Amelioration of murine beta-thalassemia through drug selection of hematopoietic stem cells transduced with a lentiviral vector encoding both gamma-globin and the MGMT drug-resistance gene.
about
Lentiviral vectors in gene therapy: their current status and future potentialTowards in vivo amplification: Overcoming hurdles in the use of hematopoietic stem cells in transplantation and gene therapyHematopoietic stem cell gene therapy:assessing the relevance of preclinical modelsAberrant methylation of different DNA repair genes demonstrates distinct prognostic value for esophageal cancerTransduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins.Future alternative therapies for β-thalassemia.Repair of O4-alkylthymine by O6-alkylguanine-DNA alkyltransferases.A zinc-finger transcriptional activator designed to interact with the gamma-globin gene promoters enhances fetal hemoglobin production in primary human adult erythroblastsIn vivo enrichment of genetically manipulated platelets corrects the murine hemophilic phenotype and induces immune tolerance even using a low multiplicity of infectionGene therapy for hemoglobinopathies: the state of the field and the future.Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer.Gene therapy for canine leukocyte adhesion deficiency with lentiviral vectors using the murine stem cell virus and human phosphoglycerate kinase promoters.Cell Membrane-associated heparan sulfate is a receptor for prototype foamy virus in human, monkey, and rodent cells.Chemoselection of allogeneic HSC after murine neonatal transplantation without myeloablation or post-transplant immunosuppression.Efficiency and safety of O⁶-methylguanine DNA methyltransferase (MGMT(P140K))-mediated in vivo selection in a humanized mouse modelGene therapy for β-thalassaemia: the continuing challenge.Gene therapy in thalassemia and hemoglobinopathies.Role of stem cell factor in the reactivation of human fetal hemoglobin.Genetic strategies for the treatment of sickle cell anaemia.Lentiviral vectors and cardiovascular diseases: a genetic tool for manipulating cardiomyocyte differentiation and function.Alternative options for DNA-based experimental therapy of β-thalassemia.Recent advances in gene therapy for thalassemia.Development of gene therapy for thalassemia.Recent trends in the gene therapy of β-thalassemia.The Ongoing Challenge of Hematopoietic Stem Cell-Based Gene Therapy for β-Thalassemia.Lentiviral Transfer of γ-Globin with Fusion Gene NUP98-HOXA10HD Expands Hematopoietic Stem Cells and Ameliorates Murine β-Thalassemia.Chemoprotection in brain tumor patients: another success for stem cell gene therapy.MicroRNA-210 overexpression induces angiogenesis and neurogenesis in the normal adult mouse brain.Gene Addition Strategies for β-Thalassemia and Sickle Cell Anemia.Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia.
P2860
Q24629462-FE0D5BAA-8792-40AA-AD53-575D8F0E7C1EQ26771159-CB7FC780-E02C-4CD0-A009-36A57925A61CQ26859147-7AC2191B-D1BF-48E7-9482-AFFF779C2F18Q28240796-36A56F87-1ED5-47A4-8CBF-871D859C9CEAQ30495724-32814CF3-03C4-4172-9D18-7329E82387B5Q33659678-F5D5E11C-1580-420F-96B4-4C9E261775E2Q33707101-E9C239BF-9690-4A6A-BB60-E8BB9C764A7DQ33805970-A9D2351E-21B0-4F31-964E-EC3062F1F184Q34021880-B6C99B7C-BAF5-453E-9E79-76ADC99A4FEDQ34204480-FB294E1B-7A04-44CC-B971-1A5D2003257CQ34707143-765CD5C7-83D7-492E-B561-C80110E7ECAEQ35022870-BCBA7999-3463-4570-A26A-42EE383F8F9BQ36014113-64D3E137-62AD-4149-B71E-BE6F6335FE14Q36401055-2EF6405A-6762-436C-B1AB-4BB5ADAE7200Q37580086-AA9AF936-6EA9-49E2-85E1-6968274289BCQ37795125-ED5A25C4-8925-4839-A406-A2B99CC6BE56Q37854468-58C33C6E-2F0C-4CFB-BECB-7B10BF75168FQ37854469-F8B929D7-4101-4B8A-B31A-366E59AD778BQ37894826-9CDD18BE-92A6-495F-ACCA-F47D98F71686Q37989402-6DC22A46-93AC-4298-82D5-C2B4A266C42BQ37993118-BE7C6044-31BB-4250-95AF-C195F563DE71Q38038167-62BA03FB-DD92-4137-AC02-9F9007B89F8DQ38057725-75811206-B5A8-481E-8F34-0FB65D546963Q38367473-8AE78809-A33D-4978-AAE7-2BFDA64D464FQ39749114-E36EA29A-280E-4AEB-ABC6-D2558661EBD1Q40338871-A3A327C4-D75E-4E19-BE5B-58B78861B420Q42226731-302F9BAB-3058-4A87-9B6E-C228132045A4Q42260328-35268411-AD92-4881-91B3-A8DC0148A32DQ45874313-FA4E8D7F-6434-4DE7-B01D-3253DEF58FCDQ45888439-AB68D8A6-76F4-4D23-8B8D-7161A7B9317A
P2860
Amelioration of murine beta-thalassemia through drug selection of hematopoietic stem cells transduced with a lentiviral vector encoding both gamma-globin and the MGMT drug-resistance gene.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 13 April 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@en
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@nl
type
label
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@en
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@nl
prefLabel
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@en
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@nl
P2093
P2860
P1433
P1476
Amelioration of murine beta-th ...... the MGMT drug-resistance gene.
@en
P2093
Derek A Persons
Huifen Zhao
Md Nasimuzzaman
Perdeep Mehta
Phillip W Hargrove
Tamara I Pestina
P2860
P304
P356
10.1182/BLOOD-2008-10-186684
P407
P577
2009-04-13T00:00:00Z