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Publication Programs: Platform

Multiplex Deletion of Myeloid Antigens by Base Editing in Human Hematopoietic Stem and Progenitor Cells (HSPCs) Enables Potential for Next Generation Transplant for Acute Myeloid Leukemia (AML) Treatment

ESGCT – 2022 – Poster Presentation P432 […]

Read More… from Multiplex Deletion of Myeloid Antigens by Base Editing in Human Hematopoietic Stem and Progenitor Cells (HSPCs) Enables Potential for Next Generation Transplant for Acute Myeloid Leukemia (AML) Treatment

Efficient Knockout of Both CD33 and CLL-1 by Multiplex Genome Editing of Human Hematopoietic Stem Cells Enhances the Potential of Next- Generation Transplants for Acute Myeloid Leukemia (AML) Treatment

ESGCT – 2022 – Poster Presentation P150 […]

Read More… from Efficient Knockout of Both CD33 and CLL-1 by Multiplex Genome Editing of Human Hematopoietic Stem Cells Enhances the Potential of Next- Generation Transplants for Acute Myeloid Leukemia (AML) Treatment

Automated Closed Cell Processing System De-Risks Gene-Edited CD34+ Hematopoietic Stem Cell Manufacturing

Bioprocess International – 2022 – Poster Presentation CT11 […]

Read More… from Automated Closed Cell Processing System De-Risks Gene-Edited CD34+ Hematopoietic Stem Cell Manufacturing

TransACT Enhances Detection and Characterization of Translocation Events from High-Throughput Sequencing Data at Base-Pair Resolution for Gene Editing Products

ISMB – 2022 – Poster Presentation 859 […]

Read More… from TransACT Enhances Detection and Characterization of Translocation Events from High-Throughput Sequencing Data at Base-Pair Resolution for Gene Editing Products

Multiplex Deletion of Myeloid Antigens CD33 and CLL-1 by CRISPR/Cas9 in Human Hematopoietic Stem Cells Highlights the Potential of Next-Generation Transplantation for AML Treatment

EHA – 2022 – Poster Presentation 1429 […]

Read More… from Multiplex Deletion of Myeloid Antigens CD33 and CLL-1 by CRISPR/Cas9 in Human Hematopoietic Stem Cells Highlights the Potential of Next-Generation Transplantation for AML Treatment

A Novel Scalable Electroporation Platform for the Manufacturing of Gene Modified Hematopoietic Stem and Progenitor Cell Therapies

ASGCT – 2022 – Poster Presentation Tu-117 […]

Read More… from A Novel Scalable Electroporation Platform for the Manufacturing of Gene Modified Hematopoietic Stem and Progenitor Cell Therapies

Novel Automated, Functionally Closed System for Rapid Immunomagnetic Negative Selection of T Cells

ISGCT – 2022 – Poster Presentation 933 […]

Read More… from Novel Automated, Functionally Closed System for Rapid Immunomagnetic Negative Selection of T Cells

Multiplex Editing of Hematopoietic Stem and Progenitor Cells (HSPCs) with CRISPR Cas Nucleases Achieves High On Target Editing with Undetectable Translocations

Keystone Symposia – 2022 – Poster Presentation 3002 […]

Read More… from Multiplex Editing of Hematopoietic Stem and Progenitor Cells (HSPCs) with CRISPR Cas Nucleases Achieves High On Target Editing with Undetectable Translocations

Multiplex Base Editing in Human Hematopoietic Stem and Progenitor Cells (HSPCs) Enables Efficient Removal of Multiple Surface Antigens in Acute Myeloid Leukemia (AML) Immunotherapy

Keystone Symposia – 2022 – Poster Presentation 3001 […]

Read More… from Multiplex Base Editing in Human Hematopoietic Stem and Progenitor Cells (HSPCs) Enables Efficient Removal of Multiple Surface Antigens in Acute Myeloid Leukemia (AML) Immunotherapy

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All employment opportunities at Vor Biopharma are managed by our in-house Human Resources Department. Therefore, agency staff and independent recruiters must contact the Human Resources Department directly in order to present candidates or inquire about openings. Please do not contact other Vor Bipharma employees. Your ability to comply with this request will significantly impact any decision we may make about doing business with you.

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