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

Ingebrigt Sylte

Showing results (81-90 of 96) with videos related to

Pageof 10
Sort By:
The Journal of Steroid Biochemistry and Molecular Biology|November 5, 2011
The liver X receptor modulator 22(S)-hydroxycholesterol exerts cell-type specific effects on lipid and glucose metabolismNina Pettersen Hessvik, Siril Skaret Bakke, Robert Smith, et al.
Biophysical Journal|November 6, 2007
Theoretical calculations of the catalytic triad in short-chain alcohol dehydrogenases/reductasesOsman A B S M Gani, Olayiwola A Adekoya, Laura Giurato, et al.
European Journal of Medicinal Chemistry|March 14, 2015
Synthesis, biological evaluation and molecular modeling studies of the PPARβ/δ antagonist CC618Åsmund Kaupang, Steinar Martin Paulsen, Calin C Steindal, et al.
Environmental Science & Technology|September 8, 2016
Environmental Chemicals Modulate Polar Bear (Ursus maritimus) Peroxisome Proliferator-Activated Receptor Gamma (PPARG) and Adipogenesis in VitroHeli Routti, Roger Lille-Langøy, Mari K Berg, et al.
Steroids|May 18, 2018
Synthesis, molecular modeling and biological evaluation of potent analogs of 2-methoxyestradiolNora Al-Kazaale, Phuong T Tran, Farhad Haidari, et al.
European Journal of Medicinal Chemistry|February 8, 2012
Synthesis, in vitro binding studies and docking of long-chain arylpiperazine nitroquipazine analogues, as potential serotonin transporter inhibitorsMałgorzata Jarończyk, Karol Wołosewicz, Mari Gabrielsen, et al.
Plos One|August 4, 2018
The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteasesIngebrigt Sylte, Rangita Dawadi, Nabin Malla, et al.
European Journal of Medicinal Chemistry|December 3, 2014
Inhibition of pseudolysin and thermolysin by hydroxamate-based MMP inhibitorsOlayiwola A Adekoya, Stian Sjøli, Yimingjiang Wuxiuer, et al.
Bioorganic & Medicinal Chemistry|July 29, 2019
Molecular modelling, synthesis, and biological evaluations of a 3,5-disubstituted isoxazole fatty acid analogue as a PPARα-selective agonistHenriette Arnesen, Nadia Nabil Haj-Yasein, Jørn E Tungen, et al.
Bioorganic & Medicinal Chemistry|April 9, 2008
1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogues of combretastatin A-4: Synthesis, molecular modeling and evaluation as cytotoxic agents and inhibitors of tubulinKristin Odlo, Jean Hentzen, Jérémie Fournier dit Chabert, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
The Journal of Steroid Biochemistry and Molecular Biology|November 5, 2011
The liver X receptor modulator 22(S)-hydroxycholesterol exerts cell-type specific effects on lipid and glucose metabolismNina Pettersen Hessvik, Siril Skaret Bakke, Robert Smith, et al.
Biophysical Journal|November 6, 2007
Theoretical calculations of the catalytic triad in short-chain alcohol dehydrogenases/reductasesOsman A B S M Gani, Olayiwola A Adekoya, Laura Giurato, et al.
European Journal of Medicinal Chemistry|March 14, 2015
Synthesis, biological evaluation and molecular modeling studies of the PPARβ/δ antagonist CC618Åsmund Kaupang, Steinar Martin Paulsen, Calin C Steindal, et al.
Environmental Science & Technology|September 8, 2016
Environmental Chemicals Modulate Polar Bear (Ursus maritimus) Peroxisome Proliferator-Activated Receptor Gamma (PPARG) and Adipogenesis in VitroHeli Routti, Roger Lille-Langøy, Mari K Berg, et al.
Steroids|May 18, 2018
Synthesis, molecular modeling and biological evaluation of potent analogs of 2-methoxyestradiolNora Al-Kazaale, Phuong T Tran, Farhad Haidari, et al.
European Journal of Medicinal Chemistry|February 8, 2012
Synthesis, in vitro binding studies and docking of long-chain arylpiperazine nitroquipazine analogues, as potential serotonin transporter inhibitorsMałgorzata Jarończyk, Karol Wołosewicz, Mari Gabrielsen, et al.
Plos One|August 4, 2018
The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteasesIngebrigt Sylte, Rangita Dawadi, Nabin Malla, et al.
European Journal of Medicinal Chemistry|December 3, 2014
Inhibition of pseudolysin and thermolysin by hydroxamate-based MMP inhibitorsOlayiwola A Adekoya, Stian Sjøli, Yimingjiang Wuxiuer, et al.
Bioorganic & Medicinal Chemistry|July 29, 2019
Molecular modelling, synthesis, and biological evaluations of a 3,5-disubstituted isoxazole fatty acid analogue as a PPARα-selective agonistHenriette Arnesen, Nadia Nabil Haj-Yasein, Jørn E Tungen, et al.
Bioorganic & Medicinal Chemistry|April 9, 2008
1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogues of combretastatin A-4: Synthesis, molecular modeling and evaluation as cytotoxic agents and inhibitors of tubulinKristin Odlo, Jean Hentzen, Jérémie Fournier dit Chabert, et al.
Pageof 10