Vice President Of Research
Current• Head of Discovery Research• Head of Translational Science
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@sentibio.com
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Brian Garrison is listed as Vice President at Senti Biosciences at Senti Biosciences, based in South San Francisco, California, United States. AeroLeads shows a work email signal at sentibio.com, phone signal with area code 650, 707, 617, and a matched LinkedIn profile for Brian Garrison.
Brian Garrison previously worked as Vice President of Research at Senti Biosciences and Senior Director of Research at Senti Biosciences. Brian Garrison holds Phd, Microbiology And Immunology from Stanford University.
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Brian Garrison is Vice President of Research at Senti Biosciences in South San Francisco, CA, where he is Head of both Discovery Research (encompassing 3 teams - Bioinformatics, Gene Circuit Research, Cell Therapy Research) and Translational Research. In his role as Head of Discovery Research, Brian leads discovery and technology development within Senti's cell therapy pipeline, including both liquid and solid tumors. He leads 3 teams whose goal is to use collaborative approaches across cell biology, immunology, synthetic biology, biological programming, and bioinformatics to develop truly innovative “smarter” living medicines with the ability to target diseases in a more focused, controlled, and effective manner. In his role as Head of Translational Research, Brian leads a team who plays key roles in performing IND-enabling studies as well as correlative studies within Senti's clinical trial(s). Brian's commitment to innovation is evident by the multiple cell therapy programs he has overseen, including logic gated and multi-armed CAR-NK/T cell therapy programs. Brian truly believes that innovation is the key to cell therapy success, and that such innovation will require a team effort.
Listed skills include Cell Biology, Molecular Biology, Stem Cells, Cell Culture, and 35 others.
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South San Francisco, Ca, Us
• Head of Discovery Research• Head of Translational Science
South San Francisco, Ca, Us
◦ Head of Discovery Research, encompassing 3 teams (Bioinformatics, Gene Circuit Research, Cell Therapy Research)◦ Lead discovery and technology development within Senti Bio's cell therapy pipeline◦ Oversee strategic early pipeline planning, with direct oversight of multiple CAR cell therapy programs from target identification through to DC Selection and IND-enabling studies◦ Lead cross-functional collaborations to develop Senti Bio’s allogeneic CAR-NK cell platform and pipeline programs◦ Lead external collaborations to further Senti's technology development◦ Forecast and maintain the Discovery Research departmental budget, and collaboratively help manage the broader R&D budget◦ Inform and confer with Senti leadership on status of pipeline programs, challenges, and potential solutions◦ Successfully completed SBIR contract, receiving highest marks◦ Engage, promote, and educate the scientific community about Senti Bio's innovative technologies, often including multiple conference presentation per year◦ Dedicated to providing a positive and supportive work environment that follows Senti Bio's core values: Be Bold! Better Together! Build to Last!
South San Francisco, Ca, Us
◦ Head of logic gated CAR-NK cell program for AML◦ Successfully led Senti's first CAR-NK cell program to DC Selection◦ PI on SBIR contract from the NCI for clinical translation of CAR NK cell program◦ Align and support other research teams to ensure fulfillment of R&D and corporate goals
South San Francisco, Ca, Us
◦ Head of logic gated CAR-NK cell program for AML◦ Enhanced collaborative team efforts through improved communication and deconstructing of informational silos◦ Successfully led Senti's first CAR-NK cell program through lead selection, which required significant novel technology development for both the activating and inhibitory CARs
South San Francisco, Ca, Us
◦ Led Senti's first CAR T cell therapy team, for the treatment of AML◦ Successfully led efforts to identify the ideal tumor target antigen pair for a bivalent activating CAR approach for logic gated T/NK cell AML programs◦ Successfully led efforts to identify the ideal inhibitory CAR target for protection of healthy cells from on-target off-tumor toxicity within logic gated CAR T/NK cell AML programs
South San Francisco, Ca, Us
◦ Led a team responsible for identifying and optimizing new cell therapy technologies for Senti Bio
South San Francisco, Ca, Us
◦ Developed Senti Bio's first cell platform for the design, testing, and development of new gene circuit technologies (PMID: 34210826; co-author)
Cambridge, Massachusetts, Us
• Generated and comparatively analyzed transcriptomics data to identify hematopoietic stem cell (HSC)-specific transcription factors, which were then characterized using a variety of in vitro and in vivo functional assays (PMID: 24319662; co-first author)• Identified the transcription factor Zfp521 as a regulator of HSC pool size and MLL-AF9-mediated leukemic disease (PMID: 28615219; co-first author)• Identified Hlf as a key HSC regulator by demonstrating it could imbue progenitors with stem cell-like attributes• In collaboration with Dr. Timothy Springer laboratory, generated bone marrow-derived microglia for successful therapeutic treatment of a neurological disease caused by defective TGFβ signaling (PMID: 29909984; co-first author)• Utilized HSC transcription factor expertise in collaboration to reprogram hematopoietic cells to a stem cell fate (PMID: 24766805; co-author)• Utilized my HSC and microglia experience in collaboration to achieve engraftment of microglia-like cells in the brain (PMID: 29226242; co-author)• Collaborated with laboratory colleagues on several HSC aging projects (PMID: 25274507, PMID: 23415915; co-author), as well as the first demonstration of CRISPR/Cas9-based ablation of clinically relevant genes in human hematopoietic cells (PMID: 25517468; co-author)(Laboratory of Dr. Derrick J. Rossi)
Boston, Ma, Us
• Generated and comparatively analyzed transcriptomics data to identify hematopoietic stem cell (HSC)-specific transcription factors, which were then characterized using a variety of in vitro and in vivo functional assays (PMID: 24319662; co-first author)• Identified the transcription factor Zfp521 as a regulator of HSC pool size and MLL-AF9-mediated leukemic disease (PMID: 28615219; co-first author)• Identified Hlf as a key HSC regulator by demonstrating it could imbue progenitors with stem cell-like attributes• In collaboration with Dr. Timothy Springer laboratory, generated bone marrow-derived microglia for successful therapeutic treatment of a neurological disease caused by defective TGFβ signaling (PMID: 29909984; co-first author)• Utilized HSC transcription factor expertise in collaboration to reprogram hematopoietic cells to a stem cell fate (PMID: 24766805; co-author)• Utilized my HSC and microglia experience in collaboration to achieve engraftment of microglia-like cells in the brain (PMID: 29226242; co-author)• Collaborated with laboratory colleagues on several HSC aging projects (PMID: 25274507, PMID: 23415915; co-author), as well as the first demonstration of CRISPR/Cas9-based ablation of clinically relevant genes in human hematopoietic cells (PMID: 25517468; co-author)(Laboratory of Dr. Derrick J. Rossi)
Boston, Ma, Us
• Utilized a microarray-based approach to identify HSC-specific regulators for possible therapeutic manipulation• Genes of interest were ectopically expressed or knocked-down within in vitro and in vivo functional assays for stem and progenitor cell activity• Studied the role of p57 in biological pathways unique to HSCs, including quiescence and self-renewal• Collaborated with laboratory colleagues on several HSC microenvironment projects (PMID: 18682243; co-author)• Collaborator for study of MLL-AF9-mediated leukemic disease (PMID: 28615219; co-first author)(Laboratory of Dr. David T. Scadden)
Stanford, Ca, Us
• Optimized transposon-mediated gene addition strategies for human gene therapy• Uncovered the extent of post-integrative silencing potential in transposon-mediated gene therapy approaches (PMID: 17938204; first author) while concurrently studying transposon integration site preferences (PMID: 15743807; co-author)(Laboratory of Dr. Mark A. Kay)
Davis, California, Us
• Used forward genetic screens to identify and characterize regulators of autophagy (PMID: 10712513; co-author)• Studied the assembly of the yeast vacuolar proton-translocating ATPase (PMID: 9195975; co-author)(Laboratory of Dr. Daniel J. Klionsky)
Quick answers generated from the profile data available on this page.
Brian Garrison works for Senti Biosciences.
Brian Garrison is listed as Vice President at Senti Biosciences at Senti Biosciences.
AeroLeads has found 1 work email signal at @sentibio.com for Brian Garrison at Senti Biosciences.
AeroLeads has found 6 phone signal(s) with area code 650, 707, 617 for Brian Garrison at Senti Biosciences.
Brian Garrison is based in South San Francisco, California, United States while working with Senti Biosciences.
Brian Garrison has worked for Senti Biosciences, Harvard University, Boston Children'S Hospital, Massachusetts General Hospital, and Stanford University.
You can use AeroLeads to view verified contact signals for Brian Garrison at Senti Biosciences, including work email, phone, and LinkedIn data when available.
Brian Garrison holds Phd, Microbiology And Immunology from Stanford University.
Brian Garrison is listed with skills including Cell Biology, Molecular Biology, Stem Cells, Cell Culture, Cell, Clinical Research, Biochemistry, and Genetics.
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