From CFTR to a CF signalling network: a systems biology approach to study Cystic Fibrosis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: From CFTR to a CF signalling network: a systems biology approach to study Cystic Fibrosis ; volume:25 ; number:1 ; day:28 ; month:9 ; year:2024 ; pages:1-22 ; date:12.2024
BMC genomics ; 25, Heft 1 (28.9.2024), 1-22, 12.2024

Creator: Najm, Matthieu
Martignetti, Loredana
Cornet, Matthieu
Kelly-Aubert, Mairead
Sermet, Isabelle
Calzone, Laurence
Stoven, Véronique

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12864-024-10752-x

URN: urn:nbn:de:101:1-2412142102051.208691625327

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:37 AM CEST

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Najm, Matthieu
Martignetti, Loredana
Cornet, Matthieu
Kelly-Aubert, Mairead
Sermet, Isabelle
Calzone, Laurence
Stoven, Véronique
SpringerLink (Online service)

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From CFTR to a CF signalling network: a systems biology approach to study Cystic Fibrosis

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Other Objects (12)

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Rationale and design of the HIT-CF organoid study: stratifying cystic fibrosis patients based on intestinal organoid response to different CFTR-modulators

The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis

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CF Fungal Disease in the Age of CFTR Modulators

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Lived experiences of individuals with cystic fibrosis on CFTR-modulators

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Phenotyping ciliary dynamics and coordination in response to CFTR-modulators in Cystic Fibrosis respiratory epithelial cells

Targeted therapies to improve CFTR function in cystic fibrosis

Vectorized peptidic Inhibitors to rescue F508del-CFTR in Cystic Fibrosis

Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis

Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis

Rationale and design of the HIT-CF organoid study: stratifying cystic fibrosis patients based on intestinal organoid response to different CFTR-modulators

The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis

Targeting protein–protein interactions to rescue Δf508‐cftr: a novel corrector approach to treat cystic fibrosis

CF Fungal Disease in the Age of CFTR Modulators

The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability

Lived experiences of individuals with cystic fibrosis on CFTR-modulators

Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function

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Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis

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Rationale and design of the HIT-CF organoid study: stratifying cystic fibrosis patients based on intestinal organoid response to different CFTR-modulators

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Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function

Phenotyping ciliary dynamics and coordination in response to CFTR-modulators in Cystic Fibrosis respiratory epithelial cells

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