Pages that link to "Q36556391"

The following pages link to Cystic fibrosis mouse models (Q36556391):

Displaying 50 items.

• Pass the bicarb: the importance of HCO3– for mucin release (Q22306298) (← links)
• A novel host defense system of airways is defective in cystic fibrosis (Q24657774) (← links)
• Animal Models of Cystic Fibrosis Pathology: Phenotypic Parallels and Divergences (Q26747210) (← links)
• Microscale imaging of cilia-driven fluid flow (Q26826635) (← links)
• Gene therapy: light is finally in the tunnel (Q27000091) (← links)
• Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats (Q27316635) (← links)
• Airway Gland Structure and Function (Q28082284) (← links)
• Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer (Q28271767) (← links)
• The Pig: A Relevant Model for Evaluating the Neutrophil Serine Protease Activities during Acute Pseudomonas aeruginosa Lung Infection (Q28555083) (← links)
• Barriers to inhaled gene therapy of obstructive lung diseases: A review (Q29248141) (← links)
• The role of the UPS in cystic fibrosis (Q33307871) (← links)
• Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis mice (Q33327433) (← links)
• Tissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTR (Q33586056) (← links)
• Lung phenotype of juvenile and adult cystic fibrosis transmembrane conductance regulator-knockout ferrets. (Q33799679) (← links)
• Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis (Q33870016) (← links)
• Distribution and size of mucous glands in the ferret tracheobronchial tree. (Q33894239) (← links)
• Pathophysiological preconditions promoting mixed "black" pigment plus cholesterol gallstones in a DeltaF508 mouse model of cystic fibrosis (Q33994808) (← links)
• Generation of multipotent lung and airway progenitors from mouse ESCs and patient-specific cystic fibrosis iPSCs (Q34031395) (← links)
• Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis. (Q34090196) (← links)
• Completion of the swine genome will simplify the production of swine as a large animal biomedical model (Q34476881) (← links)
• Ferret and pig models of cystic fibrosis: prospects and promise for gene therapy (Q35200182) (← links)
• Coordinated international action to accelerate genome-to-phenome with FAANG, the Functional Annotation of Animal Genomes project (Q35215891) (← links)
• Efficient production of Fah-null heterozygote pigs by chimeric adeno-associated virus-mediated gene knockout and somatic cell nuclear transfer. (Q35249273) (← links)
• Cystic fibrosis: an inherited disease affecting mucin-producing organs (Q35665456) (← links)
• Porcine models of digestive disease: the future of large animal translational research. (Q35691021) (← links)
• Processing and function of CFTR-DeltaF508 are species-dependent (Q35991100) (← links)
• Chloride secretion by cultures of pig tracheal gland cells (Q35994809) (← links)
• 5'-adenosine monophosphate mediated cooling treatment enhances ΔF508-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) stability in vivo (Q36024047) (← links)
• Murine and human CFTR exhibit different sensitivities to CFTR potentiators (Q36122891) (← links)
• The pig as a model for investigating the role of neutrophil serine proteases in human inflammatory lung diseases. (Q36382772) (← links)
• Keratin K18 increases cystic fibrosis transmembrane conductance regulator (CFTR) surface expression by binding to its C-terminal hydrophobic patch (Q36418881) (← links)
• The Peter Pan paradigm (Q36473575) (← links)
• The cystic fibrosis gene: a molecular genetic perspective (Q36554624) (← links)
• Salt, chloride, bleach, and innate host defense (Q36608150) (← links)
• New animal models of cystic fibrosis: what are they teaching us? (Q36679834) (← links)
• Comparative biology of cystic fibrosis animal models (Q36744020) (← links)
• Loss of Cftr function exacerbates the phenotype of Na(+) hyperabsorption in murine airways (Q36770683) (← links)
• The porcine lung as a potential model for cystic fibrosis (Q36846439) (← links)
• Airway acidification initiates host defense abnormalities in cystic fibrosis mice. (Q36857687) (← links)
• Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs (Q36944556) (← links)
• The cystic fibrosis intestine (Q37122355) (← links)
• Postentry processing of recombinant adeno-associated virus type 1 and transduction of the ferret lung are altered by a factor in airway secretions. (Q37158813) (← links)
• Advances in mouse models of prostate cancer (Q37185527) (← links)
• Is Quorum Sensing Interference a Viable Alternative to Treat Pseudomonas aeruginosa Infections? (Q37254245) (← links)
• Pathophysiological basis of liver disease in cystic fibrosis employing a DeltaF508 mouse model (Q37269561) (← links)
• In vitro and murine efficacy and toxicity studies of nebulized SCC1, a methylated caffeine-silver(I) complex, for treatment of pulmonary infections (Q37274684) (← links)
• Relevance of granulocyte apoptosis to resolution of inflammation at the respiratory mucosa. (Q37349730) (← links)
• Influence of genetic background on genetically engineered mouse phenotypes (Q37407922) (← links)
• Proteases and antiproteases in chronic neutrophilic lung disease - relevance to drug discovery (Q37447482) (← links)
• Generation of SV40-transformed rabbit tracheal-epithelial-cell-derived blastocyst by somatic cell nuclear transfer (Q37522146) (← links)