EXTRAPULMONARY PHYSIOLOGY & PATHOPHYSIOLOGY

(572) Changes in total IgE levels and fungal acquisition in People with CF before and after Elexacaftor/Tezacaftor/Ivacaftor Initiation

(573) Intravenous versus oral iron supplementation for iron deficiency in people with CF

(574) Determining the Minimal Clinically Important Difference for the 22-Question SinoNasal Outcome Test (SNOT-22) in People with Cystic Fibrosis

(575) Chronic rhinosinusitis in cystic fibrosis: a review of surgical management and our surgical experience.

(577) SGLT1 is associated with ER stress response in CF and transcriptionally regulated by XBP1s

(578) Single-cell RNA sequencing and CFTR functional analysis of human eccrine sweat glands establish a viable method for investigating CF genotypic-phenotypic heterogeneity

(579) Integrin activation in monocytes as a novel potential test for CFTR targeted compounds in Cystic Fibrosis.

(580) Preservation of β-cell Function in Pancreatic Insufficient Cystic Fibrosis with Highly Effective CFTR Modulator therapy.

(581) Effects of Cftr genotype on circadian system function

(582) Cystic Fibrosis Porcine Pancreatic Duct Cell Culture Models to Study Disease Pathophysiology

(583) Loss of AGTR2 Confers Protection from Hepatic Steatosis and Mortality in Ketogenic CF Mice

(584) Prominent role of gut dysbiosis in the pathogenesis of cystic fibrosis related cholangiopathy

(585) CFTR Contributes to Chloride Homeostasis in Swine Sensory Neurons

(586) ΔF508-CFTR mutation in C57BL/6 and Collaborative Cross mice to unravel the contribution of genetic background in the CF disease phenotype

(587) Evaluation of the extrapulmonary benefits after initiation of elexacaftor/tezacaftor/ivacaftor in pediatric patients

(588) The Relationship between Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction and Impairment in Limb Muscle Contractile Function in Adults with Cystic Fibrosis