-
1
-
-
0002783769
-
-
Jacobson, K. A., Jarvis, M., Eds., Wiley: New York
-
Burnstock, G. In Purinergic Approaches in Experimental Therapeutics; Jacobson, K. A., Jarvis, M., Eds., Wiley: New York, 1997.
-
(1997)
Purinergic Approaches in Experimental Therapeutics
-
-
Burnstock, G.1
-
2
-
-
0028183014
-
Nomenclature and classification of purinoceptors
-
Fredholm, B. B.; Abbracchio, M. P.; Burnstock, G.; Daly, J. W.; Harden, T. K.; Jacobson, K. A.; Leff, P.; Williams, M. Nomenclature and classification of purinoceptors. Pharmacol. Rev. 1994, 46, 143-156.
-
(1994)
Pharmacol. Rev.
, vol.46
, pp. 143-156
-
-
Fredholm, B.B.1
Abbracchio, M.P.2
Burnstock, G.3
Daly, J.W.4
Harden, T.K.5
Jacobson, K.A.6
Leff, P.7
Williams, M.8
-
3
-
-
0029741183
-
Numbering of cloned P2 purinoceptors
-
Burnstock, G.; King, B. F. Numbering of cloned P2 purinoceptors. Drug Dev. Res. 1996, 35, 67-71.
-
(1996)
Drug Dev. Res.
, vol.35
, pp. 67-71
-
-
Burnstock, G.1
King, B.F.2
-
4
-
-
0027310852
-
Cloning and functional expression of a brain G protein-coupled ATP receptor
-
Webb, T. E.; Simon, J.; Krishek, B. J.; Bateson, A. N.; Smart, T. G.; King, B. F.; Burnstock, G.; Barnard, E. A. Cloning and functional expression of a brain G protein-coupled ATP receptor. FEBS Lett. 1993, 324, 219-225.
-
(1993)
FEBS Lett.
, vol.324
, pp. 219-225
-
-
Webb, T.E.1
Simon, J.2
Krishek, B.J.3
Bateson, A.N.4
Smart, T.G.5
King, B.F.6
Burnstock, G.7
Barnard, E.A.8
-
5
-
-
0029414435
-
Modelling the P2Y purinoceptor using rhodopsin as template
-
van Rhee, A. M.; Fischer, B.; van Galen, P. J. M.; Jacobson, K. A. Modelling the P2Y purinoceptor using rhodopsin as template. Drug Design Discovery 1995, 13, 133-154.
-
(1995)
Drug Design Discovery
, vol.13
, pp. 133-154
-
-
Van Rhee, A.M.1
Fischer, B.2
Van Galen, P.J.M.3
Jacobson, K.A.4
-
6
-
-
0024022311
-
Phosphoinositide hydrolysis by guanosine 5′-(gamma-thio)tri phosphate-activated phospholipase C of turkey erythrocyte membranes
-
Harden, T. K.; Hawkins, P. T.; Stephens, L.; Boyer, J. L.; Downes. P. Phosphoinositide hydrolysis by guanosine 5′-(gamma-thio)tri phosphate-activated phospholipase C of turkey erythrocyte membranes. Biochem. J. 1988, 252, 583-593.
-
(1988)
Biochem. J.
, vol.252
, pp. 583-593
-
-
Harden, T.K.1
Hawkins, P.T.2
Stephens, L.3
Boyer, J.L.4
Downes, P.5
-
7
-
-
0002626643
-
Structure activity relationships of P2 receptor agonists and antagonists. Chapter 4 in the P2 Nucleotide Receptors
-
Turner, J. T., Weisman, G., Fedan, J., Eds.; Humana Press: Clifton, NJ
-
Jacobson, K. A.; Kim, Y.-C.; Camaioni, E.; van Rhee, A. M. Structure activity relationships of P2 receptor agonists and antagonists. Chapter 4 in The P2 Nucleotide Receptors. In The Receptors; Turner, J. T., Weisman, G., Fedan, J., Eds.; Humana Press: Clifton, NJ, 1997; pp 81-107.
-
(1997)
The Receptors
, pp. 81-107
-
-
Jacobson, K.A.1
Kim, Y.-C.2
Camaioni, E.3
Van Rhee, A.M.4
-
9
-
-
0028987857
-
2U purinoceptors-positively charged amino acids in transmembrane helix-6 and helix-7 affect agonist potency and specificity
-
2U purinoceptors-positively charged amino acids in transmembrane helix-6 and helix-7 affect agonist potency and specificity. J. Biol. Chem. 1995, 270, 4185-4188.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 4185-4188
-
-
Erb, L.1
Garrad, R.2
Wang, Y.J.3
Quinn, T.4
Turner, J.T.5
Weisman, G.A.6
-
10
-
-
0030758832
-
1 receptor
-
1 receptor. Mol. Pharmacol. 1997, 52, 499-507.
-
(1997)
Mol. Pharmacol.
, vol.52
, pp. 499-507
-
-
Jiang, Q.1
Guo, D.2
Lee, B.X.3
Van Rhee, A.M.4
Kirn, Y.C.5
Nicholas, R.6
Schachter, J.7
Harden, T.K.8
Jacobson, K.A.9
-
12
-
-
0020640836
-
A cDNA cloning vector that permits expression of cDNA inserts in mammalian cells
-
Okayama, H.; Berg, P. A. A cDNA cloning vector that permits expression of cDNA inserts in mammalian cells. Mol. Cell. Biol. 1983, 3, 280-289.
-
(1983)
Mol. Cell. Biol.
, vol.3
, pp. 280-289
-
-
Okayama, H.1
Berg, P.A.2
-
13
-
-
85016731055
-
Using PCR to Engineer DNA
-
Ehrlich, H. A., Ed.; Stockton Press: New York
-
Higuchi, R. Using PCR to Engineer DNA. In PCR Technology; Ehrlich, H. A., Ed.; Stockton Press: New York, 1989; pp 61-70.
-
(1989)
PCR Technology
, pp. 61-70
-
-
Higuchi, R.1
-
14
-
-
0017681196
-
DNA sequencing with chain-terminating inhibitors
-
Sanger, R.; Nicklen, S.; Coulson, A. R. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. U.S.A. 1977, 74, 5463-5467.
-
(1977)
Proc. Natl. Acad. Sci. U.S.A.
, vol.74
, pp. 5463-5467
-
-
Sanger, R.1
Nicklen, S.2
Coulson, A.R.3
-
15
-
-
0030070457
-
2A-adenosine receptors with hexahistidine and the FLAG epitope. Development of an efficient generic protein purification procedure
-
2A-adenosine receptors with hexahistidine and the FLAG epitope. Development of an efficient generic protein purification procedure. Biochem. Pharmacol. 1996, 51, 545-555.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 545-555
-
-
Robeva, A.S.1
Woodard, R.2
Luthin, D.R.3
Linden J, T.H.E.4
-
16
-
-
0023084134
-
Use of eukaryotic expression technology in the functional analysis of cloned genes
-
Cullen, B. R. Use of eukaryotic expression technology in the functional analysis of cloned genes. Methods Enzymol. 1987, 152, 684-704.
-
(1987)
Methods Enzymol.
, vol.152
, pp. 684-704
-
-
Cullen, B.R.1
-
17
-
-
0020595443
-
Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides
-
Berridge, M. J.; Dawson, R. M.; Downes, C. P.; Heslop, J. P.; Irvine, R. F. Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides. Biochem J. 1983, 212, 473-482.
-
(1983)
Biochem J.
, vol.212
, pp. 473-482
-
-
Berridge, M.J.1
Dawson, R.M.2
Downes, C.P.3
Heslop, J.P.4
Irvine, R.F.5
-
18
-
-
84920294520
-
-
The program SYBYL 6.3 is available from TRIPOS Associates, St. Louis, MO, 1993
-
The program SYBYL 6.3 is available from TRIPOS Associates, St. Louis, MO, 1993.
-
-
-
-
19
-
-
84986437005
-
MacroModel-An Integrated Software System for Modeling Organic and Bioorganic Molecules using Molecular Mechanics
-
Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendrickson, T.; Still, W. C. MacroModel-An Integrated Software System for Modeling Organic and Bioorganic Molecules using Molecular Mechanics. J. Comput. Chem. 1990, 11, 440-450.
-
(1990)
J. Comput. Chem.
, vol.11
, pp. 440-450
-
-
Mohamadi, F.1
Richards, N.G.J.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Caufield, C.6
Chang, G.7
Hendrickson, T.8
Still, W.C.9
-
20
-
-
0020475449
-
A simple method for displaying the hydrophobic character of a protein
-
Kyte, J.; Doolittle, R. F. A simple method for displaying the hydrophobic character of a protein. J. Mol. Biol. 1982 757, 105-132
-
(1982)
J. Mol. Biol.
, vol.757
, pp. 105-132
-
-
Kyte, J.1
Doolittle, R.F.2
-
21
-
-
84988053694
-
An all-atom force field for simulation of protein and nucleic acids
-
Weiner, S. J.; Kollman, P. A.; Nguyen, D. T.; Case, D. A. An all-atom force field for simulation of protein and nucleic acids. J. Comput. Chem. 1986, 7, 230-252.
-
(1986)
J. Comput. Chem.
, vol.7
, pp. 230-252
-
-
Weiner, S.J.1
Kollman, P.A.2
Nguyen, D.T.3
Case, D.A.4
-
22
-
-
0020338576
-
Sequence and structure of yeast phosphoglycerate kinase
-
Watson, H. C.; Walker, N. P.; Shaw, P. J.; Bryant, T. N.; Wendell, P. L.; Fothergill, L. A.; Perkins, R. E.; Conroy, S. C.; Dobson, M. J.; Tuite, M. F. Sequence and structure of yeast phosphoglycerate kinase. EMBO J. 1982, 1, 1635-1640.
-
(1982)
EMBO J.
, vol.1
, pp. 1635-1640
-
-
Watson, H.C.1
Walker, N.P.2
Shaw, P.J.3
Bryant, T.N.4
Wendell, P.L.5
Fothergill, L.A.6
Perkins, R.E.7
Conroy, S.C.8
Dobson, M.J.9
Tuite, M.F.10
-
23
-
-
0842341771
-
AM1: A new general purpose quantum mechanical molecular model
-
Dewar, M. J. S. E.; Zoebisch, G.; Healy, E. F. AM1: A new general purpose quantum mechanical molecular model. J. Am. Chem. Soc. 1985, 707, 3902-3909.
-
(1985)
J. Am. Chem. Soc.
, vol.707
, pp. 3902-3909
-
-
Dewar, M.J.S.E.1
Zoebisch, G.2
Healy, E.F.3
-
24
-
-
84920294519
-
-
MOPAC 6.0 available from Quantum Chemistry Program Exchange
-
MOPAC 6.0 available from Quantum Chemistry Program Exchange.
-
-
-
-
25
-
-
0019872825
-
Helix to helix packing in proteins
-
Chiota, C.; Levitt, M.; Richardson, D. Helix to helix packing in proteins. J. Mol. Biol. 1981, 145, 215-250.
-
(1981)
J. Mol. Biol.
, vol.145
, pp. 215-250
-
-
Chiota, C.1
Levitt, M.2
Richardson, D.3
-
26
-
-
0027190359
-
Projection structure of rhodopsin
-
Schertler, G. F.; Villa, C.; Henderson, R. Projection structure of rhodopsin. Nature 1993, 362, 770-772.
-
(1993)
Nature
, vol.362
, pp. 770-772
-
-
Schertler, G.F.1
Villa, C.2
Henderson, R.3
-
27
-
-
0030775615
-
Arrangement of rhodopsin transmenbrane α-helices
-
Urger, V. M.; Hargrave, P. A.; Baldwin, J. M.; Schertler, G. F. X. Arrangement of rhodopsin transmenbrane α-helices. Nature 1997, 389, 203-206.
-
(1997)
Nature
, vol.389
, pp. 203-206
-
-
Urger, V.M.1
Hargrave, P.A.2
Baldwin, J.M.3
Schertler, G.F.X.4
-
29
-
-
0029043501
-
Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor
-
Kim, J.; Wess, J.; van Rhee, M. A.; Schoneberg, T.; Jacobson, K. A. Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor. J. Biol. Chem. 1995, 270, 13987-13997.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 13987-13997
-
-
Kim, J.1
Wess, J.2
Van Rhee, M.A.3
Schoneberg, T.4
Jacobson, K.A.5
-
30
-
-
0027133429
-
Identification of potent, selective P2Y-purinoceptor agonists - Structure - activity-relationships for 2-thioether derivatives of adenosine 5′-triphosphate
-
Fischer, B.; Boyer, J. L.; Hoyle, C. H. V.; Ziganshin, A. U.; Brizzolara, A. L.; Knight, G. E.; Zimmet, J.; Burnstock, G.; Harden, T. K.; Jacobson, K. A. Identification of potent, selective P2Y-purinoceptor agonists - structure - activity-relationships for 2-thioether derivatives of adenosine 5′-triphosphate. J. Med. Chem. 1993, 36, 3937-3946.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3937-3946
-
-
Fischer, B.1
Boyer, J.L.2
Hoyle, C.H.V.3
Ziganshin, A.U.4
Brizzolara, A.L.5
Knight, G.E.6
Zimmet, J.7
Burnstock, G.8
Harden, T.K.9
Jacobson, K.A.10
-
31
-
-
0030831364
-
2-adrenergic receptor that exploits the domain structure of G-protein-coupled receptors
-
2-adrenergic receptor that exploits the domain structure of G-protein-coupled receptors. J. Med. Chem. 1997, 40, 3871-3886.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3871-3886
-
-
Gouldson, P.R.1
Snell, C.R.2
Reynolds, C.A.3
|