Search Results - "Banh, Lynda"
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Mapping the genomic landscape of CRISPR–Cas9 cleavage
Published in Nature methods (01-06-2017)“…SITE-Seq probes Cas9 cleavage sites in vitro and returns a comprehensive list of off-target sites at different Cas9–sgRNA concentrations. RNA-guided…”
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Harnessing type I CRISPR–Cas systems for genome engineering in human cells
Published in Nature biotechnology (01-12-2019)“…Type I CRISPR–Cas systems are the most abundant adaptive immune systems in bacteria and archaea 1 , 2 . Target interference relies on a multi-subunit,…”
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Author Correction: Mapping the genomic landscape of CRISPR–Cas9 cleavage
Published in Nature methods (01-12-2023)Get full text
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Conformational control of Cas9 by CRISPR hybrid RNA-DNA guides mitigates off-target activity in T cells
Published in Molecular cell (02-09-2021)“…The off-target activity of the CRISPR-associated nuclease Cas9 is a potential concern for therapeutic genome editing applications. Although high-fidelity Cas9…”
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Allogeneic chimeric antigen receptor-T cells with CRISPR-disrupted programmed death-1 checkpoint exhibit enhanced functional fitness
Published in Cytotherapy (Oxford, England) (01-07-2023)“…Therapeutic disruption of immune checkpoints has significantly advanced the armamentarium of approaches for treating cancer. The prominent role of the…”
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CB-011, a BCMA-Specific Allogeneic CAR-T Cell Therapy, Engineered with Next-Generation CRISPR Technology to Express an HLA-E Fusion Transgene to Prevent Immune Cell-Mediated Rejection, for r/r Multiple Myeloma
Published in Transplantation and cellular therapy (01-02-2023)Get full text
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524 - CB-011, a BCMA-Specific Allogeneic CAR-T Cell Therapy, Engineered with Next-Generation CRISPR Technology to Express an HLA-E Fusion Transgene to Prevent Immune Cell-Mediated Rejection, for r/r Multiple Myeloma
Published in Transplantation and cellular therapy (01-02-2023)Get full text
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Highly Specific Cas9 and Cas12a Engineering of Human T Cells for Generation of Novel Allogeneic Cell Therapies
Published in Transplantation and cellular therapy (01-02-2024)“…CRISPR-based genome editing of primary human T cells has the potential to revolutionize disease-modifying therapies. However, substantial improvements in…”
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Abstract LB009: A BCMA-specific allogeneic CAR-T cell therapy (CB-011) genome-engineered to express an HLA-E fusion transgene to prevent immune cell rejection
Published in Cancer research (Chicago, Ill.) (15-06-2022)“…Abstract The approval and commercial launch of multiple first-generation CD19- or BCMA-directed, autologous CAR-T cell products have laid the foundation and…”
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