Rebecca Minso

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

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Found 11 publications

CFTR activity in nasal potential difference of adults with idiopathic bronchiectasis.

CFTR activity in nasal potential difference of adults with idiopathic bronchiectasis.

Journal: Respiratory research

Published: November 25, 2025

Genotype and transcript processing of the tumour necrosis factor receptor TNFRSF1A in epithelial cells: implications for survival in cystic fibrosis.

Genotype and transcript processing of the tumour necrosis factor receptor TNFRSF1A in epithelial cells: implications for survival in cystic fibrosis.

Journal: EBioMedicine

Published: October 10, 2024

The Cystic Fibrosis Upper and Lower Airway Metagenome.

The Cystic Fibrosis Upper and Lower Airway Metagenome.

Journal: Microbiology spectrum

Published: March 09, 2023

Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depending on age and lung disease severity.

Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depending on age and lung disease severity.

Journal: Frontiers in pharmacology

Published: February 22, 2023

Differential effects of ELX/TEZ/IVA on organ-specific CFTR function in two patients with the rare CFTR splice mutations c.273+1G>A and c.165-2A>G.

Differential effects of ELX/TEZ/IVA on organ-specific CFTR function in two patients with the rare CFTR splice mutations c.273+1G>A and c.165-2A>G.

Journal: Frontiers in pharmacology

Published: January 29, 2023

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.

Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.

Journal: Frontiers in pharmacology

Published: December 02, 2022

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles.

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles.

Journal: American journal of respiratory and critical care medicine

Published: December 22, 2021

Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters.

Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: March 13, 2021

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.

Journal: BMJ open respiratory research

Published: August 04, 2020

Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases.

Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases.

Journal: ERJ open research

Published: June 20, 2020

Functional analysis of the p.[Arg74Trp;Val201Met;Asp1270Asn]/p.Phe508del CFTR mutation genotype in human native colon.

Functional analysis of the p.[Arg74Trp;Val201Met;Asp1270Asn]/p.Phe508del CFTR mutation genotype in human native colon.

Journal: Molecular genetics & genomic medicine

Published: October 11, 2017

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Last Updated: 09/26/2026