Journal of CF

Posting content from the Journal of Cystic Fibrosis, European Cystic Fibrosis Society and Cystic Fibrosis Research News. Follows do not indicate endorsement.

[Journal of CF @JournalofCF]

We are seeking an early career researcher to run this Twitter feed, promoting #JournalCF content and European #cysticfibrosis Society events/news. This is a voluntary role. To apply, please DM a CV and a letter of interest/qualifications by 31st January.

[Journal of CF @JournalofCF]

Seeking applications for an Administrative & Communication Assistant. It is a full time position, split equally between #cysticfibrosis Europe and the ECFS patient registry. Deadline for applications is 1st February 2020. For more information, visit https://t.co/tWKmnlyEtk

[Journal of CF @JournalofCF]

The Second Announcement of the #ECFS2020 #cysticfibrosis Conference in Lyon is available: https://t.co/WxOBojn8tk

[Journal of CF @JournalofCF]

#JournalCF Letter to the Editor explores the utility of n-of-1 trials to expand access to CFTR modulators for rare #cysticfibrosis mutations.
https://t.co/s2v30TcUMp

[Journal of CF @JournalofCF]

To foster basic and translational research on #cysticfibrosis, a number of European Post-Doctoral 2-year duration Research Fellowships will be supported the ECFS and CF Europe.
More information on: https://t.co/NtQzZJOKjk

[Journal of CF @JournalofCF]

#openaccess publication in #JournalCF on how rescue of #cysticfibrosis W1282X-CFTR requires inhibition of nonsense mediated decay alongside corrector and potentiator therapy. https://t.co/OnkqS9jock

[Journal of CF @JournalofCF]

The abstract submission deadline for the ECFS #cysticfibrosis Basic Science Conference is this Friday 10 January 23:59 (CET)!! Submit your abstract here https://t.co/1djJvwJ8Ca

[Journal of CF @JournalofCF]

Data from a recent #JournalCF manuscript finds strong toll-like receptor responses in #cysticfibrosis patients are associated with higher lung function.
https://t.co/iZF58nXBta

[Journal of CF @JournalofCF]

Read in #JournalCF an #openaccess review of intestinal organoid models for #cysticfibrosis research. https://t.co/2HoiRv6MLm

[Journal of CF @JournalofCF]

Also #openaccess in #JournalCF, alterations of bone microarchitecture and composition at birth in #cysticfibrosis pigs suggest bone defects may be a primary aspect of disease.
https://t.co/b8SPCnUIPf

[Journal of CF @JournalofCF]

An #openaccess #JournalCF publication on use of ivacaftor in #cysticfibrosis with residual function: Lung function results from an N-of-1 study. https://t.co/lPDNx59ljc

[Journal of CF @JournalofCF]

Published in #JournalCF is new evidence demonstrating the utility of lung clearance index as an effective primary endpoint in #cysticfibrosis phase III clinical trial. https://t.co/cTz6WNsCuw

[Journal of CF @JournalofCF]

#JournalCF Letter to the Editor - positive clinical outcomes following ivacaftor treatment of #cysticfibrosis genotype 3272–26A > G/Q493X. https://t.co/AHljFeQBjC

[Journal of CF @JournalofCF]

Read results from a survey of #cysticfibrosis community and clinicians about treatment withdrawal research to reduce treatment burden. #JournalCF https://t.co/VcSD2JtvMP

[Journal of CF @JournalofCF]

New evidence is emerging that has to be considered as an additional opportunistic pathogen in #cysticfibrosis. Read further in #JournalCF. https://t.co/L3lT3cWKEb

[Journal of CF @JournalofCF]

Read a review of the new insights gained into how small molecules for #cysticfibrosis can rescue CFTR structure and function. #JournalCF https://t.co/glHUfzAJbn

[Journal of CF @JournalofCF]

New #JournalCF study asks - Can exercise replace airway clearance techniques in #cysticfibrosis? A survey of patients and healthcare professionals. https://t.co/EY5m6A6MNS

[Journal of CF @JournalofCF]

#JournalCF study used a questionnaire to summarise the lived experience of #cysticfibrosis treatment burden and suggest research themes aimed at reducing burden. https://t.co/hkrzdwbME2

[Journal of CF @JournalofCF]

Intestinal organoids function varied between #cysticfibrosis subjects with homozygous F508del, correlates with pulmonary and nutritional parameters and may underly clinical heterogeneity. #JournalCF https://t.co/xVbJozw1g2

[Journal of CF @JournalofCF]

#CFResearchNews: Could quality improvement programs improve adherence to #cysticfibrosis related diabetes screening and management guidelines? https://t.co/RuNy8ccCce