High-Efficiency Lentiviral Transduction of Human CD34

hematopoietic stem cells lentiviral vector transduction efficiency

Journal

Molecular therapy. Methods & clinical development
ISSN: 2329-0501
Titre abrégé: Mol Ther Methods Clin Dev
Pays: United States
ID NLM: 101624857

Informations de publication

Date de publication:
14 Jun 2019
Historique:
received: 11 10 2018
accepted: 16 01 2019
entrez: 22 2 2019
pubmed: 23 2 2019
medline: 23 2 2019
Statut: epublish

Résumé

Hematopoietic stem cell (HSC) gene therapy is curative for various hereditary diseases; however, high-efficiency transduction in HSCs remains crucial to improve the prospects for hemoglobinopathies. We previously optimized lentiviral transduction in human CD34

Identifiants

pubmed: 30788387
doi: 10.1016/j.omtm.2019.01.005
pii: S2329-0501(19)30008-7
pmc: PMC6370599
doi:

Types de publication

Journal Article

Langues

eng

Pagination

187-196

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Auteurs

Naoya Uchida (N)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Tina Nassehi (T)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Claire M Drysdale (CM)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Jackson Gamer (J)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Morgan Yapundich (M)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Selami Demirci (S)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Juan J Haro-Mora (JJ)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Alexis Leonard (A)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Matthew M Hsieh (MM)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

John F Tisdale (JF)

Cellular and Molecular Therapeutics Branch, National Heart Lung and Blood Institutes (NHLBI) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.

Classifications MeSH