Search Results - "Clapp, D"

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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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    Journal Article
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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, D. Wade, 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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    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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    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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    Baseline Characteristics of Participants in the Randomized National Lung Screening Trial by Aberle, Denise R., Adams, Amanda M., Berg, Christine D., Clapp, Jonathan D., Clingan, Kathy L., Gareen, Ilana F., Lynch, David A., Marcus, Pamela M., Pinsky, Paul F.

    “…Background The National Lung Screening Trial (NLST), a randomized study conducted at 33 US sites, is comparing lung cancer mortality among persons screened…”
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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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    Cdkn2a (Arf) loss drives NF1-associated atypical neurofibroma and malignant transformation by Rhodes, Steven D, He, Yongzheng, Smith, Abbi, Jiang, Li, Lu, Qingbo, Mund, Julie, Li, Xiaohong, Bessler, Waylan, Qian, Shaomin, Dyer, William, Sandusky, George E, Horvai, Andrew E, Armstrong, Amy E, Clapp, D Wade

    Published in Human molecular genetics (15-08-2019)
    “…Plexiform neurofibroma (PN) tumors are a hallmark manifestation of neurofibromatosis type 1 (NF1) that arise in the Schwann cell (SC) lineage. NF1 is a common…”
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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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    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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    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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