Get started
Author

M. Luz Lozano

Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia
2019 · Paula Río, Susana Navarro, et al. · Nature Medicine · 167
Lentiviral-mediated Genetic Correction of Hematopoietic and Mesenchymal Progenitor Cells From Fanconi Anemia Patients
2009 · Ariana Jacome, Susana Navarro, et al. · Molecular Therapy · 50
PDF
Lentiviral vector integration sites in human NOD/SCID repopulating cells
2006 · Stephanie Laufs, Guillermo Guenechea, et al. · The Journal of Gene Medicine · 49
Development of Lentiviral Vectors with Optimized Transcriptional Activity for the Gene Therapy of Patients with Fanconi Anemia
2009 · África González-Murillo, M. Luz Lozano, et al. · Human Gene Therapy · 48
Unaltered repopulation properties of mouse hematopoietic stem cells transduced with lentiviral vectors
2008 · Africa Gonzalez-Murillo, M. Luz Lozano, et al. · Blood · 27
PDF
Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs
2015 · F. Molina-Estevez, Ali Nowrouzi, et al. · Current Gene Therapy · 23
Generation of iPSCs from Genetically Corrected Brca2 Hypomorphic Cells: Implications in Cell Reprogramming and Stem Cell Therapy
2013 · S. Navarro, V. Moleiro, et al. · Stem Cells · 15
PDF
Brief Report: Impaired Cell Reprogramming in Nonhomologous End Joining Deficient Cells
2013 · F. Javier Molina-Estevez, M. Luz Lozano, et al. · Stem Cells · 13
PDF
Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1
2021 · Carlos Carrascoso-Rubio, Hidde A. Zittersteijn, et al. · Stem Cell Research & Therapy · 6
PDF
Gene Therapy for Lad-I Immunodeficiency: Preclinical Evaluation of HSC Transduction Under Optimized GMP-Conditions
2019 · Elena Almarza, Cristina Mesa-Núñez, et al. · Blood · 4
Targeted gene therapy into a safe harbor site in human hematopoietic progenitor cells
2020 · Fatima Rodriguez-Fornes, Oscar Quintana-Bustamante, et al. · Gene Therapy · 3
Impaired cell reprogramming in non-homologous end joining deficient cells
2013 · F Javier Molina-Estevez, M. Luz Lozano, et al. · MDC Repository (Max-Delbrueck-Center for Molecular Medicine) · 2
Premature ageing of lung alveoli and bone marrow cells from Terc deficient mice with different telomere lengths
2025 · Rosa Guerrero-López, Cristina Manguán-García, et al. · Scientific Reports · 1
PDF
Optimization of lentiviral vectors for the gene therapy of fanconi anemia
2008 · Africa Gonzalez-Murillo, M. Luz Lozano, et al. · Blood Cells Molecules and Diseases
Works count: 18
Citation count: 408
H-index: 8
I10-index: 8
Year
Topic
Type