Chui‐Se Tham - Concepedia

Concepedia

Author

Chui‐Se Tham

University of British Columbia

Also Known As

C S Tham, C.-S. Tham, Chui-Se Tham, Chui-se Tham, Chui‐Se Tham

18

Publications

1.3K

Citations

16

H-Index

47

Concepts

All Affiliations

University of British Columbia Johnson & Johnson (United States)General Atomics (United States)

CT

About

Chui‐Se Tham is an author at University of British Columbia specializing in medicine, neuroscience, and neuropharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	784
2	Social Sciences	3	3	124
3	Biochemistry	2	2	165
4	Cell Biology	2	2	277
5	Health Sciences	1	1	108

Chui‐Se Tham

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16

Publications

1.3K

Citations

16

H-Index

	Year	Citations
Sphingosine 1-phosphate receptor agonists attenuate relapsing–remitting experimental autoimmune encephalitis in SJL mice Michael Webb, Chui‐Se Tham, Fen‐Fen Lin, Journal of Neuroimmunology Molecular ImmunologySjl MiceAutoimmune DiseaseImmune Cell DevelopmentImmunology	2004	222
ALX 5407: A Potent, Selective Inhibitor of the hGlyT1 Glycine Transporter B N Atkinson, Stanley C. Bell, Michael De Vivo, Molecular Pharmacology	2001	171
Dopaminergic regulation of striatal acetylcholine release: importance of D1 and N-methyl-D-aspartate receptors. G. Damsma, George S. Robertson, Chui‐Se Tham, Journal of Pharmacology and Experimental Therapeutics	1991	128
Microglial activation state and lysophospholipid acid receptor expression Chui‐Se Tham, Fen‐Fen Lin, Tadimeti S. Rao, International Journal of Developmental Neuroscience	2003	119
Dopamine D1 receptor stimulation increases striatal acetylcholine release in the rat G. Damsma, Chui‐Se Tham, George S. Robertson, European Journal of Pharmacology Striatal Acetylcholine ReleaseHealth SciencesNeurophysiologyPhysiologyNeurotransmitter	1990	108
Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase John M. Keith, Richard L. Apodaca, Wei Xiao, Bioorganic & Medicinal Chemistry Letters BiochemistryMedicineDrug DevelopmentPharmacologyInhibitory Activity	2008	91
Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase Mark J. Karbarz, Lin Luo, Leon Chang, Anesthesia & Analgesia Lipid SynthesisBiochemistrySelective Faah InhibitorMedicine-Piperazine-1-carboxylic Acid Phenylamide	2008	74
Receptor mechanisms mediating clozapine-inducedc-fos expression in the forebrain N. Guo, Mark A. Klitenick, Chui‐Se Tham, Neuroscience MedicineNeurotransmitterNeuropeptide ReceptorNeuropharmacologyClozapine-inducedc-fos Expression	1995	68
Induction of Oligodendrocyte Differentiation and In Vitro Myelination by Inhibition of Rho-Associated Kinase Carlos E. Pedraza, Christopher M. Taylor, Albertina Pereira, ASN NEURO Vitro MyelinationCellular NeurobiologyCellular PhysiologySocial SciencesNeuroinflammation	2014	55
Inhibition of microglial fatty acid amide hydrolase modulates LPS stimulated release of inflammatory mediators Chui‐Se Tham, John N. Whitaker, Lin Luo, FEBS Letters Pge2 ReleaseNeuroinflammationInflammationSupplemental Exogenous AnandamideNeurology	2007	54

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