R. El Kouhen

发表

[3H]A-778317 [1-((R)-5-tert-Butyl-indan-1-yl)-3-isoquinolin-5-yl-urea]: a Novel, Stereoselective, High-Affinity Antagonist Is a Useful Radioligand for the Human Transient Receptor Potential Vanilloid-1 (TRPV1) Receptor

A. Gomtsyan, Chih-Hung Lee, T. Neelands, 2007, Journal of Pharmacology and Experimental Therapeutics.

Stimulation of dopamine release by nicotinic acetylcholine receptor ligands in rat brain slices correlates with the profile of high, but not low, sensitivity alpha4beta2 subunit combination.

C. Briggs, M. Håkerud, M. Gopalakrishnan, 2009, Biochemical pharmacology.

The Absence of a Direct Correlation between the Loss of [d-Ala2,MePhe4,Gly5-ol]Enkephalin Inhibition of Adenylyl Cyclase Activity and Agonist-induced μ-Opioid Receptor Phosphorylation*

H. Loh, P. Law, R. El Kouhen, 1999, The Journal of Biological Chemistry.

Phosphorylation of Ser363, Thr370, and Ser375 Residues within the Carboxyl Tail Differentially Regulates μ-Opioid Receptor Internalization*

H. Loh, P. Law, Chia-Yu Chang, 2001, The Journal of Biological Chemistry.

A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel Transient Receptor Potential Type V1 Receptor Antagonist, Relieves Pathophysiological Pain Associated with Inflammation and Tissue Injury in Rats

A. Gomtsyan, J. Sullivan, Chih-Hung Lee, 2005, Journal of Pharmacology and Experimental Therapeutics.

A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel and Selective Transient Receptor Potential Type V1 Receptor Antagonist, Blocks Channel Activation by Vanilloids, Heat, and Acid

A. Gomtsyan, J. Sullivan, Chih-Hung Lee, 2005, Journal of Pharmacology and Experimental Therapeutics.

Naphthalene dicarboxaldehyde as an electrophilic fluorogenic moiety for affinity labeling: application to opioid receptor affinity labels with greatly improved fluorogenic properties.

P. Law, P. Portoghese, T. Metzger, 2002, Journal of medicinal chemistry.

Affinity labels as tools for the identification of opioid receptor recognition sites.

H. Loh, P. Law, P. Portoghese, 2001, Farmaco.

(R)-(5-tert-Butyl-2,3-dihydro-1H-inden-1-yl)-3-(1H-indazol-4-yl)-urea (ABT-102) Blocks Polymodal Activation of Transient Receptor Potential Vanilloid 1 Receptors in Vitro and Heat-Evoked Firing of Spinal Dorsal Horn Neurons in Vivo

A. Gomtsyan, J. Sullivan, Chih-Hung Lee, 2008, Journal of Pharmacology and Experimental Therapeutics.

Capsaicin infused into the PAG affects rat tail flick responses to noxious heat and alters neuronal firing in the RVM.

E. Burgard, M. Jarvis, C. Faltynek, 2003, Journal of neurophysiology.

Characterization of the receptor and translocator domains of colicin N.

M. Steiert, F. Pattus, H. Fierobe, 1993, European journal of biochemistry.

Reporter affinity labels: an o-phthalaldehyde derivative of beta-naltrexamine as a fluorogenic ligand for opioid receptors.

H. Loh, P. Law, P. Portoghese, 2000, Journal of medicinal chemistry.

Colicin N interaction with sensitive Escherichia coli cells: in situ and kinetic approaches.

J. Pagés, A. Bernadac, R. El Kouhen, 1998, Research in microbiology.

Dynamic aspects of colicin N translocation through the Escherichia coli outer membrane

J. Pagés, R. El Kouhen, 1996, Journal of bacteriology.

Modulation of human TRPV1 receptor activity by extracellular protons and host cell expression system.

Chih-Hung Lee, R. Moreland, M. Jarvis, 2006, European journal of pharmacology.

Covalently induced activation of the delta opioid receptor by a fluorogenic affinity label, 7'-(phthalaldehydecarboxamido)naltrindole (PNTI).

D. Ferguson, G. Poda, H. Loh, 2001, Journal of Medicinal Chemistry.

Binding of [(3)H]A-778317 to native transient receptor potential vanilloid-1 (TRPV1) channels in rat dorsal root ganglia and spinal cord.

Jun Chen, B. Bianchi, P. Puttfarcken, 2010, European journal of pharmacology.

In vitro approaches to investigation of the early steps of colicin-OmpF interaction.

A. Hoenger, A. Engel, J. Pagés, 1994, European journal of biochemistry.

(R)-(5-tert-Butyl-2,3-dihydro-1H-inden-1-yl)-3-(1H-indazol-4-yl)-urea (ABT-102) Blocks Polymodal Activation of Transient Receptor Potential Vanilloid 1 Receptors in Vitro and Heat-Evoked Firing of Spinal Dorsal Horn Neurons in Vivo

A. Gomtsyan, J. Sullivan, Chih-Hung Lee, 2008, Journal of Pharmacology and Experimental Therapeutics.