Pages that link to "Q45674295"
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The following pages link to Efficient gene transfer into rhesus repopulating hematopoietic stem cells using a simian immunodeficiency virus-based lentiviral vector system (Q45674295):
Displaying 50 items.
- Distinct genomic integration of MLV and SIV vectors in primate hematopoietic stem and progenitor cells (Q24796392) (← links)
- The use of retroviral vectors for gene therapy-what are the risks? A review of retroviral pathogenesis and its relevance to retroviral vector-mediated gene delivery (Q24804110) (← links)
- Hematopoietic stem cell gene therapy:assessing the relevance of preclinical models (Q26859147) (← links)
- Alix-mediated assembly of the actomyosin-tight junction polarity complex preserves epithelial polarity and epithelial barrier (Q27313202) (← links)
- Engineered drug resistant γδ T cells kill glioblastoma cell lines during a chemotherapy challenge: a strategy for combining chemo- and immunotherapy (Q28485036) (← links)
- Ultrasensitive fluorescent proteins for imaging neuronal activity (Q29616778) (← links)
- Transduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins (Q30495724) (← links)
- Recruitment of a SAP18-HDAC1 complex into HIV-1 virions and its requirement for viral replication (Q33463283) (← links)
- Protection of stem cell-derived lymphocytes in a primate AIDS gene therapy model after in vivo selection (Q33514823) (← links)
- Comparison of factor VIII transgenes bioengineered for improved expression in gene therapy of hemophilia A (Q33688429) (← links)
- Transient in vivo beta-globin production after lentiviral gene transfer to hematopoietic stem cells in the nonhuman primate (Q33688435) (← links)
- Directed engineering of a high-expression chimeric transgene as a strategy for gene therapy of hemophilia A. (Q33713758) (← links)
- Mobilization and mechanism of transcription of integrated self-inactivating lentiviral vectors (Q33843471) (← links)
- Integration-specific In Vitro Evaluation of Lentivirally Transduced Rhesus CD34( ) Cells Correlates With In Vivo Vector Copy Number. (Q33902257) (← links)
- Decitabine suspends human CD34 cell differentiation and proliferation during lentiviral transduction (Q33999887) (← links)
- Large animal models of hematopoietic stem cell gene therapy (Q34039922) (← links)
- A self-inactivating lentiviral vector for SCID-X1 gene therapy that does not activate LMO2 expression in human T cells (Q34074917) (← links)
- Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo (Q34170361) (← links)
- Stem cell gene transfer--efficacy and safety in large animal studies. (Q34344216) (← links)
- Chicken HS4 insulators have minimal barrier function among progeny of human hematopoietic cells transduced with an HIV1-based lentiviral vector. (Q34473330) (← links)
- Viral-genetic tracing of the input-output organization of a central noradrenaline circuit. (Q34483073) (← links)
- The murine stem cell virus promoter drives correlated transgene expression in the leukocytes and cerebellar Purkinje cells of transgenic mice (Q34506207) (← links)
- Highly efficient retrograde gene transfer into motor neurons by a lentiviral vector pseudotyped with fusion glycoprotein (Q35006070) (← links)
- A neuron-based screening platform for optimizing genetically-encoded calcium indicators (Q35025522) (← links)
- Modeling of the human alveolar rhabdomyosarcoma Pax3-Foxo1 chromosome translocation in mouse myoblasts using CRISPR-Cas9 nuclease (Q35058021) (← links)
- Contributions of gene marking to cell and gene therapies. (Q35059829) (← links)
- Porcine endogenous retrovirus integration sites in the human genome: features in common with those of murine leukemia virus (Q35139582) (← links)
- Effects of vector backbone and pseudotype on lentiviral vector-mediated gene transfer: studies in infant ADA-deficient mice and rhesus monkeys (Q35596574) (← links)
- Pigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies (Q35664334) (← links)
- Lentiviral Fluorescent Protein Expression Vectors for Biotinylation Proteomics (Q35756010) (← links)
- Cytokine-independent growth and clonal expansion of a primary human CD8 T-cell clone following retroviral transduction with the IL-15 gene (Q35839860) (← links)
- Increased Engraftment of Human Short Term Repopulating Hematopoietic Cells in NOD/SCID/IL2rγnull Mice by Lentiviral Expression of NUP98-HOXA10HD (Q35892883) (← links)
- Construction of stable producer cells to make high-titer lentiviral vectors for dendritic cell-based vaccination (Q35899079) (← links)
- Nonmyeloablative conditioning regimen to increase engraftment of gene-modified hematopoietic stem cells in young rhesus monkeys (Q35939500) (← links)
- Stem cell factor-displaying simian immunodeficiency viral vectors together with a low conditioning regimen allow for long-term engraftment of gene-marked autologous hematopoietic stem cells in macaques. (Q36114246) (← links)
- Stem cell gene transfer: insights into integration and hematopoiesis from primate genetic marking studies (Q36164528) (← links)
- Vector design for expression of O6-methylguanine-DNA methyltransferase in hematopoietic cells (Q36248825) (← links)
- Real-time quantitative PCR for the design of lentiviral vector analytical assays (Q36288916) (← links)
- High-efficiency transduction of rhesus hematopoietic repopulating cells by a modified HIV1-based lentiviral vector (Q36298679) (← links)
- Evaluation of engraftment and immunological tolerance after reduced intensity conditioning in a rhesus hematopoietic stem cell gene therapy model (Q36424560) (← links)
- Gene therapy for treatment of inherited haematological disorders (Q36446948) (← links)
- Genotoxicity of retroviral integration in hematopoietic cells. (Q36453658) (← links)
- Retrovirus vectors: toward the plentivirus? (Q36457016) (← links)
- Can gene delivery close the door to HIV-1 entry after escape? (Q36548748) (← links)
- Territories of heterologous inputs onto Purkinje cell dendrites are segregated by mGluR1-dependent parallel fiber synapse elimination (Q36646309) (← links)
- The genetic engineering of hematopoietic stem cells: the rise of lentiviral vectors, the conundrum of the ltr, and the promise of lineage-restricted vectors (Q36709988) (← links)
- Efficient transduction of pigtailed macaque hematopoietic repopulating cells with HIV-based lentiviral vectors (Q36713507) (← links)
- Reconstitution of the myeloid and lymphoid compartments after the transplantation of autologous and genetically modified CD34 bone marrow cells, following gamma irradiation in cynomolgus macaques (Q36766589) (← links)
- Gene therapy for childhood immunological diseases (Q36997726) (← links)
- Combinatorial incorporation of enhancer-blocking components of the chicken beta-globin 5'HS4 and human T-cell receptor alpha/delta BEAD-1 insulators in self-inactivating retroviral vectors reduces their genotoxic potential (Q37021156) (← links)