-
1
-
-
0034783960
-
Mechanisms of estrogen action
-
Nilsson, S., Makela, S., Treuter, E., Tujague, M., Thomsen, J., Andersson, G., Enmark, E., Pettersson, K., Warner, M., and Gustafsson J. A. (2001) Mechanisms of estrogen action, Physiol. Rev. 81, 1535-1565.
-
(2001)
Physiol. Rev.
, vol.81
, pp. 1535-1565
-
-
Nilsson, S.1
Makela, S.2
Treuter, E.3
Tujague, M.4
Thomsen, J.5
Anders-Son, G.6
Enmark, E.7
Pettersson, K.8
Warner, M.9
Gustafsson, J.A.10
-
2
-
-
0033780783
-
Estrogen-induced activation of Erk-1 and Erk-2 requires the G protein-coupled receptor homolog, GPR30, and occurs via trans-activation of the epidermal growth factor receptor through release of HB-EGF
-
Filardo, E. J., Quinn, J. A., Bland, K. I., and Frackelton, A. R. Jr. (2000) Estrogen-induced activation of Erk-1 and Erk-2 requires the G protein-coupled receptor homolog, GPR30, and occurs via trans-activation of the epidermal growth factor receptor through release of HB-EGF, Mol. Endocrinol. 14,1649-1660.
-
(2000)
Mol. Endocrinol.
, vol.14
, pp. 1649-1660
-
-
Filardo, E.J.1
Quinn, J.A.2
Bland, K.I.3
Frackelton Jr., A.R.4
-
3
-
-
14844343093
-
A transmembrane intracellular estrogen receptor mediates rapid cell signaling
-
Revankar, C. M., Cimino, D. F., Sklar, L A., Arterburn, J. B., and Prossnitz, E. R. (2005) A transmembrane intracellular estrogen receptor mediates rapid cell signaling, Science 307,1625-1630.
-
(2005)
Science
, vol.307
, pp. 1625-1630
-
-
Revankar, C.M.1
Cimino, D.F.2
Sklar, L.A.3
Arterburn, J.B.4
Prossnitz, E.R.5
-
4
-
-
12344307170
-
Identityofan estrogen membrane receptor coupled to a G protein in human breast cancer cells
-
Thomas, P., Pang, Y., Filardo, E.J., and Dong, J. (2005) Identityofan estrogen membrane receptor coupled to a G protein in human breast cancer cells, Endocrinology 146, 624-632.
-
(2005)
Endocrinology
, vol.146
, pp. 624-632
-
-
Thomas, P.1
Pang, Y.2
Filardo, E.J.3
Dong, J.4
-
5
-
-
35348857513
-
Synthetic estrogen derivatives demonstrate the functionality of intracellular GPR30
-
Revankar, C. M., Mitchell, H. D., Field, A. S., Burai, R., Corona, C., Ramesh, C., Sklar, L A., Arterburn, J. B., and Prossnitz, E. R. (2007) Synthetic estrogen derivatives demonstrate the functionality of intracellular GPR30, ACS Chem. Biol. 2, 536-544.
-
(2007)
ACS Chem. Biol.
, vol.2
, pp. 536-544
-
-
Revankar, C.M.1
Mitchell, H.D.2
Field, A.S.3
Burai, R.4
Corona, C.5
Ramesh, C.6
Sklar, L.A.7
Arterburn, J.B.8
Prossnitz, E.R.9
-
6
-
-
34347238583
-
Activation of the novel estrogen receptor G protein-coupled receptor 30 (GPR30) at the plasma membrane
-
Filardo, E., Quinn, J., Pang, Y., Graeber, C., Shaw, S., Dong, J., and Thomas, P. (2007) Activation of the novel estrogen receptor G protein-coupled receptor 30 (GPR30) at the plasma membrane, Endocrinology 148, 3236-3245.
-
(2007)
Endocrinology
, vol.148
, pp. 3236-3245
-
-
Filardo, E.1
Quinn, J.2
Pang, Y.3
Graeber, C.4
Shaw, S.5
Dong, J.6
Thomas, P.7
-
7
-
-
33646366423
-
Virtual and biomolecular screening converge on a selective agonist for GPR30
-
Bologa, C. G., Revankar, C. M., Young, S. M., Edwards, B. S., Arterburn, J. B., Kiselyov, A. S., Parker, M. A., Tkachenko, S. E., Savchuck, N. P., Sklar, L A., Oprea, T. I., and Prossnitz, E. R. (2006) Virtual and biomolecular screening converge on a selective agonist for GPR30, Nat. Chem. Biol. 2, 207-212.
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 207-212
-
-
Bologa, C.G.1
Revankar, C.M.2
Young, S.M.3
Edwards, B.S.4
Arterburn, J.B.5
Kiselyov, A.S.6
Parker, M.A.7
Tkachenko, S.E.8
Savchuck, N.P.9
Sklar, L.A.10
Oprea, T.I.11
Prossnitz, E.R.12
-
8
-
-
67349140294
-
In vivo effects of a GPR30 antagonist
-
Dennis, M. K., Burai, R., Ramesh, C., Petrie, W. K., Alcon, S. N., Nayak, T. K., Bologa, C. G., Leitao, A., Brailoiu, E., Deliu, E., Dun, N. J., Sklar, L A., Hathaway, H. J., Arterburn, J. B., Oprea, T. I., and Prossnitz, E. R. (2009) In vivo effects of a GPR30 antagonist, Nat. Chem. Biol. 5, 421-427.
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 421-427
-
-
Dennis, M.K.1
Burai, R.2
Ramesh, C.3
Petrie, W.K.4
Alcon, S.N.5
Nayak, T.K.6
Bologa, C.G.7
Leitao, A.8
Brailoiu, E.9
Deliu, E.10
Dun, N.J.11
Sklar, L.A.12
Hathaway, H.J.13
Arterburn, J.B.14
Oprea, T.I.15
Prossnitz, E.R.16
-
9
-
-
69949166203
-
Beneficial role of the GPR30 agonist G-1 in an animal model of multiple sclerosis
-
Blasko, E., Haskell, C. A., Leung, S., Gualtieri, G., Halks-Miller, M., Mahmoudi, M., Dennis, M. K., Prossnitz, E. R., Karpus, W. J., and Horuk, R. (2009) Beneficial role of the GPR30 agonist G-1 in an animal model of multiple sclerosis, J. Neuroimmunol. 214, 67-77.
-
(2009)
J. Neuroimmunol.
, vol.214
, pp. 67-77
-
-
Blasko, E.1
Haskell, C.A.2
Leung, S.3
Gualtieri, G.4
Halks-Miller, M.5
Mahmoudi, M.6
Dennis, M.K.7
Prossnitz, E.R.8
Karpus, W.J.9
Horuk, R.10
-
10
-
-
60149091560
-
Extranuclear estrogen receptor GPR30 regulates serotonin function in rat hypothalamus
-
Xu, H., Qin, S., Carrasco, G. A., Dai, Y., Filardo, E. J., Prossnitz, E. R., Battaglia, G., Doncarlos, L L., and Muma, N. A. (2009) Extranuclear estrogen receptor GPR30 regulates serotonin function in rat hypothalamus, Neuroscience 158,1599-1607.
-
(2009)
Neuroscience
, vol.158
, pp. 1599-1607
-
-
Xu, H.1
Qin, S.2
Carrasco, G.A.3
Dai, Y.4
Filardo, E.J.5
Prossnitz, E.R.6
Battaglia, G.7
Doncarlos, L.L.8
Muma, N.A.9
-
11
-
-
61949405394
-
Regulatory role of G protein-coupled estrogen receptor for vascular function and obesity
-
Haas, E., Bhattacharya, I., Brailoiu, E., Damjanovic, M., Brailoiu, G. C., Gao, X., Mueller-Guerre, L., Marjon, N. A., Gut, A., Minotti, R., Meyer, M. R., Amann, K., Ammann, E., Perez-Dominguez, A., Genoni, M., Clegg, D.J., Dun, N.J., Resta, T. C., Prossnitz, E. R., and Barton, M. (2009) Regulatory role of G protein-coupled estrogen receptor for vascular function and obesity, Circ. Res. 104, 288-291.
-
(2009)
Circ. Res.
, vol.104
, pp. 288-291
-
-
Haas, E.1
Bhattacharya, I.2
Brailoiu, E.3
Damjanovic, M.4
Brailoiu, G.C.5
Gao, X.6
Mueller-Guerre, L.7
Marjon, N.A.8
Gut, A.9
Minotti, R.10
Meyer, M.R.11
Amann, K.12
Ammann, E.13
Perez-Dominguez, A.14
Genoni, M.15
Clegg, D.J.16
Dun, N.J.17
Resta, T.C.18
Prossnitz, E.R.19
Barton, M.20
more..
-
12
-
-
47949092800
-
The G protein-coupled receptor GPR30 inhibits human urothelial cell proliferation
-
Teng, J., Wang, Z. Y., Prossnitz, E. R., and Bjorling, D. E. (2008) The G protein-coupled receptor GPR30 inhibits human urothelial cell proliferation, Endocrinology 149,4024-4034.
-
(2008)
Endocrinology
, vol.149
, pp. 4024-4034
-
-
Teng, J.1
Wang, Z.Y.2
Prossnitz, E.R.3
Bjorling, D.E.4
-
13
-
-
70349401677
-
GPR30/GPER1: Searching for a role in estrogen physiology
-
Olde, B., and Leeb-Lundberg, L M. (2009) GPR30/GPER1: searching for a role in estrogen physiology, Trends Endocrinol. Metab. 20, 409-416.
-
(2009)
Trends Endocrinol. Metab.
, vol.20
, pp. 409-416
-
-
Olde, B.1
Leeb-Lundberg, L.M.2
-
14
-
-
59649122739
-
Deletion of the G protein-coupled receptor 30 impairs glucose tolerance, reduces bone growth, increases blood pressure, and eliminates estradiol-stimulated insulin release in female mice
-
Martensson, U. E., Salehi, S.A., Windahl, S., Gomez, M. F., Sward, K., Daszkiewicz-Nilsson, J., Wendt, A., Andersson, N., Hellstrand, P., Grande, P. O., Owman, C., Rosen, C. J., Adamo, M. L., Lundquist, I., Rorsman, P., Nilsson, B. O., Ohlsson, C., Olde, B., and Leeb-Lundberg, L. M. (2009) Deletion of the G protein-coupled receptor 30 impairs glucose tolerance, reduces bone growth, increases blood pressure, and eliminates estradiol-stimulated insulin release in female mice, Endocrinology 150, 687-698.
-
(2009)
Endocrinology
, vol.150
, pp. 687-698
-
-
Martensson, U.E.1
Salehi, S.A.2
Windahl, S.3
Gomez, M.F.4
Sward, K.5
Daszkiewicz-Nilsson, J.6
Wendt, A.7
Andersson, N.8
Hellstrand, P.9
Grande, P.O.10
Owman, C.11
Rosen, C.J.12
Adamo, M.L.13
Lundquist, I.14
Rorsman, P.15
Nilsson, B.O.16
Ohlsson, C.17
Olde, B.18
Leeb-Lundberg, L.M.19
-
15
-
-
33751272253
-
Distribution of GPR30, a seven membrane-spanning estrogen receptor, in primary breast cancer and its association with clinicopathologic determinants of tumor progression
-
Filardo, E.J., Graeber, C.T., Quinn, J. A., Resnick, M. B., Giri, D., DeLellis, R. A., Steinhoff, M. M., and Sabo, E. (2006) Distribution of GPR30, a seven membrane-spanning estrogen receptor, in primary breast cancer and its association with clinicopathologic determinants of tumor progression, Clin. Cancer Res. 12, 6359-6366.
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 6359-6366
-
-
Filardo, E.J.1
Graeber, C.T.2
Quinn, J.A.3
Resnick, M.B.4
Giri, D.5
DeLellis, R.A.6
Steinhoff, M.M.7
Sabo, E.8
-
16
-
-
33947697810
-
GPR30: A novel indicator of poor survival for endometrial carcinoma
-
discussion e389-311
-
Smith, H. O., Leslie, K. K., Singh, M., Qualls, C. R., Revankar, C. M., Joste, N. E., and Prossnitz, E. R. (2007) GPR30: a novel indicator of poor survival for endometrial carcinoma, Am. J. Obstet. Gynecol. 196, e381-389; discussion e389-311.
-
(2007)
Am. J. Obstet. Gynecol.
, vol.196
-
-
Smith, H.O.1
Leslie, K.K.2
Singh, M.3
Qualls, C.R.4
Revankar, C.M.5
Joste, N.E.6
Prossnitz, E.R.7
-
17
-
-
67749119671
-
GPR30 predicts poor survival for ovarian cancer
-
Smith, H. O., Arias-Pulido, H., Kuo, D. Y., Howard, T., Qualls, C. R., Lee, S. J., Verschraegen, C. F., Hathaway, H. J., Joste, N. E., and Prossnitz, E. R. (2009) GPR30 predicts poor survival for ovarian cancer, Gynecol. Oncol. 114,465-471.
-
(2009)
Gynecol. Oncol.
, vol.114
, pp. 465-471
-
-
Smith, H.O.1
Arias-Pulido, H.2
Kuo, D.Y.3
Howard, T.4
Qualls, C.R.5
Lee, S.J.6
Verschraegen, C.F.7
Hathaway, H.J.8
Joste, N.E.9
Prossnitz, E.R.10
-
18
-
-
0029979129
-
Positron emission tomography with 2-[18F]fluoro-2-deoxy-D-glucose and 16α-[18F]fluoro-17β-estradiol in breast cancer: Correlation with estrogen receptor status and response to systemic therapy
-
Mortimer, J. E., Dehdashti, F., Siegel, B. A., Katzenellenbogen, J. A., Fracasso, P., and Welch, M.J. (1996) Positron emission tomography with 2-[18F]fluoro-2-deoxy-D-glucose and 16α-[18F]fluoro-17β-estradiol in breast cancer: correlation with estrogen receptor status and response to systemic therapy, Clin. Cancer Res. 2, 933-939.
-
(1996)
Clin. Cancer Res.
, vol.2
, pp. 933-939
-
-
Mortimer, J.E.1
Dehdashti, F.2
Siegel, B.A.3
Katzenellenbogen, J.A.4
Fracasso, P.5
Welch, M.J.6
-
19
-
-
49049103406
-
Uterine tumors: Pathophysiologic imagingwith 16α-[18F]fluoro- 17β-estradioland 18Ffluorodeoxyglu-cose PET - Initial experience
-
Tsujikawa, T., Yoshida, Y., Mori, T., Kurokawa, T., Fujibayashi, Y., Kotsuji, F., and Okazawa, H. (2008) Uterine tumors: pathophysiologic imagingwith 16α-[18F]fluoro-17β-estradioland 18Ffluorodeoxyglu-cose PET - initial experience, Radiology 248, 599-605.
-
(2008)
Radiology
, vol.248
, pp. 599-605
-
-
Tsujikawa, T.1
Yoshida, Y.2
Mori, T.3
Kurokawa, T.4
Fujibayashi, Y.5
Kotsuji, F.6
Okazawa, H.7
-
20
-
-
70450221982
-
Positron emission tomography in ovarian cancer: 18F-deoxy-glucose and 16α-18F-fluoro-17β-estradiol PET
-
Yoshida, Y., Kurokawa, T., Tsujikawa, T., Okazawa, H., and Kotsuji, F. (2009) Positron emission tomography in ovarian cancer: 18F-deoxy-glucose and 16α-18F-fluoro-17β-estradiol PET, J. Ovarian Res. 2, 7.
-
(2009)
J. Ovarian Res.
, vol.2
, pp. 7
-
-
Yoshida, Y.1
Kurokawa, T.2
Tsujikawa, T.3
Okazawa, H.4
Kotsuji, F.5
-
21
-
-
33846921573
-
The positron emission tomography with F18 17β-estradiol has the potential to benefit diagnosis and treatment of endometrial cancer
-
Yoshida, Y., Kurokawa, T., Sawamura, Y., Shinagawa, A., Okazawa, H., Fujibayashi, Y., and Kotsuji, F. (2007) The positron emission tomography with F18 17β-estradiol has the potential to benefit diagnosis and treatment of endometrial cancer, Gynecol. Oncol. 104, 764-766.
-
(2007)
Gynecol. Oncol.
, vol.104
, pp. 764-766
-
-
Yoshida, Y.1
Kurokawa, T.2
Sawamura, Y.3
Shinagawa, A.4
Okazawa, H.5
Fujibayashi, Y.6
Kotsuji, F.7
-
22
-
-
33745545477
-
Quantitative fluoroestradiol positron emission tomography imaging predicts response to endocrine treatment in breast cancer
-
Linden, H. M., Stekhova, S.A., Link, J. M., Gralow, J. R., Livingston, R. B., Ellis, G. K., Petra, P. H., Peterson, L. M., Schubert, E. K., Dunnwald, L. K., Krohn, K. A., and Mankoff, D. A. (2006) Quantitative fluoroestradiol positron emission tomography imaging predicts response to endocrine treatment in breast cancer, J. Clin. Oncol. 24, 2793-2799.
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 2793-2799
-
-
Linden, H.M.1
Stekhova, S.A.2
Link, J.M.3
Gralow, J.R.4
Livingston, R.B.5
Ellis, G.K.6
Petra, P.H.7
Peterson, L.M.8
Schubert, E.K.9
Dunnwald, L.K.10
Krohn, K.A.11
Mankoff, D.A.12
-
23
-
-
58549097114
-
PET-based estradiol challenge as a predictive biomarker of response to endocrine therapy in women with estrogen-receptor-positive breast cancer
-
Dehdashti, F., Mortimer, J. E., Trinkaus, K., Naughton, M. J., Ellis, M., Katzenellenbogen, J. A., Welch, M. J., and Siegel, B. A. (2009) PET-based estradiol challenge as a predictive biomarker of response to endocrine therapy in women with estrogen-receptor-positive breast cancer, Breast Cancer Res. Treat. 113,509-517.
-
(2009)
Breast Cancer Res. Treat.
, vol.113
, pp. 509-517
-
-
Dehdashti, F.1
Mortimer, J.E.2
Trinkaus, K.3
Naughton, M.J.4
Ellis, M.5
Katzenellenbogen, J.A.6
Welch, M.J.7
Siegel, B.A.8
-
24
-
-
77249119272
-
Synthesis and characterization of iodinated tetrahydroquinolines targeting the G protein-coupled estrogen receptor GPR30
-
Ramesh, C., Nayak, T. K., Burai, R., Dennis, M. K., Hathaway, H. J., Sklar, L. A., Prossnitz, E. R., and Arterburn J. B. (2010) Synthesis and characterization of iodinated tetrahydroquinolines targeting the G protein-coupled estrogen receptor GPR30, J. Med. Chem. 53, 1004-1014.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1004-1014
-
-
Ramesh, C.1
Nayak, T.K.2
Burai, R.3
Dennis, M.K.4
Hathaway, H.J.5
Sklar, L.A.6
Prossnitz, E.R.7
Arterburn, J.B.8
-
25
-
-
0036973248
-
Synthesis and estrogen receptor affinity of a 4-hydroxytamoxifen-labeled ligand for diagnostic imaging
-
Lashley, M. R., Niedzinski, E. J., Rogers, J. M., Denison, M. S., and Nantz, M. H. (2002) Synthesis and estrogen receptor affinity of a 4-hydroxytamoxifen-labeled ligand for diagnostic imaging, Bioorg. Med. Chem. 10,4075-4082.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 4075-4082
-
-
Lashley, M.R.1
Niedzinski, E.J.2
Rogers, J.M.3
Denison, M.S.4
Nantz, M.H.5
-
26
-
-
20344383981
-
An estradiol-conjugate for radio-labelling with 177Lu: An attempt to prepare a radiotherapeutic agent
-
Banerjee, S., Das, T., Chakraborty, S., Samuel, G., Korde, A., Venkatesh, M., and Pillai, M. R. (2005) An estradiol-conjugate for radio-labelling with 177Lu: an attempt to prepare a radiotherapeutic agent Bioorg. Med. Chem. 13,4315-4322.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4315-4322
-
-
Banerjee, S.1
Das, T.2
Chakraborty, S.3
Samuel, G.4
Korde, A.5
Venkatesh, M.6
Pillai, M.R.7
-
27
-
-
0029904131
-
Synthesis, biodistribution, and estrogen receptorscintigraphy of indium-111-diethylenetriaminepentaacetic acid-tamoxifen analogue
-
Delpassand, E. S., Yang, D. J., Wallace, S., Cherif, A., Quadri, S. M., Price, J., Joubert, A., Inoue, T., and Podoloff, D. A. (1996) Synthesis, biodistribution, and estrogen receptorscintigraphy of indium-111- diethylenetriaminepentaacetic acid-tamoxifen analogue, J. Pharm. Sci. 85, 553-559.
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 553-559
-
-
Delpassand, E.S.1
Yang, D.J.2
Wallace, S.3
Cherif, A.4
Quadri, S.M.5
Price, J.6
Joubert, A.7
Inoue, T.8
Podoloff, D.A.9
-
28
-
-
34648840361
-
Water-soluble contrast agents targeted at the estrogen receptor for molecular magnetic resonance imaging
-
Gunanathan, C., Pais, A., Furman-Haran, E., Seger, D., Eyal, E., Mukhopadhyay, S., Ben-David, Y., Leitus, G., Cohen, H., Vilan, A., Degani, H., and Milstein, D. (2007) Water-soluble contrast agents targeted at the estrogen receptor for molecular magnetic resonance imaging, Bioconjugate Chem. 18,1361-1365.
-
(2007)
Bioconjugate Chem.
, vol.18
, pp. 1361-1365
-
-
Gunanathan, C.1
Pais, A.2
Furman-Haran, E.3
Seger, D.4
Eyal, E.5
Mukhopadhyay, S.6
Ben-David, Y.7
Leitus, G.8
Cohen, H.9
Vilan, A.10
Degani, H.11
Milstein, D.12
-
29
-
-
0028535424
-
A facile, watersoluble method for modification of proteins with DOTA. Use of elevated temperature and optimized pH to achieve high specific activity and high chelate stability in radiolabeled immunoconjugates
-
Lewis, M. R., Raubitschek, A., and Shively, J. E. (1994) A facile, watersoluble method for modification of proteins with DOTA. Use of elevated temperature and optimized pH to achieve high specific activity and high chelate stability in radiolabeled immunoconjugates, Bioconjugate Chem. 5, 565-576.
-
(1994)
Bioconjugate Chem.
, vol.5
, pp. 565-576
-
-
Lewis, M.R.1
Raubitschek, A.2
Shively, J.E.3
-
30
-
-
0025237122
-
Yttrium-90-labeled monoclonal antibody for therapy: Labeling by a new macrocyclic bifunctionalchelating agent
-
Deshpande, S. V., DeNardo, S. J., Kukis, D. L., Moi, M. K., McCall, M. J., DeNardo, G. L., and Meares, C. F. (1990) Yttrium-90-labeled monoclonal antibody for therapy: labeling by a new macrocyclic bifunctionalchelating agent, J. Nucl. Med. 31, 473-479.
-
(1990)
J. Nucl. Med.
, vol.31
, pp. 473-479
-
-
Deshpande, S.V.1
DeNardo, S.J.2
Kukis, D.L.3
Moi, M.K.4
McCall, M.J.5
DeNardo, G.L.6
Meares, C.F.7
-
31
-
-
0001401522
-
Kinetics of formation of Ca(2+) complexes of acyclic and macrocyclic poly-(amino carboxylate) ligands: Bimolecular rate constants forthefullydeprotonated ligands reveal the effect of macrocyclic ligand constraints on the rate-determining conversions of rapidly-formed intermediates to the final complexes
-
Wu, S. L., Johnson, K. A., and Horrocks, W. D., Jr. (1997) Kinetics of formation of Ca(2+) complexes of acyclic and macrocyclic poly-(amino carboxylate) ligands: bimolecular rate constants forthefullydeprotonated ligands reveal the effect of macrocyclic ligand constraints on the rate-determining conversions of rapidly-formed intermediates to the final complexes, Inorg. Chem. 36, 1884-1889.
-
(1997)
Inorg. Chem.
, vol.36
, pp. 1884-1889
-
-
Wu, S.L.1
Johnson, K.A.2
Horrocks Jr., W.D.3
-
32
-
-
33751004697
-
Linkage effects on binding affinity and activation of GPR30 and estrogen receptors ERα/β with tridentate pyridin-2-yl hydrazine tricarbonyl-Re/(99m)Tc(I) chelates
-
Ramesh, C., Bryant, B., Nayak, T., Revankar, CM., Anderson, T., Carlson, K. E., Katzenellenbogen, J. A., Sklar, L. A., Norenberg, J. P., Prossnitz, E. R., and Arterburn, J. B. (2006) Linkage effects on binding affinity and activation of GPR30 and estrogen receptors ERα/β with tridentate pyridin-2-yl hydrazine tricarbonyl-Re/(99m)Tc(I) chelates, J. Am. Chem. Soc. 128, 14476-14477.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14476-14477
-
-
Ramesh, C.1
Bryant, B.2
Nayak, T.3
Revankar, C.M.4
Anderson, T.5
Carlson, K.E.6
Katzenellenbogen, J.A.7
Sklar, L.A.8
Norenberg, J.P.9
Prossnitz, E.R.10
Arterburn, J.B.11
-
33
-
-
44849115355
-
Preclinical development of a neutral, estrogen receptor-targeted, tridentate 99mTc(I)-estradiol-pyridin-2-yl hydrazine derivative for imaging of breast and endometrial cancers
-
Nayak, T. K., Hathaway, H. J., Ramesh, C., Arterburn, J. B., Dai, D., Sklar, L. A., Norenberg, J. P., and Prossnitz, E. R. (2008) Preclinical development of a neutral, estrogen receptor-targeted, tridentate 99mTc(I)-estradiol-pyridin-2-yl hydrazine derivative for imaging of breast and endometrial cancers, J. Nucl. Med. 49, 978-986.
-
(2008)
J. Nucl. Med.
, vol.49
, pp. 978-986
-
-
Nayak, T.K.1
Hathaway, H.J.2
Ramesh, C.3
Arterburn, J.B.4
Dai, D.5
Sklar, L.A.6
Norenberg, J.P.7
Prossnitz, E.R.8
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