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Matthias Engel

Showing results (11-20 of 79) with videos related to

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Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|July 26, 2020
Menthacarin attenuates experimental colitisKorina Alliger, Mohammad Khalil, Beatrix König, et al.
Environmental Microbiology|February 2, 2011
Depicting more accurate pictures of protistan community complexity using pyrosequencing of hypervariable SSU rRNA gene regionsAnke Behnke, Matthias Engel, Richard Christen, et al.
Journal of Medicinal Chemistry|March 15, 2017
First Bispecific Inhibitors of the Epidermal Growth Factor Receptor Kinase and the NF-κB Activity As Novel Anticancer AgentsMostafa M Hamed, Sarah S Darwish, Jennifer Herrmann, et al.
Journal of Medicinal Chemistry|July 18, 2013
Highly potent and selective nonsteroidal dual inhibitors of CYP17/CYP11B2 for the treatment of prostate cancer to reduce risks of cardiovascular diseasesMariano A E Pinto-Bazurco Mendieta, Qingzhong Hu, Matthias Engel, et al.
FEMS Microbiology Ecology|November 19, 2011
Sample pooling obscures diversity patterns in intertidal ciliate community composition and structureMatthias Engel, Anke Behnke, Sara Bauerfeld, et al.
European Journal of Medicinal Chemistry|September 8, 2018
Development of novel 2,4-bispyridyl thiophene-based compounds as highly potent and selective Dyrk1A inhibitors. Part I: Benzamide and benzylamide derivativesSarah S Darwish, Mohammad Abdel-Halim, Mohamed Salah, et al.
Medicinal Research Reviews|October 20, 2022
An overview of cdc2-like kinase 1 (Clk1) inhibitors and their therapeutic indicationsAhmed K ElHady, Dalia S El-Gamil, Ashraf H Abadi, et al.
ACS Chemical Neuroscience|September 24, 2014
First selective dual inhibitors of tau phosphorylation and Beta-amyloid aggregation, two major pathogenic mechanisms in Alzheimer's diseaseMarica Mariano, Christian Schmitt, Parisa Miralinaghi, et al.
Steroids|June 9, 2015
New biaryl-chalcone derivatives of pregnenolone via Suzuki-Miyaura cross-coupling reaction. Synthesis, CYP17 hydroxylase inhibition activity, QSAR, and molecular docking studyNajim A Al-Masoudi, Rawaa A Kadhim, Nabeel A Abdul-Rida, et al.
Journal of Medicinal Chemistry|July 25, 2014
Discovery and optimization of 1,3,5-trisubstituted pyrazolines as potent and highly selective allosteric inhibitors of protein kinase C-ζMohammad Abdel-Halim, Britta Diesel, Alexandra K Kiemer, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|July 26, 2020
Menthacarin attenuates experimental colitisKorina Alliger, Mohammad Khalil, Beatrix König, et al.
Environmental Microbiology|February 2, 2011
Depicting more accurate pictures of protistan community complexity using pyrosequencing of hypervariable SSU rRNA gene regionsAnke Behnke, Matthias Engel, Richard Christen, et al.
Journal of Medicinal Chemistry|March 15, 2017
First Bispecific Inhibitors of the Epidermal Growth Factor Receptor Kinase and the NF-κB Activity As Novel Anticancer AgentsMostafa M Hamed, Sarah S Darwish, Jennifer Herrmann, et al.
Journal of Medicinal Chemistry|July 18, 2013
Highly potent and selective nonsteroidal dual inhibitors of CYP17/CYP11B2 for the treatment of prostate cancer to reduce risks of cardiovascular diseasesMariano A E Pinto-Bazurco Mendieta, Qingzhong Hu, Matthias Engel, et al.
FEMS Microbiology Ecology|November 19, 2011
Sample pooling obscures diversity patterns in intertidal ciliate community composition and structureMatthias Engel, Anke Behnke, Sara Bauerfeld, et al.
European Journal of Medicinal Chemistry|September 8, 2018
Development of novel 2,4-bispyridyl thiophene-based compounds as highly potent and selective Dyrk1A inhibitors. Part I: Benzamide and benzylamide derivativesSarah S Darwish, Mohammad Abdel-Halim, Mohamed Salah, et al.
Medicinal Research Reviews|October 20, 2022
An overview of cdc2-like kinase 1 (Clk1) inhibitors and their therapeutic indicationsAhmed K ElHady, Dalia S El-Gamil, Ashraf H Abadi, et al.
ACS Chemical Neuroscience|September 24, 2014
First selective dual inhibitors of tau phosphorylation and Beta-amyloid aggregation, two major pathogenic mechanisms in Alzheimer's diseaseMarica Mariano, Christian Schmitt, Parisa Miralinaghi, et al.
Steroids|June 9, 2015
New biaryl-chalcone derivatives of pregnenolone via Suzuki-Miyaura cross-coupling reaction. Synthesis, CYP17 hydroxylase inhibition activity, QSAR, and molecular docking studyNajim A Al-Masoudi, Rawaa A Kadhim, Nabeel A Abdul-Rida, et al.
Journal of Medicinal Chemistry|July 25, 2014
Discovery and optimization of 1,3,5-trisubstituted pyrazolines as potent and highly selective allosteric inhibitors of protein kinase C-ζMohammad Abdel-Halim, Britta Diesel, Alexandra K Kiemer, et al.
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