Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.
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Instability of the insertional mutation in CftrTgH(neoim)Hgu cystic fibrosis mouse modelEpithelial Anion Transport as Modulator of Chemokine SignalingAnimal Models of Cystic Fibrosis Pathology: Phenotypic Parallels and DivergencesBarriers to inhaled gene therapy of obstructive lung diseases: A reviewRole of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.Pathophysiological preconditions promoting mixed "black" pigment plus cholesterol gallstones in a DeltaF508 mouse model of cystic fibrosis.Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model.Azithromycin reduces spontaneous and induced inflammation in DeltaF508 cystic fibrosis mice.Species-specific differences in mouse and human airway epithelial biology of recombinant adeno-associated virus transduction.Lentiviral vector gene transfer to porcine airways.Comparative biology of cystic fibrosis animal modelsGeneration of a conditional null allele for Cftr in mice.Pathophysiological basis of liver disease in cystic fibrosis employing a DeltaF508 mouse modelDisease-causing mutations in the cystic fibrosis transmembrane conductance regulator determine the functional responses of alveolar macrophagesThe cystic fibrosis of exocrine pancreasMechanosensitivity of wild-type and G551D cystic fibrosis transmembrane conductance regulator (CFTR) controls regulatory volume decrease in simple epithelia.Ceramide in cystic fibrosis: a potential new target for therapeutic intervention.Airway disease phenotypes in animal models of cystic fibrosis.A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies.Cystic fibrosis presenting with corneal perforation and crystalline lens extrusion.
P2860
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P2860
Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@ast
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@en
type
label
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@ast
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@en
prefLabel
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@ast
Cystic fibrosis mice carrying ...... notype-phenotype correlations.
@en
P2093
P2860
P1433
P1476
Cystic fibrosis mice carrying ...... enotype-phenotype correlations
@en
P2093
B J Wainwright
D J Porteous
P K Lovelock
S A Thomson
P2860
P304
P356
10.1002/J.1460-2075.1996.TB00432.X
P407
P577
1996-03-01T00:00:00Z