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BMC Genetics|April 11, 2008
Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis miceBalázs Tóth, Martina Wilke, Frauke Stanke, et al.Nature Nanotechnology|January 30, 2019
Self-assembled peptide-poloxamine nanoparticles enable in vitro and in vivo genome restoration for cystic fibrosisShan Guan, Antje Munder, Silke Hedtfeld, et al.Journal of Medical Genetics|September 15, 2010
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epitheliaFrauke Stanke, Tim Becker, Vinod Kumar, et al.BMJ Open Respiratory Research|October 6, 2020
Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat testRebecca Minso, Angela Schulz, Christian Dopfer, et al.Stem Cell Research & Therapy|October 20, 2025
Human induced pluripotent stem cells for in vitro modeling of impaired mucociliary clearance in cystic fibrosis lung diseaseMark-Christian Klassen, Anita Balázs, Janina Zöllner, et al.Ebiomedicine|July 11, 2025
Genotype and transcript processing of the tumour necrosis factor receptor TNFRSF1A in epithelial cells: implications for survival in cystic fibrosisAlexander Uden, Inga Dunsche, Sabina Janciauskiene, et al.Human Mutation|May 23, 2009
Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like diseaseAbul Kalam Azad, Robert Rauh, François Vermeulen, et al.Pageof 5