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

Manylion Llyfryddiaeth
Prif Awduron:	Sergijenko, A, Moiseenko, A, Pineault, K, Nafchi, NAM, Chan, M, Gamlen, T, Gill, D, Hyde, S, Kreuz, S, Griesenbach, U, Alton, EWFW
Fformat:	Conference item
Iaith:	English
Cyhoeddwyd:	Wiley 2020

Eitemau Tebyg

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Assessment of F/HN-pseudotyped lentivirus as a clinically relevant vector for lung gene therapy.
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Cyhoeddwyd: (2012)

ASSESSMENT OF F/HN-PSEUDOTYPED LENTIVIRUS AS A CLINICALLY RELEVANT VECTOR FOR LUNG GENE THERAPY
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Towards a first-in-human trial with a pseudotyped lentivirus
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Cyhoeddwyd: (2020)

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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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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Sendai F/HN pseudotyped lentiviral vector transduces human ciliated and non-ciliated airway cells using α 2,3 sialylated receptors
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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
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CFTR Modulator Therapies: Potential Impact on Airway Infections in Cystic Fibrosis
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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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Eucalyptus Essential Oil Inhibits Cell Infection by SARS-CoV-2 Spike Pseudotyped Lentivirus
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Transgenesis and Genome Editing of Mouse Spermatogonial Stem Cells by Lentivirus Pseudotyped with Sendai Virus F Protein
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Cell-targeted gene modification by delivery of CRISPR-Cas9 ribonucleoprotein complexes in pseudotyped lentivirus-derived nanoparticles
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CFTR targeted therapies: recent advances in cystic fibrosis and possibilities in other diseases of the airways
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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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