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Mario Milani

Showing results (91-100 of 101) with videos related to

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Nature Communications|August 2, 2020
Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral SclerosisLuca Muzio, Riccardo Sirtori, Davide Gornati, et al.
Scientific Reports|August 6, 2025
Identification of new selective CD36 inhibitors to potentiate HER2-targeted therapy in HER2-positive breast cancerLorenzo Castagnoli, Francesco Bonì, Martina Bigliardi, et al.
Journal of Medicinal Chemistry|June 7, 2021
Synthesis and Characterization of Novel Mono- and Bis-Guanyl Hydrazones as Potent and Selective ASIC1 Inhibitors Able to Reduce Brain Ischemic InsultDavide Gornati, Roselia Ciccone, Antonio Vinciguerra, et al.
Bioorganic & Medicinal Chemistry|October 16, 2012
Dimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part II: Structural and biological characterizationDaniele Lecis, Eloise Mastrangelo, Laura Belvisi, et al.
British Journal of Haematology|October 6, 2004
Intravascular lymphoma: clinical presentation, natural history, management and prognostic factors in a series of 38 cases, with special emphasis on the 'cutaneous variant'Andrés J M Ferreri, Elías Campo, John F Seymour, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 15, 2003
Prognostic scoring system for primary CNS lymphomas: the International Extranodal Lymphoma Study Group experienceAndrés J M Ferreri, Jean-Yves Blay, Michele Reni, et al.
ACS Infectious Diseases|August 3, 2024
4-(3-Phenylsulfonylindol-2-yl)-1-(pyridin-2-yl)piperazinyl-methanones as Potent Inhibitors of both SARS-CoV-2 and HCoV-OC43 VirusesMichela Puxeddu, Manuela Donalisio, Joachim Jakob Bugert, et al.
Bioorganic & Medicinal Chemistry|July 22, 2009
Rational design, synthesis and characterization of potent, non-peptidic Smac mimics/XIAP inhibitors as proapoptotic agents for cancer therapyPierfausto Seneci, Aldo Bianchi, Cristina Battaglia, et al.
Antiviral Research|December 1, 2009
Structure and functionality in flavivirus NS-proteins: perspectives for drug designMichela Bollati, Karin Alvarez, René Assenberg, et al.
Iscience|October 12, 2023
A quinolin-8-ol sub-millimolar inhibitor of UGGT, the ER glycoprotein folding quality control checkpointKevin P Guay, Roberta Ibba, J L Kiappes, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Nature Communications|August 2, 2020
Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral SclerosisLuca Muzio, Riccardo Sirtori, Davide Gornati, et al.
Scientific Reports|August 6, 2025
Identification of new selective CD36 inhibitors to potentiate HER2-targeted therapy in HER2-positive breast cancerLorenzo Castagnoli, Francesco Bonì, Martina Bigliardi, et al.
Journal of Medicinal Chemistry|June 7, 2021
Synthesis and Characterization of Novel Mono- and Bis-Guanyl Hydrazones as Potent and Selective ASIC1 Inhibitors Able to Reduce Brain Ischemic InsultDavide Gornati, Roselia Ciccone, Antonio Vinciguerra, et al.
Bioorganic & Medicinal Chemistry|October 16, 2012
Dimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part II: Structural and biological characterizationDaniele Lecis, Eloise Mastrangelo, Laura Belvisi, et al.
British Journal of Haematology|October 6, 2004
Intravascular lymphoma: clinical presentation, natural history, management and prognostic factors in a series of 38 cases, with special emphasis on the 'cutaneous variant'Andrés J M Ferreri, Elías Campo, John F Seymour, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 15, 2003
Prognostic scoring system for primary CNS lymphomas: the International Extranodal Lymphoma Study Group experienceAndrés J M Ferreri, Jean-Yves Blay, Michele Reni, et al.
ACS Infectious Diseases|August 3, 2024
4-(3-Phenylsulfonylindol-2-yl)-1-(pyridin-2-yl)piperazinyl-methanones as Potent Inhibitors of both SARS-CoV-2 and HCoV-OC43 VirusesMichela Puxeddu, Manuela Donalisio, Joachim Jakob Bugert, et al.
Bioorganic & Medicinal Chemistry|July 22, 2009
Rational design, synthesis and characterization of potent, non-peptidic Smac mimics/XIAP inhibitors as proapoptotic agents for cancer therapyPierfausto Seneci, Aldo Bianchi, Cristina Battaglia, et al.
Antiviral Research|December 1, 2009
Structure and functionality in flavivirus NS-proteins: perspectives for drug designMichela Bollati, Karin Alvarez, René Assenberg, et al.
Iscience|October 12, 2023
A quinolin-8-ol sub-millimolar inhibitor of UGGT, the ER glycoprotein folding quality control checkpointKevin P Guay, Roberta Ibba, J L Kiappes, et al.
Pageof 11