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Volumn 3, Issue 9, 2015, Pages 684-691

Corrections to Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: A randomised, double-blind, placebo-controlled, phase 2b trial, [Lancet Respir Med, (2015)] DOI: 10.1016/S2213-2600(15)00245-3;Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: A randomised, double-blind, placebo-controlled, phase 2b trial

(80)  Alton, Eric W F W b   Armstrong, David K g   Ashby, Deborah b   Bayfield, Katie J b   Bilton, Diana a   Bloomfield, Emily V b   Boyd, A Christopher f   Brand, June f   Buchan, Ruaridh c   Calcedo, Roberto i   Carvelli, Paula b   Chan, Mario b   Cheng, Seng H j   Collie, D David S e   Cunningham, Steve g   Davidson, Heather E f   Davies, Gwyneth b   Davies, Jane C b   Davies, Lee A h   Dewar, Maria H c   more..


Author keywords

[No Author keywords available]

Indexed keywords

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; LIPOSOME; PLACEBO; PLASMID VECTOR; CFTR PROTEIN, HUMAN;

EID: 84941179388     PISSN: 22132600     EISSN: 22132619     Source Type: Journal    
DOI: 10.1016/S2213-2600(15)00314-8     Document Type: Erratum
Times cited : (349)

References (25)
  • 1
    • 84884802285 scopus 로고    scopus 로고
    • Moving forward: cystic fibrosis gene therapy
    • Griesenbach U, Alton EW Moving forward: cystic fibrosis gene therapy. Hum Mol Genet 2013, 22:R52-R58.
    • (2013) Hum Mol Genet , vol.22 , pp. R52-R58
    • Griesenbach, U.1    Alton, E.W.2
  • 3
    • 84909583944 scopus 로고    scopus 로고
    • Delivery of genes into the CF airway
    • Gill DR, Hyde SC Delivery of genes into the CF airway. Thorax 2014, 69:962-964.
    • (2014) Thorax , vol.69 , pp. 962-964
    • Gill, D.R.1    Hyde, S.C.2
  • 5
    • 80054087238 scopus 로고    scopus 로고
    • Pre-clinical evaluation of three non-viral gene transfer agents for cystic fibrosis after aerosol delivery to the ovine lung
    • McLachlan G, Davidson H, Holder E, et al. Pre-clinical evaluation of three non-viral gene transfer agents for cystic fibrosis after aerosol delivery to the ovine lung. Gene Ther 2011, 18:996-1005.
    • (2011) Gene Ther , vol.18 , pp. 996-1005
    • McLachlan, G.1    Davidson, H.2    Holder, E.3
  • 6
    • 84885388155 scopus 로고    scopus 로고
    • The safety profile of a cationic lipid-mediated cystic fibrosis gene transfer agent following repeated monthly aerosol administration to sheep
    • Alton EW, Baker A, Baker E, et al. The safety profile of a cationic lipid-mediated cystic fibrosis gene transfer agent following repeated monthly aerosol administration to sheep. Biomaterials 2013, 34:10267-10277.
    • (2013) Biomaterials , vol.34 , pp. 10267-10277
    • Alton, E.W.1    Baker, A.2    Baker, E.3
  • 7
    • 84891742682 scopus 로고    scopus 로고
    • Toxicology study assessing efficacy and safety of repeated administration of lipid/DNA complexes to mouse lung
    • Alton EW, Boyd AC, Cheng SH, et al. Toxicology study assessing efficacy and safety of repeated administration of lipid/DNA complexes to mouse lung. Gene Ther 2014, 21:89-95.
    • (2014) Gene Ther , vol.21 , pp. 89-95
    • Alton, E.W.1    Boyd, A.C.2    Cheng, S.H.3
  • 8
    • 43449111490 scopus 로고    scopus 로고
    • CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression
    • Hyde SC, Pringle IA, Abdullah S, et al. CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression. Nat Biotechnol 2008, 26:549-551.
    • (2008) Nat Biotechnol , vol.26 , pp. 549-551
    • Hyde, S.C.1    Pringle, I.A.2    Abdullah, S.3
  • 9
    • 84867065315 scopus 로고    scopus 로고
    • Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample
    • Quittner AL, Sawicki GS, McMullen A, et al. Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample. Qual Life Res 2012, 21:1267-1278.
    • (2012) Qual Life Res , vol.21 , pp. 1267-1278
    • Quittner, A.L.1    Sawicki, G.S.2    McMullen, A.3
  • 10
    • 84904016376 scopus 로고    scopus 로고
    • Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial
    • Kerem E, Konstan MW, De Boeck K, et al. Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial. Lancet Respir Med 2014, 2:539-547.
    • (2014) Lancet Respir Med , vol.2 , pp. 539-547
    • Kerem, E.1    Konstan, M.W.2    De Boeck, K.3
  • 11
    • 0033531143 scopus 로고    scopus 로고
    • Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group
    • Ramsey BW, Pepe MS, Quan JM, et al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group. N Engl J Med 1999, 340:23-30.
    • (1999) N Engl J Med , vol.340 , pp. 23-30
    • Ramsey, B.W.1    Pepe, M.S.2    Quan, J.M.3
  • 12
    • 0141816759 scopus 로고    scopus 로고
    • Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial
    • Saiman L, Marshall BC, Mayer-Hamblett N, et al. Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA 2003, 290:1749-1756.
    • (2003) JAMA , vol.290 , pp. 1749-1756
    • Saiman, L.1    Marshall, B.C.2    Mayer-Hamblett, N.3
  • 13
    • 84904002908 scopus 로고    scopus 로고
    • A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial
    • Boyle MP, Bell SC, Konstan MW, et al. A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial. Lancet Respir Med 2014, 2:527-538.
    • (2014) Lancet Respir Med , vol.2 , pp. 527-538
    • Boyle, M.P.1    Bell, S.C.2    Konstan, M.W.3
  • 14
    • 0029318990 scopus 로고
    • Cell proliferation in bronchial epithelium and submucosal glands of cystic fibrosis patients
    • Leigh MW, Kylander JE, Yankaskas JR, Boucher RC Cell proliferation in bronchial epithelium and submucosal glands of cystic fibrosis patients. Am J Respir Cell Mol Biol 1995, 12:605-612.
    • (1995) Am J Respir Cell Mol Biol , vol.12 , pp. 605-612
    • Leigh, M.W.1    Kylander, J.E.2    Yankaskas, J.R.3    Boucher, R.C.4
  • 15
    • 9844237019 scopus 로고    scopus 로고
    • Safety of a single aerosol administration of escalating doses of the cationic lipid GL-67/DOPE/DMPE-PEG5000 formulation to the lungs of normal volunteers
    • Chadwick SL, Kingston HD, Stern M, et al. Safety of a single aerosol administration of escalating doses of the cationic lipid GL-67/DOPE/DMPE-PEG5000 formulation to the lungs of normal volunteers. Gene Ther 1997, 4:937-942.
    • (1997) Gene Ther , vol.4 , pp. 937-942
    • Chadwick, S.L.1    Kingston, H.D.2    Stern, M.3
  • 16
    • 0033586375 scopus 로고    scopus 로고
    • Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial
    • Alton EW, Stern M, Farley R, et al. Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial. Lancet 1999, 353:947-954.
    • (1999) Lancet , vol.353 , pp. 947-954
    • Alton, E.W.1    Stern, M.2    Farley, R.3
  • 17
    • 8244238394 scopus 로고    scopus 로고
    • A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis
    • Gill DR, Southern KW, Mofford KA, et al. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis. Gene Ther 1997, 4:199-209.
    • (1997) Gene Ther , vol.4 , pp. 199-209
    • Gill, D.R.1    Southern, K.W.2    Mofford, K.A.3
  • 18
    • 0030759153 scopus 로고    scopus 로고
    • Comparison of DNA-lipid complexes and DNA alone for gene transfer to cystic fibrosis airway epithelia in vivo
    • Zabner J, Cheng SH, Meeker D, et al. Comparison of DNA-lipid complexes and DNA alone for gene transfer to cystic fibrosis airway epithelia in vivo. J Clin Invest 1997, 100:1529-1537.
    • (1997) J Clin Invest , vol.100 , pp. 1529-1537
    • Zabner, J.1    Cheng, S.H.2    Meeker, D.3
  • 19
    • 80054070494 scopus 로고    scopus 로고
    • The significance of plasmid DNA preparations contaminated with bacterial genomic DNA on inflammatory responses following delivery of lipoplexes to the murine lung
    • Bazzani RP, Cai Y, Hebel HL, Hyde SC, Gill DR The significance of plasmid DNA preparations contaminated with bacterial genomic DNA on inflammatory responses following delivery of lipoplexes to the murine lung. Biomaterials 2011, 32:9854-9865.
    • (2011) Biomaterials , vol.32 , pp. 9854-9865
    • Bazzani, R.P.1    Cai, Y.2    Hebel, H.L.3    Hyde, S.C.4    Gill, D.R.5
  • 20
    • 0033924663 scopus 로고    scopus 로고
    • Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis
    • Hyde SC, Southern KW, Gileadi U, et al. Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis. Gene Ther 2000, 7:1156-1165.
    • (2000) Gene Ther , vol.7 , pp. 1156-1165
    • Hyde, S.C.1    Southern, K.W.2    Gileadi, U.3
  • 21
    • 0036791579 scopus 로고    scopus 로고
    • Optimisation of real-time quantitative RT-PCR for the evaluation of non-viral mediated gene transfer to the airways
    • Rose AC, Goddard CA, Colledge WH, Cheng SH, Gill DR, Hyde SC Optimisation of real-time quantitative RT-PCR for the evaluation of non-viral mediated gene transfer to the airways. Gene Ther 2002, 9:1312-1320.
    • (2002) Gene Ther , vol.9 , pp. 1312-1320
    • Rose, A.C.1    Goddard, C.A.2    Colledge, W.H.3    Cheng, S.H.4    Gill, D.R.5    Hyde, S.C.6
  • 22
    • 19944398726 scopus 로고    scopus 로고
    • Compacted DNA nanoparticles administered to the nasal mucosa of cystic fibrosis subjects are safe and demonstrate partial to complete cystic fibrosis transmembrane regulator reconstitution
    • Konstan MW, Davis PB, Wagener JS, et al. Compacted DNA nanoparticles administered to the nasal mucosa of cystic fibrosis subjects are safe and demonstrate partial to complete cystic fibrosis transmembrane regulator reconstitution. Hum Gene Ther 2004, 15:1255-1269.
    • (2004) Hum Gene Ther , vol.15 , pp. 1255-1269
    • Konstan, M.W.1    Davis, P.B.2    Wagener, J.S.3
  • 24
    • 84862184691 scopus 로고    scopus 로고
    • Azithromycin maintenance therapy in patients with cystic fibrosis: a dose advice based on a review of pharmacokinetics, efficacy, and side effects
    • Wilms EB, Touw DJ, Heijerman HG, van der Ent CK Azithromycin maintenance therapy in patients with cystic fibrosis: a dose advice based on a review of pharmacokinetics, efficacy, and side effects. Pediatr Pulmonol 2012, 47:658-665.
    • (2012) Pediatr Pulmonol , vol.47 , pp. 658-665
    • Wilms, E.B.1    Touw, D.J.2    Heijerman, H.G.3    van der Ent, C.K.4


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