The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance—challenges and future research opportunities
CLR Barratt, L Björndahl, CJ De Jonge… - Human reproduction …, 2017 - academic.oup.com
BACKGROUND Herein, we describe the consensus guideline methodology, summarize the
evidence-based recommendations we provided to the World Health Organization (WHO) for …
evidence-based recommendations we provided to the World Health Organization (WHO) for …
[HTML][HTML] Pseudomonas aeruginosa infection in patients with cystic fibrosis: scientific evidence regarding clinical impact, diagnosis, and treatment
LVRF Silva Filho, FA Ferreira, FJC Reis… - Jornal Brasileiro de …, 2013 - SciELO Brasil
Evidence-based techniques have been increasingly used in the creation of clinical
guidelines and the development of recommendations for medical practice. The use of levels …
guidelines and the development of recommendations for medical practice. The use of levels …
Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145,-223, and-494 is altered in ΔF508 cystic fibrosis airway epithelium
IK Oglesby, SH Chotirmall, NG McElvaney… - The Journal of …, 2013 - journals.aai.org
Expression of the cystic fibrosis transmembrane conductance regulator (CFTR) is altered in
individuals with the ΔF508 CFTR mutation. We previously reported differential expression of …
individuals with the ΔF508 CFTR mutation. We previously reported differential expression of …
Ivacaftor improves rhinologic, psychologic, and sleep‐related quality of life in G551D cystic fibrosis patients
J McCormick, DY Cho, B Lampkin… - International forum of …, 2019 - Wiley Online Library
Background Ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR)
potentiator that improves pulmonary function in cystic fibrosis (CF) patients with at least 1 …
potentiator that improves pulmonary function in cystic fibrosis (CF) patients with at least 1 …
Lack of standardization in the procedures for mycological examination of sputum samples from CF patients: a possible cause for variations in the prevalence of …
Filamentous fungi and yeasts are increasingly isolated from respiratory secretions of
patients with cystic fibrosis (CF), and persistent fungal colonization of the airways of such …
patients with cystic fibrosis (CF), and persistent fungal colonization of the airways of such …
[HTML][HTML] Myxobacteria-derived outer membrane vesicles: potential applicability against intracellular infections
A Goes, P Lapuhs, T Kuhn, E Schulz, R Richter… - Cells, 2020 - mdpi.com
In 2019, it was estimated that 2.5 million people die from lower tract respiratory infections
annually. One of the main causes of these infections is Staphylococcus aureus, a bacterium …
annually. One of the main causes of these infections is Staphylococcus aureus, a bacterium …
Cystic fibrosis transmembrane conductance regulator–modifying medications: the future of cystic fibrosis treatment
RS Pettit - Annals of Pharmacotherapy, 2012 - journals.sagepub.com
OBJECTIVE: To review and evaluate cystic fibrosis transmembrane conductance regulator
(CFTR) modulators for the treatment of cystic fibrosis (CF). DATA SOURCES: Literature was …
(CFTR) modulators for the treatment of cystic fibrosis (CF). DATA SOURCES: Literature was …
[HTML][HTML] Cystic fibrosis related liver disease—another black box in hepatology
K Staufer, E Halilbasic, M Trauner… - International journal of …, 2014 - mdpi.com
Due to improved medical care, life expectancy in patients with cystic fibrosis (CF) has
veritably improved over the last decades. Importantly, cystic fibrosis related liver disease …
veritably improved over the last decades. Importantly, cystic fibrosis related liver disease …
[HTML][HTML] Genetics of CFTR and male infertility
JM Bieniek, CD Lapin, KA Jarvi - Translational andrology and …, 2021 - ncbi.nlm.nih.gov
Cystic fibrosis (CF) is a rare autosomal-recessive disorder manifested as multisystem organ
dysfunction. The cystic fibrosis transmembrane conductance regulator (CFTR) protein …
dysfunction. The cystic fibrosis transmembrane conductance regulator (CFTR) protein …
Non-coding RNA in cystic fibrosis
AMA Glasgow, C De Santi… - Biochemical Society …, 2018 - portlandpress.com
Non-coding RNAs (ncRNAs) are an abundant class of RNAs that include small ncRNAs,
long non-coding RNAs (lncRNA) and pseudogenes. The human ncRNA atlas includes …
long non-coding RNAs (lncRNA) and pseudogenes. The human ncRNA atlas includes …