Search Results - "CLAPP, D. Wade"

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    Fanconi Anemia Proteins Function in Mitophagy and Immunity by Sumpter, Rhea, Sirasanagandla, Shyam, Fernández, Álvaro F., Wei, Yongjie, Dong, Xiaonan, Franco, Luis, Zou, Zhongju, Marchal, Christophe, Lee, Ming Yeh, Clapp, DWade, Hanenberg, Helmut, Levine, Beth

    Published in Cell (05-05-2016)
    “…Fanconi anemia (FA) pathway genes are important tumor suppressors whose best-characterized function is repair of damaged nuclear DNA. Here, we describe an…”
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    Journal Article
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    Contributions of inflammation and tumor microenvironment to neurofibroma tumorigenesis by Liao, Chung-Ping, Booker, Reid C, Brosseau, Jean-Philippe, Chen, Zhiguo, Mo, Juan, Tchegnon, Edem, Wang, Yong, Clapp, D Wade, Le, Lu Q

    Published in The Journal of clinical investigation (02-07-2018)
    “…Neurofibromatosis type 1 associates with multiple neoplasms, and the Schwann cell tumor neurofibroma is the most prevalent. A hallmark feature of neurofibroma…”
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    Feasibility of using NF1-GRD and AAV for gene replacement therapy in NF1-associated tumors by Bai, Ren-Yuan, Esposito, Dominic, Tam, Ada J., McCormick, Frank, Riggins, Gregory J., Wade Clapp, D., Staedtke, Verena

    Published in Gene therapy (01-06-2019)
    “…Neurofibromatosis type 1, including the highly aggressive malignant peripheral nerve sheath tumors (MPNSTs), is featured by the loss of functional…”
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    Inhibition or Ablation of p21-activated Kinase (PAK1) Disrupts Glucose Homeostatic Mechanisms in Vivo by Wang, Zhanxiang, Oh, Eunjin, Clapp, D. Wade, Chernoff, Jonathan, Thurmond, Debbie C.

    Published in The Journal of biological chemistry (02-12-2011)
    “…The p21-activated kinase PAK1 is implicated in tumorigenesis, and efforts to inhibit PAK1 signaling as a means to induce tumor cell apoptosis are underway…”
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    Mast cells and the neurofibroma microenvironment by Staser, Karl, Yang, Feng-Chun, Clapp, D. Wade

    Published in Blood (15-07-2010)
    “…Neurofibromatosis type 1 (NF1) is the most common genetic disorder with a predisposition to malignancy and affects 1 in 3500 persons worldwide. NF1 is caused…”
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    A Collaborative Model for Accelerating the Discovery and Translation of Cancer Therapies by Maertens, Ophélia, McCurrach, Mila E, Braun, Benjamin S, De Raedt, Thomas, Epstein, Inbal, Huang, Tannie Q, Lauchle, Jennifer O, Lee, Hyerim, Wu, Jianqiang, Cripe, Timothy P, Clapp, D Wade, Ratner, Nancy, Shannon, Kevin, Cichowski, Karen

    Published in Cancer research (Chicago, Ill.) (01-11-2017)
    “…Preclinical studies using genetically engineered mouse models (GEMM) have the potential to expedite the development of effective new therapies; however, they…”
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    Fanconi anaemia and cancer: an intricate relationship by Nalepa, Grzegorz, Clapp, D. Wade

    Published in Nature reviews. Cancer (01-03-2018)
    “…Key Points Fanconi anaemia (FA) is a complex genetic syndrome associated with risk of congenital malformations, bone marrow failure and cancer. Diagnosis of FA…”
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    A molecular basis for neurofibroma-associated skeletal manifestations in NF1 by Ma, Yun, Gross, Andrea M., Dombi, Eva, Pemov, Alexander, Choi, Kwangmin, Chaney, Katherine, Rhodes, Steven D., Angus, Steven P., Sciaky, Noah, Clapp, D. Wade, Ratner, Nancy, Widemann, Brigitte C., Rios, Jonathan J., Elefteriou, Florent

    Published in Genetics in medicine (01-11-2020)
    “…Purpose Plexiform neurofibromas (pNF) develop in children with neurofibromatosis type 1 (NF1) and can be associated with several skeletal comorbidities…”
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    Pathogenesis of plexiform neurofibroma: tumor-stromal/hematopoietic interactions in tumor progression by Staser, Karl, Yang, Feng-Chun, Clapp, D Wade

    Published in Annual review of pathology (01-01-2012)
    “…Neurofibromatosis type 1 (NF1) is a genetic disease that results from either heritable or spontaneous autosomal dominant mutations in the NF1 gene. A…”
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    Fanconi anemia signaling network regulates the spindle assembly checkpoint by Nalepa, Grzegorz, Enzor, Rikki, Sun, Zejin, Marchal, Christophe, Park, Su-Jung, Yang, Yanzhu, Tedeschi, Laura, Kelich, Stephanie, Hanenberg, Helmut, Clapp, D Wade

    Published in The Journal of clinical investigation (01-09-2013)
    “…Fanconi anemia (FA) is a heterogenous genetic disease with a high risk of cancer. The FA proteins are essential for interphase DNA damage repair; however, it…”
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