetium-99m labelling: Synthesis, bioconjugation and evaluation as targeted SPECT imaging probes for GRP-receptor-positive tumours
-
20066690 1:CAS:528:DC%2BC3cXitVKrtbs%3D 10.1002/chem.200902011
-
Abiraj K, Mansi R, Tamma ML, Forrer F, Cescato R, Reubi JC, et al. Tetraamine-derived bifunctional chelators for technetium-99m labelling: synthesis, bioconjugation and evaluation as targeted SPECT imaging probes for GRP-receptor-positive tumours. Chemistry 2010;16:2115-24.
-
(2010)
Chemistry
, vol.16
, pp. 2115-2124
-
-
Abiraj, K.1
Mansi, R.2
Tamma, M.L.3
Forrer, F.4
Cescato, R.5
Reubi, J.C.6
-
6
-
-
0013146138
-
Detection of somatostatin receptor-positive tumours using the new 99mTc-tricine-HYNIC-D-Phe1-Tyr3-octreotide: First results in patients and comparison with 111In-DTPA-D-Phe1-octreotide
-
10901448 1:CAS:528:DC%2BD3cXjsVOgtrw%3D 10.1007/s002590050556
-
Bangard M, Béhé M, Guhlke S, Otte R, Bender H, Maecke HR, et al. Detection of somatostatin receptor-positive tumours using the new 99mTc-tricine-HYNIC-D-Phe1-Tyr3-octreotide: first results in patients and comparison with 111In-DTPA-D-Phe1-octreotide. Eur J Nucl Med 2000;27:628-37.
-
(2000)
Eur J Nucl Med
, vol.27
, pp. 628-637
-
-
Bangard, M.1
Béhé, M.2
Guhlke, S.3
Otte, R.4
Bender, H.5
Maecke, H.R.6
-
7
-
-
33746932887
-
Preparation and evaluation of 99mTc-EDDA/HYNIC-[Lys 3]-bombesin for imaging gastrin-releasing peptide receptor-positive tumours
-
16531924 1:CAS:528:DC%2BD28Xitlaku7s%3D 10.1097/01.mnm.0000202863.52046. 7f
-
Ferro-Flores G, Arteaga de Murphy C, Rodriguez-Cortés J, Pedraza-López M, Ramírez-Iglesias MT. Preparation and evaluation of 99mTc-EDDA/HYNIC-[Lys 3]-bombesin for imaging gastrin-releasing peptide receptor-positive tumours. Nucl Med Commun 2006;27:371-6.
-
(2006)
Nucl Med Commun
, vol.27
, pp. 371-376
-
-
Ferro-Flores, G.1
Arteaga De Murphy, C.2
Rodriguez-Cortés, J.3
Pedraza-López, M.4
Ramírez-Iglesias, M.T.5
-
8
-
-
45749108311
-
99mTc-labeled bombesin(7-14)NH2 with favorable properties for SPECT imaging of colon cancer
-
18491928 1:CAS:528:DC%2BD1cXmtFWhu70%3D 10.1021/bc700471z
-
Shi J, Jia B, Liu Z, Yang Z, Yu Z, Chen K, et al. 99mTc-labeled bombesin(7-14)NH2 with favorable properties for SPECT imaging of colon cancer. Bioconjug Chem 2008;19:1170-8.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 1170-1178
-
-
Shi, J.1
Jia, B.2
Liu, Z.3
Yang, Z.4
Yu, Z.5
Chen, K.6
-
9
-
-
3242752014
-
99mTc-labeling and in vitro and in vivo evaluation of HYNIC- and (Nalpha-His)acetic acid-modified [D-Glu1]-minigastrin
-
10.1021/bc0300807 1:CAS:528:DC%2BD2cXlt1yht7k%3D
-
von Guggenberg E, Behe M, Behr TM, Saurer M, Seppi T, Decristoforo C. 99mTc-labeling and in vitro and in vivo evaluation of HYNIC- and (Nalpha-His)acetic acid-modified [D-Glu1]-minigastrin. Bioconjug Chem 2004;15:864-71.
-
(2004)
Bioconjug Chem
, vol.15
, pp. 864-871
-
-
Von Guggenberg, E.1
Behe, M.2
Behr, T.M.3
Saurer, M.4
Seppi, T.5
Decristoforo, C.6
-
10
-
-
0033626271
-
99mTc-EDDA/HYNIC-TOC: A new 99mTc-labelled radiopharmaceutical for imaging somatostatin receptor-positive tumours; First clinical results and intra-patient comparison with 111In-labelled octreotide derivatives
-
11007513 1:CAS:528:DC%2BD3cXnsFCjsrc%3D 10.1007/s002590000289
-
Decristoforo C, Mather SJ, Cholewinski W, Donnemiller E, Riccabona G, Moncayo R. 99mTc-EDDA/HYNIC-TOC: a new 99mTc-labelled radiopharmaceutical for imaging somatostatin receptor-positive tumours; first clinical results and intra-patient comparison with 111In-labelled octreotide derivatives. Eur J Nucl Med 2000;27:1318-25.
-
(2000)
Eur J Nucl Med
, vol.27
, pp. 1318-1325
-
-
Decristoforo, C.1
Mather, S.J.2
Cholewinski, W.3
Donnemiller, E.4
Riccabona, G.5
Moncayo, R.6
-
11
-
-
77954986457
-
Exendin-4-based radiopharmaceuticals for glucagonlike peptide-1 receptor PET/CT and SPECT/CT
-
20595511 1:CAS:528:DC%2BC3cXhtVWmu73F 10.2967/jnumed.110.074914
-
Wild D, Wicki A, Mansi R, Béhé M, Keil B, Bernhardt P, et al. Exendin-4-based radiopharmaceuticals for glucagonlike peptide-1 receptor PET/CT and SPECT/CT. J Nucl Med 2010;51:1059-67.
-
(2010)
J Nucl Med
, vol.51
, pp. 1059-1067
-
-
Wild, D.1
Wicki, A.2
Mansi, R.3
Béhé, M.4
Keil, B.5
Bernhardt, P.6
-
12
-
-
58249137680
-
The chemistry of technetium-water complexes within the manganese triad: Challenges and perspectives
-
Alberto R. The chemistry of technetium-water complexes within the manganese triad: challenges and perspectives. Eur J Inorg Chem 2009:21-31.
-
(2009)
Eur J Inorg Chem
, pp. 21-31
-
-
Alberto, R.1
-
13
-
-
77952468760
-
Coordinating radiometals of copper, gallium, indium, yttrium, and zirconium for PET and SPECT imaging of disease
-
20415480 1:CAS:528:DC%2BC3cXltFChtro%3D 10.1021/cr900325h
-
Wadas TJ, Wong EH, Weisman GR, Anderson CJ. Coordinating radiometals of copper, gallium, indium, yttrium, and zirconium for PET and SPECT imaging of disease. Chem Rev 2010;110:2858-902.
-
(2010)
Chem Rev
, vol.110
, pp. 2858-2902
-
-
Wadas, T.J.1
Wong, E.H.2
Weisman, G.R.3
Anderson, C.J.4
-
14
-
-
84878457151
-
Radiometals (non-Tc, non-Re) and bifunctional labeling chemistry
-
A. Vértes S. Nagy Z. Klencsár R.G. Lovas F. Rösch (eds) Springer Heidelberg 10.1007/978-1-4419-0720-2-45
-
Fani M, Good S, Maecke HR. Radiometals (non-Tc, non-Re) and bifunctional labeling chemistry. In: Vértes A, Nagy S, Klencsár Z, Lovas RG, Rösch F, editors. Handbook of nuclear chemistry. Heidelberg: Springer; 2011. p. 2143-78.
-
(2011)
Handbook of Nuclear Chemistry
, pp. 2143-2178
-
-
Fani, M.1
Good, S.2
Maecke, H.R.3
-
15
-
-
79958025504
-
[68Ga]NODAGA-RGD for imaging alphavbeta3 integrin expression
-
21487838 1:CAS:528:DC%2BC3MXmvVaisLc%3D 10.1007/s00259-011-1778-0
-
Knetsch PA, Petrik M, Griessinger CM, Rangger C, Fani M, Kesenheimer C, et al. [68Ga]NODAGA-RGD for imaging alphavbeta3 integrin expression. Eur J Nucl Med Mol Imaging 2011;38:1303-12.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 1303-1312
-
-
Knetsch, P.A.1
Petrik, M.2
Griessinger, C.M.3
Rangger, C.4
Fani, M.5
Kesenheimer, C.6
-
16
-
-
34548864369
-
Radiolabeling of TETA- and CB-TE2A-conjugated peptides with copper-64
-
17406569 1:CAS:528:DC%2BD2sXhtFGjt7fJ 10.1038/nprot.2006.431
-
Wadas TJ, Anderson CJ. Radiolabeling of TETA- and CB-TE2A-conjugated peptides with copper-64. Nat Protoc 2006;1:3062-8.
-
(2006)
Nat Protoc
, vol.1
, pp. 3062-3068
-
-
Wadas, T.J.1
Anderson, C.J.2
-
17
-
-
33745834770
-
Validation of a novel CHX-A″ derivative suitable for peptide conjugation: Small animal PET/CT imaging using yttrium-86-CHX-A″- octreotide
-
16821789 1:CAS:528:DC%2BD28XmtVSitrc%3D 10.1021/jm060317v
-
Clifford T, Boswell CA, Biddlecombe GB, Lewis JS, Brechbiel MW. Validation of a novel CHX-A″ derivative suitable for peptide conjugation: small animal PET/CT imaging using yttrium-86-CHX-A″-octreotide. J Med Chem 2006;49:4297-304.
-
(2006)
J Med Chem
, vol.49
, pp. 4297-4304
-
-
Clifford, T.1
Boswell, C.A.2
Biddlecombe, G.B.3
Lewis, J.S.4
Brechbiel, M.W.5
-
18
-
-
0037700078
-
Optimising conditions for radiolabelling of DOTA-peptides with 90Y, 111In and 177Lu at high specific activities
-
12677301 1:CAS:528:DC%2BD3sXjvF2lsb4%3D 10.1007/s00259-003-1142-0
-
Breeman WA, De Jong M, Visser TJ, Erion JL, Krenning EP. Optimising conditions for radiolabelling of DOTA-peptides with 90Y, 111In and 177Lu at high specific activities. Eur J Nucl Med Mol Imaging 2003;30:917-20.
-
(2003)
Eur J Nucl Med Mol Imaging
, vol.30
, pp. 917-920
-
-
Breeman, W.A.1
De Jong, M.2
Visser, T.J.3
Erion, J.L.4
Krenning, E.P.5
-
19
-
-
2442649352
-
Microwave-supported preparation of (68)Ga bioconjugates with high specific radioactivity
-
15149183 1:CAS:528:DC%2BD2cXjt12kt78%3D 10.1021/bc030078f
-
Velikyan I, Beyer GJ, Långström B. Microwave-supported preparation of (68)Ga bioconjugates with high specific radioactivity. Bioconjug Chem 2004;15:554-60.
-
(2004)
Bioconjug Chem
, vol.15
, pp. 554-560
-
-
Velikyan, I.1
Beyer, G.J.2
Långström, B.3
-
20
-
-
0033033382
-
Radiometal-labelled macrocyclic chelator-derivatised somatostatin analogue with superb tumour-targeting properties and potential for receptor-mediated internal radiotherapy
-
1:CAS:528:DyaK1MXksVansbY%3D 10.1002/(SICI)1521-3765(19990702)5: 7<1974: AID-CHEM1974>3.0.CO;2-X
-
Heppeler A, Froidevaux S, Mäcke HR, Jermann E, Behe M, Powell P, et al. Radiometal-labelled macrocyclic chelator-derivatised somatostatin analogue with superb tumour-targeting properties and potential for receptor-mediated internal radiotherapy. Chem Eur J 1999;5:1974-81.
-
(1999)
Chem Eur J
, vol.5
, pp. 1974-1981
-
-
Heppeler, A.1
Froidevaux, S.2
MäcKe, H.R.3
Jermann, E.4
Behe, M.5
Powell, P.6
-
21
-
-
0033822875
-
A convenient synthesis of novel bifunctional prochelators for coupling to bioactive peptides for radiometal labelling
-
10999487 1:CAS:528:DC%2BD3cXmtF2ht7Y%3D 10.1016/S0960-894X(00)00413-3
-
Eisenwiener KP, Powell P, Mäcke HR. A convenient synthesis of novel bifunctional prochelators for coupling to bioactive peptides for radiometal labelling. Bioorg Med Chem Lett 2000;10:2133-5.
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 2133-2135
-
-
Eisenwiener, K.P.1
Powell, P.2
MäcKe, H.R.3
-
22
-
-
0035999707
-
NODAGATOC, a new chelator-coupled somatostatin analogue labeled with [67/68Ga] and [111In] for SPECT, PET, and targeted therapeutic applications of somatostatin receptor (hsst2) expressing tumors
-
12009943 1:CAS:528:DC%2BD38XjtVaitr4%3D 10.1021/bc010074f
-
Eisenwiener KP, Prata MI, Buschmann I, Zhang HW, Santos AC, Wenger S, et al. NODAGATOC, a new chelator-coupled somatostatin analogue labeled with [67/68Ga] and [111In] for SPECT, PET, and targeted therapeutic applications of somatostatin receptor (hsst2) expressing tumors. Bioconjug Chem 2002;13:530-41.
-
(2002)
Bioconjug Chem
, vol.13
, pp. 530-541
-
-
Eisenwiener, K.P.1
Prata, M.I.2
Buschmann, I.3
Zhang, H.W.4
Santos, A.C.5
Wenger, S.6
-
23
-
-
67650093751
-
Small-animal PET of tumors with (64)Cu-labeled RGD-bombesin heterodimer
-
19525469 1:CAS:528:DC%2BD1MXpsV2gsbY%3D 10.2967/jnumed.108.061739
-
Liu Z, Li ZB, Cao Q, Liu S, Wang F, Chen X. Small-animal PET of tumors with (64)Cu-labeled RGD-bombesin heterodimer. J Nucl Med 2009;50:1168-77.
-
(2009)
J Nucl Med
, vol.50
, pp. 1168-1177
-
-
Liu, Z.1
Li, Z.B.2
Cao, Q.3
Liu, S.4
Wang, F.5
Chen, X.6
-
24
-
-
11144228601
-
Preparation and biological evaluation of copper-64-labeled tyr3-octreotate using a cross-bridged macrocyclic chelator
-
15623652 1:CAS:528:DC%2BD2cXhtFGjsL7F 10.1158/1078-0432.CCR-04-1084
-
Sprague JE, Peng Y, Sun X, Weisman GR, Wong EH, Achilefu S, et al. Preparation and biological evaluation of copper-64-labeled tyr3-octreotate using a cross-bridged macrocyclic chelator. Clin Cancer Res 2004;10:8674-82.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 8674-8682
-
-
Sprague, J.E.1
Peng, Y.2
Sun, X.3
Weisman, G.R.4
Wong, E.H.5
Achilefu, S.6
-
25
-
-
80051700245
-
Novel (64)Cu- and (68)Ga-labeled RGD conjugates show improved PET imaging of alpha(nu)beta(3) integrin expression and facile radiosynthesis
-
21764795 1:CAS:528:DC%2BC3MXhtFKju7jN 10.2967/jnumed.111.087700
-
Dumont RA, Deininger F, Haubner R, Maecke HR, Weber WA, Fani M. Novel (64)Cu- and (68)Ga-labeled RGD conjugates show improved PET imaging of alpha(nu)beta(3) integrin expression and facile radiosynthesis. J Nucl Med 2011;52:1276-84.
-
(2011)
J Nucl Med
, vol.52
, pp. 1276-1284
-
-
Dumont, R.A.1
Deininger, F.2
Haubner, R.3
Maecke, H.R.4
Weber, W.A.5
Fani, M.6
-
26
-
-
34547630542
-
[64Cu-NOTA-8-Aoc-BBN(7-14)NH2] targeting vector for positron-emission tomography imaging of gastrin-releasing peptide receptor-expressing tissues
-
17626788 1:CAS:528:DC%2BD2sXos1ehtLw%3D 10.1073/pnas.0705347104
-
Prasanphanich AF, Nanda PK, Rold TL, Ma L, Lewis MR, Garrison JC, et al. [64Cu-NOTA-8-Aoc-BBN(7-14)NH2] targeting vector for positron-emission tomography imaging of gastrin-releasing peptide receptor-expressing tissues. Proc Natl Acad Sci U S A 2007;104:12462-7.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 12462-12467
-
-
Prasanphanich, A.F.1
Nanda, P.K.2
Rold, T.L.3
Ma, L.4
Lewis, M.R.5
Garrison, J.C.6
-
27
-
-
79960323194
-
PET of somatostatin receptor-positive tumors using 64Cu- and 68Ga-somatostatin antagonists: The chelate makes the difference
-
21680701 1:CAS:528:DC%2BC3MXpvVKltro%3D 10.2967/jnumed.111.087999
-
Fani M, Del Pozzo L, Abiraj K, Mansi R, Tamma ML, Cescato R, et al. PET of somatostatin receptor-positive tumors using 64Cu- and 68Ga-somatostatin antagonists: the chelate makes the difference. J Nucl Med 2011;52:1110-8.
-
(2011)
J Nucl Med
, vol.52
, pp. 1110-1118
-
-
Fani, M.1
Del Pozzo, L.2
Abiraj, K.3
Mansi, R.4
Tamma, M.L.5
Cescato, R.6
-
28
-
-
79952783054
-
In vitro and in vivo evaluation of 64Cu-labeled SarAr-bombesin analogs in gastrin-releasing peptide receptor-expressing prostate cancer
-
21321264 1:CAS:528:DC%2BC3MXktVGnuro%3D 10.2967/jnumed.110.082826
-
Lears KA, Ferdani R, Liang K, Zheleznyak A, Andrews R, Sherman CD, et al. In vitro and in vivo evaluation of 64Cu-labeled SarAr-bombesin analogs in gastrin-releasing peptide receptor-expressing prostate cancer. J Nucl Med 2011;52:470-7.
-
(2011)
J Nucl Med
, vol.52
, pp. 470-477
-
-
Lears, K.A.1
Ferdani, R.2
Liang, K.3
Zheleznyak, A.4
Andrews, R.5
Sherman, C.D.6
-
29
-
-
67749114523
-
Synthesis of a novel bifunctional chelator AmBaSar based on sarcophagine for peptide conjugation and (64)Cu radiolabelling
-
19565091 10.1039/b902210d 1:CAS:528:DC%2BD1MXnvVOltbs%3D
-
Cai H, Fissekis J, Conti PS. Synthesis of a novel bifunctional chelator AmBaSar based on sarcophagine for peptide conjugation and (64)Cu radiolabelling. Dalton Trans 2009;27:5395-400.
-
(2009)
Dalton Trans
, vol.27
, pp. 5395-5400
-
-
Cai, H.1
Fissekis, J.2
Conti, P.S.3
-
30
-
-
0033001991
-
Radiolabeled peptides for targeting cholecystokinin-B/gastrin receptor-expressing tumors
-
10452322 1:CAS:528:DyaK1MXktVaqsLo%3D
-
Behr TM, Jenner N, Béhé M, Angerstein C, Gratz S, Raue F, et al. Radiolabeled peptides for targeting cholecystokinin-B/gastrin receptor-expressing tumors. J Nucl Med 1999;40:1029-44.
-
(1999)
J Nucl Med
, vol.40
, pp. 1029-1044
-
-
Behr, T.M.1
Jenner, N.2
Béhé, M.3
Angerstein, C.4
Gratz, S.5
Raue, F.6
-
31
-
-
0032587186
-
Radiolabeled alpha(v)beta3 integrin antagonists: A new class of tracers for tumor targeting
-
10452325 1:CAS:528:DyaK1MXktVaqsLg%3D
-
Haubner R, Wester HJ, Reuning U, Senekowitsch-Schmidtke R, Diefenbach B, Kessler H, et al. Radiolabeled alpha(v)beta3 integrin antagonists: a new class of tracers for tumor targeting. J Nucl Med 1999;40:1061-71.
-
(1999)
J Nucl Med
, vol.40
, pp. 1061-1071
-
-
Haubner, R.1
Wester, H.J.2
Reuning, U.3
Senekowitsch-Schmidtke, R.4
Diefenbach, B.5
Kessler, H.6
-
32
-
-
0036232690
-
Use of the incretin hormone glucagon-like peptide-1 (GLP-1) for the detection of insulinomas: Initial experimental results
-
11976797 1:CAS:528:DC%2BD38XkvFSns74%3D 10.1007/s00259-002-0761-1
-
Gotthardt M, Fischer M, Naeher I, Holz JB, Jungclas H, Fritsch HW, et al. Use of the incretin hormone glucagon-like peptide-1 (GLP-1) for the detection of insulinomas: initial experimental results. Eur J Nucl Med Mol Imaging 2002;29:597-606.
-
(2002)
Eur J Nucl Med Mol Imaging
, vol.29
, pp. 597-606
-
-
Gotthardt, M.1
Fischer, M.2
Naeher, I.3
Holz, J.B.4
Jungclas, H.5
Fritsch, H.W.6
-
33
-
-
0026069670
-
N-succinimidyl 5-(trialkylstannyl)-3-pyridinecarboxylates: A new class of reagents for protein radioiodination
-
1878411 1:CAS:528:DyaK3MXhtFOksrw%3D 10.1021/bc00007a009
-
Garg S, Garg PK, Zalutsky MR. N-succinimidyl 5-(trialkylstannyl)-3- pyridinecarboxylates: a new class of reagents for protein radioiodination. Bioconjug Chem 1991;2:50-6.
-
(1991)
Bioconjug Chem
, vol.2
, pp. 50-56
-
-
Garg, S.1
Garg, P.K.2
Zalutsky, M.R.3
-
34
-
-
34248632788
-
Synthesis of N-succinimidyl 4-[18F]fluorobenzoate, an agent for labeling proteins and peptides with 18F
-
17487148 1:CAS:528:DC%2BD2sXhtFagtrbE 10.1038/nprot.2006.264
-
Vaidyanathan G, Zalutsky MR. Synthesis of N-succinimidyl 4-[18F]fluorobenzoate, an agent for labeling proteins and peptides with 18F. Nat Protoc 2006;1:1655-61.
-
(2006)
Nat Protoc
, vol.1
, pp. 1655-1661
-
-
Vaidyanathan, G.1
Zalutsky, M.R.2
-
35
-
-
33645958934
-
18F-labeled bombesin analogs for targeting GRP receptor-expressing prostate cancer
-
16513619 1:CAS:528:DC%2BD28Xlt1Kmsb4%3D
-
Zhang X, Cai W, Cao F, Schreibmann E, Wu Y, Wu JC, et al. 18F-labeled bombesin analogs for targeting GRP receptor-expressing prostate cancer. J Nucl Med 2006;47:492-501.
-
(2006)
J Nucl Med
, vol.47
, pp. 492-501
-
-
Zhang, X.1
Cai, W.2
Cao, F.3
Schreibmann, E.4
Wu, Y.5
Wu, J.C.6
-
36
-
-
2542544479
-
First (18)F-labeled tracer suitable for routine clinical imaging of sst receptor-expressing tumors using positron emission tomography
-
15173065 1:CAS:528:DC%2BD2cXksVKnsLY%3D 10.1158/1078-0432.CCR-03-0359
-
Schottelius M, Poethko T, Herz M, Reubi JC, Kessler H, Schwaiger M, et al. First (18)F-labeled tracer suitable for routine clinical imaging of sst receptor-expressing tumors using positron emission tomography. Clin Cancer Res 2004;10:3593-606.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 3593-3606
-
-
Schottelius, M.1
Poethko, T.2
Herz, M.3
Reubi, J.C.4
Kessler, H.5
Schwaiger, M.6
-
37
-
-
52249113335
-
Synthesis, 18F-labeling, and in vitro and in vivo studies of bombesin peptides modified with silicon-based building blocks
-
18754574 10.1021/bc800157h 1:CAS:528:DC%2BD1cXhtVGgurrE
-
Höhne A, Mu L, Honer M, Schubiger PA, Ametamey SM, Graham K, et al. Synthesis, 18F-labeling, and in vitro and in vivo studies of bombesin peptides modified with silicon-based building blocks. Bioconjug Chem 2008;19:1871-9.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 1871-1879
-
-
Höhne, A.1
Mu, L.2
Honer, M.3
Schubiger, P.A.4
Ametamey, S.M.5
Graham, K.6
-
38
-
-
77958193859
-
In vitro and in vivo characterization of novel 18F-labeled bombesin analogues for targeting GRPR-positive tumors
-
20857927 1:CAS:528:DC%2BC3cXhtFOru7bO 10.1021/bc100222u
-
Mu L, Honer M, Becaud J, Martic M, Schubiger PA, Ametamey SM, et al. In vitro and in vivo characterization of novel 18F-labeled bombesin analogues for targeting GRPR-positive tumors. Bioconjug Chem 2010;21:1864-71.
-
(2010)
Bioconjug Chem
, vol.21
, pp. 1864-1871
-
-
Mu, L.1
Honer, M.2
Becaud, J.3
Martic, M.4
Schubiger, P.A.5
Ametamey, S.M.6
-
39
-
-
68949220252
-
(18)F-Fluoroglucosylation of peptides, exemplified on cyclo(RGDfK)
-
19350236 1:CAS:528:DC%2BD1MXps1Cktrc%3D 10.1007/s00259-009-1122-0
-
Hultsch C, Schottelius M, Auernheimer J, Alke A, Wester HJ. (18)F-Fluoroglucosylation of peptides, exemplified on cyclo(RGDfK). Eur J Nucl Med Mol Imaging 2009;36:1469-74.
-
(2009)
Eur J Nucl Med Mol Imaging
, vol.36
, pp. 1469-1474
-
-
Hultsch, C.1
Schottelius, M.2
Auernheimer, J.3
Alke, A.4
Wester, H.J.5
-
40
-
-
80053493999
-
PET of insulinoma using (18)F-FBEM-EM3106B, a new GLP-1 analogue
-
21800885 1:CAS:528:DC%2BC3MXhtVemu73F 10.1021/mp200141x
-
Gao H, Niu G, Yang M, Quan Q, Ma Y, Murage EN, et al. PET of insulinoma using (18)F-FBEM-EM3106B, a new GLP-1 analogue. Mol Pharm 2011;8:1775-82.
-
(2011)
Mol Pharm
, vol.8
, pp. 1775-1782
-
-
Gao, H.1
Niu, G.2
Yang, M.3
Quan, Q.4
Ma, Y.5
Murage, E.N.6
-
41
-
-
45749108297
-
Synthesis and application of [18F]FDG-maleimidehexyloxime ([18F]FDG-MHO): A [18F]FDG-based prosthetic group for the chemoselective 18F-labeling of peptides and proteins
-
18481886 1:CAS:528:DC%2BD1cXlvFaku7w%3D 10.1021/bc8000112
-
Wuest F, Berndt M, Bergmann R, van den Hoff J, Pietzsch J. Synthesis and application of [18F]FDG-maleimidehexyloxime ([18F]FDG-MHO): a [18F]FDG-based prosthetic group for the chemoselective 18F-labeling of peptides and proteins. Bioconjug Chem 2008;19:1202-10.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 1202-1210
-
-
Wuest, F.1
Berndt, M.2
Bergmann, R.3
Van Den Hoff, J.4
Pietzsch, J.5
-
42
-
-
53549125801
-
In vivo positron emission tomography (PET) imaging with an alphavbeta6 specific peptide radiolabeled using 18F-"click" chemistry: Evaluation and comparison with the corresponding 4-[18F]fluorobenzoyl- and 2-[18F]fluoropropionyl-peptides
-
18785727 1:CAS:528:DC%2BD1cXhtFaqtLrE 10.1021/jm800608s
-
Hausner SH, Marik J, Gagnon MK, Sutcliffe JL. In vivo positron emission tomography (PET) imaging with an alphavbeta6 specific peptide radiolabeled using 18F-"click" chemistry: evaluation and comparison with the corresponding 4-[18F]fluorobenzoyl- and 2-[18F]fluoropropionyl-peptides. J Med Chem 2008;51:5901-4.
-
(2008)
J Med Chem
, vol.51
, pp. 5901-5904
-
-
Hausner, S.H.1
Marik, J.2
Gagnon, M.K.3
Sutcliffe, J.L.4
-
43
-
-
34347338806
-
Click labeling" with 2-[18f]fluoroethylazide for positron emission tomography
-
17429938 1:CAS:528:DC%2BD2sXktFynsbk%3D 10.1021/bc060301j
-
Glaser M, Arstad E. "Click labeling" with 2-[18f] fluoroethylazide for positron emission tomography. Bioconjug Chem 2007;18:989-93.
-
(2007)
Bioconjug Chem
, vol.18
, pp. 989-993
-
-
Glaser, M.1
Arstad, E.2
-
44
-
-
80052615497
-
Targeting somatostatin receptors: Preclinical evaluation of novel 18F-fluoroethyltriazole-Tyr3-octreotate analogs for PET
-
21852355 1:CAS:528:DC%2BC3MXht1yisrrL 10.2967/jnumed.111.088906
-
Leyton J, Iddon L, Perumal M, Indrevoll B, Glaser M, Robins E, et al. Targeting somatostatin receptors: preclinical evaluation of novel 18F-fluoroethyltriazole-Tyr3-octreotate analogs for PET. J Nucl Med 2011;52:1441-8.
-
(2011)
J Nucl Med
, vol.52
, pp. 1441-1448
-
-
Leyton, J.1
Iddon, L.2
Perumal, M.3
Indrevoll, B.4
Glaser, M.5
Robins, E.6
-
45
-
-
77950348936
-
A novel facile method of labeling octreotide with (18)F-fluorine
-
20150268 1:CAS:528:DC%2BC3cXksVylsrs%3D 10.2967/jnumed.109.066902
-
Laverman P, McBride WJ, Sharkey RM, Eek A, Joosten L, Oyen WJ, et al. A novel facile method of labeling octreotide with (18)F-fluorine. J Nucl Med 2010;51:454-61.
-
(2010)
J Nucl Med
, vol.51
, pp. 454-461
-
-
Laverman, P.1
McBride, W.J.2
Sharkey, R.M.3
Eek, A.4
Joosten, L.5
Oyen, W.J.6
-
46
-
-
0034924612
-
Somatostatin receptor sst1-sst5 expression in normal and neoplastic human tissues using receptor autoradiography with subtype-selective ligands
-
11504080 1:CAS:528:DC%2BD3MXkvVWltL0%3D 10.1007/s002590100541
-
Reubi JC, Waser B, Schaer JC, Laissue JA. Somatostatin receptor sst1-sst5 expression in normal and neoplastic human tissues using receptor autoradiography with subtype-selective ligands. Eur J Nucl Med 2001;28:836-46.
-
(2001)
Eur J Nucl Med
, vol.28
, pp. 836-846
-
-
Reubi, J.C.1
Waser, B.2
Schaer, J.C.3
Laissue, J.A.4
-
47
-
-
0034033495
-
Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use
-
10774879 1:CAS:528:DC%2BD3cXhsVWns7w%3D 10.1007/s002590050034
-
Reubi JC, Schar JC, Waser B, Wenger S, Heppeler A, Schmitt JS, et al. Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use. Eur J Nucl Med 2000;27:273-82.
-
(2000)
Eur J Nucl Med
, vol.27
, pp. 273-282
-
-
Reubi, J.C.1
Schar, J.C.2
Waser, B.3
Wenger, S.4
Heppeler, A.5
Schmitt, J.S.6
-
48
-
-
79958120505
-
Somatostatin receptors as targets for nuclear medicine imaging and radionuclide treatment
-
21571797 1:CAS:528:DC%2BC3MXot1yisL0%3D 10.2967/jnumed.110.084236
-
Maecke HR, Reubi JC. Somatostatin receptors as targets for nuclear medicine imaging and radionuclide treatment. J Nucl Med 2011;52:841-4.
-
(2011)
J Nucl Med
, vol.52
, pp. 841-844
-
-
Maecke, H.R.1
Reubi, J.C.2
-
49
-
-
33744547026
-
Imaging of neuroendocrine tumors
-
16762613 10.1053/j.semnuclmed.2006.03.007
-
Rufini V, Calcagni ML, Baum RP. Imaging of neuroendocrine tumors. Semin Nucl Med 2006;36:228-47.
-
(2006)
Semin Nucl Med
, vol.36
, pp. 228-247
-
-
Rufini, V.1
Calcagni, M.L.2
Baum, R.P.3
-
51
-
-
33747822854
-
99mTc-EDDA/HYNIC-octreotate scintigraphy, an efficient method for the detection and staging of carcinoid tumours: Results of 3 years' experience
-
16721571 1:STN:280:DC%2BD28rnvVGiug%3D%3D 10.1007/s00259-006-0113-7
-
Hubalewska-Dydejczyk A, Fröss-Baron K, Mikolajczak R, Maecke HR, Huszno B, Pach D, et al. 99mTc-EDDA/HYNIC-octreotate scintigraphy, an efficient method for the detection and staging of carcinoid tumours: results of 3 years' experience. Eur J Nucl Med Mol Imaging 2006;33:1123-33.
-
(2006)
Eur J Nucl Med Mol Imaging
, vol.33
, pp. 1123-1133
-
-
Hubalewska-Dydejczyk, A.1
Fröss-Baron, K.2
Mikolajczak, R.3
Maecke, H.R.4
Huszno, B.5
Pach, D.6
-
52
-
-
67651124762
-
Molecular imaging of cancer with copper-64 radiopharmaceuticals and positron emission tomography (PET)
-
19530674 1:CAS:528:DC%2BD1MXnt1Cmu7w%3D 10.1021/ar800255q
-
Shokeen M, Anderson CJ. Molecular imaging of cancer with copper-64 radiopharmaceuticals and positron emission tomography (PET). Acc Chem Res 2009;42:832-41.
-
(2009)
Acc Chem Res
, vol.42
, pp. 832-841
-
-
Shokeen, M.1
Anderson, C.J.2
-
53
-
-
33749674563
-
Design, synthesis, and biological evaluation of somatostatin-based radiopeptides
-
17052612 1:CAS:528:DC%2BD28XhtFSktL%2FI 10.1016/j.chembiol.2006.08.012
-
Ginj M, Schmitt JS, Chen J, Waser B, Reubi JC, de Jong M, et al. Design, synthesis, and biological evaluation of somatostatin-based radiopeptides. Chem Biol 2006;13:1081-90.
-
(2006)
Chem Biol
, vol.13
, pp. 1081-1090
-
-
Ginj, M.1
Schmitt, J.S.2
Chen, J.3
Waser, B.4
Reubi, J.C.5
De Jong, M.6
-
54
-
-
12944329895
-
Preclinical evaluation of new and highly potent analogues of octreotide for predictive imaging and targeted radiotherapy
-
15709181 1:CAS:528:DC%2BD2MXht1ynt7s%3D
-
Ginj M, Chen J, Walter MA, Eltschinger V, Reubi JC, Maecke HR. Preclinical evaluation of new and highly potent analogues of octreotide for predictive imaging and targeted radiotherapy. Clin Cancer Res 2005;11:1136-45.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 1136-1145
-
-
Ginj, M.1
Chen, J.2
Walter, M.A.3
Eltschinger, V.4
Reubi, J.C.5
Maecke, H.R.6
-
55
-
-
34250349188
-
Are radiogallium-labelled DOTA-conjugated somatostatin analogues superior to those labelled with other radiometals?
-
17225119 1:CAS:528:DC%2BD2sXmtl2jtL8%3D 10.1007/s00259-006-0317-x
-
Antunes P, Ginj M, Zhang H, Waser B, Baum RP, Reubi JC, et al. Are radiogallium-labelled DOTA-conjugated somatostatin analogues superior to those labelled with other radiometals? Eur J Nucl Med Mol Imaging 2007;34:982-93.
-
(2007)
Eur J Nucl Med Mol Imaging
, vol.34
, pp. 982-993
-
-
Antunes, P.1
Ginj, M.2
Zhang, H.3
Waser, B.4
Baum, R.P.5
Reubi, J.C.6
-
56
-
-
79851489455
-
Radiolabeled bicyclic somatostatin-based analogs: A novel class of potential radiotracers for SPECT/PET of neuroendocrine tumors
-
20956465 10.2967/jnumed.110.076695
-
Fani M, Mueller A, Tamma ML, Nicolas G, Rink HR, Cescato R, et al. Radiolabeled bicyclic somatostatin-based analogs: a novel class of potential radiotracers for SPECT/PET of neuroendocrine tumors. J Nucl Med 2010;51:1771-9.
-
(2010)
J Nucl Med
, vol.51
, pp. 1771-1779
-
-
Fani, M.1
Mueller, A.2
Tamma, M.L.3
Nicolas, G.4
Rink, H.R.5
Cescato, R.6
-
57
-
-
0037027926
-
A new peptidic somatostatin agonist with high affinity to all five somatostatin receptors
-
12450568 1:CAS:528:DC%2BD38XovFCjt7c%3D 10.1016/S0014-2999(02)02651-1
-
Reubi JC, Eisenwiener KP, Rink H, Waser B, Mäcke HR. A new peptidic somatostatin agonist with high affinity to all five somatostatin receptors. Eur J Pharmacol 2002;456:45-9.
-
(2002)
Eur J Pharmacol
, vol.456
, pp. 45-49
-
-
Reubi, J.C.1
Eisenwiener, K.P.2
Rink, H.3
Waser, B.4
MäcKe, H.R.5
-
58
-
-
42249083915
-
New pansomatostatin ligands and their chelated versions: Affinity profile, agonist activity, internalization, and tumor targeting
-
18381940 1:CAS:528:DC%2BD1cXkt1akuro%3D 10.1158/1078-0432.CCR-07-1687
-
Ginj M, Zhang H, Eisenwiener KP, Wild D, Schulz S, Rink H, et al. New pansomatostatin ligands and their chelated versions: affinity profile, agonist activity, internalization, and tumor targeting. Clin Cancer Res 2008;14:2019-27.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 2019-2027
-
-
Ginj, M.1
Zhang, H.2
Eisenwiener, K.P.3
Wild, D.4
Schulz, S.5
Rink, H.6
-
59
-
-
73549093367
-
Agonist-biased signaling at the sst2A receptor: The multi-somatostatin analogs KE108 and SOM230 activate and antagonize distinct signaling pathways
-
19910453 1:CAS:528:DC%2BC3cXmtVGgsw%3D%3D 10.1210/me.2009-0321
-
Cescato R, Loesch KA, Waser B, Mäcke HR, Rivier JE, Reubi JC, et al. Agonist-biased signaling at the sst2A receptor: the multi-somatostatin analogs KE108 and SOM230 activate and antagonize distinct signaling pathways. Mol Endocrinol 2010;24:240-9.
-
(2010)
Mol Endocrinol
, vol.24
, pp. 240-249
-
-
Cescato, R.1
Loesch, K.A.2
Waser, B.3
MäcKe, H.R.4
Rivier, J.E.5
Reubi, J.C.6
-
60
-
-
33750823665
-
Radiolabeled somatostatin receptor antagonists are preferable to agonists for in vivo peptide receptor targeting of tumors
-
17056720 1:CAS:528:DC%2BD28Xht1WmsLjJ 10.1073/pnas.0607761103
-
Ginj M, Zhang H, Waser B, Cescato R, Wild D, Wang X, et al. Radiolabeled somatostatin receptor antagonists are preferable to agonists for in vivo peptide receptor targeting of tumors. Proc Natl Acad Sci U S A 2006;103:16436-41.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 16436-16441
-
-
Ginj, M.1
Zhang, H.2
Waser, B.3
Cescato, R.4
Wild, D.5
Wang, X.6
-
61
-
-
46849089935
-
Design and in vitro characterization of highly sst2-selective somatostatin antagonists suitable for radiotargeting
-
18543899 1:CAS:528:DC%2BD1cXntVygtLs%3D 10.1021/jm701618q
-
Cescato R, Erchegyi J, Waser B, Piccand V, Maecke HR, Rivier JE, et al. Design and in vitro characterization of highly sst2-selective somatostatin antagonists suitable for radiotargeting. J Med Chem 2008;51:4030-7.
-
(2008)
J Med Chem
, vol.51
, pp. 4030-4037
-
-
Cescato, R.1
Erchegyi, J.2
Waser, B.3
Piccand, V.4
Maecke, H.R.5
Rivier, J.E.6
-
62
-
-
80052631663
-
First clinical evidence that imaging with somatostatin receptor antagonists is feasible
-
21852357 1:CAS:528:DC%2BC3MXht1yisrrI 10.2967/jnumed.111.088922
-
Wild D, Fani M, Behe M, Brink I, Rivier JE, Reubi JC, et al. First clinical evidence that imaging with somatostatin receptor antagonists is feasible. J Nucl Med 2011;52:1412-7.
-
(2011)
J Nucl Med
, vol.52
, pp. 1412-1417
-
-
Wild, D.1
Fani, M.2
Behe, M.3
Brink, I.4
Rivier, J.E.5
Reubi, J.C.6
-
63
-
-
0033754433
-
Technetium-99m RP527, a GRP analogue for visualisation of GRP receptor-expressing malignancies: A feasibility study
-
11105826 10.1007/s002590000355
-
Van de Wiele C, Dumont F, Vanden Broecke R, Oosterlinck W, Cocquyt V, Serreyn R, et al. Technetium-99m RP527, a GRP analogue for visualisation of GRP receptor-expressing malignancies: a feasibility study. Eur J Nucl Med 2000;27:1694-9.
-
(2000)
Eur J Nucl Med
, vol.27
, pp. 1694-1699
-
-
Van De Wiele, C.1
Dumont, F.2
Vanden Broecke, R.3
Oosterlinck, W.4
Cocquyt, V.5
Serreyn, R.6
-
64
-
-
38949198118
-
Bombesin receptor antagonists may be preferable to agonists for tumor targeting
-
18199616 1:CAS:528:DC%2BD1cXivVOltb8%3D 10.2967/jnumed.107.045054
-
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;49:318-26.
-
(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
-
65
-
-
12244301557
-
Radiochemical investigations of (99m)Tc-N(3)S-X-BBN[7-14]NH(2): An in vitro/in vivo structure-activity relationship study where X = 0-, 3-, 5-, 8-, and 11-carbon tethering moieties
-
12526698 1:CAS:528:DC%2BD38XpsFWmtrY%3D 10.1021/bc020034r
-
Smith CJ, Gali H, Sieckman GL, Higginbotham C, Volkert WA, Hoffman TJ. Radiochemical investigations of (99m)Tc-N(3)S-X-BBN[7-14]NH(2): an in vitro/in vivo structure-activity relationship study where X = 0-, 3-, 5-, 8-, and 11-carbon tethering moieties. Bioconjug Chem 2003;14:93-102.
-
(2003)
Bioconjug 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
-
66
-
-
43149086083
-
Radiolabeled bombesin analogs for prostate cancer diagnosis: Preclinical studies
-
18482677 1:CAS:528:DC%2BD1cXlvF2qt7o%3D 10.1016/j.nucmedbio.2008.02.005
-
Faintuch BL, Teodoro R, Duatti A, Muramoto E, Faintuch S, Smith CJ. Radiolabeled bombesin analogs for prostate cancer diagnosis: preclinical studies. Nucl Med Biol 2008;35:401-11.
-
(2008)
Nucl Med Biol
, vol.35
, pp. 401-411
-
-
Faintuch, B.L.1
Teodoro, R.2
Duatti, A.3
Muramoto, E.4
Faintuch, S.5
Smith, C.J.6
-
67
-
-
33845934020
-
Chemical and biological characterization of new Re(CO)3/[99mTc](CO)3 bombesin analogues
-
17210458 10.1016/j.nucmedbio.2006.10.004 1:CAS:528:DC%2BD2sXisVWqug%3D%3D
-
García Garayoa E, Rüegg D, Bläuenstein P, Zwimpfer M, Khan IU, Maes V, et al. Chemical and biological characterization of new Re(CO)3/[99mTc](CO)3 bombesin analogues. Nucl Med Biol 2007;34:17-28.
-
(2007)
Nucl Med Biol
, vol.34
, pp. 17-28
-
-
García Garayoa, E.1
Rüegg, D.2
Bläuenstein, P.3
Zwimpfer, M.4
Khan, I.U.5
Maes, V.6
-
68
-
-
34249684449
-
New [99mTc]bombesin analogues with improved biodistribution for targeting gastrin releasing-peptide receptor-positive tumors
-
17372572
-
García Garayoa E, Schweinsberg C, Maes V, Rüegg D, Blanc A, Bläuenstein P, et al. New [99mTc]bombesin analogues with improved biodistribution for targeting gastrin releasing-peptide receptor-positive tumors. Q J Nucl Med Mol Imaging 2007;51:42-50.
-
(2007)
Q J Nucl Med Mol Imaging
, vol.51
, pp. 42-50
-
-
García Garayoa, E.1
Schweinsberg, C.2
Maes, V.3
Rüegg, D.4
Blanc, A.5
Bläuenstein, P.6
-
69
-
-
56649115222
-
Novel glycated [99mTc(CO)3]-labeled bombesin analogues for improved targeting of gastrin-releasing peptide receptor-positive tumors
-
19053304 1:CAS:528:DC%2BD1cXhtl2nsrbK 10.1021/bc800319g
-
Schweinsberg C, Maes V, Brans L, Bläuenstein P, Tourwé DA, Schubiger PA, et al. Novel glycated [99mTc(CO)3]-labeled bombesin analogues for improved targeting of gastrin-releasing peptide receptor-positive tumors. Bioconjug Chem 2008;19:2432-9.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 2432-2439
-
-
Schweinsberg, C.1
Maes, V.2
Brans, L.3
Bläuenstein, P.4
Tourwé, D.A.5
Schubiger, P.A.6
-
70
-
-
58149096143
-
Influence of the molecular charge on the biodistribution of bombesin analogues labeled with the [99mTc(CO)3]-core
-
18998719 10.1021/bc800262m 1:CAS:528:DC%2BD1cXhtlGku7bE
-
García Garayoa E, Schweinsberg C, Maes V, Brans L, Bläuenstein P, Tourwe DA, et al. Influence of the molecular charge on the biodistribution of bombesin analogues labeled with the [99mTc(CO)3]-core. Bioconjug Chem 2008;19:2409-16.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 2409-2416
-
-
García Garayoa, E.1
Schweinsberg, C.2
Maes, V.3
Brans, L.4
Bläuenstein, P.5
Tourwe, D.A.6
-
71
-
-
52249089417
-
Evaluation of the pharmacokinetic effects of various linking group using the 111In-DOTA-X-BBN(7-14)NH2 structural paradigm in a prostate cancer model
-
18712899 1:CAS:528:DC%2BD1cXhtVShtLbK 10.1021/bc8001375
-
Garrison JC, Rold TL, Sieckman GL, Naz F, Sublett SV, Figueroa SD, et al. Evaluation of the pharmacokinetic effects of various linking group using the 111In-DOTA-X-BBN(7-14)NH2 structural paradigm in a prostate cancer model. Bioconjug Chem 2008;19:1803-12.
-
(2008)
Bioconjug Chem
, vol.19
, pp. 1803-1812
-
-
Garrison, J.C.1
Rold, T.L.2
Sieckman, G.L.3
Naz, F.4
Sublett, S.V.5
Figueroa, S.D.6
-
72
-
-
34547730701
-
In vivo evaluation and small-animal PET/CT of a prostate cancer mouse model using 64Cu bombesin analogs: Side-by-side comparison of the CB-TE2A and DOTA chelation systems
-
17631556 1:CAS:528:DC%2BD2sXhtVSktbzP 10.2967/jnumed.107.039487
-
Garrison JC, Rold TL, Sieckman GL, Figueroa SD, Volkert WA, Jurisson SS, et al. In vivo evaluation and small-animal PET/CT of a prostate cancer mouse model using 64Cu bombesin analogs: side-by-side comparison of the CB-TE2A and DOTA chelation systems. J Nucl Med 2007;48:1327-37.
-
(2007)
J Nucl Med
, vol.48
, pp. 1327-1337
-
-
Garrison, J.C.1
Rold, T.L.2
Sieckman, G.L.3
Figueroa, S.D.4
Volkert, W.A.5
Jurisson, S.S.6
-
73
-
-
0032545948
-
Identification of a unique ligand which has high affinity for all four bombesin receptor subtypes
-
9570477 1:CAS:528:DyaK1cXhsFejtbk%3D 10.1016/S0014-2999(97)01527-6
-
Pradhan TK, Katsuno T, Taylor JE, Kim SH, Ryan RR, Mantey SA, et al. Identification of a unique ligand which has high affinity for all four bombesin receptor subtypes. Eur J Pharmacol 1998;343:275-87.
-
(1998)
Eur J Pharmacol
, vol.343
, pp. 275-287
-
-
Pradhan, T.K.1
Katsuno, T.2
Taylor, J.E.3
Kim, S.H.4
Ryan, R.R.5
Mantey, S.A.6
-
74
-
-
4644360336
-
Synthesis and evaluation of bombesin derivatives on the basis of pan-bombesin peptides labeled with indium-111, lutetium-177, and yttrium-90 for targeting bombesin receptor-expressing tumors
-
15374988 1:CAS:528:DC%2BD2cXnsFOksro%3D 10.1158/0008-5472.CAN-03-3845
-
Zhang H, Chen J, Waldherr C, Hinni K, Waser B, Reubi JC, et al. Synthesis and evaluation of bombesin derivatives on the basis of pan-bombesin peptides labeled with indium-111, lutetium-177, and yttrium-90 for targeting bombesin receptor-expressing tumors. Cancer Res 2004;64:6707-15.
-
(2004)
Cancer Res
, vol.64
, pp. 6707-6715
-
-
Zhang, H.1
Chen, J.2
Waldherr, C.3
Hinni, K.4
Waser, B.5
Reubi, J.C.6
-
75
-
-
19644372238
-
GRP receptor-targeted PET of a rat pancreas carcinoma xenograft in nude mice with a 68Ga-labeled bombesin(6-14) analog
-
15809493 1:CAS:528:DC%2BD2MXjvVyqtbw%3D
-
Schuhmacher J, Zhang H, Doll J, Mäcke HR, Matys R, Hauser H, et al. GRP receptor-targeted PET of a rat pancreas carcinoma xenograft in nude mice with a 68Ga-labeled bombesin(6-14) analog. J Nucl Med 2005;46:691-9.
-
(2005)
J Nucl Med
, vol.46
, pp. 691-699
-
-
Schuhmacher, J.1
Zhang, H.2
Doll, J.3
MäcKe, H.R.4
Matys, R.5
Hauser, H.6
-
76
-
-
79551589409
-
Pharmacokinetic studies of 68Ga-labeled bombesin (68Ga-BZH3) and F-18 FDG PET in patients with recurrent gliomas and comparison to grading: Preliminary results
-
21220970 10.1097/RLU.0b013e318203bb24
-
Dimitrakopoulou-Strauss A, Seiz M, Tuettenberg J, Schmieder K, Eisenhut M, Haberkorn U, et al. Pharmacokinetic studies of 68Ga-labeled bombesin (68Ga-BZH3) and F-18 FDG PET in patients with recurrent gliomas and comparison to grading: preliminary results. Clin Nucl Med 2011;36:101-8.
-
(2011)
Clin Nucl Med
, vol.36
, pp. 101-108
-
-
Dimitrakopoulou-Strauss, A.1
Seiz, M.2
Tuettenberg, J.3
Schmieder, K.4
Eisenhut, M.5
Haberkorn, U.6
-
77
-
-
33747105269
-
177Lu-AMBA: Synthesis and characterization of a selective 177Lu-labeled GRP-R agonist for systemic radiotherapy of prostate cancer
-
16818949 1:CAS:528:DC%2BD28XnslSmtrc%3D
-
Lantry LE, Cappelletti E, Maddalena ME, Fox JS, Feng W, Chen J, et al. 177Lu-AMBA: synthesis and characterization of a selective 177Lu-labeled GRP-R agonist for systemic radiotherapy of prostate cancer. J Nucl Med 2006;47:1144-52.
-
(2006)
J Nucl Med
, vol.47
, pp. 1144-1152
-
-
Lantry, L.E.1
Cappelletti, E.2
Maddalena, M.E.3
Fox, J.S.4
Feng, W.5
Chen, J.6
-
78
-
-
33845361405
-
Selective in vitro targeting of GRP and NMB receptors in human tumours with the new bombesin tracer 177Lu-AMBA
-
16909223 1:CAS:528:DC%2BD28Xht1Ontr7I 10.1007/s00259-006-0229-9
-
Waser B, Eltschinger V, Linder K, Nunn A, Reubi JC. Selective in vitro targeting of GRP and NMB receptors in human tumours with the new bombesin tracer 177Lu-AMBA. Eur J Nucl Med Mol Imaging 2007;34:95-100.
-
(2007)
Eur J Nucl Med Mol Imaging
, vol.34
, pp. 95-100
-
-
Waser, B.1
Eltschinger, V.2
Linder, K.3
Nunn, A.4
Reubi, J.C.5
-
79
-
-
69349085452
-
177Lu-AMBA Bombesin analogue in hormone refractory prostate cancer patients: A phase i escalation study with single-cycle administrations
-
Bodei L, Ferrari M, Nunn A, Lull JB, Cremonesi M, Martano L, et al. 177Lu-AMBA Bombesin analogue in hormone refractory prostate cancer patients: a phase I escalation study with single-cycle administrations. Eur J Nucl Med Mol Imaging 2007;34 Suppl 2:S221.
-
(2007)
Eur J Nucl Med Mol Imaging
, vol.34
, Issue.SUPPL. 2
, pp. 221
-
-
Bodei, L.1
Ferrari, M.2
Nunn, A.3
Lull, J.B.4
Cremonesi, M.5
Martano, L.6
-
80
-
-
34548119893
-
DOTA-PESIN, a DOTA-conjugated bombesin derivative designed for the imaging and targeted radionuclide treatment of bombesin receptor-positive tumours
-
17262215 10.1007/s00259-006-0347-4
-
Zhang H, Schuhmacher J, Waser B, Wild D, Eisenhut M, Reubi JC, et al. DOTA-PESIN, a DOTA-conjugated bombesin derivative designed for the imaging and targeted radionuclide treatment of bombesin receptor-positive tumours. Eur J Nucl Med Mol Imaging 2007;34:1198-208.
-
(2007)
Eur J Nucl Med Mol Imaging
, vol.34
, pp. 1198-1208
-
-
Zhang, H.1
Schuhmacher, J.2
Waser, B.3
Wild, D.4
Eisenhut, M.5
Reubi, J.C.6
-
81
-
-
79551553871
-
Alpha- versus beta-particle radiopeptide therapy in a human prostate cancer model (213Bi-DOTA-PESIN and 213Bi-AMBA versus 177Lu-DOTA-PESIN)
-
21245097 1:CAS:528:DC%2BC3MXhsVCju7g%3D 10.1158/0008-5472.CAN-10-1186
-
Wild D, Frischknecht M, Zhang H, Morgenstern A, Bruchertseifer F, Boisclair J, et al. Alpha- versus beta-particle radiopeptide therapy in a human prostate cancer model (213Bi-DOTA-PESIN and 213Bi-AMBA versus 177Lu-DOTA-PESIN). Cancer Res 2011;71:1009-18.
-
(2011)
Cancer Res
, vol.71
, pp. 1009-1018
-
-
Wild, D.1
Frischknecht, M.2
Zhang, H.3
Morgenstern, A.4
Bruchertseifer, F.5
Boisclair, J.6
-
82
-
-
69349102846
-
Evaluation of a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated bombesin-based radioantagonist for the labeling with single-photon emission computed tomography, positron emission tomography, and therapeutic radionuclides
-
19671861 1:CAS:528:DC%2BD1MXpvFeit7g%3D 10.1158/1078-0432.CCR-08-3145
-
Mansi R, Wang X, Forrer F, Kneifel S, Tamma ML, Waser B, et al. Evaluation of a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated bombesin-based radioantagonist for the labeling with single-photon emission computed tomography, positron emission tomography, and therapeutic radionuclides. Clin Cancer Res 2009;15:5240-9.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 5240-5249
-
-
Mansi, R.1
Wang, X.2
Forrer, F.3
Kneifel, S.4
Tamma, M.L.5
Waser, B.6
-
83
-
-
79551537113
-
Development of a potent DOTA-conjugated bombesin antagonist for targeting GRPr-positive tumours
-
20717822 1:CAS:528:DC%2BC3cXhsF2gtLvJ 10.1007/s00259-010-1596-9
-
Mansi R, Wang X, Forrer F, Waser B, Cescato R, Graham K, et al. Development of a potent DOTA-conjugated bombesin antagonist for targeting GRPr-positive tumours. Eur J Nucl Med Mol Imaging 2011;38:97-107.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 97-107
-
-
Mansi, R.1
Wang, X.2
Forrer, F.3
Waser, B.4
Cescato, R.5
Graham, K.6
-
84
-
-
83755170780
-
Bombesin antagonist-based radioligands for translational nuclear imaging of gastrin releasing peptide receptor positive tumors
-
doi: 10.2967/jnumed.111.094375
-
Abiraj K, Mansi R, Tamma ML, Fani M, Forrer F, Nicolas G, et al. Bombesin antagonist-based radioligands for translational nuclear imaging of gastrin releasing peptide receptor positive tumors. J Nucl Med 2011. doi: 10.2967/jnumed.111.094375.
-
(2011)
J Nucl Med
-
-
Abiraj, K.1
Mansi, R.2
Tamma, M.L.3
Fani, M.4
Forrer, F.5
Nicolas, G.6
-
85
-
-
84864683522
-
Evaluation of the GRPR radioantagonist 64Cu-CB-TE2A-AR-06 in mice and men
-
Gornik G, Mansi R, Maecke H, Weber WA, et al. Evaluation of the GRPR radioantagonist 64Cu-CB-TE2A-AR-06 in mice and men. J Nucl Med 2011;52 Suppl 1:7P.
-
(2011)
J Nucl Med
, vol.52
, Issue.SUPPL. 1
-
-
Gornik, G.1
Mansi, R.2
Maecke, H.3
Weber, W.A.4
-
86
-
-
79851506832
-
18F-labeled bombesin analog for specific and effective targeting of prostate tumors expressing gastrin-releasing peptide receptors
-
21233180 1:CAS:528:DC%2BC3MXisF2ku7g%3D 10.2967/jnumed.110.081620
-
Honer M, Mu L, Stellfeld T, Graham K, Martic M, Fischer CR, et al. 18F-labeled bombesin analog for specific and effective targeting of prostate tumors expressing gastrin-releasing peptide receptors. J Nucl Med 2011;52:270-8.
-
(2011)
J Nucl Med
, vol.52
, pp. 270-278
-
-
Honer, M.1
Mu, L.2
Stellfeld, T.3
Graham, K.4
Martic, M.5
Fischer, C.R.6
-
87
-
-
0036231110
-
Cholecystokinin-B/Gastrin receptor-targeting peptides for staging and therapy of medullary thyroid cancer and other cholecystokinin-B receptor-expressing malignancies
-
11965605 10.1053/snuc.2002.31028
-
Behr TM, Béhé MP. Cholecystokinin-B/Gastrin receptor-targeting peptides for staging and therapy of medullary thyroid cancer and other cholecystokinin-B receptor-expressing malignancies. Semin Nucl Med 2002;32:97-109.
-
(2002)
Semin Nucl Med
, vol.32
, pp. 97-109
-
-
Behr, T.M.1
Béhé, M.P.2
-
88
-
-
0031968525
-
G protein-coupled receptors in gastrointestinal physiology. I. CCK receptors: An exemplary family
-
9575840 1:CAS:528:DyaK1cXislyis7c%3D
-
Wank SA. G protein-coupled receptors in gastrointestinal physiology. I. CCK receptors: an exemplary family. Am J Physiol 1998;274:G607-13.
-
(1998)
Am J Physiol
, vol.274
-
-
Wank, S.A.1
-
89
-
-
0031746335
-
Unsulfated DTPA- and DOTA-CCK analogs as specific high-affinity ligands for CCK-B receptor-expressing human and rat tissues in vitro and in vivo
-
9575243 1:CAS:528:DyaK1cXislWmtL0%3D 10.1007/s002590050247
-
Reubi JC, Waser B, Schaer JC, Laederach U, Erion J, Srinivasan A, et al. Unsulfated DTPA- and DOTA-CCK analogs as specific high-affinity ligands for CCK-B receptor-expressing human and rat tissues in vitro and in vivo. Eur J Nucl Med 1998;25:481-90.
-
(1998)
Eur J Nucl Med
, vol.25
, pp. 481-490
-
-
Reubi, J.C.1
Waser, B.2
Schaer, J.C.3
Laederach, U.4
Erion, J.5
Srinivasan, A.6
-
90
-
-
77951282548
-
Stabilized (111)in-labeled sCCK8 analogues for targeting CCK2-receptor positive tumors: Synthesis and evaluation
-
20302291 1:CAS:528:DC%2BC3cXjs1Wkurk%3D 10.1021/bc900465y
-
Roosenburg S, Laverman P, Joosten L, Eek A, Oyen WJ, de Jong M, et al. Stabilized (111)in-labeled sCCK8 analogues for targeting CCK2-receptor positive tumors: synthesis and evaluation. Bioconjug Chem 2010;21:663-70.
-
(2010)
Bioconjug Chem
, vol.21
, pp. 663-670
-
-
Roosenburg, S.1
Laverman, P.2
Joosten, L.3
Eek, A.4
Oyen, W.J.5
De Jong, M.6
-
91
-
-
2442684493
-
Two technetium-99m-labeled cholecystokinin-8 (CCK8) peptides for scintigraphic imaging of CCK receptors
-
15149184 1:CAS:528:DC%2BD2cXivFemsLY%3D 10.1021/bc034208w
-
Laverman P, Béhé M, Oyen WJ, Willems PH, Corstens FH, Behr TM, et al. Two technetium-99m-labeled cholecystokinin-8 (CCK8) peptides for scintigraphic imaging of CCK receptors. Bioconjug Chem 2004;15:561-8.
-
(2004)
Bioconjug Chem
, vol.15
, pp. 561-568
-
-
Laverman, P.1
Béhé, M.2
Oyen, W.J.3
Willems, P.H.4
Corstens, F.H.5
Behr, T.M.6
-
92
-
-
0345240929
-
Cholecystokinin-B/gastrin receptor binding peptides: Preclinical development and evaluation of their diagnostic and therapeutic potential
-
10541353 1:CAS:528:DyaK1MXnsVShtro%3D
-
Behr TM, Béhé M, Angerstein C, Gratz S, Mach R, Hagemann L, et al. Cholecystokinin-B/gastrin receptor binding peptides: preclinical development and evaluation of their diagnostic and therapeutic potential. Clin Cancer Res 1999;5:3124s-38s.
-
(1999)
Clin Cancer Res
, vol.5
-
-
Behr, T.M.1
Béhé, M.2
Angerstein, C.3
Gratz, S.4
MacH, R.5
Hagemann, L.6
-
93
-
-
0042736655
-
Improved kinetic stability of DTPA-dGlu as compared with conventional monofunctional DTPA in chelating indium and yttrium: Preclinical and initial clinical evaluation of radiometal labelled minigastrin derivatives
-
12768330 10.1007/s00259-003-1178-1 1:CAS:528:DC%2BD3sXlslGrt7o%3D
-
Béhé M, Becker W, Gotthardt M, Angerstein C, Behr TM. Improved kinetic stability of DTPA-dGlu as compared with conventional monofunctional DTPA in chelating indium and yttrium: preclinical and initial clinical evaluation of radiometal labelled minigastrin derivatives. Eur J Nucl Med Mol Imaging 2003;30:1140-6.
-
(2003)
Eur J Nucl Med Mol Imaging
, vol.30
, pp. 1140-1146
-
-
Béhé, M.1
Becker, W.2
Gotthardt, M.3
Angerstein, C.4
Behr, T.M.5
-
94
-
-
23044459663
-
Use of polyglutamic acids to reduce uptake of radiometal-labeled minigastrin in the kidneys
-
15937313
-
Béhé M, Kluge G, Becker W, Gotthardt M, Behr TM. Use of polyglutamic acids to reduce uptake of radiometal-labeled minigastrin in the kidneys. J Nucl Med 2005;46:1012-5.
-
(2005)
J Nucl Med
, vol.46
, pp. 1012-1015
-
-
Béhé, M.1
Kluge, G.2
Becker, W.3
Gotthardt, M.4
Behr, T.M.5
-
95
-
-
52449093302
-
Macrocyclic chelator-coupled gastrin-based radiopharmaceuticals for targeting of gastrin receptor-expressing tumours
-
18509636 1:CAS:528:DC%2BD1cXhtFCjtbzE 10.1007/s00259-008-0803-4
-
Good S, Walter MA, Waser B, Wang X, Müller-Brand J, Béhé MP, et al. Macrocyclic chelator-coupled gastrin-based radiopharmaceuticals for targeting of gastrin receptor-expressing tumours. Eur J Nucl Med Mol Imaging 2008;35:1868-77.
-
(2008)
Eur J Nucl Med Mol Imaging
, vol.35
, pp. 1868-1877
-
-
Good, S.1
Walter, M.A.2
Waser, B.3
Wang, X.4
Müller-Brand, J.5
Béhé, M.P.6
-
96
-
-
34248586422
-
Selection of radiolabeled gastrin analogs for peptide receptor-targeted radionuclide therapy
-
17401100 1:CAS:528:DC%2BD2sXhtVert7bN 10.2967/jnumed.106.037085
-
Mather SJ, McKenzie AJ, Sosabowski JK, Morris TM, Ellison D, Watson SA. Selection of radiolabeled gastrin analogs for peptide receptor-targeted radionuclide therapy. J Nucl Med 2007;48:615-22.
-
(2007)
J Nucl Med
, vol.48
, pp. 615-622
-
-
Mather, S.J.1
McKenzie, A.J.2
Sosabowski, J.K.3
Morris, T.M.4
Ellison, D.5
Watson, S.A.6
-
97
-
-
33644695474
-
CCK-2/gastrin receptor-targeted tumor imaging with (99m)Tc-labeled minigastrin analogs
-
16204724 1:CAS:528:DC%2BD28XitVGlt7g%3D
-
Nock BA, Maina T, Béhé M, Nikolopoulou A, Gotthardt M, Schmitt JS, et al. CCK-2/gastrin receptor-targeted tumor imaging with (99m)Tc-labeled minigastrin analogs. J Nucl Med 2005;46:1727-36.
-
(2005)
J Nucl Med
, vol.46
, pp. 1727-1736
-
-
Nock, B.A.1
Maina, T.2
Béhé, M.3
Nikolopoulou, A.4
Gotthardt, M.5
Schmitt, J.S.6
-
98
-
-
70349234164
-
Comparison of three radiolabelled peptide analogues for CCK-2 receptor scintigraphy in medullary thyroid carcinoma
-
19266197 10.1007/s00259-009-1098-9 1:CAS:528:DC%2BD1MXotl2nuro%3D
-
Fröberg AC, de Jong M, Nock BA, Breeman WA, Erion JL, Maina T, et al. Comparison of three radiolabelled peptide analogues for CCK-2 receptor scintigraphy in medullary thyroid carcinoma. Eur J Nucl Med Mol Imaging 2009;36:1265-72.
-
(2009)
Eur J Nucl Med Mol Imaging
, vol.36
, pp. 1265-1272
-
-
Fröberg, A.C.1
De Jong, M.2
Nock, B.A.3
Breeman, W.A.4
Erion, J.L.5
Maina, T.6
-
99
-
-
34548060051
-
99mTc-labelled HYNIC-minigastrin with reduced kidney uptake for targeting of CCK-2 receptor-positive tumours
-
10.1007/s00259-006-0348-3 1:CAS:528:DC%2BD2sXpsFaku7k%3D
-
von Guggenberg E, Dietrich H, Skvortsova I, Gabriel M, Virgolini IJ, Decristoforo C. 99mTc-labelled HYNIC-minigastrin with reduced kidney uptake for targeting of CCK-2 receptor-positive tumours. Eur J Nucl Med Mol Imaging 2007;34:1209-18.
-
(2007)
Eur J Nucl Med Mol Imaging
, vol.34
, pp. 1209-1218
-
-
Von Guggenberg, E.1
Dietrich, H.2
Skvortsova, I.3
Gabriel, M.4
Virgolini, I.J.5
Decristoforo, C.6
-
100
-
-
68549110407
-
Cyclic minigastrin analogues for gastrin receptor scintigraphy with technetium-99m: Preclinical evaluation
-
10.1021/jm900400w 1:CAS:528:DC%2BD1MXotl2htrg%3D
-
von Guggenberg E, Sallegger W, Helbok A, Ocak M, King R, Mather SJ, et al. Cyclic minigastrin analogues for gastrin receptor scintigraphy with technetium-99m: preclinical evaluation. J Med Chem 2009;52:4786-93.
-
(2009)
J Med Chem
, vol.52
, pp. 4786-4793
-
-
Von Guggenberg, E.1
Sallegger, W.2
Helbok, A.3
Ocak, M.4
King, R.5
Mather, S.J.6
-
101
-
-
73349124522
-
Targeting of CCK-2 receptor-expressing tumors using a radiolabeled divalent gastrin peptide
-
19910426 1:CAS:528:DC%2BC3cXjvVantQ%3D%3D 10.2967/jnumed.109.064808
-
Sosabowski JK, Matzow T, Foster JM, Finucane C, Ellison D, Watson SA, et al. Targeting of CCK-2 receptor-expressing tumors using a radiolabeled divalent gastrin peptide. J Nucl Med 2009;50:2082-9.
-
(2009)
J Nucl Med
, vol.50
, pp. 2082-2089
-
-
Sosabowski, J.K.1
Matzow, T.2
Foster, J.M.3
Finucane, C.4
Ellison, D.5
Watson, S.A.6
-
102
-
-
79955405442
-
Highly improved metabolic stability and pharmacokinetics of indium-111-DOTA-gastrin conjugates for targeting of the gastrin receptor
-
21456601 1:CAS:528:DC%2BC3MXktFGjsLk%3D 10.1021/jm101279a
-
Kolenc-Peitl P, Mansi R, Tamma M, Gmeiner-Stopar T, Sollner-Dolenc M, Waser B, et al. Highly improved metabolic stability and pharmacokinetics of indium-111-DOTA-gastrin conjugates for targeting of the gastrin receptor. J Med Chem 2011;54:2602-9.
-
(2011)
J Med Chem
, vol.54
, pp. 2602-2609
-
-
Kolenc-Peitl, P.1
Mansi, R.2
Tamma, M.3
Gmeiner-Stopar, T.4
Sollner-Dolenc, M.5
Waser, B.6
-
103
-
-
80052593793
-
Comparison of the binding and internalization properties of 12 DOTA-coupled and (111)In-labelled CCK2/gastrin receptor binding peptides: A collaborative project under COST Action BM0607
-
21523391 1:CAS:528:DC%2BC3MXotl2mtLg%3D 10.1007/s00259-011-1816-y
-
Aloj L, Aurilio M, Rinaldi V, D'ambrosio L, Tesauro D, Peitl PK, et al. Comparison of the binding and internalization properties of 12 DOTA-coupled and (111)In-labelled CCK2/gastrin receptor binding peptides: a collaborative project under COST Action BM0607. Eur J Nucl Med Mol Imaging 2011;38:1417-25.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 1417-1425
-
-
Aloj, L.1
Aurilio, M.2
Rinaldi, V.3
D'Ambrosio, L.4
Tesauro, D.5
Peitl, P.K.6
-
104
-
-
80052579110
-
Comparison of biological stability and metabolism of CCK2 receptor targeting peptides, a collaborative project under COST BM0607
-
21528387 1:CAS:528:DC%2BC3MXotl2mtLk%3D 10.1007/s00259-011-1818-9
-
Ocak M, Helbok A, Rangger C, Peitl PK, Nock BA, Morelli G, et al. Comparison of biological stability and metabolism of CCK2 receptor targeting peptides, a collaborative project under COST BM0607. Eur J Nucl Med Mol Imaging 2011;38:1426-35.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 1426-1435
-
-
Ocak, M.1
Helbok, A.2
Rangger, C.3
Peitl, P.K.4
Nock, B.A.5
Morelli, G.6
-
105
-
-
80052573912
-
Comparative biodistribution of 12 (111)In-labelled gastrin/CCK2 receptor-targeting peptides
-
21461732 1:CAS:528:DC%2BC3MXotl2mtL0%3D 10.1007/s00259-011-1806-0
-
Laverman P, Joosten L, Eek A, Roosenburg S, Peitl PK, Maina T, et al. Comparative biodistribution of 12 (111)In-labelled gastrin/CCK2 receptor-targeting peptides. Eur J Nucl Med Mol Imaging 2011;38:1410-6.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 1410-1416
-
-
Laverman, P.1
Joosten, L.2
Eek, A.3
Roosenburg, S.4
Peitl, P.K.5
Maina, T.6
-
106
-
-
0037907532
-
Concomitant expression of several peptide receptors in neuroendocrine tumours: Molecular basis for in vivo multireceptor tumour targeting
-
12707737 1:CAS:528:DC%2BD3sXjsF2ksbs%3D 10.1007/s00259-003-1184-3
-
Reubi JC, Waser B. Concomitant expression of several peptide receptors in neuroendocrine tumours: molecular basis for in vivo multireceptor tumour targeting. Eur J Nucl Med Mol Imaging 2003;30:781-93.
-
(2003)
Eur J Nucl Med Mol Imaging
, vol.30
, pp. 781-793
-
-
Reubi, J.C.1
Waser, B.2
-
107
-
-
0028169656
-
Use of 125I-[Y39]exendin-4 to characterize exendin receptors on dispersed pancreatic acini and gastric chief cells from guinea pig
-
7800858 1:CAS:528:DyaK2cXmt1anu74%3D 10.1016/0167-0115(94)90158-9
-
Singh G, Eng J, Raufman JP. Use of 125I-[Y39]exendin-4 to characterize exendin receptors on dispersed pancreatic acini and gastric chief cells from guinea pig. Regul Pept 1994;53:47-59.
-
(1994)
Regul Pept
, vol.53
, pp. 47-59
-
-
Singh, G.1
Eng, J.2
Raufman, J.P.3
-
108
-
-
34250732525
-
[Lys40(Ahx-DTPA-111In)NH2]exendin-4, a very promising ligand for glucagon-like peptide-1 (GLP-1) receptor targeting
-
17138746 1:CAS:528:DC%2BD2sXksFKntw%3D%3D
-
Wild D, Béhé M, Wicki A, Storch D, Waser B, Gotthardt M, et al. [Lys40(Ahx-DTPA-111In)NH2]exendin-4, a very promising ligand for glucagon-like peptide-1 (GLP-1) receptor targeting. J Nucl Med 2006;47:2025-33.
-
(2006)
J Nucl Med
, vol.47
, pp. 2025-2033
-
-
Wild, D.1
Béhé, M.2
Wicki, A.3
Storch, D.4
Waser, B.5
Gotthardt, M.6
-
109
-
-
33751515577
-
A new technique for in vivo imaging of specific GLP-1 binding sites: First results in small rodents
-
16930741 1:CAS:528:DC%2BD28Xht12rsLjO 10.1016/j.regpep.2006.07.005
-
Gotthardt M, Lalyko G, van Eerd-Vismale J, Keil B, Schurrat T, Hower M, et al. A new technique for in vivo imaging of specific GLP-1 binding sites: first results in small rodents. Regul Pept 2006;137:162-7.
-
(2006)
Regul Pept
, vol.137
, pp. 162-167
-
-
Gotthardt, M.1
Lalyko, G.2
Van Eerd-Vismale, J.3
Keil, B.4
Schurrat, T.5
Hower, M.6
-
110
-
-
34250722229
-
[Lys40(Ahx-DTPA-111In)NH2]-Exendin-4 is a highly efficient radiotherapeutic for glucagon-like peptide-1 receptor-targeted therapy for insulinoma
-
17575235 1:CAS:528:DC%2BD2sXmsFCqu70%3D 10.1158/1078-0432.CCR-06-2965
-
Wicki A, Wild D, Storch D, Seemayer C, Gotthardt M, Behe M, et al. [Lys40(Ahx-DTPA-111In)NH2]-Exendin-4 is a highly efficient radiotherapeutic for glucagon-like peptide-1 receptor-targeted therapy for insulinoma. Clin Cancer Res 2007;13:3696-705.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 3696-3705
-
-
Wicki, A.1
Wild, D.2
Storch, D.3
Seemayer, C.4
Gotthardt, M.5
Behe, M.6
-
111
-
-
49449085799
-
Glucagon-like peptide 1-receptor scans to localize occult insulinomas
-
18703486 1:CAS:528:DC%2BD1cXhtVSht73O 10.1056/NEJMc0802045
-
Wild D, Mäcke H, Christ E, Gloor B, Reubi JC. Glucagon-like peptide 1-receptor scans to localize occult insulinomas. N Engl J Med 2008;359:766-8.
-
(2008)
N Engl J Med
, vol.359
, pp. 766-768
-
-
Wild, D.1
MäcKe, H.2
Christ, E.3
Gloor, B.4
Reubi, J.C.5
-
112
-
-
70449111654
-
Glucagon-like peptide-1 receptor imaging for localization of insulinomas
-
19820010 1:CAS:528:DC%2BD1MXhsVejtLfK 10.1210/jc.2009-1082
-
Christ E, Wild D, Forrer F, Brändle M, Sahli R, Clerici T, et al. Glucagon-like peptide-1 receptor imaging for localization of insulinomas. J Clin Endocrinol Metab 2009;94:4398-405.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 4398-4405
-
-
Christ, E.1
Wild, D.2
Forrer, F.3
Brändle, M.4
Sahli, R.5
Clerici, T.6
-
113
-
-
79960296365
-
Glucagon-like peptide-1 versus somatostatin receptor targeting reveals 2 distinct forms of malignant insulinomas
-
21680696 10.2967/jnumed.110.085142
-
Wild D, Christ E, Caplin ME, Kurzawinski TR, Forrer F, Brändle M, et al. Glucagon-like peptide-1 versus somatostatin receptor targeting reveals 2 distinct forms of malignant insulinomas. J Nucl Med 2011;52:1073-8.
-
(2011)
J Nucl Med
, vol.52
, pp. 1073-1078
-
-
Wild, D.1
Christ, E.2
Caplin, M.E.3
Kurzawinski, T.R.4
Forrer, F.5
Brändle, M.6
-
114
-
-
77954955137
-
68Ga-labelled exendin-3, a new agent for the detection of insulinomas with PET
-
20111963 1:CAS:528:DC%2BC3cXns1Sis7s%3D 10.1007/s00259-009-1363-y
-
Brom M, Oyen WJ, Joosten L, Gotthardt M, Boerman OC. 68Ga-labelled exendin-3, a new agent for the detection of insulinomas with PET. Eur J Nucl Med Mol Imaging 2010;37:1345-55.
-
(2010)
Eur J Nucl Med Mol Imaging
, vol.37
, pp. 1345-1355
-
-
Brom, M.1
Oyen, W.J.2
Joosten, L.3
Gotthardt, M.4
Boerman, O.C.5
-
115
-
-
84864535818
-
99mTc labeled GLP-1 scintigraphy with the use of [Lys40-(Ahx-HYNIC/EDDA) NH2]-Exendin-4 in the insulinoma localization
-
Hubalewska-Dydejczyk A, Sowa-Staszczak A, Mikolajczak R, Pach D, Janota B, Tomaszuk M, et al. 99mTc labeled GLP-1 scintigraphy with the use of [Lys40-(Ahx-HYNIC/EDDA)NH2]-Exendin-4 in the insulinoma localization. J Nucl Med 2011;52 Suppl 1:561.
-
(2011)
J Nucl Med
, vol.52
, Issue.SUPPL. 1
, pp. 561
-
-
Hubalewska-Dydejczyk, A.1
Sowa-Staszczak, A.2
Mikolajczak, R.3
Pach, D.4
Janota, B.5
Tomaszuk, M.6
-
116
-
-
84864562811
-
First clinical application of 99mTc labelled long-acting agonist of GLP-1 (Exendin-4) in endocrine diagnosis
-
Sowa-Staszczak A, Stefanska A, Pach D, Tomaszuk M, Jabrocka-Hybel A, Glowa B, et al. First clinical application of 99mTc labelled long-acting agonist of GLP-1 (Exendin-4) in endocrine diagnosis. Eur J Nucl Med Mol Imaging. 2011;38 Suppl 2:S206.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, Issue.SUPPL. 2
, pp. 206
-
-
Sowa-Staszczak, A.1
Stefanska, A.2
Pach, D.3
Tomaszuk, M.4
Jabrocka-Hybel, A.5
Glowa, B.6
-
117
-
-
77954956603
-
Determination of the beta-cell mass by SPECT imaging with In-111-DTPA-Exendin-3 in rats
-
Brom M, Baumeister P, Melis M, Laverman P, Joosten L, Behe M, et al. Determination of the beta-cell mass by SPECT imaging with In-111-DTPA-Exendin-3 in rats. J Nucl Med 2009;50 Suppl 2:147.
-
(2009)
J Nucl Med
, vol.50
, Issue.SUPPL. 2
, pp. 147
-
-
Brom, M.1
Baumeister, P.2
Melis, M.3
Laverman, P.4
Joosten, L.5
Behe, M.6
-
118
-
-
84861481526
-
Ex vivo imaging of pancreatic beta cells using a radiolabeled GLP-1 receptor agonist
-
doi: 10.1007/s11307-011-0481-7
-
Connolly BM, Vanko A, McQuade P, Guenther I, Meng X, Rubins D, et al. Ex vivo imaging of pancreatic beta cells using a radiolabeled GLP-1 receptor agonist. Mol Imaging Biol 2011. doi: 10.1007/s11307-011-0481-7.
-
(2011)
Mol Imaging Biol
-
-
Connolly, B.M.1
Vanko, A.2
McQuade, P.3
Guenther, I.4
Meng, X.5
Rubins, D.6
-
119
-
-
80051751238
-
In vivo imaging of transplanted islets with 64Cu-DO3A-VS-Cys40-Exendin-4 by targeting GLP-1 receptor
-
21692471 1:CAS:528:DC%2BC3MXovVSnu78%3D 10.1021/bc200132t
-
Wu Z, Todorov I, Li L, Bading JR, Li Z, Nair I, et al. In vivo imaging of transplanted islets with 64Cu-DO3A-VS-Cys40-Exendin-4 by targeting GLP-1 receptor. Bioconjug Chem 2011;22:1587-94.
-
(2011)
Bioconjug Chem
, vol.22
, pp. 1587-1594
-
-
Wu, Z.1
Todorov, I.2
Li, L.3
Bading, J.R.4
Li, Z.5
Nair, I.6
-
120
-
-
77957134846
-
GLP-1-receptor scanning for imaging of human beta cells transplanted in muscle
-
20860517 10.1056/NEJMc1004547
-
Pattou F, Kerr-Conte J, Wild D. GLP-1-receptor scanning for imaging of human beta cells transplanted in muscle. N Engl J Med 2010;363:1289-90.
-
(2010)
N Engl J Med
, vol.363
, pp. 1289-1290
-
-
Pattou, F.1
Kerr-Conte, J.2
Wild, D.3
-
121
-
-
72949119124
-
Integrins in cancer: Biological implications and therapeutic opportunities
-
20029421 1:CAS:528:DC%2BD1MXhsF2hsLzI 10.1038/nrc2748
-
Desgrosellier JS, Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nat Rev Cancer 2010;10:9-22.
-
(2010)
Nat Rev Cancer
, vol.10
, pp. 9-22
-
-
Desgrosellier, J.S.1
Cheresh, D.A.2
-
122
-
-
77956267966
-
Positron emission tomography tracers for imaging angiogenesis
-
20559632 10.1007/s00259-010-1503-4 1:CAS:528:DC%2BC3cXpslCgsL0%3D
-
Haubner R, Beer AJ, Wang H, Chen X. Positron emission tomography tracers for imaging angiogenesis. Eur J Nucl Med Mol Imaging 2010;37 Suppl 1:S86-S103.
-
(2010)
Eur J Nucl Med Mol Imaging
, vol.37
, Issue.SUPPL. 1
-
-
Haubner, R.1
Beer, A.J.2
Wang, H.3
Chen, X.4
-
123
-
-
18244376347
-
Noninvasive visualization of the activated alphavbeta3 integrin in cancer patients by positron emission tomography and [18F]Galacto-RGD
-
15783258 10.1371/journal.pmed.0020070 1:CAS:528:DC%2BD2MXjtFyhsLg%3D
-
Haubner R, Weber WA, Beer AJ, Vabuliene E, Reim D, Sarbia M, et al. Noninvasive visualization of the activated alphavbeta3 integrin in cancer patients by positron emission tomography and [18F]Galacto-RGD. PLoS Med 2005;2:e70.
-
(2005)
PLoS Med
, vol.2
, pp. 70
-
-
Haubner, R.1
Weber, W.A.2
Beer, A.J.3
Vabuliene, E.4
Reim, D.5
Sarbia, M.6
-
124
-
-
33746032220
-
Positron emission tomography using [18F]Galacto-RGD identifies the level of integrin alpha(v)beta3 expression in man
-
16818691 1:CAS:528:DC%2BD28XmsValtLk%3D 10.1158/1078-0432.CCR-06-0266
-
Beer AJ, Haubner R, Sarbia M, Goebel M, Luderschmidt S, Grosu AL, et al. Positron emission tomography using [18F]Galacto-RGD identifies the level of integrin alpha(v)beta3 expression in man. Clin Cancer Res 2006;12:3942-9.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 3942-3949
-
-
Beer, A.J.1
Haubner, R.2
Sarbia, M.3
Goebel, M.4
Luderschmidt, S.5
Grosu, A.L.6
-
125
-
-
33750701133
-
NC-100717: A versatile RGD peptide scaffold for angiogenesis imaging
-
17000103 1:CAS:528:DC%2BD28XhtF2jsrzP 10.1016/j.bmcl.2006.09.033
-
Indrevoll B, Kindberg GM, Solbakken M, Bjurgert E, Johansen JH, Karlsen H, et al. NC-100717: a versatile RGD peptide scaffold for angiogenesis imaging. Bioorg Med Chem Lett 2006;16:6190-3.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 6190-6193
-
-
Indrevoll, B.1
Kindberg, G.M.2
Solbakken, M.3
Bjurgert, E.4
Johansen, J.H.5
Karlsen, H.6
-
126
-
-
44849137859
-
Phase i trial of the positron-emitting Arg-Gly-Asp (RGD) peptide radioligand 18F-AH111585 in breast cancer patients
-
18483090 10.2967/jnumed.107.049452
-
Kenny LM, Coombes RC, Oulie I, Contractor KB, Miller M, Spinks TJ, et al. Phase I trial of the positron-emitting Arg-Gly-Asp (RGD) peptide radioligand 18F-AH111585 in breast cancer patients. J Nucl Med 2008;49:879-86.
-
(2008)
J Nucl Med
, vol.49
, pp. 879-886
-
-
Kenny, L.M.1
Coombes, R.C.2
Oulie, I.3
Contractor, K.B.4
Miller, M.5
Spinks, T.J.6
-
127
-
-
77956268144
-
First in human evaluation of a newly developed PET tracer, 18F-RGD-K5 in patients with breast cancer: Comparison with 18F-FDG uptake pattern and microvessel density
-
1:CAS:528:DC%2BD1MXhtV2itLvJ
-
Cho HJ, Lee JD, Park JY, Yun M, Kang WJ, Walsh JC, et al. First in human evaluation of a newly developed PET tracer, 18F-RGD-K5 in patients with breast cancer: comparison with 18F-FDG uptake pattern and microvessel density. J Nucl Med 2009;50 Suppl 2:1910.
-
(2009)
J Nucl Med
, vol.50
, Issue.SUPPL. 2
, pp. 1910
-
-
Cho, H.J.1
Lee, J.D.2
Park, J.Y.3
Yun, M.4
Kang, W.J.5
Walsh, J.C.6
-
128
-
-
0842263619
-
MicroPET and autoradiographic imaging of breast cancer alpha v-integrin expression using 18F- and 64Cu-labeled RGD peptide
-
14733582 10.1021/bc0300403 1:CAS:528:DC%2BD3sXhtVWit7nE
-
Chen X, Park R, Tohme M, Shahinian AH, Bading JR, Conti PS. MicroPET and autoradiographic imaging of breast cancer alpha v-integrin expression using 18F-
-
(2004)
Bioconjug Chem
, vol.15
, pp. 41-49
-
-
Chen, X.1
Park, R.2
Tohme, M.3
Shahinian, A.H.4
Bading, J.R.5
Conti, P.S.6
-
129
-
-
48149103227
-
68Ga- and 111In-labelled DOTA-RGD peptides for imaging of alphavbeta3 integrin expression
-
18369617 10.1007/s00259-008-0757-6
-
Decristoforo C, Hernandez Gonzalez I, Carlsen J, Rupprich M, Huisman M, Virgolini I, et al. 68Ga- and 111In-labelled DOTA-RGD peptides for imaging of alphavbeta3 integrin expression. Eur J Nucl Med Mol Imaging 2008;35:1507-15.
-
(2008)
Eur J Nucl Med Mol Imaging
, vol.35
, pp. 1507-1515
-
-
Decristoforo, C.1
Hernandez Gonzalez, I.2
Carlsen, J.3
Rupprich, H.4
Huisman, M.5
Virgolini, I.6
-
130
-
-
44149120982
-
Preparation of a promising angiogenesis PET imaging agent: 68Ga-labeled c(RGDyK)-isothiocyanatobenzyl-1,4,7-triazacyclononane-1,4,7-triacetic acid and feasibility studies in mice
-
18413379 1:CAS:528:DC%2BD1cXmvVSju7k%3D 10.2967/jnumed.107.047423
-
Jeong JM, Hong MK, Chang YS, Lee YS, Kim YJ, Cheon GJ, et al. Preparation of a promising angiogenesis PET imaging agent: 68Ga-labeled c(RGDyK)-isothiocyanatobenzyl-1,4,7-triazacyclononane-1,4,7-triacetic acid and feasibility studies in mice. J Nucl Med 2008;49:830-6.
-
(2008)
J Nucl Med
, vol.49
, pp. 830-836
-
-
Jeong, J.M.1
Hong, M.K.2
Chang, Y.S.3
Lee, Y.S.4
Kim, Y.J.5
Cheon, G.J.6
-
131
-
-
13944263708
-
Pegylated Arg-Gly-Asp peptide: 64Cu labeling and PET imaging of brain tumor alphavbeta3-integrin expression
-
15471848 1:CAS:528:DC%2BD2cXpslCqsLY%3D
-
Chen X, Hou Y, Tohme M, Park R, Khankaldyyan V, Gonzales-Gomez I, et al. Pegylated Arg-Gly-Asp peptide: 64Cu labeling and PET imaging of brain tumor alphavbeta3-integrin expression. J Nucl Med 2004;45:1776-83.
-
(2004)
J Nucl Med
, vol.45
, pp. 1776-1783
-
-
Chen, X.1
Hou, Y.2
Tohme, M.3
Park, R.4
Khankaldyyan, V.5
Gonzales-Gomez, I.6
-
132
-
-
3943086376
-
MicroPET imaging of brain tumor angiogenesis with 18F-labeled PEGylated RGD peptide
-
15118844 1:CAS:528:DC%2BD2cXmtFWks7k%3D 10.1007/s00259-003-1452-2
-
Chen X, Park R, Hou Y, Khankaldyyan V, Gonzales-Gomez I, Tohme M, et al. MicroPET imaging of brain tumor angiogenesis with 18F-labeled PEGylated RGD peptide. Eur J Nucl Med Mol Imaging 2004;31:1081-9.
-
(2004)
Eur J Nucl Med Mol Imaging
, vol.31
, pp. 1081-1089
-
-
Chen, X.1
Park, R.2
Hou, Y.3
Khankaldyyan, V.4
Gonzales-Gomez, I.5
Tohme, M.6
-
133
-
-
4644327177
-
Micro-PET imaging of alphavbeta3-integrin expression with 18F-labeled dimeric RGD peptide
-
15296674 1:CAS:528:DC%2BD2cXlvFCiu7s%3D 10.1162/1535350041464892
-
Chen X, Tohme M, Park R, Hou Y, Bading JR, Conti PS. Micro-PET imaging of alphavbeta3-integrin expression with 18F-labeled dimeric RGD peptide. Mol Imaging 2004;3:96-104.
-
(2004)
Mol Imaging
, vol.3
, pp. 96-104
-
-
Chen, X.1
Tohme, M.2
Park, R.3
Hou, Y.4
Bading, J.R.5
Conti, P.S.6
-
134
-
-
33646415036
-
Quantitative PET imaging of tumor integrin alphavbeta3 expression with 18F-FRGD2
-
16391195 1:CAS:528:DC%2BD28XhsFeisL4%3D
-
Zhang X, Xiong Z, Wu Y, Cai W, Tseng JR, Gambhir SS, et al. Quantitative PET imaging of tumor integrin alphavbeta3 expression with 18F-FRGD2. J Nucl Med 2006;47:113-21.
-
(2006)
J Nucl Med
, vol.47
, pp. 113-121
-
-
Zhang, X.1
Xiong, Z.2
Wu, Y.3
Cai, W.4
Tseng, J.R.5
Gambhir, S.S.6
-
135
-
-
0036829759
-
Tumor targeting with radiolabeled alpha(v)beta(3) integrin binding peptides in a nude mouse model
-
12414640 1:CAS:528:DC%2BD38XosF2ms7w%3D
-
Janssen ML, Oyen WJ, Dijkgraaf I, Massuger LF, Frielink C, Edwards DS, et al. Tumor targeting with radiolabeled alpha(v)beta(3) integrin binding peptides in a nude mouse model. Cancer Res 2002;62:6146-51.
-
(2002)
Cancer Res
, vol.62
, pp. 6146-6151
-
-
Janssen, M.L.1
Oyen, W.J.2
Dijkgraaf, I.3
Massuger, L.F.4
Frielink, C.5
Edwards, D.S.6
-
136
-
-
79551515411
-
PET imaging of alphavbeta3 integrin expression in tumours with 68Ga-labelled mono-, di- and tetrameric RGD peptides
-
20857099 1:CAS:528:DC%2BC3cXhsF2gtLjN 10.1007/s00259-010-1615-x
-
Dijkgraaf I, Yim CB, Franssen GM, Schuit RC, Luurtsema G, Liu S, et al. PET imaging of alphavbeta3 integrin expression in tumours with 68Ga-labelled mono-, di- and tetrameric RGD peptides. Eur J Nucl Med Mol Imaging 2011;38:128-37.
-
(2011)
Eur J Nucl Med Mol Imaging
, vol.38
, pp. 128-137
-
-
Dijkgraaf, I.1
Yim, C.B.2
Franssen, G.M.3
Schuit, R.C.4
Luurtsema, G.5
Liu, S.6
-
137
-
-
34447336118
-
(64)Cu-labeled tetrameric and octameric RGD peptides for small-animal PET of tumor alpha(v)beta(3) integrin expression
-
17574975 1:CAS:528:DC%2BD2sXhtVertL7F 10.2967/jnumed.107.039859
-
Li ZB, Cai W, Cao Q, Chen K, Wu Z, He L, et al. (64)Cu-labeled tetrameric and octameric RGD peptides for small-animal PET of tumor alpha(v)beta(3) integrin expression. J Nucl Med 2007;48:1162-71.
-
(2007)
J Nucl Med
, vol.48
, pp. 1162-1171
-
-
Li, Z.B.1
Cai, W.2
Cao, Q.3
Chen, K.4
Wu, Z.5
He, L.6
-
138
-
-
67349145987
-
(68)Ga-labeled cyclic RGD dimers with Gly3 and PEG4 linkers: Promising agents for tumor integrin alphavbeta3 PET imaging
-
19159928 1:CAS:528:DC%2BD1MXls1yjsL0%3D 10.1007/s00259-008-1045-1
-
Liu Z, Niu G, Shi J, Liu S, Wang F, Chen X. (68)Ga-labeled cyclic RGD dimers with Gly3 and PEG4 linkers: promising agents for tumor integrin alphavbeta3 PET imaging. Eur J Nucl Med Mol Imaging 2009;36:947-57.
-
(2009)
Eur J Nucl Med Mol Imaging
, vol.36
, pp. 947-957
-
-
Liu, Z.1
Niu, G.2
Shi, J.3
Liu, S.4
Wang, F.5
Chen, X.6
-
139
-
-
33750598987
-
Integrin receptor imaging of breast cancer: A proof-of-concept study to evaluate 99mTc-NC100692
-
16954550 1:CAS:528:DC%2BD28XhtVCmtLbP
-
Bach-Gansmo T, Danielsson R, Saracco A, Wilczek B, Bogsrud TV, Fangberget A, et al. Integrin receptor imaging of breast cancer: a proof-of-concept study to evaluate 99mTc-NC100692. J Nucl Med 2006;47:1434-9.
-
(2006)
J Nucl Med
, vol.47
, pp. 1434-1439
-
-
Bach-Gansmo, T.1
Danielsson, R.2
Saracco, A.3
Wilczek, B.4
Bogsrud, T.V.5
Fangberget, A.6
-
140
-
-
77956264376
-
18F-labeled galacto and PEGylated RGD dimers for PET imaging of alphavbeta3 integrin expression
-
19949981 10.1007/s11307-009-0284-2
-
Liu S, Liu Z, Chen K, Yan Y, Watzlowik P, Wester HJ, et al. 18F-labeled galacto and PEGylated RGD dimers for PET imaging of alphavbeta3 integrin expression. Mol Imaging Biol 2010;12:530-8.
-
(2010)
Mol Imaging Biol
, vol.12
, pp. 530-538
-
-
Liu, S.1
Liu, Z.2
Chen, K.3
Yan, Y.4
Watzlowik, P.5
Wester, H.J.6
|