Michael Forte

Affiliations: 
Vollum Institute Oregon Health and Science University, Portland, OR 
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"Michael Forte"
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Publications

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Carraro M, Jones K, Sartori G, et al. (2020) The Unique Cysteine of F-ATP Synthase OSCP Subunit Participates in Modulation of the Permeability Transition Pore. Cell Reports. 32: 108095
Sileikyte J, Devereaux J, de Jong J, et al. (2019) Second generation inhibitors of the mitochondrial permeability transition pore with improved plasma stability. Chemmedchem
Šileikytė J, Forte M. (2019) The Mitochondrial Permeability Transition in Mitochondrial Disorders Oxidative Medicine and Cellular Longevity. 2019: 3403075-3403075
Stocco A, Schiavone M, Zulian A, et al. (2018) A mitochondrial therapy for Duchenne muscular dystrophy Biochimica Et Biophysica Acta. 1859
Antoniel M, Jones K, Antonucci S, et al. (2017) The unique histidine in OSCP subunit of F-ATP synthase mediates inhibition of the permeability transition pore by acidic pH. Embo Reports
Giorgio V, Burchell V, Schiavone M, et al. (2017) Ca(2+) binding to F-ATP synthase β subunit triggers the mitochondrial permeability transition. Embo Reports
Šileikytė J, Roy S, Schiavone M, et al. (2016) Discovery and characterization of small molecular inhibitors of the mitochondrial permeability transition pore Biochimica Et Biophysica Acta. 1857
Antoniel M, Spolaore B, Fogolari F, et al. (2016) The unique histidine of F-ATP synthase subunit OSCP mediates regulation of the permeability transition by matrix pH Biochimica Et Biophysica Acta. 1857
Šileikyte J, Forte M. (2016) Shutting down the pore: The search for small molecule inhibitors of the mitochondrial permeability transition Biochimica Et Biophysica Acta - Bioenergetics
Bernardi P, Rasola A, Forte M, et al. (2015) The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology. Physiological Reviews. 95: 1111-55
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