Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
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Animal Models of Cystic Fibrosis Pathology: Phenotypic Parallels and DivergencesCurrent progress of genetically engineered pig models for biomedical researchOrigins of cystic fibrosis lung diseasePrecision Genomic Medicine in Cystic FibrosisImmunohistochemical detection of arginase-I expression in formalin-fixed lung and other tissuesA functional anatomic defect of the cystic fibrosis airway.Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.Ferret and pig models of cystic fibrosis: prospects and promise for gene therapy.Hybrid nonviral/viral vector systems for improved piggyBac DNA transposon in vivo deliveryPorcine models of digestive disease: the future of large animal translational research.Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis PigletsRestoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutationQuantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretomePartial Restoration of CFTR Function in cftr-Null Mice following Targeted Cell Replacement Therapy.Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction.Pancreatic pathophysiology in cystic fibrosis.Immunohistochemical Detection of Markers for Translational Studies of Lung Disease in Pigs and HumansElectrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.Human, Pig, and Mouse Interferon-Induced Transmembrane Proteins Partially Restrict Pseudotyped Lentiviral Vectors.Airway acidification initiates host defense abnormalities in cystic fibrosis mice.Lessons learned from the cystic fibrosis pig.A novel culture system for adult porcine intestinal cryptsLentiviral-mediated phenotypic correction of cystic fibrosis pigs.CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypesAnchored PDE4 regulates chloride conductance in wild-type and ΔF508-CFTR human airway epithelia.Identification of the MUC2 Promoter as a Strong Promoter for Intestinal Gene Expression through Generation of Transgenic Quail Expressing GFP in Gut Epithelial CellsGenotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets.Does epithelial sodium channel hyperactivity contribute to cystic fibrosis lung disease?Genetically modified pigs to model human diseases.Anatomy and bronchoscopy of the porcine lung. A model for translational respiratory medicine.Modeling the lung: Design and development of tissue engineered macro- and micro-physiologic lung models for research use.Cystic fibrosis genetics: from molecular understanding to clinical application.Tailored Pig Models for Preclinical Efficacy and Safety Testing of Targeted Therapies.Immunohistochemical Markers for Prospective Studies in Neurofibromatosis-1 Porcine Models.Simple and reproducible approaches for the collection of select porcine ganglia.Postnatal airway growth in cystic fibrosis piglets.Genetic medicines for CF: Hype versus reality.Genome editing revolutionize the creation of genetically modified pigs for modeling human diseases.The CF gastrointestinal microbiome: Structure and clinical impact.
P2860
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P2860
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
@en
type
label
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
@en
prefLabel
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
@en
P2093
P2860
P50
P356
P1476
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.
@en
P2093
Christine Wohlford-Lenane
Drake C Bouzek
Emma E Hornick
Eugene H Chang
George A Nelson
James D McMenimen
Jeng-Haur Chen
Katrina L Bogan
Mark J Hoegger
Melissa S Samuel
P2860
P304
P356
10.1172/JCI68867
P407
P50
P577
2013-05-08T00:00:00Z