Detalhe da pesquisa
1.
Unbiased assessment of genome integrity and purging of adverse outcomes at the target locus upon editing of CD4+ T-cells for the treatment of Hyper IgM1.
EMBO J
; 42(23): e114188, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37916874
2.
Lipid nanoparticles allow efficient and harmless ex vivo gene editing of human hematopoietic cells.
Blood
; 142(9): 812-826, 2023 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37294917
3.
Intracoronary delivery of extracellular vesicles from human cardiac progenitor cells reduces infarct size in porcine acute myocardial infarction.
Eur Heart J
; 45(9): 728-732, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37787585
4.
Effect of Bone Marrow-Derived Mononuclear Cell Treatment, Early or Late After Acute Myocardial Infarction: Twelve Months CMR and Long-Term Clinical Results.
Circ Res
; 119(3): 481-90, 2016 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27267068
5.
Intracoronary injection of bone marrow-derived mononuclear cells early or late after acute myocardial infarction: effects on global left ventricular function.
Circulation
; 127(19): 1968-79, 2013 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23596006
6.
Bone marrow-derived cells for cardiovascular cell therapy: an optimized GMP method based on low-density gradient improves cell purity and function.
J Transl Med
; 12: 276, 2014 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-25260977
7.
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome.
Mol Ther
; 21(1): 175-84, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22371846
8.
IL-7 receptor expression identifies suicide gene-modified allospecific CD8+ T cells capable of self-renewal and differentiation into antileukemia effectors.
Blood
; 117(24): 6469-78, 2011 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21531977
9.
Methodologies for Scalable Production of High-Quality Purified Small Extracellular Vesicles from Conditioned Medium.
Methods Mol Biol
; 2668: 69-98, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37140791
10.
Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo.
Mol Ther Methods Clin Dev
; 30: 546-557, 2023 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37693944
11.
IL-7 and IL-15 allow the generation of suicide gene-modified alloreactive self-renewing central memory human T lymphocytes.
Blood
; 113(5): 1006-15, 2009 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-18978209
12.
GMP-Grade Methods for Cardiac Progenitor Cells: Cell Bank Production and Quality Control.
Methods Mol Biol
; 2286: 131-166, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33381854
13.
Quantitative proteomic analysis of lentiviral vectors using 2-DE.
Proteomics
; 9(14): 3666-76, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19639585
14.
Exosomes From Human Cardiac Progenitor Cells for Therapeutic Applications: Development of a GMP-Grade Manufacturing Method.
Front Physiol
; 9: 1169, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30197601
15.
Quality Control Assays for Clinical-Grade Human Mesenchymal Stromal Cells: Methods for ATMP Release.
Methods Mol Biol
; 1416: 313-37, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236681
16.
Quality Control Assays for Clinical-Grade Human Mesenchymal Stromal Cells: Validation Strategy.
Methods Mol Biol
; 1416: 339-56, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236682
17.
Long term follow up of patients after allogeneic stem cell transplantation and transfusion of HSV-TK transduced T-cells.
Front Pharmacol
; 6: 76, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25954199
18.
Combined delivery of bone marrow-derived mononuclear cells in chronic ischemic heart disease: rationale and study design.
Clin Cardiol
; 36(8): 435-41, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23720276
19.
Genetically modified donor leukocyte transfusion and graft-versus-leukemia effect after allogeneic stem cell transplantation.
Hum Gene Ther
; 22(7): 829-41, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21091264
20.
Large-scale manufacture and characterization of a lentiviral vector produced for clinical ex vivo gene therapy application.
Hum Gene Ther
; 22(3): 343-56, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21043787