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Eduardo J. Molinari

Observed names: E J Molinari, E Molinari, Eduardo J Molinari, Eduardo Molinari
OpenAlex ID: A5000402799
Stable expression, pharmacologic properties and regulation of the human neuronal nicotinic acetylcholine alpha 4 beta 2 receptor.
1996 · M Gopalakrishnan, L M Monteggia, et al. · Journal of Pharmacology and Experimental Therapeutics · 168
Regulation of Human α4β2 Neuronal Nicotinic Acetylcholine Receptors by Cholinergic Channel Ligands and Second Messenger Pathways
1997 · Murali Gopalakrishnan, Eduardo J. Molinari, et al. · Molecular Pharmacology · 127
2-[125I]Iodo-5-methoxycarbonylamino-N-acetyltryptamine: a selective radioligand for the characterization of melatonin ML2 binding sites
1996 · Eduardo J. Molinari, Peter C. North, et al. · European Journal of Pharmacology · 110
Characterization of the ATP-Sensitive Potassium Channels (KATP) Expressed in Guinea Pig Bladder Smooth Muscle Cells
1999 · Murali Gopalakrishnan, Kristi L. Whiteaker, et al. · Journal of Pharmacology and Experimental Therapeutics · 96
Wild-type gas vesicle formation requires at least ten genes in the gvp gene cluster of Halobacterium halobium plasmid pNRC100
1994 · S DasSarma, P Arora, et al. · Journal of Bacteriology · 81
ABT-089 [2-Methyl-3-(2-(S)-pyrrolidinylmethoxy)pyridine]: I. A Potent and Selective Cholinergic Channel Modulator with Neuroprotective Properties
1997 · James P. Sullivan, Diana Donnelly-Roberts, et al. · Journal of Pharmacology and Experimental Therapeutics · 79
Up-regulation of human α7 nicotinic receptors by chronic treatment with activator and antagonist ligands
1998 · Eduardo J Molinari, Osvaldo Delbono, et al. · European Journal of Pharmacology · 78
The high affinity melatonin binding site probed with conformationally restricted ligands—I. Pharmacophore and minireceptor models
1996 · Johanna M. Jansen, Swier Copinga, et al. · Bioorganic & Medicinal Chemistry · 53
(−)-(9 S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4 H)-one 1,1-Dioxide (A-278637): A Novel ATP-Sensitive Potassium Channel Opener Efficacious in Suppressing Urinary Bladder Contractions. I. In Vitro Characterization
2002 · Murali Gopalakrishnan, Steven A. Buckner, et al. · Journal of Pharmacology and Experimental Therapeutics · 40
Genetic and topological analyses of the bop promoter of Halobacterium halobium: stimulation by DNA supercoiling and non-B-DNA structure
1996 · C F Yang, J M Kim, et al. · Journal of Bacteriology · 39
Pharmacology of human sulphonylurea receptor SUR1 and inward rectifier K+ channel Kir6.2 combination expressed in HEK‐293 cells
2000 · Murali Gopalakrishnan, Eduardo J Molinari, et al. · British Journal of Pharmacology · 32
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Pharmacological and molecular characterization of ATP-sensitive K+ channels in the TE671 human medulloblastoma cell line
1999 · Thomas R Miller, Rachel Davis Taber, et al. · European Journal of Pharmacology · 29
Characterization of a novel ATP‐sensitive K + channel opener, A‐251179, on urinary bladder relaxation and cystometric parameters
2007 · C‐C Shieh, M E Brune, et al. · British Journal of Pharmacology · 21
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[125I]A-312110, a Novel High-Affinity 1,4-Dihydropyridine ATP-sensitive K+ Channel Opener: Characterization and Pharmacology of Binding
2003 · Rachel Davis-Taber, Eduardo J Molinari, et al. · Molecular Pharmacology · 18
Pharmacological characterization of a 1,4‐dihydropyridine analogue, 9‐(3,4‐dichlorophenyl)‐3,3,6,6‐tetramethyl‐3,4,6,7,9,10‐hexahydro‐1,8(2H,5H)‐acridinedione (A‐184209) as a novel KATP channel inhibitor
2003 · Murali Gopalakrishnan, Thomas R Miller, et al. · British Journal of Pharmacology · 10
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Characterization and modulation of [125I]iberiotoxin-D19Y/Y36F binding in the guinea-pig urinary bladder
2000 · Eduardo J Molinari, James P Sullivan, et al. · European Journal of Pharmacology · 5
Expression of Cloned Receptors in Mammalian Cell Lines
1998 · Murali Gopalakrishnan, Eduardo J. Molinari · Current Protocols in Pharmacology · 1
Works count: 18
Citation count: 987
H-index: 14
I10-index: 15
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