Intestinal Smooth Muscle Dysfunction Develops Postnatally in Cystic Fibrosis Mice

Cystic fibrosis growth retardation is not correlated with loss of Cftr in the intestinal epithelium

(2011) Craig A. Hodges et al.   AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY

Lack of Cystic Fibrosis Transmembrane Conductance Regulator in CD3+Lymphocytes Leads to Aberrant Cytokine Secretion and Hyperinflammatory Adaptive Immune Responses

(2010) Christian Mueller et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

Critical role of cytosolic phospholipase A2  in bronchial mucus hypersecretion in CFTR-deficient mice

(2010) F. Dif et al.   EUROPEAN RESPIRATORY JOURNAL

Fatty acid metabolism in cystic fibrosis

(2010) Birgitta Strandvik   PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS

Cyclooxygenase Allosterism, Fatty Acid-mediated Cross-talk between Monomers of Cyclooxygenase Homodimers

(2009) Chong Yuan et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator–dependent bicarbonate secretion

(2009) Mary Abigail S. Garcia et al.   JOURNAL OF CLINICAL INVESTIGATION

Expression and Distribution of Cystic Fibrosis Transmembrane Conductance Regulator in Neurons of the Human Brain

(2009) Yong Guo et al.   JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY

Enteric circular muscle dysfunction in the cystic fibrosis mouse small intestine

(2009) r. c. de lisle et al.   NEUROGASTROENTEROLOGY AND MOTILITY

Role of the Cystic Fibrosis Transmembrane Conductance Channel in Human Airway Smooth Muscle

(2008) Marie-Claire Michoud et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

Knockout mouse models for intestinal electrolyte transporters and regulatory PDZ adaptors: new insights into cystic fibrosis, secretory diarrhoea and fructose-induced hypertension

(2008) Ursula Seidler et al.   EXPERIMENTAL PHYSIOLOGY

Generation of a conditional null allele forCftrin mice

(2008) Craig A. Hodges et al.   GENESIS

Cell culture models demonstrate that CFTR dysfunction leads to defective fatty acid composition and metabolism

(2008) Charlotte Andersson et al.   JOURNAL OF LIPID RESEARCH

Altered Eicosanoid Metabolism in the Cystic Fibrosis Mouse Small Intestine

(2008) Robert C De Lisle et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis

(2008) Paul M Quinton   LANCET