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Bioscience Reports|June 16, 2022
Molecular mechanisms of cystic fibrosis - how mutations lead to misfunction and guide therapyCarlos M Farinha, Isabelle CallebautCellular and Molecular Life Sciences : CMLS|October 5, 2016
From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and traffickingCarlos M Farinha, Sara CanatoSmall Gtpases|May 3, 2017
Rab GTPases regulate the trafficking of channels and transporters - a focus on cystic fibrosisCarlos M Farinha, Paulo MatosInternational Journal of Molecular Sciences|December 24, 2021
Revisiting CFTR Interactions: Old Partners and New PlayersCarlos M Farinha, Martina GentzschThe FEBS Journal|September 30, 2015
Repairing the basic defect in cystic fibrosis - one approach is not enoughCarlos M Farinha, Paulo MatosFEBS Letters|July 6, 2026
Regulation of CFTR stability at the plasma membrane-Mechanisms and therapeutic opportunities in cystic fibrosisCarlos M Farinha, João OliveiraMolecular and Cellular Biology|June 1, 2005
Most F508del-CFTR is targeted to degradation at an early folding checkpoint and independently of calnexinCarlos M Farinha, Margarida D AmaralBiochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|May 19, 2011
Teaching biochemistry at Lisbon University-Facing the challenge of the Bologna Declaration in the 25th anniversary of the biochemistry courseCarlos M Farinha, Ana Ponces FreireCurrent Pharmaceutical Design|January 22, 2013
Rescuing mutant CFTR: a multi-task approach to a better outcome in treating cystic fibrosisMargarida D Amaral, Carlos M FarinhaJournal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 15, 2020
Exploring the basic mechanisms in Cystic Fibrosis: Promoting data presentation and discussion at the 16th ECFS Basic Science ConferenceIsabelle Callebaut, Martin Mense, Carlos M FarinhaPageof 9