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Journal of Muscle Research and Cell Motility|November 1, 2011
Ahnak1 is a tuneable modulator of cardiac Ca(v)1.2 calcium channel activityInes Pankonien, Julio L Alvarez, Anke Doller, et al.
Pflugers Archiv : European Journal of Physiology|August 13, 2016
Relationship between TMEM16A/anoctamin 1 and LRRC8ARoberta Benedetto, Lalida Sirianant, Ines Pankonien, et al.
Frontiers in Pharmacology|September 5, 2025
CFTR ion transport deficiency primes the epithelium for partial epithelial-mesenchymal transition in cystic fibrosisCláudia S Rodrigues, Matilde Canto, Raquel Torres, et al.
Life Science Alliance|November 17, 2019
TMEM16A chloride channel does not drive mucus productionFilipa B Simões, Margarida C Quaresma, Luka A Clarke, et al.
Frontiers in Molecular Biosciences|April 3, 2023
Personalized medicine: Function of CFTR variant p.Arg334Trp is rescued by currently available CFTR modulatorsVioleta Railean, Cláudia S Rodrigues, Sofia S Ramalho, et al.
Life Science Alliance|May 2, 2022
Exploring YAP1-centered networks linking dysfunctional CFTR to epithelial-mesenchymal transitionMargarida C Quaresma, Hugo M Botelho, Ines Pankonien, et al.
Respiratory Medicine|July 11, 2025
N1303K (p.Asn1303Lys) variant: Expanding frontiers in the treatment of cystic fibrosisJoana Pacheco, Leonor Almeida, Rita Boaventura, et al.
Cell Death & Disease|October 27, 2020
Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transitionMargarida C Quaresma, Ines Pankonien, Luka A Clarke, et al.
Progress in Retinal and Eye Research|September 8, 2024
The role of CFTR in the eye, and the effect of early highly effective modulator treatment for cystic fibrosis on eye healthElena K Schneider-Futschik, Yimin Zhu, Danni Li, et al.
Molecular Diagnosis & Therapy|September 13, 2025
Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular ModelsVioleta Railean, Cláudia S Rodrigues, Ines Pankonien, et al.
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