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au.\*:("LEE, Chih-Hung")

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Results 1 to 25 of 41

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Nonnucleoside inhibitors of adenosine kinaseGOMTSYAN, Arthur; LEE, Chih-Hung.Current pharmaceutical design. 2004, Vol 10, Num 10, pp 1093-1103, issn 1381-6128, 11 p.Article

Pathophysiology of chemokines and chemokine receptors in dermatological science: A focus on psoriasis and cutaneous T-cell lymphomaLEE, Chih-Hung; HWANG, Sam Tzen-Yue.Zhōnghuá pífūkē yīxué zázhì. 2012, Vol 30, Num 4, pp 128-135, issn 1027-8117, 8 p.Article

Accurate TSV Number Minimization in High-Level SynthesisLEE, Chih-Hung; HUANG, Shih-Hsu; CHENG, Chun-Hua et al.Journal of information science and engineering. 2011, Vol 27, Num 5, pp 1527-1543, issn 1016-2364, 17 p.Article

Carvedilol-induced elevation in cytosolic free Ca2+ level and apoptosis in SIRC corneal epithelial cellsSHIEH, Pochuen; LEE, Chih-Hung; NG LING YI et al.Human & experimental toxicology. 2010, Vol 29, Num 6, pp 477-487, issn 0960-3271, 11 p.Article

Defective adrenergic responses in patients with arsenic-induced peripheral vascular diseaseLEE, Chih-Hung; CHANG, Huoy-Rou; CHEN, Jau-Shiuh et al.Angiology. 2007, Vol 58, Num 2, pp 161-168, issn 0003-3197, 8 p.Article

Structure-activity relationships of α-amino acid ligands for the α2δ subunit of voltage-gated calcium channelsMORTELL, Kathleen H; ANDERSON, David J; JARVIS, Michael F et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 5, pp 1138-1141, issn 0960-894X, 4 p.Article

Synthesis and biological evaluation of pteridine and pyrazolopyrimidine based adenosine kinase inhibitorsGOMTSYAN, Arthur; DIDOMENICO, Stanley; LEE, Chih-Hung et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 16, pp 4165-4168, issn 0960-894X, 4 p.Article

Synthesis and structure-activity relationships of 5-heteroatom-substituted pyridopyrimidines as adenosine kinase inhibitorsGFESSER, Gregory A; BAYBURT, Erol K; COWART, Marlon et al.European journal of medicinal chemistry. 2003, Vol 38, Num 3, pp 245-252, issn 0223-5234, 8 p.Article

Synthesis and biological evaluation of clitocine analogues as adenosine kinase inhibitorsLEE, Chih-Hung; DAANEN, Jerome F; MEIQUN JIANG et al.Bioorganic & medicinal chemistry letters (Print). 2001, Vol 11, Num 18, pp 2419-2422, issn 0960-894XArticle

Functional Regulation of Interleukin-31 Production by its Genetic Polymorphism in Patients with Extrinsic Atopic DermatitisHONG, Chien-Hui; YU, Hsin-Su; KO, Ying-Chin et al.Acta dermato-venereologica. 2012, Vol 92, Num 4, pp 430-432, issn 0001-5555, 3 p.Article

Potentiation of analgesic efficacy but not side effects: Co-administration of an α4β2 neuronal nicotinic acetylcholine receptor agonist and its positive allosteric modulator in experimental models of pain in ratsZHU, Chang Z; CHIN, Chih-Liang; GAUVIN, Donna et al.Biochemical pharmacology. 2011, Vol 82, Num 8, pp 967-976, issn 0006-2952, 10 p.Conference Paper

Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonistsBROWN, Brian S; KEDDY, Ryan; POLAKOWSKI, James S et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 18, pp 8516-8525, issn 0968-0896, 10 p.Article

α-Μethylation at benzylic fragment of N-aryl-N'-benzyl ureas provides TRPV1 antagonists with better pharmacokinetic properties and higher efficacy in inflammatory pain modelGOMTSYAN, Arthur; BAYBURT, Erol K; SUROWY, Carol S et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 14, pp 3894-3899, issn 0960-894X, 6 p.Article

In vitro structure-activity relationship and in vivo characterization of 1 -(aryl ) -3 -(4 -(amino )benzyl )urea transient receptor potential vanilloid 1 antagonistsPERNER, Richard J; DIDOMENICO, Stanley; BROWN, Brian S et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 15, pp 3651-3660, issn 0022-2623, 10 p.Article

Design, synthesis, and structure-activity relationship of 6-alkynylpyrimidines as potent adenosine kinase inhibitorsGOMTSYAN, Arthur; DIDOMENICO, Stanley; JARVIS, Michael F et al.Journal of medicinal chemistry (Print). 2002, Vol 45, Num 17, pp 3639-3648, issn 0022-2623Article

α3* and α7 nAChR-mediated Ca2+ transient generation in IMR-32 neuroblastoma cellsWEEN, Hilde; THORIN-HAGENE, Kirsten; ANDERSEN, Elisabeth et al.Neurochemistry international. 2010, Vol 57, Num 3, pp 269-277, issn 0197-0186, 9 p.Article

Differential effects of arsenic on cutaneous and systemic immunity: focusing on CD4+ cell apoptosis in patients with arsenic-induced Bowen's diseaseLIAO, Wei-Ting; YU, Chia-Li; LAN, Cheng-Che E et al.Carcinogenesis (New York. Print). 2009, Vol 30, Num 6, pp 1064-1072, issn 0143-3334, 9 p.Article

5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido-[2,3-d]pyrimidin-4-ylamine : structure-activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitorsMATULENKO, Mark A; LEE, Chih-Hung; MCKIE, Jeffery A et al.Bioorganic & medicinal chemistry. 2005, Vol 13, Num 11, pp 3705-3720, issn 0968-0896, 16 p.Article

Discovery of 4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin-3-yl)pyrido[2,3-d]pyrimidine, an orally active, non-nucleoside adenosine kinase inhibitorLEE, Chih-Hung; MEIQUN JIANG; STEWART, Andrew O et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 13, pp 2133-2138, issn 0022-2623Article

Pyridopyrimidine analogues as novel adenosine kinase inhibitorsGUO ZHU ZHENG; LEE, Chih-Hung; MUCHMORE, Steve et al.Bioorganic & medicinal chemistry letters (Print). 2001, Vol 11, Num 16, pp 2071-2074, issn 0960-894XArticle

Use of Arsenic-Induced Palmoplantar Hyperkeratosis and Skin Cancers to Predict Risk of Subsequent Internal MalignancyHSU, Ling-I; CHEN, Gwo-Shing; LEE, Chih-Hung et al.American journal of epidemiology. 2013, Vol 177, Num 3, pp 202-212, issn 0002-9262, 11 p.Article

α4β2 neuronal nicotinic receptor positive allosteric modulation: An approach for improving the therapeutic index of α4β2 nAChR agonists in painLEE, Chih-Hung; CHANG ZHU; MALYSZ, John et al.Biochemical pharmacology. 2011, Vol 82, Num 8, pp 959-966, issn 0006-2952, 8 p.Conference Paper

4-amino-5-aryl-6-arylethynylpyrimidines : Structure-activity relationships of non-nucleoside adenosine kinase inhibitorsMATULENKO, Mark A; PAIGHT, Ernest S; ALEXANDER, Karen M et al.Bioorganic & medicinal chemistry. 2007, Vol 15, Num 4, pp 1586-1605, issn 0968-0896, 20 p.Article

Defective β1-integrins expression in arsenical keratosis and arsenic-treated cultured human keratinocytesLEE, Chih-Hung; CHEN, Jau-Shiuh; SUN, Yu-Lan et al.Journal of cutaneous pathology. 2006, Vol 33, Num 2, pp 129-138, issn 0303-6987, 10 p.Article

Effects of A-317491, a novel and selective P2X3/P2X2/3 receptor antagonist, on neuropathic, inflammatory and chemogenic nociception following intrathecal and intraplantar administrationMCGARAUGHTY, Steve; WISMER, Carol T; ZHU, Chang Z et al.British journal of pharmacology. 2003, Vol 140, Num 8, pp 1381-1388, issn 0007-1188, 8 p.Article

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