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Results:
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Results: 25
Authors:
VANHOOFT JA
SPIER AD
YAKEL JL
LUMMIS SCR
VIJVERBERG HPM
Citation: Ja. Vanhooft et al., PROMISCUOUS COASSEMBLY OF SEROTONIN 5-HT3 AND NICOTINIC ALPHA-4 RECEPTOR SUBUNITS INTO CA2-PERMEABLE ION CHANNELS(), Proceedings of the National Academy of Sciences of the United Statesof America, 95(19), 1998, pp. 11456-11461
Authors:
LUMMIS SCR
FLETCHER EJ
GREEN T
Citation: Scr. Lummis et al., NMDA RECEPTOR NR2 SUBUNITS CONTAIN AMINO-ACIDS INVOLVED IN GLUTAMATE BINDING, Journal of physiology, 506P, 1998, pp. 76-76
Authors:
NIEMEYER MI
LUMMIS SCR
Citation: Mi. Niemeyer et Scr. Lummis, DIFFERENT EFFICACY OF SPECIFIC AGONISTS AT 5-HT3 RECEPTOR SPLICE VARIANTS - THE ROLE OF THE EXTRA 6 AMINO-ACID SEGMENT, British Journal of Pharmacology, 123(4), 1998, pp. 661-666
Authors:
LUMMIS SCR
BAKER J
Citation: Scr. Lummis et J. Baker, RADIOLIGAND BINDING AND PHOTOAFFINITY-LABELING STUDIES SHOW A DIRECT INTERACTION OF PHENOTHIAZINES AT 5-HT3 RECEPTORS, Neuropharmacology, 36(4-5), 1997, pp. 665-670
Authors:
LUMMIS SCR
FLETCHER EJ
GREEN T
Citation: Scr. Lummis et al., IDENTIFICATION OF AMINO-ACIDS IN THE N-METHYL-D-ASPARTATE (NMDA) RECEPTOR NR2 SUBUNIT THAT CONTRIBUTE TO THE GLUTAMATE BINDING-SITE, British Journal of Pharmacology, 122, 1997, pp. 5-5
Authors:
SPIER AD
LUMMIS SCR
Citation: Ad. Spier et Scr. Lummis, THE ROLE OF TRYPTOPHAN RESIDUES IN THE 5-HT3 RECEPTOR-BINDING SITE, British Journal of Pharmacology, 122, 1997, pp. 251-251
Authors:
GUNTHORPE MJ
LUMMIS SCR
Citation: Mj. Gunthorpe et Scr. Lummis, SUBSTITUTION OF A CHARGED RESIDUE, LYSINE-282, IN THE M2 DOMAIN OF THE 5-HT3 RECEPTOR AFFECTS THE RATE OF DESENSITIZATION, British Journal of Pharmacology, 122, 1997, pp. 252-252
Authors:
NIEMEYER MI
LUMMIS SCR
Citation: Mi. Niemeyer et Scr. Lummis, CA2-INHIBITION OF AGONIST-EVOKED CURRENTS IN THE 5-HT3 RECEPTOR(), British Journal of Pharmacology, 122, 1997, pp. 421-421
Authors:
HARGREAVES AC
GUNTHORPE MJ
TAYLOR CW
LUMMIS SCR
Citation: Ac. Hargreaves et al., DIRECT INHIBITION OF 5-HYDROXYTRYPTAMINE(3) RECEPTORS BY ANTAGONISTS OF L-TYPE CA2+ CHANNELS, Molecular pharmacology, 50(5), 1996, pp. 1284-1294
Authors:
GUNTHORPE MJ
FLETCHER EJ
LUMMIS SCR
Citation: Mj. Gunthorpe et al., CONVERSION OF THE ION SELECTIVITY OF THE 5-HT3 RECEPTOR FROM CATIONICTO ANIONIC - A CONSERVED FEATURE OF THE LIGAND-GATED ION-CHANNEL SUPERFAMILY, British Journal of Pharmacology, 119, 1996, pp. 259-259
Authors:
SPIER AD
LUMMIS SCR
Citation: Ad. Spier et Scr. Lummis, IMMUNOLOGICAL CHARACTERIZATION OF 5-HT3 RECEPTOR TRANSMEMBRANE TOPOLOGY, British Journal of Pharmacology, 119, 1996, pp. 260-260
Authors:
NIEMEYER MI
LUMMIS SCR
Citation: Mi. Niemeyer et Scr. Lummis, EFFECTS OF AGONISTS ON THE LONG AND SHORT SPLICE VARIANTS OF 5-HT3 RECEPTOR STABLY EXPRESSED IN HEK-293 CELLS, British Journal of Pharmacology, 119, 1996, pp. 261-261
Authors:
LUMMIS SCR
FLETCHER EJ
Citation: Scr. Lummis et Ej. Fletcher, FUNCTIONAL AND BINDING-STUDIES OF GLYCOSYLATION SITE MUTANTS OF 5-HT3RECEPTORS, British Journal of Pharmacology, 119, 1996, pp. 291-291
Authors:
HARGREAVES AC
TAYLOR CW
LUMMIS SCR
Citation: Ac. Hargreaves et al., MODULATION OF 5-HT3 RECEPTOR-EVOKED CURRENTS BY L-TYPE CA2+ CHANNEL ANTAGONISTS, British Journal of Pharmacology, 117, 1996, pp. 313-313
Authors:
BUCKINGHAM SD
BALK ML
LUMMIS SCR
JEWESS P
SATTELLE DB
Citation: Sd. Buckingham et al., ACTIONS OF NITROMETHYLENES ON AN ALPHA-BUNGAROTOXIN-SENSITIVE NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR, Neuropharmacology, 34(6), 1995, pp. 591-597
Authors:
GREEN T
STAUFFER KA
LUMMIS SCR
Citation: T. Green et al., EXPRESSION OF RECOMBINANT HOMOOLIGOMERIC 5-HYDROXYTRYPTAMINE(3) RECEPTORS PROVIDES NEW INSIGHTS INTO THEIR MATURATION AND STRUCTURE, The Journal of biological chemistry, 270(11), 1995, pp. 6056-6061
Authors:
HARGREAVES AC
LUMMIS SCR
TAYLOR CW
Citation: Ac. Hargreaves et al., DIRECT INHIBITION OF 5-HT3 RECEPTOR FUNCTION BY L-TYPE CA2+ CHANNEL ANTAGONISTS, British Journal of Pharmacology, 115, 1995, pp. 23-23
Authors:
LUMMIS SCR
Citation: Scr. Lummis, RADIOLIGAND BINDING CHARACTERISTICS OF 5-HT3 RECEPTOR SPLICE VARIANTS- EVIDENCE THAT PHOSPHORYLATION DOES NOT AFFECT RECEPTOR-BINDING AFFINITY, British Journal of Pharmacology, 115, 1995, pp. 24-24
Authors:
SEPULVEDA MI
BAKER J
LUMMIS SCR
Citation: Mi. Sepulveda et al., CHLORPROMAZINE AND QX222 BLOCK 5-HT3, RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS, Neuropharmacology, 33(3-4), 1994, pp. 493-499
Authors:
HARGREAVES AC
LUMMIS SCR
TAYLOR CW
Citation: Ac. Hargreaves et al., CA2-HYDROXYTRYPTAMINE TYPE-3 RECEPTORS( PERMEABILITY OF CLONED AND NATIVE 5), Molecular pharmacology, 46(6), 1994, pp. 1120-1128
Authors:
HARGREAVES AC
LUMMIS SCR
TAYLOR CW
Citation: Ac. Hargreaves et al., EFFECTS OF THE SELECTIVE 5-HT3 RECEPTOR AGONIST 1-(M-CHLOROPHENYL)-BIGUANIDE ON INTRACELLULAR FREE CA2-115 NEUROBLASTOMA-CELLS( CONCENTRATION IN UNDIFFERENTIATED N1E), British Journal of Pharmacology, 112, 1994, pp. 210000052-210000052
Authors:
SEPULVEDA MI
LUMMIS SCR
Citation: Mi. Sepulveda et Scr. Lummis, 5-HT3 AGONISTS CAN DISTINGUISH CLONED 5-HT3 RECEPTORS FROM NCB20 AND NG108-15 CELL-LINES, British Journal of Pharmacology, 112, 1994, pp. 210000160-210000160
Authors:
BUCKINGHAM SD
LUMMIS SCR
BALK ML
SCHROEDER M
SATTELLE DB
Citation: Sd. Buckingham et al., ACTIONS OF VESAMICOL ON AN ALPHA-BUNGAROTOXIN-SENSITIVE NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR, Journal of Experimental Biology, 182, 1993, pp. 255-264
Authors:
LUMMIS SCR
SEPULVEDA MI
KILPATRICK GJ
BAKER J
Citation: Scr. Lummis et al., CHARACTERIZATION OF [H-3] META-CHLOROPHENYLBIGUANIDE BINDING TO 5-HT(3) RECEPTORS IN N1E-115 NEUROBLASTOMA-CELLS, European journal of pharmacology, 243(1), 1993, pp. 7-11
Authors:
LUMMIS SCR
MARTIN IL
Citation: Scr. Lummis et Il. Martin, SOLUBILIZATION, PURIFICATION, AND FUNCTIONAL RECONSTITUTION OF 5-HYDROXYTRYPTAMINE3 RECEPTORS FROM N1E-115 NEUROBLASTOMA-CELLS, Molecular pharmacology, 41(1), 1992, pp. 18-23
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