-
2
-
-
2442467014
-
The neurobiology of dopamine signaling
-
Girault J-A, Greengard P. The neurobiology of dopamine signaling. Arch Neurol. 2004;61:641-644.
-
(2004)
Arch Neurol.
, vol.61
, pp. 641-644
-
-
Girault, J.-A.1
Greengard, P.2
-
3
-
-
0033536020
-
Isolation and characterization of a dualsubstrate phosphodiesterase gene family: Pde10a
-
Soderling SH, Bayuga SJ, Beavo JA. Isolation and characterization of a dualsubstrate phosphodiesterase gene family: PDE10A. Proc Natl Acad Sci USA. 1999;96:7071-7076.
-
(1999)
Proc Natl Acad Sci USA.
, vol.96
, pp. 7071-7076
-
-
Soderling, S.H.1
Bayuga, S.J.2
Beavo, J.A.3
-
4
-
-
33750314788
-
Immunohistochemical localization of phosphodiesterase 10a in multiple mammalian species
-
Coskran TM, Morton D, Menniti FS, et al. Immunohistochemical localization of phosphodiesterase 10A in multiple mammalian species. J Histochem Cytochem. 2006;54:1205-1213.
-
(2006)
J Histochem Cytochem.
, vol.54
, pp. 1205-1213
-
-
Coskran, T.M.1
Morton, D.2
Menniti, F.S.3
-
5
-
-
34547396908
-
Phosphodiesterase 10a inhibitors as a novel therapeutic approach for schizophrenia
-
Siuciak JA, Strick CA. Phosphodiesterase 10A inhibitors as a novel therapeutic approach for schizophrenia. Expert Opin Drug Discov. 2007;2:1001-1009.
-
(2007)
Expert Opin Drug Discov.
, vol.2
, pp. 1001-1009
-
-
Siuciak, J.A.1
Strick, C.A.2
-
6
-
-
42449099422
-
Preclinical characterization of selective phosphodiesterase 10a inhibitors: A new therapeutic approach to the treatment of schizophrenia
-
Schmidt CJ, Chapin DS, Cianfrogna J, et al. Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophrenia. J Pharmacol Exp Ther. 2008;325:681-690.
-
(2008)
J Pharmacol Exp Ther.
, vol.325
, pp. 681-690
-
-
Schmidt, C.J.1
Chapin, D.S.2
Cianfrogna, J.3
-
7
-
-
78650779872
-
Chronic suppression of phosphodiesterase 10a alters striatal expression of genes responsible for neurotransmitter synthesis, neurotransmission, and signaling pathways implicated in huntington's disease
-
Kleiman RJ, Kimmel LH, Bove SE, et al. Chronic suppression of phosphodiesterase 10A alters striatal expression of genes responsible for neurotransmitter synthesis, neurotransmission, and signaling pathways implicated in Huntington's disease. J Pharmacol Exp Ther. 2011;336:64-76.
-
(2011)
J Pharmacol Exp Ther.
, vol.336
, pp. 64-76
-
-
Kleiman, R.J.1
Kimmel, L.H.2
Bove, S.E.3
-
8
-
-
79955945166
-
Pde10a and pde10a-dependent camp catabolism are dysregulated oppositely in striatum and nucleus accumbens after lesion of midbrain dopamine neurons in rat: A key step in parkinsonism physiopathology
-
Giorgi M, Melchiorri G, Nuccetelli V, et al. PDE10A and PDE10A-dependent cAMP catabolism are dysregulated oppositely in striatum and nucleus accumbens after lesion of midbrain dopamine neurons in rat: a key step in parkinsonism physiopathology. Neurobiol Dis. 2011;43:293-303.
-
(2011)
Neurobiol Dis.
, vol.43
, pp. 293-303
-
-
Giorgi, M.1
Melchiorri, G.2
Nuccetelli, V.3
-
9
-
-
80051693428
-
Radiosynthesis and in vivo evaluation of [11c]mp-10 as a positron emission tomography radioligand for phosphodiesterase 10a
-
Plisson C, Salinas C, Weinzimmer D, et al. Radiosynthesis and in vivo evaluation of [11C]MP-10 as a positron emission tomography radioligand for phosphodiesterase 10A. Nucl Med Biol. 2011;38:875-884.
-
(2011)
Nucl Med Biol.
, vol.38
, pp. 875-884
-
-
Plisson, C.1
Salinas, C.2
Weinzimmer, D.3
-
10
-
-
79952186381
-
Radiosynthesis and in vivo evaluation of [11c]mp-10 as a pet probe for imaging pde10a in rodent and non-human primate brain
-
Tu Z, Fan J, Li S, et al. Radiosynthesis and in vivo evaluation of [11C]MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain. Bioorg Med Chem. 2011;19:1666-1673.
-
(2011)
Bioorg Med Chem.
, vol.19
, pp. 1666-1673
-
-
Tu, Z.1
Fan, J.2
Li, S.3
-
11
-
-
79851490485
-
Preclinical evaluation of 18f-jnj41510417 as a radioligand for pet imaging of phosphodiesterase-10a in the brain
-
Celen S, Koole M, De Angelis M, et al. Preclinical evaluation of 18F-JNJ41510417 as a radioligand for PET imaging of phosphodiesterase-10A in the brain. J Nucl Med. 2010;51:1584-1591.
-
(2010)
J Nucl Med.
, vol.51
, pp. 1584-1591
-
-
Celen, S.1
Koole, M.2
De Angelis, M.3
-
12
-
-
80051897157
-
Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10 inhibitors as candidates for positron emission tomography imaging
-
Andrés J-I, De Angelis M, Alcazar J, et al. Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10 inhibitors as candidates for positron emission tomography imaging. J Med Chem. 2011;54: 5820-5835.
-
(2011)
J Med Chem.
, vol.54
, pp. 5820-5835
-
-
Andrés, J.-I.1
De Angelis, M.2
Alcazar, J.3
-
14
-
-
84857677917
-
Radiosynthesis and radiotracer properties of a 7-(2-[18f]fluoroethoxy)-6- methoxypyrrolidinylquinazoline for imaging of phosphodiesterase 10a with pet
-
Funke U, Deuther-Conrad W, Schwan G, et al. Radiosynthesis and radiotracer properties of a 7-(2-[18F]Fluoroethoxy)-6- methoxypyrrolidinylquinazoline for imaging of phosphodiesterase 10A with PET. Pharmaceuticals. 2012;5: 169-188.
-
(2012)
Pharmaceuticals.
, vol.5
, pp. 169-188
-
-
Funke, U.1
Deuther-Conrad, W.2
Schwan, G.3
-
16
-
-
84881404106
-
Quantification of 18f-jnj-42259152 a novel phosphodiesterase 10a pet tracer: Kinetic modeling and test-retest study in human brain
-
Van Laere K, Ahmad RU, Hudyana H, et al. Quantification of 18F-JNJ-42259152, a novel phosphodiesterase 10A PET tracer: kinetic modeling and test-retest study in human brain. J Nucl Med. 2013;54:1285-1293.
-
(2013)
J Nucl Med.
, vol.54
, pp. 1285-1293
-
-
Van Laere, K.1
Ahmad, R.U.2
Hudyana, H.3
-
17
-
-
84901326139
-
First in vivo assessment of two pde10 tracers [18f]mni654 and [18f]mni659 [abstract]
-
Barret O, Thomae D, Alagille D, et al. First in vivo assessment of two PDE10 tracers [18F]MNI654 and [18F]MNI659 [abstract]. J Nucl Med. 2012;53(suppl):110P.
-
(2012)
J Nucl Med.
, vol.53
, Issue.SUPPL.
-
-
Barret, O.1
Thomae, D.2
Alagille, D.3
-
18
-
-
84901307194
-
Inventors
-
Eiji Kawanishi, Mitsuya Hongu, Yoshihito Tanaka, original assignee. WO2011/105628. Dec. 6
-
Kawanishi E, Hongu M, Tanaka Y, inventors; Eiji Kawanishi, Mitsuya Hongu, Yoshihito Tanaka, original assignee. Pyrazolopyrimidine compounds and their use as PDE10 inhibitors. WO2011/105628. Dec. 6, 2012.
-
(2012)
Pyrazolopyrimidine Compounds and Their use as PDE10 Inhibitors
-
-
Kawanishi, E.1
Hongu, M.2
Tanaka, Y.3
-
19
-
-
0033546738
-
Characterization and phosphorylation of pde10a2, a novel alternative splice variant of human phosphodiesterase that hydrolyzes camp and cgmp
-
Kotera J, Fujishige K, Yuasa K, Omori K. Characterization and phosphorylation of PDE10A2, a novel alternative splice variant of human phosphodiesterase that hydrolyzes cAMP and cGMP. Biochem Biophys Res Commun. 1999;261: 551-557.
-
(1999)
Biochem Biophys Res Commun.
, vol.261
, pp. 551-557
-
-
Kotera, J.1
Fujishige, K.2
Yuasa, K.3
Omori, K.4
-
20
-
-
0034333326
-
Characterization and effects of methyl-2-(4-aminophenyl) 1,2-dihydro-1-oxo-7-(2-pyridinylmethoxy)-4-(3,45-trimethoxyphenyl) -3-isoquinoline carboxylate sulfate (t-1032) a novel potent inhibitor of cgmp-binding cgmp-specific phosphodiesterase (pde5)
-
Kotera J, Fujishige K, Michibata H, et al. Characterization and effects of methyl-2-(4-aminophenyl)-1,2-dihydro-1-oxo-7-(2-pyridinylmethoxy)-4-(3,4,5- trimethoxyphenyl)-3-isoquinoline carboxylate sulfate (T-1032), a novel potent inhibitor of cGMP-binding cGMP-specific phosphodiesterase (PDE5). Biochem Pharmacol. 2000;60:1333-1341.
-
(2000)
Biochem Pharmacol
, vol.60
, pp. 1333-1341
-
-
Kotera, J.1
Fujishige, K.2
Michibata, H.3
-
21
-
-
0042379865
-
Immunohistochemical localization of pde10a in the rat brain
-
Seeger TF, Bartlett B, Coskran TM, et al. Immunohistochemical localization of PDE10A in the rat brain. Brain Res. 2003;985:113-126.
-
(2003)
Brain Res.
, vol.985
, pp. 113-126
-
-
Seeger, T.F.1
Bartlett, B.2
Coskran, T.M.3
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