Showing results (321-330 of 343) with videos related to
Sort By:
Pageof 35
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|July 27, 2021
Insomnia episodes, new-onset pharmacological treatments, and other sleep disturbances during the COVID-19 pandemic: a nationwide cross-sectional study in Brazilian health care professionalsLuciano F Drager, Daniela V Pachito, Claudia R C Moreno, et al.The Journal of Biological Chemistry|September 2, 2000
The neuropeptide processing enzyme EC 3.4.24.15 is modulated by protein kinase A phosphorylationJ W Tullai, P M Cummins, A Pabon, et al.Bioorganic & Medicinal Chemistry Letters|October 25, 2013
4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable Stearoyl-CoA desaturase-1 (SCD1) inhibitors. Part 1: urea-based analogsShyh-Ming Yang, Yuting Tang, Rui Zhang, et al.Biochemical and Biophysical Research Communications|September 15, 1998
Neuropeptide specificity and inhibition of recombinant isoforms of the endopeptidase 3.4.24.16 family: comparison with the related recombinant endopeptidase 3.4.24.15V Rioli, A Kato, F C Portaro, et al.Journal of the American Academy of Dermatology|October 20, 1998
Finasteride in the treatment of men with androgenetic alopecia. Finasteride Male Pattern Hair Loss Study GroupK D Kaufman, E A Olsen, D Whiting, et al.Journal of the American Academy of Dermatology|October 26, 2000
Lack of efficacy of finasteride in postmenopausal women with androgenetic alopeciaV H Price, J L Roberts, M Hordinsky, et al.European Journal of Pharmacology|December 6, 2001
In vitro activity of LY393558, an inhibitor of the 5-hydroxytryptamine transporter with 5-HT(1B/1D/2) receptor antagonist propertiesI A Pullar, J R Boot, S L Carney, et al.Science (New York, N.Y.)|November 3, 1995
Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid developmentS M Russell, N Tayebi, H Nakajima, et al.Clinical & Experimental Metastasis|March 1, 1996
Effect of matrix metalloproteinase inhibitors on tumor growth and spontaneous metastasisJ G Conway, S J Trexler, J A Wakefield, et al.Bioorganic & Medicinal Chemistry Letters|January 11, 2014
4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable stearoyl-CoA desaturase-1 (SCD1) inhibitors: part 2. Pyridazine-based analogsShyh-Ming Yang, Yuting Tang, Thomas Rano, et al.Pageof 35