OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
In silico analysis and theratyping of an ultra-rare CFTR genotype (W57G/A234D) in primary human rectal and nasal epithelial cells
Karina Kleinfelder, Virginia Lotti, Adriana Eramo, et al.
iScience (2023) Vol. 26, Iss. 11, pp. 108180-108180
Open Access | Times Cited: 8
Karina Kleinfelder, Virginia Lotti, Adriana Eramo, et al.
iScience (2023) Vol. 26, Iss. 11, pp. 108180-108180
Open Access | Times Cited: 8
Showing 8 citing articles:
Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in a Cystic Fibrosis Child With L1077P Mutation
Angela Sepe, Alice Castaldo, Chiara Cimbalo, et al.
Pediatric Pulmonology (2025) Vol. 60, Iss. 2
Closed Access
Angela Sepe, Alice Castaldo, Chiara Cimbalo, et al.
Pediatric Pulmonology (2025) Vol. 60, Iss. 2
Closed Access
How Effectively Can Oxidative Stress and Inflammation Be Reversed When CFTR Function Is Pharmacologically Improved?
Valeria Rachela Villella, Alice Castaldo, Filippo Scialò, et al.
Antioxidants (2025) Vol. 14, Iss. 3, pp. 310-310
Open Access
Valeria Rachela Villella, Alice Castaldo, Filippo Scialò, et al.
Antioxidants (2025) Vol. 14, Iss. 3, pp. 310-310
Open Access
Elexacaftor/Tezacaftor/Ivacaftor Efficacy in a Cohort of Italian Patients with CFTR Rare Mutations
Francesca Lucca, Sonia Volpi, Mirco Ros, et al.
International Journal of Translational Medicine (2025) Vol. 5, Iss. 1, pp. 11-11
Open Access
Francesca Lucca, Sonia Volpi, Mirco Ros, et al.
International Journal of Translational Medicine (2025) Vol. 5, Iss. 1, pp. 11-11
Open Access
Mouse intestine as a useful model for CFTR electrophysiology function analysis
Speranza Esposito, Fatima Domenica Elisa De Palma, Gustavo Cernera, et al.
Methods in cell biology (2025)
Closed Access
Speranza Esposito, Fatima Domenica Elisa De Palma, Gustavo Cernera, et al.
Methods in cell biology (2025)
Closed Access
Identification of an ultra-rare Alu insertion in the CFTR gene: Pitfalls and challenges in genetic test interpretation
Speranza Esposito, Immacolata Zollo, Valeria Rachela Villella, et al.
Clinica Chimica Acta (2024) Vol. 558, pp. 118317-118317
Open Access | Times Cited: 2
Speranza Esposito, Immacolata Zollo, Valeria Rachela Villella, et al.
Clinica Chimica Acta (2024) Vol. 558, pp. 118317-118317
Open Access | Times Cited: 2
Cystic Fibrosis Modulator Therapies: Bridging Insights from CF to other Membrane Protein Misfolding Diseases
Minsoo Kim, Lars Plate
Israel Journal of Chemistry (2024) Vol. 64, Iss. 12
Closed Access | Times Cited: 1
Minsoo Kim, Lars Plate
Israel Journal of Chemistry (2024) Vol. 64, Iss. 12
Closed Access | Times Cited: 1
Benchmarking organ-specific responses to therapies in tissues differentiated from Cystic Fibrosis patient derived iPSCs
Abdelkader Daoud, Sunny Xia, Onofrio Laselva, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Abdelkader Daoud, Sunny Xia, Onofrio Laselva, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Non pathological sweat test, pancreatic insufficiency and Cystic Fibrosis: an unusual case in a child with F508del-duplication of exons 1–3 CFTR genotype
Vito Terlizzi, Cristina Fevola, Alice Castaldo, et al.
BMC Pediatrics (2024) Vol. 24, Iss. 1
Open Access
Vito Terlizzi, Cristina Fevola, Alice Castaldo, et al.
BMC Pediatrics (2024) Vol. 24, Iss. 1
Open Access
