Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis. - Wikidata - awgldk - TriplyDB

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

http://www.wikidata.org/entity/Q36254246

about

Cystic fibrosis chronic rhinosinusitis: a comprehensive review Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats Origins of cystic fibrosis lung disease Precision Genomic Medicine in Cystic Fibrosis Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor.Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis.Lentiviral vector gene transfer to porcine airways.Acidic pH increases airway surface liquid viscosity in cystic fibrosis Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies Lessons learned from the cystic fibrosis pig.Lentiviral-mediated phenotypic correction of cystic fibrosis pigs.CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypes New insights into the pathogenesis of cystic fibrosis sinusitis Management of the upper airway in cystic fibrosis.Tailored Pig Models for Preclinical Efficacy and Safety Testing of Targeted Therapies.Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model Characterization of primary rat nasal epithelial cultures in CFTR knockout rats as a model for CF sinus disease.Sinus hypoplasia in the cystic fibrosis rat resolves in the absence of chronic infection.Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.Roadmap for an early gene therapy for cystic fibrosis airway disease.Innate immunity and chronic rhinosinusitis: What we have learned from animal models.Temporal bone pneumatization in cystic fibrosis: a correlation with genotype?Paranasal sinus size is decreased in CFTR heterozygotes with chronic rhinosinusitis.Prospective transfrontal sheep model of skull-base reconstruction using vascularized mucosa.Medical and Surgical Advancements in the Management of Cystic Fibrosis Chronic Rhinosinusitis.The influence of norepinephrine and phenylephrine on cerebral perfusion and oxygenation during propofol-remifentanil and propofol-remifentanil-dexmedetomidine anaesthesia in piglets.Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs.Clinician assessment of paranasal sinus pneumatization is correlated with total sinus volume.

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P2860

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

http://www.wikidata.org/entity/Q36254246

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

@zh-cn

name

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

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Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

@en

type

label

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

@ast

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

@en

prefLabel

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

@ast

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

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The Laryngoscope

P1476

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

@en

P2093

Andrea E Potash

http://www.w3.org/2001/XMLSchema#string

Eugene H Chang

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Michael J Welsh

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Nicholas D Gansemer

http://www.w3.org/2001/XMLSchema#string

Philip H Karp

http://www.w3.org/2001/XMLSchema#string

Sarah Ernst

http://www.w3.org/2001/XMLSchema#string

Tanner J Wallen

http://www.w3.org/2001/XMLSchema#string

Thomas O Moninger

http://www.w3.org/2001/XMLSchema#string

P2860

Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

Impact of sinusitis in cystic fibrosis.

Management of sinusitis in cystic fibrosis by endoscopic surgery and serial antimicrobial lavage. Reduction in recurrence requiring surgery.

Discovery of glycine hydrazide pore-occluding CFTR inhibitors: mechanism, structure-activity analysis, and in vivo efficacy.

Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth.

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.

Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia.

The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs.

Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.

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1898-1905

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scholarly article

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10.1002/LARY.23392

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9

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122

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David Meyerholz

Alejandro A Pezzulo

Leah R Reznikov

Jessica C Sieren

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2012-06-18T00:00:00Z

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227342963

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22711071

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cystic fibrosis

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3449319

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