Search Results - "Cutmore, Lauren C"

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  1. 1

    Optimization of anti-CD19 CAR T cell production for treatment of patients with chronic lymphocytic leukemia by Amatya, Christina, Weissler, Katherine A., Fellowes, Vicki, Lam, Norris, Cutmore, Lauren C., Natrakul, Danielle A., Highfill, Steven L., Kochenderfer, James N.

    “…T cells expressing anti-CD19 chimeric antigen receptors (CARs) have activity against chronic lymphocytic leukemia (CLL), but complete response rates range from…”
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    Journal Article
  2. 2

    Ligand-bound integrin αvβ6 internalisation and trafficking by Meecham, Amelia, Cutmore, Lauren C, Protopapa, Pantelitsa, Rigby, Lauren G, Marshall, John F

    “…The integrin αvβ6 is expressed at low levels in most normal healthy tissue but is very often upregulated in a disease context including cancer and fibrosis…”
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    Journal Article
  3. 3

    Current Perspectives on the Use of off the Shelf CAR-T/NK Cells for the Treatment of Cancer by Cutmore, Lauren C, Marshall, John F

    Published in Cancers (16-04-2021)
    “…CAR T cells have revolutionised the treatment of haematological malignancies. Despite this, several obstacles still prohibit their widespread use and efficacy…”
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    Journal Article
  4. 4

    Syngeneic Mouse Models for Pre-Clinical Evaluation of CAR T Cells by Ahmed, Eman N, Cutmore, Lauren C, Marshall, John F

    Published in Cancers (18-09-2024)
    “…Chimeric antigen receptor (CAR) T cells have revolutionized the treatment of hematological malignancies. Unfortunately, this improvement has yet to be…”
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    Journal Article
  5. 5
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    Adoptive Transfer of T Cells Genetically Engineered to Express T-Cell Receptors Targeting Neoantigens Arising from p53 and Ras Hotspot Mutations in Hematologic Malignancies by Cappell, Kathryn M, Kim, Sanghyun P, Levin, Noam, Lam, Norris, Amatya, Christina, Cutmore, Lauren C, Beyer, Rachel, Rosenberg, Steven A, Kochenderfer, James N

    Published in Blood (02-11-2023)
    “…The tumor suppressor gene p53 and the oncogenes NRAS and KRAS (shortened to Ras) are frequently mutated in many difficult-to-treat hematologic malignancies…”
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    Journal Article