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Volumn 3, Issue 9, 1996, Pages 797-801

A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction

Author keywords

Cystic fibrosis; Gene therapy; Mouse models

Indexed keywords

CHLORIDE ION; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0029813969     PISSN: 09697128     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (130)

References (16)
  • 1
    • 0030026844 scopus 로고    scopus 로고
    • Somatic gene therapy: Optimism tempered by reality
    • Dorin J. Somatic gene therapy: optimism tempered by reality. Br Med J 1996; 312: 323-324.
    • (1996) Br Med J , vol.312 , pp. 323-324
    • Dorin, J.1
  • 2
    • 0027310432 scopus 로고
    • Gene therapy for cystic fibrosis - Where and when?
    • Porteous DJ, Dorin JR. Gene therapy for cystic fibrosis - where and when? Hum Mol Genet 1993; 2: 211-212.
    • (1993) Hum Mol Genet , vol.2 , pp. 211-212
    • Porteous, D.J.1    Dorin, J.R.2
  • 3
    • 0015824267 scopus 로고
    • The control of flux. Symp Soc
    • Kacser H, Burns JA. The control of flux. Symp Soc Exp Biol 1973; 27: 65-104
    • (1973) Exp Biol , vol.27 , pp. 65-104
    • Kacser, H.1    Burns, J.A.2
  • 4
    • 0019869334 scopus 로고
    • Molecular basis of dominance
    • Kacser H, Burns JA. Molecular basis of dominance. Genetics 1981; 97: 638-666.
    • (1981) Genetics , vol.97 , pp. 638-666
    • Kacser, H.1    Burns, J.A.2
  • 5
    • 0026649122 scopus 로고
    • An animal model for cystic fibrosis made by gene targeting
    • Snouwaert JN et al. An animal model for cystic fibrosis made by gene targeting. Science 1992; 257: 1083-1088.
    • (1992) Science , vol.257 , pp. 1083-1088
    • Snouwaert, J.N.1
  • 6
    • 0026730466 scopus 로고
    • Cystic fibrosis in the mouse by targeted insertional mutagenesis
    • Dorin JR et al Cystic fibrosis in the mouse by targeted insertional mutagenesis. Nature 1992; 359: 211-215.
    • (1992) Nature , vol.359 , pp. 211-215
    • Dorin, J.R.1
  • 7
    • 0028003254 scopus 로고
    • Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type CFTR gene expression
    • Dorm JR et al. Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type CFTR gene expression. Mammal Genome 1994; 5: 465-472.
    • (1994) Mammal Genome , vol.5 , pp. 465-472
    • Dorm, J.R.1
  • 8
    • 0027361622 scopus 로고
    • Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice
    • Alton EWFW et al. Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice. Nat Genet 1993; 5: 135-142.
    • (1993) Nat Genet , vol.5 , pp. 135-142
    • Alton, E.W.F.W.1
  • 9
    • 0025912486 scopus 로고
    • Maturation and function of cystic fibrosis trans-membrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2
    • Gregory RJ et al. Maturation and function of cystic fibrosis trans-membrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2. Mol Cell Biol 1991; 11: 3886-3893.
    • (1991) Mol Cell Biol , vol.11 , pp. 3886-3893
    • Gregory, R.J.1
  • 10
    • 0028982894 scopus 로고
    • Cftr as a cAMP-dependent regulator of sodium channels
    • Stutts MJ et al. Cftr as a cAMP-dependent regulator of sodium channels. Science 1995; 269: 847-850.
    • (1995) Science , vol.269 , pp. 847-850
    • Stutts, M.J.1
  • 11
    • 0026918861 scopus 로고
    • Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis
    • Johnson LG et al. Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis. Nat Genet 1992; 2: 21-25.
    • (1992) Nat Genet , vol.2 , pp. 21-25
    • Johnson, L.G.1
  • 12
    • 0027377523 scopus 로고
    • Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis
    • Zabner J et al. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. Cell 1993; 75: 207-216.
    • (1993) Cell , vol.75 , pp. 207-216
    • Zabner, J.1
  • 13
    • 0028913411 scopus 로고
    • Lipsome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis
    • Caplen NJ et al. Lipsome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis. Nature Med 1995; 1: 39-46.
    • (1995) Nature Med , vol.1 , pp. 39-46
    • Caplen, N.J.1
  • 14
    • 9044236531 scopus 로고    scopus 로고
    • Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations
    • Delaney SJ et al. Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations. EMBO J 1996; 15: 955-963.
    • (1996) EMBO J , vol.15 , pp. 955-963
    • Delaney, S.J.1
  • 15
    • 0028913376 scopus 로고
    • Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens
    • Davidson DJ et al. Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens. Nat Genet 1995; 9: 351-357.
    • (1995) Nat Genet , vol.9 , pp. 351-357
    • Davidson, D.J.1
  • 16
    • 0027231473 scopus 로고
    • Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblasts
    • Mouiller P, Bohl D, Heard J-M, Danos O. Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblasts. Nat Genet 1993; 4: 154-159.
    • (1993) Nat Genet , vol.4 , pp. 154-159
    • Mouiller, P.1    Bohl, D.2    Heard, J.-M.3    Danos, O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.