Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Parish

Showing results (71-80 of 212) with videos related to

Pageof 22
Sort By:
JAMA Network Open|April 21, 2020
Association of Formulary Prior Authorization Policies With Buprenorphine-Naloxone Prescriptions and Hospital and Emergency Department Use Among Medicare BeneficiariesTami L Mark, William J Parish, Gary A Zarkin
The Journal of Biological Chemistry|December 10, 1980
15-Oxygenated sterols. Enzymatic conversion of [2,4]3H]5 alpha-cholest-8(14)-en-3 beta-ol-15-one to cholesterol in rat liver homogenate preparationsD J Monger, E J Parish, G J Schroepfer
Plos One|January 11, 2018
Dynamics of co-authorship and productivity across different fields of scientific researchAustin J Parish, Kevin W Boyack, John P A Ioannidis
The Journal of Biological Chemistry|April 15, 1989
Inhibition of cholesterol synthesis and cell growth by 24(R,S),25-iminolanosterol and triparanol in cultured rat hepatoma cellsG Popják, A Meenan, E J Parish, et al.
Psychiatric Services (Washington, D.C.)|May 16, 2018
Impact of Medical Homes on Expenditures and Utilization for Beneficiaries With Behavioral Health ConditionsMelissa A Romaire, Vincent Keyes, William J Parish, et al.
Biochemical and Biophysical Research Communications|April 14, 1980
Inhibitors of sterol synthesis. Hypocholesterolemic action of dietary 9 alpha-fluoro-5 alpha-cholest-8(14)-en-3 beta-ol-15-oneG J Schroepfer, V Walker, E J Parish, et al.
Chemistry and Physics of Lipids|October 1, 1988
A facile synthesis of lanost-8-en-3 beta-ol-24-one (24-ketolanosterol). An inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductaseE J Parish, H Honda, S Chitrakorn, et al.
Lipids|March 30, 2007
Syntheses of ring C oxysterols: inhibitors of sterol biosynthesisEdward J Parish, Chi Luo, Thomas Webb, et al.
Chemistry and Physics of Lipids|December 1, 1984
Chemical synthesis of 4,4'-dimethyl-7-oxygenated sterols. Inhibitors of 3-hydroxy-3-methylglutaryl reductaseE J Parish, S Chitrakorn, F R Taylor, et al.
Steroids|March 1, 1989
Studies of the oxysterol inhibition of tumor cell growthE J Parish, S Chitrakorn, B Luu, et al.
Pageof 22

Showing results (71-80 of 212) with videos related to

Sort By:
Pageof 22
JAMA Network Open|April 21, 2020
Association of Formulary Prior Authorization Policies With Buprenorphine-Naloxone Prescriptions and Hospital and Emergency Department Use Among Medicare BeneficiariesTami L Mark, William J Parish, Gary A Zarkin
The Journal of Biological Chemistry|December 10, 1980
15-Oxygenated sterols. Enzymatic conversion of [2,4]3H]5 alpha-cholest-8(14)-en-3 beta-ol-15-one to cholesterol in rat liver homogenate preparationsD J Monger, E J Parish, G J Schroepfer
Plos One|January 11, 2018
Dynamics of co-authorship and productivity across different fields of scientific researchAustin J Parish, Kevin W Boyack, John P A Ioannidis
The Journal of Biological Chemistry|April 15, 1989
Inhibition of cholesterol synthesis and cell growth by 24(R,S),25-iminolanosterol and triparanol in cultured rat hepatoma cellsG Popják, A Meenan, E J Parish, et al.
Psychiatric Services (Washington, D.C.)|May 16, 2018
Impact of Medical Homes on Expenditures and Utilization for Beneficiaries With Behavioral Health ConditionsMelissa A Romaire, Vincent Keyes, William J Parish, et al.
Biochemical and Biophysical Research Communications|April 14, 1980
Inhibitors of sterol synthesis. Hypocholesterolemic action of dietary 9 alpha-fluoro-5 alpha-cholest-8(14)-en-3 beta-ol-15-oneG J Schroepfer, V Walker, E J Parish, et al.
Chemistry and Physics of Lipids|October 1, 1988
A facile synthesis of lanost-8-en-3 beta-ol-24-one (24-ketolanosterol). An inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductaseE J Parish, H Honda, S Chitrakorn, et al.
Lipids|March 30, 2007
Syntheses of ring C oxysterols: inhibitors of sterol biosynthesisEdward J Parish, Chi Luo, Thomas Webb, et al.
Chemistry and Physics of Lipids|December 1, 1984
Chemical synthesis of 4,4'-dimethyl-7-oxygenated sterols. Inhibitors of 3-hydroxy-3-methylglutaryl reductaseE J Parish, S Chitrakorn, F R Taylor, et al.
Steroids|March 1, 1989
Studies of the oxysterol inhibition of tumor cell growthE J Parish, S Chitrakorn, B Luu, et al.
Pageof 22