Search Results - "Millar, Hillary"

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    Extracellular matrix metalloproteinase inducer stimulates tumor angiogenesis by elevating vascular endothelial cell growth factor and matrix metalloproteinases by YI TANG, NAKADA, Marian T, KESAVAN, Prabakaran, MCCABE, Francis, MILLAR, Hillary, RAFFERTY, Patricia, BUGELSKI, Peter, LI YAN

    Published in Cancer research (Chicago, Ill.) (15-04-2005)
    “…Matrix metalloproteinases (MMPs) are endopeptidases that play pivotal roles in promoting tumor disease progression, including tumor angiogenesis. In many solid…”
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    Regulation of Vascular Endothelial Growth Factor Expression by EMMPRIN via the PI3K-Akt Signaling Pathway by Tang, Yi, Nakada, Marian T, Rafferty, Patricia, Laraio, Jenny, McCabe, Francis L, Millar, Hillary, Cunningham, Mark, Snyder, Linda A, Bugelski, Peter, Yan, Li

    Published in Molecular cancer research (01-06-2006)
    “…Extracellular matrix metalloproteinase (MMP) inducer (EMMPRIN) is a cell surface glycoprotein overexpressed in many solid tumors. In addition to its ability to…”
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    CNTO 859, a humanized anti‐tissue factor monoclonal antibody, is a potent inhibitor of breast cancer metastasis and tumor growth in xenograft models by Ngo, Cam V., Picha, Kristen, McCabe, Francis, Millar, Hillary, Tawadros, Richard, Tam, Susan H., Nakada, Marian T., Anderson, G. Mark

    Published in International journal of cancer (15-03-2007)
    “…Thromboembolic complications are frequently associated with advanced cancer. Interestingly, one of the major initiators of blood coagulation, tissue factor…”
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    Circulating Human Interleukin-8 as an Indicator of Cancer Progression in a Nude Rat Orthotopic Human Non–Small Cell Lung Carcinoma Model by MILLAR, Hillary J, NEMETH, Jeffrey A, MCCABE, Francis L, PIKOUNIS, Bill, WICKSTROM, Eric

    “…Clinically relevant animal models of human cancer are necessary for the evaluation of putative therapeutics. We hypothesized that circulating human lung…”
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    αv Integrin-Targeted Immunoconjugates Regress Established Human Tumors in Xenograft Models by QIMING CHEN, MILLAR, Hillary J, ANDERSON, G. Mark, MCCABE, Francis L, MANNING, Carol D, STEEVES, Rita, LAI, Kate, KELLOGG, Brenda, LUTZ, Robert J, TRIKHA, Mohit, NAKADA, Marian T

    Published in Clinical cancer research (15-06-2007)
    “…Purpose: Targeted delivery of cytotoxic agents to solid tumors through cell surface antigens can potentially reduce systemic toxicity and increase the efficacy…”
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    Abstract 36: The discovery of a novel CD19xCD22 dual-targeting CAR for the development of an IPSC-derived cell therapy by Carton, Jill M., Wheeler, John, Dower, Chris, Campion, Liam, Millar, Hillary J., Beqiri, Marilda, Morse, Barry, Gurung, Buddha, Genovese, Rebecca, DeLuca, Steven, Dominick, Charles, Naso, Michael, Levitsky, Hy

    Published in Cancer research (Chicago, Ill.) (22-03-2024)
    “…Dual-targeting cell therapies to address CD19 antigen loss in heme malignancies are being explored by Century Therapeutics and others for unmet clinical need…”
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    Abstract 6802: CXCR4 transgene improves in vivo migration and efficacy of engineered iPSC-derived natural killer cells by Millar, Hillary J., Walker, David, Campion, Liam R., Budd, Ciara, Kolluri, Aarti, Sharma, Harsh, Gurung, Buddha, Carton, Jill M., Perry, Daniel J., Alexander, Nicholas, Levitsky, Hyam, Naso, Michael, Morse, Barry A.

    Published in Cancer research (Chicago, Ill.) (22-03-2024)
    “…Chimeric antigen receptor (CAR)-engineered induced pluripotent stem cell (iPSC)-derived natural killer (iNK) cells have shown a favorable safety profile and…”
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    Abstract 1492: Development of a CD123xCD3 bispecific antibody to treat acute myeloid leukemia (AML) by Gaudet, Francois, Nemeth, Jennifer F., McDaid, Ronan, Li, Yingzhe, Harman, Benjamin, Millar, Hillary, Teplyakov, Alexey, Wheeler, John, Luo, Jinquan, Tam, Susan, Wu, Sheng-Jiun, Chen, Emily, Babich, Alexander, Elsayed, Yusri, Attar, Ricardo

    Published in Cancer research (Chicago, Ill.) (15-07-2016)
    “…AML is a heterogeneous disease characterized by uncontrolled clonal expansion of leukemic stem cells (LSCs). Current therapies for AML are not curative, in…”
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    Abstract C189: CD24 plays an important role on NSCLC cell functions relevant to tumor growth by Macedo, Luciana F., Kaiser, Elizabeth, Jiang, Haiyan, Millar, Hillary, Pietsch, E. Christine, Kaplan, Fred, Wiley, Diana, Snyder, Linda A., Marshall, Debbie

    Published in Molecular cancer therapeutics (01-11-2013)
    “…CD24 is a heavily glycosylated glycosylphosphatidylinositol-anchored protein that is over-expressed in many different tumor types including lung cancer (NSCLC…”
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