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Current Gene Therapy|September 30, 2015
Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCsF Javier Molina-Estevez, Ali Nowrouzi, M Luz Lozano, et al.
Human Gene Therapy|December 17, 2009
Development of lentiviral vectors with optimized transcriptional activity for the gene therapy of patients with Fanconi anemiaAfrica González-Murillo, M Luz Lozano, Lara Alvarez, et al.
Stem Cell Research & Therapy|January 30, 2021
Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1Carlos Carrascoso-Rubio, Hidde A Zittersteijn, Laura Pintado-Berninches, et al.
Blood|September 25, 2008
In vivo proliferation advantage of genetically corrected hematopoietic stem cells in a mouse model of Fanconi anemia FA-D1Paula Río, Néstor W Meza, Africa González-Murillo, et al.
Stem Cells (Dayton, Ohio)|September 2, 2014
Conversion of human fibroblasts into monocyte-like progenitor cellsJulian Pulecio, Emmanuel Nivet, Ignacio Sancho-Martinez, et al.
The Journal of Gene Medicine|September 9, 2006
Lentiviral vector integration sites in human NOD/SCID repopulating cellsStephanie Laufs, Guillermo Guenechea, Africa Gonzalez-Murillo, et al.
Human Molecular Genetics|April 4, 2017
Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shorteningJaime Carrillo, Oriol Calvete, Laura Pintado-Berninches, et al.
Nucleic Acids Research|April 29, 2025
Donor insertion into CX3CR1 allows epigenetic modulation of a constitutive promoter on hematopoietic stem cells and its activation upon myeloid differentiationIris Ramos-Hernández, Carla Fuster-García, Araceli Aguilar-González, et al.
Scientific Reports|February 19, 2025
Premature ageing of lung alveoli and bone marrow cells from Terc deficient mice with different telomere lengthsRosa Guerrero-López, Cristina Manguán-García, Carlos Carrascoso-Rubio, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2009
Lentiviral-mediated genetic correction of hematopoietic and mesenchymal progenitor cells from Fanconi anemia patientsAriana Jacome, Susana Navarro, Paula Río, et al.
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