Generation and characterization of a delta F508 cystic fibrosis mouse model.
about
Correctors (specific therapies for class II CFTR mutations) for cystic fibrosisInstability 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 DivergencesCancer predisposition caused by elevated mitotic recombination in Bloom miceModulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epitheliaProduction of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transferPathophysiology of gene-targeted mouse models for cystic fibrosisAssessment of CFTR chloride channel openers in intact normal and cystic fibrosis murine epitheliaBarriers to inhaled gene therapy of obstructive lung diseases: A reviewThe role of the UPS in cystic fibrosis.DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.Salmonella typhi uses CFTR to enter intestinal epithelial cells.Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.Electrolyte transport in the mammalian colon: mechanisms and implications for disease.Hypersusceptibility of cystic fibrosis mice to chronic Pseudomonas aeruginosa oropharyngeal colonization and lung infection.The mousetrap: what we can learn when the mouse model does not mimic the human disease.Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model.Chloride channels in the kidney: lessons learned from knockout animals.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.Targeting genes for self-excision in the germ lineCystic fibrosis growth retardation is not correlated with loss of Cftr in the intestinal epithelium.Regulation of chemokine expression by NaCl occurs independently of cystic fibrosis transmembrane conductance regulator in macrophages.Processing and function of CFTR-DeltaF508 are species-dependent.Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cells.In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epitheliumGeneration and characterization of a complete null estrogen receptor alpha mouse using Cre/LoxP technology.Lentiviral vector gene transfer to porcine airways.Novel role for CFTR in fluid absorption from the distal airspaces of the lungCystic fibrosis mouse models.Comparative biology of cystic fibrosis animal modelsFeline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defectWhat have we learned from mouse models for cystic fibrosis?Generation of a conditional null allele for Cftr in mice.Animal models of chronic lung infection with Pseudomonas aeruginosa: useful tools for cystic fibrosis studies.Pathophysiological basis of liver disease in cystic fibrosis employing a DeltaF508 mouse modelImpaired estrogen feedback and infertility in female mice with pituitary-specific deletion of estrogen receptor alpha (ESR1).Animal models of human disease for gene therapy
P2860
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P2860
Generation and characterization of a delta F508 cystic fibrosis mouse model.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@en
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@nl
type
label
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@en
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@nl
prefLabel
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@en
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@nl
P2093
P2860
P356
P1433
P1476
Generation and characterization of a delta F508 cystic fibrosis mouse model.
@en
P2093
Anderson JR
Colledge WH
Cuthbert AW
MacVinish LJ
Ratcliff R
Southern KW
P2860
P2888
P304
P356
10.1038/NG0895-445
P407
P577
1995-08-01T00:00:00Z