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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family

Frontiers in genetics, 2018-03, Vol.9, p.85-85

2018

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CD105 (endoglin)-negative murine mesenchymal stromal cells define a new multipotent subpopulation with distinct differentiation and immunomodulatory capacities

PloS one, 2013-10, Vol.8 (10), p.e76979-e76979

2013

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Comparison of Zinc Finger Nucleases Versus CRISPR-Specific Nucleases for Genome Editing of the Wiskott-Aldrich Syndrome Locus

Human gene therapy, 2018-03, Vol.29 (3), p.366-380

2018

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A chimeric HS4-SAR insulator (IS2) that prevents silencing and enhances expression of lentiviral vectors in pluripotent stem cells

PloS one, 2014-01, Vol.9 (1), p.e84268-e84268

2014

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Gene-modified mesenchymal stromal cells: A VIP experience

Inflammation and Regeneration, 2014, Vol.34(4), pp.176-183

2014

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

PloS one, 2011-08, Vol.6 (8), p.e23734

2011

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Mesenchymal Stromal Cells Express GARP/LRRC32 on Their Surface: Effects on Their Biology and Immunomodulatory Capacity

Stem cells (Dayton, Ohio), 2015-01, Vol.33 (1), p.183-195

2015

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Mesenchymal Stem Cells Expressing Vasoactive Intestinal Peptide Ameliorate Symptoms in a Model of Chronic Multiple Sclerosis

Cell transplantation, 2013-05, Vol.22 (5), p.839-854

2013

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Gene Therapy Corrects Mitochondrial Dysfunction in Hematopoietic Progenitor Cells and Fibroblasts from Coq9R239X Mice

PloS one, 2016-06, Vol.11 (6), p.e0158344-e0158344

2016

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Lent-On-Plus Lentiviral vectors for conditional expression in human stem cells

Scientific reports, 2016-11, Vol.6 (1), p.37289, Article 37289

2016

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Exosomes from human lymphoblastoid B cells express enzymatically active CD38 that is associated with signaling complexes containing CD81, Hsc-70 and Lyn

Experimental cell research, 2010-10, Vol.316 (16), p.2692-2706

2010

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Absence of WASp Enhances Hematopoietic and Megakaryocytic Differentiation in a Human Embryonic Stem Cell Model

Molecular therapy, 2016-02, Vol.24 (2), p.342-353

2016

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Specific marking of hESCs-derived hematopoietic lineage by WAS-promoter driven lentiviral vectors

PloS one, 2012-06, Vol.7 (6), p.e39091-e39091

2012

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Increased Expression of Musashi-1 Evidences Mesenchymal Repair in Maxillary Sinus Floor Elevation

Scientific reports, 2018-08, Vol.8 (1), p.12243-9, Article 12243

2018

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Use of zinc-finger nucleases to knock out the WAS gene in K562 cells: a human cellular model for Wiskott-Aldrich syndrome

Disease models & mechanisms, 2013-03, Vol.6 (2), p.544-554

2013

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SCL/TAL1-mediated Transcriptional Network Enhances Megakaryocytic Specification of Human Embryonic Stem Cells

Molecular therapy, 2015-01, Vol.23 (1), p.158-170

2015

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SCL/TAL1- mediated transcriptional network enhances megakaryocytic specification of human embryonic stem cells

Experimental hematology, 2014-08, Vol.42 (8), p.S50-S50

2014

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

Human gene therapy, 2009-11, Vol.20 (11), p.1279-1290

2009

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

Human gene therapy, 2008-02, Vol.19 (2), p.179-198

2008

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A Chimeric HS4-SAR Insulator (IS2) That Prevents Silencing and Enhances Expression of Lentiviral Vectors in Pluripotent Stem Cells: e84268

PloS one, 2014-01, Vol.9 (1)

2014

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Gene-modified mesenchymal stromal cells: A VIP experience

Inflammation and regeneration, 2014, Vol.34 (4), p.176-183

2014

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Gene Therapy Corrects Mitochondrial Dysfunction in Hematopoietic Progenitor Cells and Fibroblasts from Coq9.sup.R239X Mice

PloS one, 2016-06, Vol.11 (6)

2016

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A Chimeric HS4-SAR Insulator

PloS one, 2014-01, Vol.9 (1), p.e84268

2014

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342. Gene Edition for Wiskott-Aldrich Syndrome Gene Therapy

Molecular therapy, 2015-05, Vol.23, p.S136-S136

2015

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

Arthritis and rheumatism, 2008-04, Vol.58 (4), p.1026-1037

2008

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family

CD105 (endoglin)-negative murine mesenchymal stromal cells define a new multipotent subpopulation with distinct differentiation and immunomodulatory capacities

Comparison of Zinc Finger Nucleases Versus CRISPR-Specific Nucleases for Genome Editing of the Wiskott-Aldrich Syndrome Locus

A chimeric HS4-SAR insulator (IS2) that prevents silencing and enhances expression of lentiviral vectors in pluripotent stem cells

Gene-modified mesenchymal stromal cells: A VIP experience

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

Mesenchymal Stromal Cells Express GARP/LRRC32 on Their Surface: Effects on Their Biology and Immunomodulatory Capacity

Mesenchymal Stem Cells Expressing Vasoactive Intestinal Peptide Ameliorate Symptoms in a Model of Chronic Multiple Sclerosis

Gene Therapy Corrects Mitochondrial Dysfunction in Hematopoietic Progenitor Cells and Fibroblasts from Coq9R239X Mice

Lent-On-Plus Lentiviral vectors for conditional expression in human stem cells

Exosomes from human lymphoblastoid B cells express enzymatically active CD38 that is associated with signaling complexes containing CD81, Hsc-70 and Lyn

Absence of WASp Enhances Hematopoietic and Megakaryocytic Differentiation in a Human Embryonic Stem Cell Model

Specific marking of hESCs-derived hematopoietic lineage by WAS-promoter driven lentiviral vectors

Increased Expression of Musashi-1 Evidences Mesenchymal Repair in Maxillary Sinus Floor Elevation

Use of zinc-finger nucleases to knock out the WAS gene in K562 cells: a human cellular model for Wiskott-Aldrich syndrome

SCL/TAL1-mediated Transcriptional Network Enhances Megakaryocytic Specification of Human Embryonic Stem Cells

SCL/TAL1- mediated transcriptional network enhances megakaryocytic specification of human embryonic stem cells

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

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

A Chimeric HS4-SAR Insulator (IS2) That Prevents Silencing and Enhances Expression of Lentiviral Vectors in Pluripotent Stem Cells: e84268

Gene-modified mesenchymal stromal cells: A VIP experience

Gene Therapy Corrects Mitochondrial Dysfunction in Hematopoietic Progenitor Cells and Fibroblasts from Coq9.sup.R239X Mice

A Chimeric HS4-SAR Insulator

342. Gene Edition for Wiskott-Aldrich Syndrome Gene Therapy

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

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