Search Results - Apiz, Juan

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  1. 1
    Tumor interstitial fluid analysis enables the study of microenvironment–cell interactions in cancers

    Tumor interstitial fluid analysis enables the study of microenvironment–cell interactions in cancers by Apiz Saab, Juan J, Muir, Alexander

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  2. 2
    Pancreatic tumors exhibit myeloid-driven amino acid stress and upregulate arginine biosynthesis

    Pancreatic tumors exhibit myeloid-driven amino acid stress and upregulate arginine biosynthesis by Apiz Saab, Juan J, Dzierozynski, Lindsey N, Jonker, Patrick B, AminiTabrizi, Roya, Shah, Hardik, Menjivar, Rosa Elena, Scott, Andrew J, Nwosu, Zeribe C, Zhu, Zhou, Chen, Riona N, Oh, Moses, Sheehan, Colin, Wahl, Daniel R, Pasca di Magliano, Marina, Lyssiotis, Costas A, Macleod, Kay F, Weber, Christopher R, Muir, Alexander

    Published in eLife
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  3. 3
    Uridine-derived ribose fuels glucose-restricted pancreatic cancer

    Uridine-derived ribose fuels glucose-restricted pancreatic cancer by Nwosu, Zeribe C., Ward, Matthew H., Sajjakulnukit, Peter, Poudel, Pawan, Ragulan, Chanthirika, Kasperek, Steven, Radyk, Megan, Sutton, Damien, Menjivar, Rosa E., Andren, Anthony, Apiz-Saab, Juan J., Tolstyka, Zachary, Brown, Kristee, Lee, Ho-Joon, Dzierozynski, Lindsey N., He, Xi, PS, Hari, Ugras, Julia, Nyamundanda, Gift, Zhang, Li, Halbrook, Christopher J., Carpenter, Eileen S., Shi, Jiaqi, Shriver, Leah P., Patti, Gary J., Muir, Alexander, Pasca di Magliano, Marina, Sadanandam, Anguraj, Lyssiotis, Costas A.

    Published in Nature (London)
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  4. 4
    Abstract 2177: Myeloid-derived arginase depletes microenvironmental arginine in PDAC tumors and leads to activation of arginine de novo biosynthesis in cancer cells

    Abstract 2177: Myeloid-derived arginase depletes microenvironmental arginine in PDAC tumors and leads to activation of arginine de novo biosynthesis in cancer cells by Apiz-Saab, Juan, Muir, Alex

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  5. 5
    Erratum: Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells

    Erratum: Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells by Santana-Rivera, Yasmarie, Rabelo-Fernández, Robert J, Quiñones-Díaz, Blanca I, Grafals-Ruíz, Nilmary, Santiago-Sánchez, Ginette, Lozada-Delgado, Eunice L, Echevarría-Vargas, Ileabett M, Apiz, Juan, Soto, Daniel, Rosado, Andrea, Meléndez, Loyda, Valiyeva, Fatima, Vivas-Mejía, Pablo E

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  6. 6
    Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells

    Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells by Santana-Rivera, Yasmarie, Rabelo-Fernández, Robert J, Quiñones-Díaz, Blanca I, Grafals-Ruíz, Nilmary, Santiago-Sánchez, Ginette, Lozada-Delgado, Eunice L, Echevarría-Vargas, Ileabett M, Apiz, Juan, Soto, Daniel, Rosado, Andrea, Meléndez, Loyda, Valiyeva, Fatima, Vivas-Mejía, Pablo E

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  7. 7
    Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells

    Reduced expression of enolase-1 correlates with high intracellular glucose levels and increased senescence in cisplatin-resistant ovarian cancer cells by Santana-Rivera, Yasmarie, Rabelo-Fernández, Robert J, Quiñones-Díaz, Blanca I, Grafals-Ruíz, Nilmary, Santiago-Sánchez, Ginette, Lozada-Delgado, Eunice L, Echevarría-Vargas, Ileabett M, Apiz, Juan, Soto, Daniel, Rosado, Andrea, Meléndez, Loyda, Valiyeva, Fatima, Vivas-Mejía, Pablo E

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  8. 8
    Abstract B003: Pancreatic cancer cells activate arginine biosynthesis to adapt to myeloid-driven amino acid stress in the tumor microenvironment

    Abstract B003: Pancreatic cancer cells activate arginine biosynthesis to adapt to myeloid-driven amino acid stress in the tumor microenvironment by Saab, Juan J. Apiz, Dzierozynski, Lindsey N., Jonker, Patrick B., Zhu, Zhou, Chen, Riona N., Oh, Moses, Sheehan, Colin, Macleod, Kay F., Weber, Christopher R., Muir, Alexander

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