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Journal Francais D'Ophtalmologie|January 11, 2021
[Immunosuppressive therapy in severe or chronic pediatric uveitis: Review of the literature]N Stolowy, E Zanin, A Comet, et al.Bioorganic & Medicinal Chemistry Letters|March 27, 2001
Structure-activity relationship on the human EP3 prostanoid receptor by use of solid-support chemistryH Juteau, Y Gareau, M Labelle, et al.Biochemical and Biophysical Research Communications|May 24, 1996
White adipose tissue nitric oxide synthase: a potential source for NO productionC Ribiere, A M Jaubert, N Gaudiot, et al.Molecular Pharmacology|May 17, 2001
Key structural features of prostaglandin E(2) and prostanoid analogs involved in binding and activation of the human EP(1) prostanoid receptorM D Ungrin, M C Carrière, D Denis, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 1, 1994
Long-term (3 years) prevention of trabecular postmenopausal bone loss with low-dose intermittent nasal salmon calcitoninJ Y Reginster, D Denis, R Deroisy, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|May 2, 2018
Acanthopanax senticosus reduces brain injury in mice exposed to low linear energy transfer radiationA Yingyu Zhou, B Wei Song, C Yilei Fu, et al.Journal of Medicinal Chemistry|September 17, 1993
Substituted thiopyrano[2,3,4-c,d]indoles as potent, selective, and orally active inhibitors of 5-lipoxygenase. Synthesis and biological evaluation of L-691,816J H Hutchinson, D Riendeau, C Brideau, et al.Canadian Journal of Physiology and Pharmacology|May 1, 1989
L-663,536 (MK-886) (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2,2 - dimethylpropanoic acid), a novel, orally active leukotriene biosynthesis inhibitorJ Gillard, A W Ford-Hutchinson, C Chan, et al.Canadian Journal of Physiology and Pharmacology|December 1, 1986
L-648,051, sodium 4-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)- propylsulfonyl]-gamma-oxo-benzenebutanoate: a leukotriene D4 receptor antagonistT R Jones, Y Guindon, R Young, et al.Bioorganic & Medicinal Chemistry|August 16, 2001
Structure-activity relationship of cinnamic acylsulfonamide analogues on the human EP3 prostanoid receptorH Juteau, Y Gareau, M Labelle, et al.Pageof 16