-
1
-
-
0028839684
-
Activation and selective inhibition of a cyclic AMP-specific phosphodiesterase, PDE-4D3
-
Alvarez R., Sette C., Yang D., Eglen R.M., Wilhelm R., Shelton E.R., Conti M. Activation and selective inhibition of a cyclic AMP-specific phosphodiesterase, PDE-4D3. Mol. Pharmacol. 48:1995;616-622
-
(1995)
Mol. Pharmacol.
, vol.48
, pp. 616-622
-
-
Alvarez, R.1
Sette, C.2
Yang, D.3
Eglen, R.M.4
Wilhelm, R.5
Shelton, E.R.6
Conti, M.7
-
2
-
-
0032445219
-
Effects of sildenafil on the relaxation of human corpus cavernosum tissue in vitro and on the activities of cyclic nucleotide phosphodiesterase isozymes
-
Ballard S.A., Gingell C.J., Tang K., Turner L.A., Price M.E., Naylor A.M. Effects of sildenafil on the relaxation of human corpus cavernosum tissue in vitro and on the activities of cyclic nucleotide phosphodiesterase isozymes. J. Urol. 159:1998;2164-2171
-
(1998)
J. Urol.
, vol.159
, pp. 2164-2171
-
-
Ballard, S.A.1
Gingell, C.J.2
Tang, K.3
Turner, L.A.4
Price, M.E.5
Naylor, A.M.6
-
3
-
-
0031911575
-
SB 207499 (Ariflo), a potent and selective second-generation phosphodiesterase 4 inhibitor: In vitro anti-inflammatory actions
-
Barnette M.S., Christensen S.B., Essayan D.M., Grous M., Prabhakar U., Rush J.A., Kagey-Sobotka A., Torphy T.J. SB 207499 (Ariflo), a potent and selective second-generation phosphodiesterase 4 inhibitor. in vitro anti-inflammatory actions J. Pharmacol. Exp. Ther. 284:1998;420-426
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.284
, pp. 420-426
-
-
Barnette, M.S.1
Christensen, S.B.2
Essayan, D.M.3
Grous, M.4
Prabhakar, U.5
Rush, J.A.6
Kagey-Sobotka, A.7
Torphy, T.J.8
-
4
-
-
0028802726
-
Cyclic nucleotide phosphodiesterases: Functional implications of multiple isoforms
-
Beavo J.A. Cyclic nucleotide phosphodiesterases. functional implications of multiple isoforms Physiol. Rev. 75:1995;725-748
-
(1995)
Physiol. Rev.
, vol.75
, pp. 725-748
-
-
Beavo, J.A.1
-
5
-
-
0036729478
-
Cyclic nucleotide research-still expanding after half a century
-
Beavo J.A., Brunton L.L. Cyclic nucleotide research-still expanding after half a century. Nat. Rev. Mol. Cell Biol. 3:2002;710-718
-
(2002)
Nat. Rev. Mol. Cell Biol.
, vol.3
, pp. 710-718
-
-
Beavo, J.A.1
Brunton, L.L.2
-
6
-
-
9944249758
-
-
December 1993. Trisubstituted phenyl derivatives as selective phosphodiesterase IV inhibitors. World-wide patent WO93/25517.
-
Beeley, N.R.A., and Millican, T.A. (1993). December 1993. Trisubstituted phenyl derivatives as selective phosphodiesterase IV inhibitors. World-wide patent WO93/25517.
-
(1993)
-
-
Beeley, N.R.A.1
Millican, T.A.2
-
7
-
-
0041856176
-
Attenuation of the activity of the cAMP-specific phosphodiesterase PDE4A5 by interaction with the immunophilin XAP2
-
Bolger G.B., Peden A.H., Steele M.R., MacKenzie C., McEwan D.G., Wallace D.A., Huston E., Baillie G.S., Houslay M.D. Attenuation of the activity of the cAMP-specific phosphodiesterase PDE4A5 by interaction with the immunophilin XAP2. J. Biol. Chem. 278:2003;33351-33363
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 33351-33363
-
-
Bolger, G.B.1
Peden, A.H.2
Steele, M.R.3
MacKenzie, C.4
McEwan, D.G.5
Wallace, D.A.6
Huston, E.7
Baillie, G.S.8
Houslay, M.D.9
-
8
-
-
3543012707
-
Crystallography & NMR system: A new software suite for macromolecular structure determination
-
Brünger A.T., Adams P.D., Clore G.M., DeLano W.L., Gros P., Grosse-Kunstleve R.W., Jiang J.S., Kuszewski J., Nilges M., Pannu N.S., et al. Crystallography & NMR system. a new software suite for macromolecular structure determination Acta Crystallogr. D Biol. Crystallogr. 54:1998;905-921
-
(1998)
Acta Crystallogr. D Biol. Crystallogr.
, vol.54
, pp. 905-921
-
-
Brünger, A.T.1
Adams, P.D.2
Clore, G.M.3
Delano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiang, J.S.7
Kuszewski, J.8
Nilges, M.9
Pannu, N.S.10
-
9
-
-
0035078823
-
In vivo efficacy in airway disease models of roflumilast, a novel orally active PDE4 inhibitor
-
Bundschuh D.S., Eltze M., Barsig J., Wollin L., Hatzelmann A., Beume R. In vivo efficacy in airway disease models of roflumilast, a novel orally active PDE4 inhibitor. J. Pharmacol. Exp. Ther. 297:2001;280-290
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.297
, pp. 280-290
-
-
Bundschuh, D.S.1
Eltze, M.2
Barsig, J.3
Wollin, L.4
Hatzelmann, A.5
Beume, R.6
-
10
-
-
0022419375
-
Aromatic-aromatic interaction: A mechanism of protein structure stabilization
-
Burley S.K., Petsko G.A. Aromatic-aromatic interaction. a mechanism of protein structure stabilization Science. 229:1985;23-28
-
(1985)
Science
, vol.229
, pp. 23-28
-
-
Burley, S.K.1
Petsko, G.A.2
-
11
-
-
9944254875
-
-
October 1993. Compounds useful for treating allergic and inflammatory diseases. World-wide patent WO93/19479.
-
Christensen, S.B. (1993). October 1993. Compounds useful for treating allergic and inflammatory diseases. World-wide patent WO93/19479.
-
(1993)
-
-
Christensen, S.B.1
-
12
-
-
0033761535
-
Phosphodiesterases and cyclic nucleotide signaling in endocrine cells
-
Conti M. Phosphodiesterases and cyclic nucleotide signaling in endocrine cells. Mol. Endocrinol. 14:2000;1317-1327
-
(2000)
Mol. Endocrinol.
, vol.14
, pp. 1317-1327
-
-
Conti, M.1
-
13
-
-
0032605044
-
The molecular biology of cyclic nucleotide phosphodiesterases
-
Conti M., Jin S.L. The molecular biology of cyclic nucleotide phosphodiesterases. Prog. Nucleic Acid Res. Mol. Biol. 63:1999;1-38
-
(1999)
Prog. Nucleic Acid Res. Mol. Biol.
, vol.63
, pp. 1-38
-
-
Conti, M.1
Jin, S.L.2
-
14
-
-
0033553509
-
Cyclic GMP phosphodiesterase-5: Target of sildenafil
-
Corbin J.D., Francis S.H. Cyclic GMP phosphodiesterase-5. target of sildenafil J. Biol. Chem. 274:1999;13729-13732
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 13729-13732
-
-
Corbin, J.D.1
Francis, S.H.2
-
15
-
-
0036332629
-
Pharmacology of phosphodiesterase-5 inhibitors
-
Corbin J.D., Francis S.H. Pharmacology of phosphodiesterase-5 inhibitors. Int. J. Clin. Pract. 56:2002;453-459
-
(2002)
Int. J. Clin. Pract.
, vol.56
, pp. 453-459
-
-
Corbin, J.D.1
Francis, S.H.2
-
16
-
-
9944241000
-
November 2000. Tetracyclic cyclic GMP-specific phosphodiesterase inhibitors, process of preparation and use
-
Daugan A.C., Gellibert F. November 2000. Tetracyclic cyclic GMP-specific phosphodiesterase inhibitors, process of preparation and use. U.S. patent. 6:2000;143,746
-
(2000)
U.S. Patent
, vol.6
, pp. 143
-
-
Daugan, A.C.1
Gellibert, F.2
-
19
-
-
9944253075
-
-
January 1995. Fluoroalkoxy-substituted benzamides and their use as cyclic nucleotide phosphodiesterase inhibitors. World-wide patent WO95/01338.
-
Flockerzi, D., Gutterer, B., Hatzelmann, A., Schudt, C., Beume, R., Kilian, U., and Wolf, H. January 1995. Fluoroalkoxy-substituted benzamides and their use as cyclic nucleotide phosphodiesterase inhibitors. World-wide patent WO95/01338.
-
-
-
Flockerzi, D.1
Gutterer, B.2
Hatzelmann, A.3
Schudt, C.4
Beume, R.5
Kilian, U.6
Wolf, H.7
-
21
-
-
0037195229
-
Erectile dysfunction: Comparison of efficacy and side effects of the PDE-5 inhibitors sildenafil, vardenafil and tadalafil-review of the literature
-
Gresser U., Gleiter C.H. Erectile dysfunction. comparison of efficacy and side effects of the PDE-5 inhibitors sildenafil, vardenafil and tadalafil-review of the literature Eur. J. Med. Res. 7:2002;435-446
-
(2002)
Eur. J. Med. Res.
, vol.7
, pp. 435-446
-
-
Gresser, U.1
Gleiter, C.H.2
-
22
-
-
0037170832
-
Imidazo[5,1-f]triazin-4(3H)-ones, a new class of potent PDE 5 inhibitors
-
Haning H., Niewohner U., Schenke T., Es-Sayed M., Schmidt G., Lampe T., Bischoff E. Imidazo[5,1-f]triazin-4(3H)-ones, a new class of potent PDE 5 inhibitors. Bioorg. Med. Chem. Lett. 12:2002;865-868
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 865-868
-
-
Haning, H.1
Niewohner, U.2
Schenke, T.3
Es-Sayed, M.4
Schmidt, G.5
Lampe, T.6
Bischoff, E.7
-
23
-
-
0035084103
-
Anti-inflammatory and immunomodulatory potential of the novel PDE4 inhibitor roflumilast in vitro
-
Hatzelmann A., Schudt C. Anti-inflammatory and immunomodulatory potential of the novel PDE4 inhibitor roflumilast in vitro. J. Pharmacol. Exp. Ther. 297:2001;267-279
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.297
, pp. 267-279
-
-
Hatzelmann, A.1
Schudt, C.2
-
24
-
-
1242274650
-
Automated protein crystal structure determination using ELVES
-
Holton J., Alber T. Automated protein crystal structure determination using ELVES. Proc. Natl. Acad. Sci. USA. 101:2004;1537-1542
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 1537-1542
-
-
Holton, J.1
Alber, T.2
-
25
-
-
0032044238
-
Adaptation in cyclic AMP signalling processes: A central role for cyclic AMP phosphodiesterases
-
Houslay M.D. Adaptation in cyclic AMP signalling processes. a central role for cyclic AMP phosphodiesterases Semin. Cell Dev. Biol. 9:1998;161-167
-
(1998)
Semin. Cell Dev. Biol.
, vol.9
, pp. 161-167
-
-
Houslay, M.D.1
-
26
-
-
0037443097
-
PDE4 cAMP phosphodiesterases: Modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization
-
Houslay M.D., Adams D.R. PDE4 cAMP phosphodiesterases. modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization Biochem. J. 370:2003;1-18
-
(2003)
Biochem. J.
, vol.370
, pp. 1-18
-
-
Houslay, M.D.1
Adams, D.R.2
-
27
-
-
0242401840
-
The crystal structure of AMP-bound PDE4 suggests a mechanism for phosphodiesterase catalysis
-
a
-
Huai Q., Colicelli J., Ke H. The crystal structure of AMP-bound PDE4 suggests a mechanism for phosphodiesterase catalysis. Biochemistry. 42:2003;13220-13226. a
-
(2003)
Biochemistry
, vol.42
, pp. 13220-13226
-
-
Huai, Q.1
Colicelli, J.2
Ke, H.3
-
28
-
-
1842581748
-
Crystal structures of phosphodiesterases 4 and 5 in complex with inhibitor IBMX suggest a conformation determinant of inhibitor selectivity
-
b
-
Huai Q., Liu Y., Francis S.H., Corbin J.D., Ke H. Crystal structures of phosphodiesterases 4 and 5 in complex with inhibitor IBMX suggest a conformation determinant of inhibitor selectivity. J. Biol. Chem. 279:2003;13095-13101. b
-
(2003)
J. Biol. Chem.
, vol.279
, pp. 13095-13101
-
-
Huai, Q.1
Liu, Y.2
Francis, S.H.3
Corbin, J.D.4
Ke, H.5
-
29
-
-
0038154006
-
Three-dimensional structures of PDE4D in complex with roliprams and implication on inhibitor selectivity
-
c
-
Huai Q., Wang H., Sun Y., Kim H.Y., Liu Y., Ke H. Three-dimensional structures of PDE4D in complex with roliprams and implication on inhibitor selectivity. Structure (Camb). 11:2003;865-873. c
-
(2003)
Structure (Camb).
, vol.11
, pp. 865-873
-
-
Huai, Q.1
Wang, H.2
Sun, Y.3
Kim, H.Y.4
Liu, Y.5
Ke, H.6
-
30
-
-
3042795876
-
Crystal structure of phosphodiesterase 9 shows orientation variation of inhibitor 3-isobutyl-1-methylxanthine binding
-
Huai Q., Wang H., Zhang W., Colman R.W., Robinson H., Ke H. Crystal structure of phosphodiesterase 9 shows orientation variation of inhibitor 3-isobutyl-1-methylxanthine binding. Proc. Natl. Acad. Sci. USA. 101:2004;9624-9629
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 9624-9629
-
-
Huai, Q.1
Wang, H.2
Zhang, W.3
Colman, R.W.4
Robinson, H.5
Ke, H.6
-
31
-
-
0037188511
-
Induction of the cyclic nucleotide phosphodiesterase PDE4B is essential for LPS-activated TNF-alpha responses
-
Jin S.L., Conti M. Induction of the cyclic nucleotide phosphodiesterase PDE4B is essential for LPS-activated TNF-alpha responses. Proc. Natl. Acad. Sci. USA. 99:2002;7628-7633
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 7628-7633
-
-
Jin, S.L.1
Conti, M.2
-
32
-
-
84889120137
-
Improved methods for building protein models in electron density maps and the location of errors in these models
-
Jones T.A., Zou J.Y., Cowan S.W., Kjeldgaard M. Improved methods for building protein models in electron density maps and the location of errors in these models. Acta Crystallogr. A. 47:1991;110-119
-
(1991)
Acta Crystallogr. a
, vol.47
, pp. 110-119
-
-
Jones, T.A.1
Zou, J.Y.2
Cowan, S.W.3
Kjeldgaard, M.4
-
33
-
-
9944261572
-
-
May 1997. Chiral methylphenyl oxazolidinones. World-wide patent WO97/15561.
-
Laurent, H., Ottow, E., Kirsch, G., Wachtel, H., Schneider, H., Faulds, D., and Dinter, H. (1997). May 1997. Chiral methylphenyl oxazolidinones. World-wide patent WO97/15561.
-
(1997)
-
-
Laurent, H.1
Ottow, E.2
Kirsch, G.3
Wachtel, H.4
Schneider, H.5
Faulds, D.6
Dinter, H.7
-
34
-
-
0037163858
-
Crystal structure of phosphodiesterase 4D and inhibitor complex
-
Lee M.E., Markowitz J., Lee J.O., Lee H. Crystal structure of phosphodiesterase 4D and inhibitor complex. FEBS Lett. 530:2002;53-58
-
(2002)
FEBS Lett.
, vol.530
, pp. 53-58
-
-
Lee, M.E.1
Markowitz, J.2
Lee, J.O.3
Lee, H.4
-
35
-
-
0033212815
-
Integration of macromolecular diffraction data
-
Leslie A.G. Integration of macromolecular diffraction data. Acta Crystallogr. D Biol. Crystallogr. 55:1999;1696-1702
-
(1999)
Acta Crystallogr. D Biol. Crystallogr.
, vol.55
, pp. 1696-1702
-
-
Leslie, A.G.1
-
36
-
-
9944230167
-
-
June 1992. Oxime-carbamates and oxime-carbonates as bronchodilatorsand anti-inflammatory agents. U.S. patent 5,124,455.
-
Lombardo, L.J. (1992). June 1992. Oxime-carbamates and oxime-carbonates as bronchodilatorsand anti-inflammatory agents. U.S. patent 5,124,455.
-
(1992)
-
-
Lombardo, L.J.1
-
37
-
-
0033597139
-
Association with the SRC family tyrosyl kinase LYN triggers a conformational change in the catalytic region of human cAMP-specific phosphodiesterase HSPDE4A4B. Consequences for rolipram inhibition
-
McPhee I., Yarwood S.J., Scotland G., Huston E., Beard M.B., Ross A.H., Houslay E.S., Houslay M.D. Association with the SRC family tyrosyl kinase LYN triggers a conformational change in the catalytic region of human cAMP-specific phosphodiesterase HSPDE4A4B. Consequences for rolipram inhibition. J. Biol. Chem. 274:1999;11796-11810
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 11796-11810
-
-
McPhee, I.1
Yarwood, S.J.2
Scotland, G.3
Huston, E.4
Beard, M.B.5
Ross, A.H.6
Houslay, E.S.7
Houslay, M.D.8
-
38
-
-
0036134416
-
Cyclic nucleotide phosphodiesterases and their role in endocrine cell signaling
-
Mehats C., Andersen C.B., Filopanti M., Jin S.L., Conti M. Cyclic nucleotide phosphodiesterases and their role in endocrine cell signaling. Trends Endocrinol. Metab. 13:2002;29-35
-
(2002)
Trends Endocrinol. Metab.
, vol.13
, pp. 29-35
-
-
Mehats, C.1
Andersen, C.B.2
Filopanti, M.3
Jin, S.L.4
Conti, M.5
-
39
-
-
0032897075
-
Efficient anisotropic refinement of macromolecular structures using FFT
-
Murshudov G.N., Vagin A.A., Lebedev A., Wilson K.S., Dodson E.J. Efficient anisotropic refinement of macromolecular structures using FFT. Acta Crystallogr. D Biol. Crystallogr. 55:1999;247-255
-
(1999)
Acta Crystallogr. D Biol. Crystallogr.
, vol.55
, pp. 247-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Lebedev, A.3
Wilson, K.S.4
Dodson, E.J.5
-
40
-
-
20844435031
-
-
May 1999. 2-Phenyl-substituted imidazotriazinones as phosphodiesterase inhibitors. World-wide patent WO99/24433.
-
Niewohner, U., Es-Sayed, M., Haning, H., Schenke, T., Schlemmer, K.H., Keldenich, J., Bischoff, E., Perzborn, E., Dembowsky, K., Serno, P., and Nowakowski, M. (1999). May 1999. 2-Phenyl-substituted imidazotriazinones as phosphodiesterase inhibitors. World-wide patent WO99/24433.
-
(1999)
-
-
Niewohner, U.1
Es-Sayed, M.2
Haning, H.3
Schenke, T.4
Schlemmer, K.H.5
Keldenich, J.6
Bischoff, E.7
Perzborn, E.8
Dembowsky, K.9
Serno, P.10
Nowakowski, M.11
-
41
-
-
0036197133
-
IC351 (tadalafil, Cialis) update on clinical experience
-
Porst H. IC351 (tadalafil, Cialis). update on clinical experience Int. J. Impot. Res. 14:2002;S57-S64
-
(2002)
Int. J. Impot. Res.
, vol.14
-
-
Porst, H.1
-
42
-
-
0036790480
-
Deletion of phosphodiesterase 4D in mice shortens alpha(2)-adrenoceptor- mediated anesthesia, a behavioral correlate of emesis
-
Robichaud A., Stamatiou P.B., Jin S.L., Lachance N., MacDonald D., Laliberte F., Liu S., Huang Z., Conti M., Chan C.C. Deletion of phosphodiesterase 4D in mice shortens alpha(2)-adrenoceptor-mediated anesthesia, a behavioral correlate of emesis. J. Clin. Invest. 110:2002;1045-1052
-
(2002)
J. Clin. Invest.
, vol.110
, pp. 1045-1052
-
-
Robichaud, A.1
Stamatiou, P.B.2
Jin, S.L.3
Lachance, N.4
MacDonald, D.5
Laliberte, F.6
Liu, S.7
Huang, Z.8
Conti, M.9
Chan, C.C.10
-
43
-
-
0030702945
-
Human recombinant phosphodiesterase 4B2B binds (R)-rolipram at a single site with two affinities
-
Rocque W.J., Tian G., Wiseman J.S., Holmes W.D., Zajac-Thompson I., Willard D.H., Patel I.R., Wisely G.B., Clay W.C., Kadwell S.H., et al. Human recombinant phosphodiesterase 4B2B binds (R)-rolipram at a single site with two affinities. Biochemistry. 36:1997;14250-14261
-
(1997)
Biochemistry
, vol.36
, pp. 14250-14261
-
-
Rocque, W.J.1
Tian, G.2
Wiseman, J.S.3
Holmes, W.D.4
Zajac-Thompson, I.5
Willard, D.H.6
Patel, I.R.7
Wisely, G.B.8
Clay, W.C.9
Kadwell, S.H.10
-
44
-
-
0036717930
-
Phosphodiesterase 5 inhibitors: Current status and potential applications
-
Rotella D.P. Phosphodiesterase 5 inhibitors. current status and potential applications Nat. Rev. Drug Discov. 1:2002;674-682
-
(2002)
Nat. Rev. Drug Discov.
, vol.1
, pp. 674-682
-
-
Rotella, D.P.1
-
45
-
-
2442700405
-
Crystal structure of human phosphodiesterase 3B: Atomic basis for substrate and inhibitor specificity
-
Scapin G., Patel S.B., Chung C., Varnerin J.P., Edmondson S.D., Mastracchio A., Parmee E.R., Singh S.B., Becker J.W., Van Der Ploeg L.H., et al. Crystal structure of human phosphodiesterase 3B. atomic basis for substrate and inhibitor specificity Biochemistry. 43:2004;6091-6100
-
(2004)
Biochemistry
, vol.43
, pp. 6091-6100
-
-
Scapin, G.1
Patel, S.B.2
Chung, C.3
Varnerin, J.P.4
Edmondson, S.D.5
Mastracchio, A.6
Parmee, E.R.7
Singh, S.B.8
Becker, J.W.9
Van Der Ploeg, L.H.10
-
46
-
-
0025832697
-
Zardaverine as a selective inhibitor of phosphodiesterase isozymes
-
Schudt C., Winder S., Muller B., Ukena D. Zardaverine as a selective inhibitor of phosphodiesterase isozymes. Biochem. Pharmacol. 42:1991;153-162
-
(1991)
Biochem. Pharmacol.
, vol.42
, pp. 153-162
-
-
Schudt, C.1
Winder, S.2
Muller, B.3
Ukena, D.4
-
47
-
-
0034130633
-
Immunosuppressive and anti-inflammatory effects of cyclic AMP phosphodiesterase (PDE) type 4 inhibitors
-
Souness J.E., Aldous D., Sargent C. Immunosuppressive and anti-inflammatory effects of cyclic AMP phosphodiesterase (PDE) type 4 inhibitors. Immunopharmacology. 47:2000;127-162
-
(2000)
Immunopharmacology
, vol.47
, pp. 127-162
-
-
Souness, J.E.1
Aldous, D.2
Sargent, C.3
-
48
-
-
0041321268
-
Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules
-
Sung B.J., Yeon Hwang K., Ho Jeon Y., Lee J.I., Heo Y.S., Hwan Kim J., Moon J., Min Yoon J., Hyun Y.L., Kim E., et al. Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules. Nature. 425:2003;98-102
-
(2003)
Nature
, vol.425
, pp. 98-102
-
-
Sung, B.J.1
Yeon Hwang, K.2
Ho Jeon, Y.3
Lee, J.I.4
Heo, Y.S.5
Hwan Kim, J.6
Moon, J.7
Min Yoon, J.8
Hyun, Y.L.9
Kim, E.10
-
49
-
-
0038573885
-
Occupancy of the catalytic site of the PDE4A4 cyclic AMP phosphodiesterase by rolipram triggers the dynamic redistribution of this specific isoform in living cells through a cyclic AMP independent process
-
Terry R., Cheung Y.F., Praestegaard M., Baillie G.S., Huston E., Gall I., Adams D.R., Houslay M.D. Occupancy of the catalytic site of the PDE4A4 cyclic AMP phosphodiesterase by rolipram triggers the dynamic redistribution of this specific isoform in living cells through a cyclic AMP independent process. Cell. Signal. 15:2003;955-971
-
(2003)
Cell. Signal.
, vol.15
, pp. 955-971
-
-
Terry, R.1
Cheung, Y.F.2
Praestegaard, M.3
Baillie, G.S.4
Huston, E.5
Gall, I.6
Adams, D.R.7
Houslay, M.D.8
-
50
-
-
0034625541
-
Atomic structure of PDE4: Insights into phosphodiesterase mechanism and specificity
-
Xu R.X., Hassell A.M., Vanderwall D., Lambert M.H., Holmes W.D., Luther M.A., Rocque W.J., Milburn M.V., Zhao Y., Ke H., Nolte R.T. Atomic structure of PDE4. insights into phosphodiesterase mechanism and specificity Science. 288:2000;1822-1825
-
(2000)
Science
, vol.288
, pp. 1822-1825
-
-
Xu, R.X.1
Hassell, A.M.2
Vanderwall, D.3
Lambert, M.H.4
Holmes, W.D.5
Luther, M.A.6
Rocque, W.J.7
Milburn, M.V.8
Zhao, Y.9
Ke, H.10
Nolte, R.T.11
-
51
-
-
1442323778
-
Crystal structures of the catalytic domain of phosphodiesterase 4B complexed with amp 8-br-AMP, and rolipram
-
Xu R.X., Rocque W.J., Lambert M.H., Vanderwall D.E., Luther M.A., Nolte R.T. Crystal structures of the catalytic domain of phosphodiesterase 4B complexed with amp 8-br-AMP, and rolipram. J. Mol. Biol. 337:2004;355-365
-
(2004)
J. Mol. Biol.
, vol.337
, pp. 355-365
-
-
Xu, R.X.1
Rocque, W.J.2
Lambert, M.H.3
Vanderwall, D.E.4
Luther, M.A.5
Nolte, R.T.6
-
52
-
-
4344676386
-
A glutamine switch mechanism for nucleotide selectivity by phosphodiesterases
-
Zhang K.Y.J., Card G.L., Suzuki Y., Artis D.R., Fong D., Gillette S., Hsieh D., Neiman J., West B.L., Zhang C., et al. A glutamine switch mechanism for nucleotide selectivity by phosphodiesterases. Mol. Cell. 15:2004;279-286
-
(2004)
Mol. Cell
, vol.15
, pp. 279-286
-
-
Zhang, K.Y.J.1
Card, G.L.2
Suzuki, Y.3
Artis, D.R.4
Fong, D.5
Gillette, S.6
Hsieh, D.7
Neiman, J.8
West, B.L.9
Zhang, C.10
|