Development of lentiviral vectors with optimized transcriptional activity for the gene therapy of patients with Fanconi anemia.
about
Scavenger receptors and their potential as therapeutic targets in the treatment of cardiovascular diseaseProstate cancer-specific and potent antitumor effect of a DD3-controlled oncolytic virus harboring the PTEN gene.Gene therapy of chronic granulomatous disease: the engraftment dilemmaModelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCsStem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting.Generation of an optimized lentiviral vector encoding a high-expression factor VIII transgene for gene therapy of hemophilia ALentiviral Vector-Mediated Correction of a Mouse Model of Leukocyte Adhesion Deficiency Type I.Semi-automated closed system manufacturing of lentivirus gene-modified haematopoietic stem cells for gene therapyFanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults.Lentiviral gene therapy using cellular promoters cures type 1 Gaucher disease in mice.Targeting expression to megakaryocytes and platelets by lineage-specific lentiviral vectors.Comparison of haematopoietic stem cell engraftment through the retro-orbital venous sinus and the lateral vein: alternative routes for bone marrow transplantation in mice.Targeted gene therapy and cell reprogramming in Fanconi anemia.Development of safer gene delivery systems to minimize the risk of insertional mutagenesis-related malignancies: a critical issue for the field of gene therapy.Gene therapy for Fanconi anemia: one step closer to the clinic.Therapeutic gene editing in CD34+ hematopoietic progenitors from Fanconi anemia patients.Generation of transgenic mice expressing EGFP protein fused to NP68 MHC class I epitope using lentivirus vectors.High-efficiency transduction of spinal cord motor neurons by intrauterine delivery of integration-deficient lentiviral vectors.Measles virus envelope pseudotyped lentiviral vectors transduce quiescent human HSCs at an efficiency without precedentPerspectives on gene therapy for Fanconi anemia
P2860
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P2860
Development of lentiviral vectors with optimized transcriptional activity for the gene therapy of patients with Fanconi anemia.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
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2010年學術文章
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2010年學術文章
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name
Development of lentiviral vect ...... patients with Fanconi anemia.
@en
Development of lentiviral vect ...... patients with Fanconi anemia.
@nl
type
label
Development of lentiviral vect ...... patients with Fanconi anemia.
@en
Development of lentiviral vect ...... patients with Fanconi anemia.
@nl
prefLabel
Development of lentiviral vect ...... patients with Fanconi anemia.
@en
Development of lentiviral vect ...... patients with Fanconi anemia.
@nl
P2093
P50
P356
P1433
P1476
Development of lentiviral vect ...... patients with Fanconi anemia.
@en
P2093
Africa González-Murillo
Helmut Hanenberg
Lara Alvarez
M Luz Lozano
Susana Navarro
P304
P356
10.1089/HUM.2009.141
P577
2010-05-01T00:00:00Z