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Volumn 312, Issue 7027, 1996, Pages 323-324

Somatic gene therapy

Author keywords

[No Author keywords available]

Indexed keywords

CONGENITAL DISORDER; CYSTIC FIBROSIS; EDITORIAL; FAMILIAL HYPERCHOLESTEROLEMIA; GENE EXPRESSION; GENE TARGETING; GENE THERAPY; LIVER CELL; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

EID: 0030026844     PISSN: 09598138     EISSN: 14685833     Source Type: Journal    
DOI: 10.1136/bmj.312.7027.323     Document Type: Editorial
Times cited : (8)

References (12)
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    • T lymphocyte- directed gene therapy for ADA-SCID: initial trial results after 4 years
    • Blaese RM, Culver KW, Miller AD, Carter CS, Fleisher T, Clerici M, et al. T lymphocyte- directed gene therapy for ADA-SCID: initial trial results after 4 years. Science 1995; 270: 475–481.
    • (1995) Science , vol.270 , pp. 475-481
    • Blaese, R.M.1    Culver, K.W.2    Miller, A.D.3    Carter, C.S.4    Fleisher, T.5    Clerici, M.6
  • 2
    • 0028793489 scopus 로고
    • A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemia
    • Grossman M, Rader DJ, Muller DWM, Kolansky DM, Kozarsky K, et al. A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemia. Nature Medicine 1995; 1: 1148–54.
    • (1995) Nature Medicine , vol.1 , pp. 1148-1154
    • Grossman, M.1    Rader, D.J.2    Muller, D.W.M.3    Kolansky, D.M.4    Kozarsky, K.5
  • 3
    • 0028875936 scopus 로고
    • Transfer of genes to humans: early lessons and obstacles to success
    • Crystal RG. Transfer of genes to humans: early lessons and obstacles to success. Science 1995; 270: 404–410.
    • (1995) Science , vol.270 , pp. 404-410
    • Crystal, R.G.1
  • 4
    • 0027967986 scopus 로고
    • Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans
    • Grubb BR, Pickles RJ, Ye H, Yankaskas JR, Vick RN, Engelhardt JF, et al. Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans. Nature 1994; 371: 802–806.
    • (1994) Nature , vol.371 , pp. 802-806
    • Grubb, B.R.1    Pickles, R.J.2    Ye, H.3    Yankaskas, J.R.4    Vick, R.N.5    Engelhardt, J.F.6
  • 5
    • 0029100239 scopus 로고
    • A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis
    • Knowles MR, Hohneker KW, Zhaoqing Z, Olsen JC, Noah TL, Ping-Chuan, et al. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. N Engl J Med 1995; 333: 823–831.
    • (1995) N Engl J Med , vol.333 , pp. 823-831
    • Knowles, M.R.1    Hohneker, K.W.2    Zhaoqing, Z.3    Olsen, J.C.4    Noah, T.L.5    Ping-Chuan6
  • 6
    • 0028978493 scopus 로고
    • Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung
    • Yang Y, Trinchieri G, Wilson JM. Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung. Nature Medicine 1995; 1: 890–893.
    • (1995) Nature Medicine , vol.1 , pp. 890-893
    • Yang, Y.1    Trinchieri, G.2    Wilson, J.M.3
  • 7
    • 0027361622 scopus 로고
    • Noninvasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice
    • Alton EWFW, Middleton PG, Caplen NJ, Smith SN, Steel DM, Munkonge FM, et al. Noninvasive 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    Middleton, P.G.2    Caplen, N.J.3    Smith, S.N.4    Steel, D.M.5    Munkonge, F.M.6
  • 8
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    • Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy
    • Hyde S, Gill D, Higgins CF, Trezise A, MacVinish L, Cuthbert A, et al. Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy. Nature 1993; 362: 250–255.
    • (1993) Nature , vol.362 , pp. 250-255
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    • Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblasts
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  • 11
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    • Phenotypic consequence of CFTR modulation in mutant mice: implications for somatic gene therapy
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    • Dorin, J.R.1    Webb, S.2    Farini, E.3    Delaney, S.4    Wainwright, B.5    Smith, S.6
  • 12
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    • Kascer, H.1    Burns, J.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.