메뉴 건너뛰기




Volumn 211, Issue 1, 1998, Pages 117-123

In-frame elimination of exon 10 in Cftr(tm1Unc) CF mice

Author keywords

Animal models; DNA sequencing; Gene expression; RT PCR; Therapy

Indexed keywords

MESSENGER RNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0032574625     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00090-0     Document Type: Article
Times cited : (6)

References (43)
  • 3
    • 0027502580 scopus 로고
    • Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
    • Chu C.S., Trapnell B.C., Curristin S., Cutting G.R., Crystal R.G. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nature Genet. 3:1993;151-156.
    • (1993) Nature Genet. , vol.3 , pp. 151-156
    • Chu, C.S.1    Trapnell, B.C.2    Curristin, S.3    Cutting, G.R.4    Crystal, R.G.5
  • 5
    • 0026640380 scopus 로고
    • Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis
    • Clarke L.L., Grubb B.R., Gabriel S.E., Smithies O., Koller B.H., Boucher R.C. Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis. Science. 257:1992;1125-1128.
    • (1992) Science , vol.257 , pp. 1125-1128
    • Clarke, L.L.1    Grubb, B.R.2    Gabriel, S.E.3    Smithies, O.4    Koller, B.H.5    Boucher, R.C.6
  • 8
    • 0026523829 scopus 로고
    • Cystic fibrosis: Molecular biology and therapeutic implications
    • Collins F. Cystic fibrosis: molecular biology and therapeutic implications. Science. 256:1992;774-779.
    • (1992) Science , vol.256 , pp. 774-779
    • Collins, F.1
  • 9
    • 0028907339 scopus 로고
    • Positional cloning moves from perditional to traditional
    • Collins F.S. Positional cloning moves from perditional to traditional. Nature Genet. 9:1995;347-357.
    • (1995) Nature Genet. , vol.9 , pp. 347-357
    • Collins, F.S.1
  • 10
    • 0028324903 scopus 로고
    • Alternative splicing of the first nucleotide binding fold of CFTR in mouse testes is associated with specific stages of spermatogenesis
    • Delaney S.J., Koopman P., Lovelock P.K., Wainwright B.J. Alternative splicing of the first nucleotide binding fold of CFTR in mouse testes is associated with specific stages of spermatogenesis. Genomics. 20:1994;517-518.
    • (1994) Genomics , vol.20 , pp. 517-518
    • Delaney, S.J.1    Koopman, P.2    Lovelock, P.K.3    Wainwright, B.J.4
  • 12
    • 0028136599 scopus 로고
    • Maintenance of an open reading frame as an additional level of scrutiny during splice site selection
    • Dietz H.C., Kendzior R.J. Jr. Maintenance of an open reading frame as an additional level of scrutiny during splice site selection. Nature Genet. 8:1994;183-188.
    • (1994) Nature Genet. , vol.8 , pp. 183-188
    • Dietz, H.C.1    Kendzior R.J., Jr.2
  • 15
    • 0028272099 scopus 로고
    • Analysis of mutations and alternative splicing patterns in the CFTR gene using mRNA derived from nasal epithelial cells
    • Hull J., Shackleton S., Harris A. Analysis of mutations and alternative splicing patterns in the CFTR gene using mRNA derived from nasal epithelial cells. Hum. Mol. Genet. 3:1994;1141-1146.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1141-1146
    • Hull, J.1    Shackleton, S.2    Harris, A.3
  • 17
    • 0026778147 scopus 로고
    • Expression and chromosome localization of the murine cystic fibrosis transmembrane conductance regulator
    • Kelley K., Stamm S., Kozak C. Expression and chromosome localization of the murine cystic fibrosis transmembrane conductance regulator. Genomics. 13:1992;381-388.
    • (1992) Genomics , vol.13 , pp. 381-388
    • Kelley, K.1    Stamm, S.2    Kozak, C.3
  • 19
    • 0025880897 scopus 로고
    • Toward an animal model of cystic fibrosis: Targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in stem cells
    • Koller B.H., Kim H.-S., Latour A.M., Brigman K., Boucher R.C., Scambler P., Wainwright B., Smithies O. Toward an animal model of cystic fibrosis: targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in stem cells. Proc. Natl. Acad. Sci. USA. 88:1991;10730-10734.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 10730-10734
    • Koller, B.H.1    Kim, H.-S.2    Latour, A.M.3    Brigman, K.4    Boucher, R.C.5    Scambler, P.6    Wainwright, B.7    Smithies, O.8
  • 20
    • 0027177717 scopus 로고
    • Nonsense mutations and diminished mRNA levels
    • McIntosh I., Hamosh A., Dietz H.C. Nonsense mutations and diminished mRNA levels. Nature Genet. 4:1993;219.
    • (1993) Nature Genet. , vol.4 , pp. 219
    • McIntosh, I.1    Hamosh, A.2    Dietz, H.C.3
  • 23
    • 0026894881 scopus 로고
    • Disruption of the cystic fibrosis transmembrane conductance regulator gene in embyronic stem cells by gene targeting
    • Ratcliff R., Evans M.J., Doran J., Wainwright B.J., Williamson R., Colledge W.H. Disruption of the cystic fibrosis transmembrane conductance regulator gene in embyronic stem cells by gene targeting. Transgenic Res. 1:1992;177-181.
    • (1992) Transgenic Res. , vol.1 , pp. 177-181
    • Ratcliff, R.1    Evans, M.J.2    Doran, J.3    Wainwright, B.J.4    Williamson, R.5    Colledge, W.H.6
  • 26
    • 0025098474 scopus 로고
    • Exon definition may facilitate splice site selection in RNAs with multiple exons
    • Robberson B., Cote G., Berget S. Exon definition may facilitate splice site selection in RNAs with multiple exons. Mol. Cell Biol. 10:1990;84-94.
    • (1990) Mol. Cell Biol. , vol.10 , pp. 84-94
    • Robberson, B.1    Cote, G.2    Berget, S.3
  • 28
    • 0026800854 scopus 로고
    • Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts
    • Slomski R., Schloesser M., Berg L.P., Wagner M., Kakkar V.V., Cooper D.N., Reiss J. Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts. Hum. Genet. 89:1992;615-619.
    • (1992) Hum. Genet. , vol.89 , pp. 615-619
    • Slomski, R.1    Schloesser, M.2    Berg, L.P.3    Wagner, M.4    Kakkar, V.V.5    Cooper, D.N.6    Reiss, J.7
  • 31
    • 0027310434 scopus 로고
    • Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance
    • Strong T.V., Wilkinson D.J., Mansoura M.K., Devor D.C., Henze K., Yang Y., Wilson J.M., Cohn J.A., Dawson D.C., Frizzell R.A.et al. Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance. Hum. Mol. Genet. 2:1993;225-230.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 225-230
    • Strong, T.V.1    Wilkinson, D.J.2    Mansoura, M.K.3    Devor, D.C.4    Henze, K.5    Yang, Y.6    Wilson, J.M.7    Cohn, J.A.8    Dawson, D.C.9    Frizzell, R.A.10
  • 34
    • 0027316155 scopus 로고
    • Testis-specific, alternative splicing of rodent CFTR mRNA
    • Trezise A.E., Buchwald M., Higgins C.F. Testis-specific, alternative splicing of rodent CFTR mRNA. Hum. Mol. Genet. 2:1993;801-802.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 801-802
    • Trezise, A.E.1    Buchwald, M.2    Higgins, C.F.3
  • 36
    • 0027034365 scopus 로고
    • Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium
    • Tsui L. Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the cystic fibrosis genetic analysis consortium. Human Mutat. 1:1992;197-203.
    • (1992) Human Mutat. , vol.1 , pp. 197-203
    • Tsui, L.1
  • 37
    • 0026641782 scopus 로고
    • The spectrum of cystic fibrosis mutations
    • Tsui L.C. The spectrum of cystic fibrosis mutations. Trends Genet. 8:1992;392-398.
    • (1992) Trends Genet. , vol.8 , pp. 392-398
    • Tsui, L.C.1
  • 39
    • 0024349521 scopus 로고
    • Nonsense mutations in the dihydrofolate reductase gene affect RNA processing
    • Urlaub B., Mitchell P.J., Ciudada C.J., Chasin L.A. Nonsense mutations in the dihydrofolate reductase gene affect RNA processing. Mol. Cell Biol. 9:1989;2868-2880.
    • (1989) Mol. Cell Biol. , vol.9 , pp. 2868-2880
    • Urlaub, B.1    Mitchell, P.J.2    Ciudada, C.J.3    Chasin, L.A.4
  • 42
    • 0028557095 scopus 로고
    • Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR
    • Zhou L., Dey C.R., Wert S.E., DuVall M.D., Frizzell R.A., Whitsett J.A. Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR. Science. 266:1994;1705-1708.
    • (1994) Science , vol.266 , pp. 1705-1708
    • Zhou, L.1    Dey, C.R.2    Wert, S.E.3    Duvall, M.D.4    Frizzell, R.A.5    Whitsett, J.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.