B cell-specific lentiviral gene therapy leads to sustained B-cell functional recovery in a murine model of X-linked agammaglobulinemia.
about
Advances of gene therapy for primary immunodeficienciesGene therapy for primary immunodeficienciesCurrent translational and clinical practices in hematopoietic cell and gene therapyDaedalus: a robust, turnkey platform for rapid production of decigram quantities of active recombinant proteins in human cell lines using novel lentiviral vectorsDevelopment of B-lineage predominant lentiviral vectors for use in genetic therapies for B cell disordersProgressive engineering of a homing endonuclease genome editing reagent for the murine X-linked immunodeficiency locus.Successful targeting and disruption of an integrated reporter lentivirus using the engineered homing endonuclease Y2 I-AniI.Gene transfer into hematopoietic stem cells as treatment for primary immunodeficiency diseases.Intraosseous delivery of lentiviral vectors targeting factor VIII expression in platelets corrects murine hemophilia A.Generation of a lentiviral vector producer cell clone for human Wiskott-Aldrich syndrome gene therapy.Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndrome.Altered B cell homeostasis is associated with type I diabetes and carriers of the PTPN22 allelic variant.A genome editing primer for the hematologistGenotoxicity of retroviral hematopoietic stem cell gene therapy.New frontiers of primary antibody deficiencies.Primary antibody deficiencies.Agammaglobulinemia: causative mutations and their implications for novel therapies.Gene therapy for primary immunodeficiencies.Safe and Effective Gene Therapy for Murine Wiskott-Aldrich Syndrome Using an Insulated Lentiviral VectorSingle cell imaging of Bruton's tyrosine kinase using an irreversible inhibitor.Gene delivery in malignant B cells using the combination of lentiviruses conjugated to anti-transferrin receptor antibodies and an immunoglobulin promoter.Evolving Gene Therapy in Primary Immunodeficiency.Targeting expression to megakaryocytes and platelets by lineage-specific lentiviral vectors.Bruton's tyrosine kinase: from X-linked agammaglobulinemia toward targeted therapy for B-cell malignancies.Developmentally regulated expression of MEF2C limits the response to BCR engagement in transitional B cellsSuccessful hematopoietic cell transplantation in a patient with X-linked agammaglobulinemia and acute myeloid leukemia.Biology and novel treatment options for XLA, the most common monogenetic immunodeficiency in man.IgM Augments Complement Bactericidal Activity with Serum from a Patient with a Novel CD79a Mutation.
P2860
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P2860
B cell-specific lentiviral gene therapy leads to sustained B-cell functional recovery in a murine model of X-linked agammaglobulinemia.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@ast
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@en
type
label
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@ast
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@en
prefLabel
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@ast
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@en
P2093
P2860
P1433
P1476
B cell-specific lentiviral gen ...... f X-linked agammaglobulinemia.
@en
P2093
Alexander Astrakhan
Blythe D Sather
Brigid V Stirling
Byoung Y Ryu
David J Rawlings
Denny Liggitt
Hannah M Kerns
Stephanie Humblet-Baron
P2860
P304
P356
10.1182/BLOOD-2009-09-241869
P407
P577
2010-01-21T00:00:00Z