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Journal of Medicinal Chemistry|June 25, 2013
Rational design of sulfonated A3 adenosine receptor-selective nucleosides as pharmacological tools to study chronic neuropathic painSilvia Paoletta, Dilip K Tosh, Amanda Finley, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5'-ribofuran-uronamide moietyZhan-Guo Gao, Bhalchandra V Joshi, Athena M Klutz, et al.
Nucleosides, Nucleotides & Nucleic Acids|October 27, 2005
Synthesis of 3'-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptorMoon Woo Chun, Hyouk Woo Lee, Ae Yil Kim, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 4, 2014
[Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review]Hai-hua Zhang, Li-guo Gao, Jing-min Wang, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 21, 2011
Protection from myocardial ischemia/reperfusion injury by a positive allosteric modulator of the A₃ adenosine receptorLili Du, Zhan-Guo Gao, Kasem Nithipatikom, et al.
Journal of Medicinal Chemistry|March 21, 2017
Scaffold Repurposing of Nucleosides (Adenosine Receptor Agonists): Enhanced Activity at the Human Dopamine and Norepinephrine Sodium SymportersDilip K Tosh, Aaron Janowsky, Amy J Eshleman, et al.
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