Low levels of CFTR gene transfer with F/HN pseudotyped lentivirus are sufficient to generate ion transport correction in airway cell cultures from cystic fibrosis patients

Low levels of CFTR gene transfer with F/HN pseudotyped lentivirus are sufficient to generate ion transport correction in airway cell cultures from cystic fibrosis patients

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Sergijenko, A, Moiseenko, A, Pineault, K, Nafchi, NAM, Chan, M, Gamlen, T, Gill, D, Hyde, S, Kreuz, S, Griesenbach, U, Alton, EWFW
التنسيق:	Conference item
اللغة:	English
منشور في:	Wiley 2020

مواد مشابهة

Assessment of the air-liquid interface culture model as a tool to validate efficacy of a rSIV.F/HN-CFTR vector
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Assessment of F/HN-pseudotyped lentivirus as a clinically relevant vector for lung gene therapy.
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ASSESSMENT OF F/HN-PSEUDOTYPED LENTIVIRUS AS A CLINICALLY RELEVANT VECTOR FOR LUNG GENE THERAPY
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منشور في: (2012)

Towards a first-in-human trial with a pseudotyped lentivirus
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Single cell assays for quantifying MRNA and protein during cystic fibrosis gene therapy trials
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Production of SIV-F/HN: a new Lentivirus vector for CF gene therapy
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منشور في: (2015)

Development of lentiviral vector respiratory tract dosing methods in anticipation of rodent GLP toxicology assessment
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SAFETY AND EXPRESSION OF A SINGLE DOSE OF LIPID-MEDIATED CFTR GENE THERAPY TO THE UPPER AND LOWER AIRWAYS OF PATIENTS WITH CYSTIC FIBROSIS
حسب: Davies, G, وآخرون
منشور في: (2011)

Development of protocols for mouse GLP-toxicology studies
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Lentiviral vector pseudotyped with sendai virus F and HN proteins uses sialylated glycan receptors to efficiently target human airway cells
حسب: Munday, RJ, وآخرون
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F/HN pseudotyped lentiviral vector uses alpha 2,3 sialylated N-acetyllactosamine to efficiently transduce human airway cells
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Sendai F/HN pseudotyped lentiviral vector transduces human ciliated and non-ciliated airway cells using α 2,3 sialylated receptors
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Preparation for a first-in-man lentivirus trial in cystic fibrosis patients
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Sendai F/HN pseudotyped lentiviral vector transduces human ciliated and non-ciliated airway cells using α 2,3 sialylated receptors
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SAFETY AND EXPRESSION OF A SINGLE DOSE OF LIPID-MEDIATED CFTR GENE THERAPY TO THE UPPER AND LOWER AIRWAYS OF PATIENTS WITH CF
حسب: Davies, J, وآخرون
منشور في: (2011)

Rapid determination of rSIV.F/HN lentiviral vector titre
حسب: Conway, CC, وآخرون
منشور في: (2020)

Assessment of CFTR function after gene transfer in vitro and in vivo.
حسب: Griesenbach, U, وآخرون
منشور في: (2008)

Preparation for a first-in-man lentivirus trial in patients with cystic fibrosis.
حسب: Alton, E, وآخرون
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Lentivirus gene therapy for autoimmune pulmonary alveolar proteinosis
حسب: Palau, H, وآخرون
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Sendai virus-mediated CFTR gene transfer to the airway epithelium.
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Large-scale, high-throughput production of rSIV.F/HN vectors
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597: Protocol development for mouse toxicology studies using lentiviral gene therapy
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CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways
حسب: Min Wu, وآخرون
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Changes in the Cystic Fibrosis Airway Microbiome in Response to CFTR Modulator Therapy
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Non-viral CFTR gene delivery to the lungs of Cystic Fibrosis patients
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منشور في: (2013)

Eucalyptus Essential Oil Inhibits Cell Infection by SARS-CoV-2 Spike Pseudotyped Lentivirus
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Self-reactive CFTR T cells in humans: implications for gene therapy.
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Lentivirus GM-CSF gene therapy ameliorates autoimmune pulmonary alveolar proteinosis
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Design and Development of a Pseudotyped-lentivirus for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
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Adenovirus-mediated in utero expression of CFTR does not improve survival of CFTR knockout mice.
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Gene therapy for respiratory diseases; progress and a changing context
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Expression of gain-of-function CFTR in cystic fibrosis airway cells restores epithelial function better than wild-type or codon-optimized CFTR
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