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Cystic Fibrosis

Cystic Fibrosis diagram by medicalstocks, Shutterstock
medicalstocks, Shutterstock

Cystic fibrosis is an autosomal recessive disease, which is the result of a genetic defect in the cystic fibrosis transmembrane conductance regulator (cftr) gene. Here is the latest research on this disease

Top 20 most recent papers
Nature Medicine

A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance

Nature MedicineJanuary 22, 2020
Raghu R ChivukulaDavid M Sabatini
89
2
Cell

A Therapy for Most with Cystic Fibrosis

CellJanuary 25, 2020
Christine E Bear
2
1
Nature Medicine

Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure

Nature MedicineJanuary 22, 2020
Hillary S HaydenLucas R Hoffman
9
1
European Journal of Public Health

Associations between health literacy and patient outcomes in adolescents and young adults with cystic fibrosis

European Journal of Public HealthJanuary 25, 2020
Abaigeal D JacksonGerardine Doyle
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society

Abnormal glucose tolerance and the 50-gram glucose challenge test in Cystic fibrosis

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis SocietyJanuary 25, 2020
Saba SheikhRonald C Rubenstein
Journal of Cell Science

What biologists want from their chloride reporters - a conversation between chemists and biologists

Journal of Cell ScienceJanuary 25, 2020
Matthew ZajacYamuna Krishnan
Analytical Biochemistry

Nanograss sensor for selective detection of Pseudomonas aeruginosa by pyocyanin identification in airway samples

Analytical BiochemistryJanuary 26, 2020
Fatima AlZahra'a AlatraktchiWinnie E Svendsen
1
Open Forum Infectious Diseases

Clinical Outcomes Associated With Escherichia coli Infections in Adults With Cystic Fibrosis: A Cohort Study

Open Forum Infectious DiseasesJanuary 25, 2020
B D EdwardsMichael D Parkins
1
Cellular and Molecular Life Sciences : CMLS

A SYK/SHC1 pathway regulates the amount of CFTR in the plasma membrane

Cellular and Molecular Life Sciences : CMLSJanuary 25, 2020
Cláudia Almeida LoureiroPeter Jordan
Antimicrobial Agents and Chemotherapy

A Phase I, dose-escalating study of safety and pharmacokinetics of inhaled dry powder vancomycin (AeroVanc) in volunteers and patients with cystic fibrosis: a new approach to therapy for methicillin-resistant Staphylococcus aureus

Antimicrobial Agents and ChemotherapyJanuary 23, 2020
Grant WatererTaneli Jouhikainen
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society

Identification of Mycobacterium porcinum in patients with cystic Fibrosis: Pathogen or contaminant?

Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis SocietyJanuary 27, 2020
Grace R PaulStella Antonara
Journal of Pediatric Genetics

Recurrent Metabolic Alkalosis in a Cystic Fibrosis Patient: Coexistence with Congenital Chloride Diarrhea

Journal of Pediatric GeneticsJanuary 25, 2020
Etna MasipCarmen Ribes-Koninckx
Journal of Pediatric Gastroenterology and Nutrition

Pancreatoscopy-directed Electrohydraulic Lithotripsy in a Pediatric Patient With Pancreas Divisum and Cystic Fibrosis

Journal of Pediatric Gastroenterology and NutritionJanuary 25, 2020
Karen QuelizaDouglas S Fishman
Clinical Nutrition : Official Journal of the European Society of Parenteral and Enteral Nutrition

Overweight, obesity and significant weight gain in adult patients with cystic fibrosis association with lung function and cardiometabolic risk factors

Clinical Nutrition : Official Journal of the European Society of Parenteral and Enteral NutritionJanuary 27, 2020
Anne BonhoureRémi Rabasa-Lhoret
BMJ Open

KMBARC registry: protocol for a multicentre observational cohort study on non-cystic fibrosis bronchiectasis in Korea

BMJ OpenJanuary 22, 2020
Hyun LeeKMBARC
1
World Journal of Hepatology

Lumacaftor/ivacaftor therapy is associated with reduced hepatic steatosis in cystic fibrosis patients

World Journal of HepatologyJanuary 23, 2020
Katherine KutneyBeth Kaminski
Scientific Reports

Plasma microRNA levels in male and female children with cystic fibrosis

Scientific ReportsJanuary 26, 2020
C MooneyC M Greene
Prenatal Diagnosis

Outcome of fetal echogenic bowel: a systematic review and meta-analysis

Prenatal DiagnosisJanuary 26, 2020
Alice D'AmicoFrancesco D'Antonio
1
Pediatric Pulmonology

Clinical communication preferences in cystic fibrosis and strategies to optimize care

Pediatric PulmonologyJanuary 25, 2020
Laura CooleyAnna M Georgiopoulos
1
Pathogens

Hypermutation as an Evolutionary Mechanism for Achromobacter xylosoxidans in Cystic Fibrosis Lung Infection

PathogensJanuary 25, 2020
Laura VeschettiGiovanni Malerba

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