Martin F - Search Results

1

Development of an all-in-one lentiviral vector system based on the original TetR for the easy generation of Tet-ON cell lines.

Benabdellah K, Cobo M, Muñoz P, Toscano MG, Martin F. Benabdellah K, et al. Among authors: martin f. PLoS One. 2011;6(8):e23734. doi: 10.1371/journal.pone.0023734. Epub 2011 Aug 18. PLoS One. 2011. PMID: 21876765 Free PMC article.

2

Efficient lentiviral transduction of Herpesvirus saimiri immortalized T cells as a model for gene therapy in primary immunodeficiencies.

Toscano MG, Frecha C, Ortega C, Santamaría M, Martín F, Molina IJ. Toscano MG, et al. Among authors: martin f. Gene Ther. 2004 Jun;11(12):956-61. doi: 10.1038/sj.gt.3302259. Gene Ther. 2004. PMID: 15029233

3

Lentiviral vectors transcriptionally targeted to hematopoietic cells by WASP gene proximal promoter sequences.

Martín F, Toscano MG, Blundell M, Frecha C, Srivastava GK, Santamaría M, Thrasher AJ, Molina IJ. Martín F, et al. Gene Ther. 2005 Apr;12(8):715-23. doi: 10.1038/sj.gt.3302457. Gene Ther. 2005. PMID: 15750617

4

Transplantation of human CD34+ stem cells from umbilical cord blood to rats with thioacetamide-induced liver cirrhosis.

Sáez-Lara MJ, Frecha C, Martín F, Abadía F, Toscano M, Gil A, Fontana L. Sáez-Lara MJ, et al. Among authors: martin f. Xenotransplantation. 2006 Nov;13(6):529-35. doi: 10.1111/j.1399-3089.2006.00344.x. Xenotransplantation. 2006. PMID: 17059580

5

Hematopoietic-specific lentiviral vectors circumvent cellular toxicity due to ectopic expression of Wiskott-Aldrich syndrome protein.

Toscano MG, Frecha C, Benabdellah K, Cobo M, Blundell M, Thrasher AJ, García-Olivares E, Molina IJ, Martin F. Toscano MG, et al. Among authors: martin f. Hum Gene Ther. 2008 Feb;19(2):179-97. doi: 10.1089/hum.2007.098. Hum Gene Ther. 2008. PMID: 18240968

6

Improved lentiviral vectors for Wiskott-Aldrich syndrome gene therapy mimic endogenous expression profiles throughout haematopoiesis.

Frecha C, Toscano MG, Costa C, Saez-Lara MJ, Cosset FL, Verhoeyen E, Martin F. Frecha C, et al. Among authors: martin f. Gene Ther. 2008 Jun;15(12):930-41. doi: 10.1038/gt.2008.20. Epub 2008 Mar 6. Gene Ther. 2008. PMID: 18323794

7

In vivo delivery of lentiviral vectors expressing vasoactive intestinal peptide complementary DNA as gene therapy for collagen-induced arthritis.

Delgado M, Toscano MG, Benabdellah K, Cobo M, O'Valle F, Gonzalez-Rey E, Martín F. Delgado M, et al. Among authors: martin f. Arthritis Rheum. 2008 Apr;58(4):1026-37. doi: 10.1002/art.23283. Arthritis Rheum. 2008. PMID: 18383372 Free article.

8

Safer vectors for gene therapy of primary immunodeficiencies.

Romero Z, Toscano MG, Unciti JD, Molina I, Martín F. Romero Z, et al. Among authors: martin f. Curr Gene Ther. 2009 Aug;9(4):291-305. doi: 10.2174/156652309788921080. Curr Gene Ther. 2009. PMID: 19534652 Review.

9

Was cDNA sequences modulate transgene expression of was promoter-driven lentiviral vectors.

Toscano MG, Benabdellah K, Muñoz P, Frecha C, Cobo M, Martín F. Toscano MG, et al. Among authors: martin f. Hum Gene Ther. 2009 Nov;20(11):1279-90. doi: 10.1089/hum.2009.118. Hum Gene Ther. 2009. PMID: 19630517

10

Dendritic cells transduced with lentiviral vectors expressing VIP differentiate into VIP-secreting tolerogenic-like DCs.

Toscano MG, Delgado M, Kong W, Martin F, Skarica M, Ganea D. Toscano MG, et al. Among authors: martin f. Mol Ther. 2010 May;18(5):1035-45. doi: 10.1038/mt.2009.293. Epub 2010 Jan 12. Mol Ther. 2010. PMID: 20068554 Free PMC article.

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