-
1
-
-
0034280739
-
Selective activation of mGlu4 metabotropic glutamate receptors is protective against excitotoxic neuronal death
-
BRUNO, V., BATTAGLIA, G., KSIAZEK, I., VAN DER PUTTEN, H., CATANIA, M.V., GIUFFRIDA, R., LUKIC, S., LEONHARDT, T., INDERBITZIN, W., GASPARINI, F., KUHN, R., HAMPSON, D.R., NICOLETTI, F. & FLOR, P.J. (2000a). Selective activation of mGlu4 metabotropic glutamate receptors is protective against excitotoxic neuronal death. J. Neurosci., 20, 6413-6420.
-
(2000)
J. Neurosci.
, vol.20
, pp. 6413-6420
-
-
Bruno, V.1
Battaglia, G.2
Ksiazek, I.3
Van Der Putten, H.4
Catania, M.V.5
Giuffrida, R.6
Lukic, S.7
Leonhardt, T.8
Inderbitzin, W.9
Gasparini, F.10
Kuhn, R.11
Hampson, D.R.12
Nicoletti, F.13
Flor, P.J.14
-
2
-
-
17044444317
-
Selective blockade of metabotropic glutamate receptor subtype 5 is neuroprotective
-
BRUNO, V., KSIAZEK, I., BATTAGLIA, G., LUKIC, S., LEONHARDT, T., SAUER, D., GASPARINI, F., KUHN, R., NICOLETTI, F. & FLOR, P.J. (2000b). Selective blockade of metabotropic glutamate receptor subtype 5 is neuroprotective. Neuropharmacology, 39, 2223-2230.
-
(2000)
Neuropharmacology
, vol.39
, pp. 2223-2230
-
-
Bruno, V.1
Ksiazek, I.2
Battaglia, G.3
Lukic, S.4
Leonhardt, T.5
Sauer, D.6
Gasparini, F.7
Kuhn, R.8
Nicoletti, F.9
Flor, P.J.10
-
3
-
-
0036258990
-
G protein-coupled receptor allosterism and complexing
-
CHRISTOPOULOS, A. & KENAKIN, T. (2002). G protein-coupled receptor allosterism and complexing. Pharmacol. Rev., 54, 323-374.
-
(2002)
Pharmacol. Rev.
, vol.54
, pp. 323-374
-
-
Christopoulos, A.1
Kenakin, T.2
-
4
-
-
0030995878
-
Pharmacology and functions of metabotropic glutamate receptors
-
CONN, P.J. & PIN, J.P. (1997). Pharmacology and functions of metabotropic glutamate receptors. Annu. Rev. Pharmacol. Toxicol., 37, 205-237.
-
(1997)
Annu. Rev. Pharmacol. Toxicol.
, vol.37
, pp. 205-237
-
-
Conn, P.J.1
Pin, J.P.2
-
5
-
-
0036462446
-
Allosteric modulators of group I metabotropic glutamate receptors: Novel subtype-selective ligands and therapeutic perspectives
-
GASPARINI, F., KUHN, R. & PIN, J.P. (2002). Allosteric modulators of group I metabotropic glutamate receptors: novel subtype-selective ligands and therapeutic perspectives. Curr. Opin. Pharmacol., 2, 43-49.
-
(2002)
Curr. Opin. Pharmacol.
, vol.2
, pp. 43-49
-
-
Gasparini, F.1
Kuhn, R.2
Pin, J.P.3
-
6
-
-
0032853255
-
2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist
-
GASPARINI, F., LINGENHOHL, K., STOEHR, N., FLOR, P.J., HEINRICH, M., VRANESIC, I., BIOLLAZ, M., ALLGEIER, H., HECKENDORN, R., URWYLER, S., VARNEY, M.A., JOHNSON, E.C., HESS, S.D., RAO, S.P., SACAAN, A.I., SANTORI, E.M., VELICELEBI, G. & KUHN, R. (1999). 2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist. Neuropharmacology, 38, 1493-1503.
-
(1999)
Neuropharmacology
, vol.38
, pp. 1493-1503
-
-
Gasparini, F.1
Lingenhohl, K.2
Stoehr, N.3
Flor, P.J.4
Heinrich, M.5
Vranesic, I.6
Biollaz, M.7
Allgeier, H.8
Heckendorn, R.9
Urwyler, S.10
Varney, M.A.11
Johnson, E.C.12
Hess, S.D.13
Rao, S.P.14
Sacaan, A.I.15
Santori, E.M.16
Velicelebi, G.17
Kuhn, R.18
-
7
-
-
0033669603
-
Modeling the functional effects of allosteric modulators at pharmacological receptors: An extension of the two-state model of receptor activation
-
HALL, D.A. (2000). Modeling the functional effects of allosteric modulators at pharmacological receptors: an extension of the two-state model of receptor activation. Mol. Pharmacol., 58, 1412-1423.
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 1412-1423
-
-
Hall, D.A.1
-
8
-
-
0035818605
-
Positive allosteric modulators of metabotropic glutamate 1 receptor: Characterization, mechanism of action, and binding site
-
KNOFLACH, F., MUTEL, V., JOLIDON, S., KEW, J.N., MALHERBE, P., VIEIRA, E., WICHMANN, J. & KEMP, J.A. (2001). Positive allosteric modulators of metabotropic glutamate 1 receptor: characterization, mechanism of action, and binding site. Proc. Natl. Acad. Sci. U.S.A., 98, 13402-13407.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 13402-13407
-
-
Knoflach, F.1
Mutel, V.2
Jolidon, S.3
Kew, J.N.4
Malherbe, P.5
Vieira, E.6
Wichmann, J.7
Kemp, J.A.8
-
9
-
-
0031595204
-
A [35S]GTPgammaS binding assessment of metabotropic glutamate receptor standards in Chinese hamster ovary cell lines expressing the human metabotropic receptor subtypes 2 and 4
-
KOWAL, D., HSIAO, C.L., GE, A., WARDWELL-SWANSON, J., GHOSH, K. & TASSE, R. (1998). A [35S]GTPgammaS binding assessment of metabotropic glutamate receptor standards in Chinese hamster ovary cell lines expressing the human metabotropic receptor subtypes 2 and 4. Neuropharmacology, 37, 179-187.
-
(1998)
Neuropharmacology
, vol.37
, pp. 179-187
-
-
Kowal, D.1
Hsiao, C.L.2
Ge, A.3
Wardwell-Swanson, J.4
Ghosh, K.5
Tasse, R.6
-
10
-
-
0034718925
-
Structural basis of glutamaterecognition by a dimeric metabotropic glutamate receptor
-
KUNISHIMA, N., SHIMADA, Y., TSUJI, Y., SATO, T., YAMAMOTO, M., KUMASAKA, T., NAKANISHI, S., JINGAMI, H. & MORIKAWA, K. (2000). Structural basis of glutamaterecognition by a dimeric metabotropic glutamate receptor. Nature, 407, 971-977.
-
(2000)
Nature
, vol.407
, pp. 971-977
-
-
Kunishima, N.1
Shimada, Y.2
Tsuji, Y.3
Sato, T.4
Yamamoto, M.5
Kumasaka, T.6
Nakanishi, S.7
Jingami, H.8
Morikawa, K.9
-
11
-
-
0032734779
-
Effect of the umami peptides on the ligand binding and function of rat mGlu4a receptor might implicate this receptor in the monosodium glutamate taste transduction
-
MONASTYRSKAIA, K., LUNDSTROM, K., PLAHL, D., ACUNA, G., SCHWEITZER, C., MALHERBE, P. & MUTEL, V. (1999). Effect of the umami peptides on the ligand binding and function of rat mGlu4a receptor might implicate this receptor in the monosodium glutamate taste transduction. Br. J. Pharmacol., 128, 1027-1034.
-
(1999)
Br. J. Pharmacol.
, vol.128
, pp. 1027-1034
-
-
Monastyrskaia, K.1
Lundstrom, K.2
Plahl, D.3
Acuna, G.4
Schweitzer, C.5
Malherbe, P.6
Mutel, V.7
-
12
-
-
0001820063
-
Analyzing radioligand binding data
-
ed. Crawley, J., Gerfen, C., Mckay, R., Rogawski, M., Sibley, D., & Skolnick, P. New York: John Wiley & Sons, Inc.
-
MOTULSKY, H. & NEUBIG, R. (1997). Analyzing radioligand binding data. In Current Protocols in Neuroscience. ed. Crawley, J., Gerfen, C., Mckay, R., Rogawski, M., Sibley, D., & Skolnick, P. pp. 7.5.1-7.5.56. New York: John Wiley & Sons, Inc.
-
(1997)
Current Protocols in Neuroscience
, pp. 751-7556
-
-
Motulsky, H.1
Neubig, R.2
-
13
-
-
0035197286
-
mGluR5 antagonists 2-methyl-6-(phenylethynyl)-pyridine and (E)-2-methyl-6-(2-phenylethenyl)-pyridine reduce traumatic neuronal injury in vitro and in vivo by antagonizing N-methyl-D-aspartate receptors
-
MOVSESYAN, V.A., O'LEARY, D.M., FAN, L., BAO, W., MULLINS, P.G., KNOBLACH, S.M. & FADEN, A.I. (2001). mGluR5 antagonists 2-methyl-6-(phenylethynyl)-pyridine and (E)-2-methyl-6-(2-phenylethenyl)-pyridine reduce traumatic neuronal injury in vitro and in vivo by antagonizing N-methyl-D-aspartate receptors. J. Pharmacol. Exp. Ther., 296, 41-47.
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.296
, pp. 41-47
-
-
Movsesyan, V.A.1
O'Leary, D.M.2
Fan, L.3
Bao, W.4
Mullins, P.G.5
Knoblach, S.M.6
Faden, A.I.7
-
14
-
-
0033638723
-
Selective mGluR5 antagonists MPEP and SIB-1893 decrease NMDA or glutamate-mediated neuronal toxicity through actions that reflect NMDA receptor antagonism
-
O'LEARY, D.M., MOVSESYAN, V., VICINI, S. & FADEN, A.I. (2000). Selective mGluR5 antagonists MPEP and SIB-1893 decrease NMDA or glutamate-mediated neuronal toxicity through actions that reflect NMDA receptor antagonism. Br. J. Pharmacol., 131, 1429-1437.
-
(2000)
Br. J. Pharmacol.
, vol.131
, pp. 1429-1437
-
-
O'Leary, D.M.1
Movsesyan, V.2
Vicini, S.3
Faden, A.I.4
-
15
-
-
0028076043
-
L-glutamate uptake inhibitors may stimulate phosphoinositide hydrolysis in baby hamster kidney cells expressing mGluR1a via heteroexchange with L-glutamate without direct activation of mGluR1a
-
THOMSEN, C., HANSEN, L. & SUZDAK, P.D. (1994). L-glutamate uptake inhibitors may stimulate phosphoinositide hydrolysis in baby hamster kidney cells expressing mGluR1a via heteroexchange with L-glutamate without direct activation of mGluR1a. J. Neurochem., 63, 2038-2047.
-
(1994)
J. Neurochem.
, vol.63
, pp. 2038-2047
-
-
Thomsen, C.1
Hansen, L.2
Suzdak, P.D.3
-
16
-
-
0034760504
-
Positive allosteric modulation of native and recombinant gamma-aminobutyric acid(B) receptors by 2,6-Di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol (CGP7930) and its aldehyde analog CGP13501
-
URWYLER, S., MOSBACHER, J., LINGENHOEHL, K., HEID, J., HOFSTETTER, K., FROESTL, W., BETTLER, B. & KAUPMANN, K. (2001). Positive allosteric modulation of native and recombinant gamma-aminobutyric acid(B) receptors by 2,6-Di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol (CGP7930) and its aldehyde analog CGP13501. Mol. Pharmacol., 60, 963-971.
-
(2001)
Mol. Pharmacol.
, vol.60
, pp. 963-971
-
-
Urwyler, S.1
Mosbacher, J.2
Lingenhoehl, K.3
Heid, J.4
Hofstetter, K.5
Froestl, W.6
Bettler, B.7
Kaupmann, K.8
-
17
-
-
0033004276
-
SIB-1757 and SIB-1893: Selective, noncompetitive antagonists of metabotropic glutamate receptor type 5
-
VARNEY, M.A., COSFORD, N.D., JACHEC, C., RAO, S.P., SACAAN, A., LIN, F.F., BLEICHER, L., SANTORI, E.M., FLOR, P.J., ALLGEIER, H., GASPARINI, F., KUHN, R., HESS, S.D., VELICELEBI, G. & JOHNSON, E.C. (1999). SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5. J Pharmacol. Exp. Ther., 290, 170-181.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 170-181
-
-
Varney, M.A.1
Cosford, N.D.2
Jachec, C.3
Rao, S.P.4
Sacaan, A.5
Lin, F.F.6
Bleicher, L.7
Santori, E.M.8
Flor, P.J.9
Allgeier, H.10
Gasparini, F.11
Kuhn, R.12
Hess, S.D.13
Velicelebi, G.14
Johnson, E.C.15
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