Search Results - "McNeill, Robert S."

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  1. 1

    Transformation of quiescent adult oligodendrocyte precursor cells into malignant glioma through a multistep reactivation process by Galvao, Rui Pedro, Kasina, Anita, McNeill, Robert S, Harbin, Jordan E, Foreman, Oded, Verhaak, Roel G W, Nishiyama, Akiko, Miller, C Ryan, Zong, Hui

    “…How malignant gliomas arise in a mature brain remains a mystery, hindering the development of preventive and therapeutic interventions. We previously showed…”
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    Journal Article
  2. 2

    Intrinsic Astrocyte Heterogeneity Influences Tumor Growth in Glioma Mouse Models by Irvin, David M., McNeill, Robert S., Bash, Ryan E., Miller, C. Ryan

    Published in Brain pathology (Zurich, Switzerland) (01-01-2017)
    “…The influence of cellular origin on glioma pathogenesis remains elusive. We previously showed that mutations inactivating Rb and Pten and activating Kras…”
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  3. 3

    PIK3CA missense mutations promote glioblastoma pathogenesis, but do not enhance targeted PI3K inhibition by McNeill, Robert S, Stroobant, Emily E, Smithberger, Erin, Canoutas, Demitra A, Butler, Madison K, Shelton, Abigail K, Patel, Shrey D, Limas, Juanita C, Skinner, Kasey R, Bash, Ryan E, Schmid, Ralf S, Miller, C Ryan

    Published in PloS one (05-07-2018)
    “…Glioblastoma (GBM) is the most common adult primary brain tumor. Multimodal treatment is empiric and prognosis remains poor. Recurrent PIK3CA missense…”
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    Journal Article
  4. 4

    Genomic profiles of low-grade murine gliomas evolve during progression to glioblastoma by Vitucci, Mark, Irvin, David M, McNeill, Robert S, Schmid, Ralf S, Simon, Jeremy M, Dhruv, Harshil D, Siegel, Marni B, Werneke, Andrea M, Bash, Ryan E, Kim, Seungchan, Berens, Michael E, Miller, C Ryan

    Published in Neuro-oncology (Charlottesville, Va.) (01-09-2017)
    “…Gliomas are diverse neoplasms with multiple molecular subtypes. How tumor-initiating mutations relate to molecular subtypes as these tumors evolve during…”
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  5. 5

    Contemporary murine models in preclinical astrocytoma drug development by McNeill, Robert S, Vitucci, Mark, Wu, Jing, Miller, C Ryan

    Published in Neuro-oncology (Charlottesville, Va.) (01-01-2015)
    “…Despite 6 decades of research, only 3 drugs have been approved for astrocytomas, the most common malignant primary brain tumors. However, clinical drug…”
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  6. 6

    BRAF Mutations Open Doors for N-Ethyl-N-Nitrosourea–Induced Gliomagenesis by McNeill, Robert S, Irvin, David M, Miller, C. Ryan

    Published in The American journal of pathology (01-10-2016)
    “…This commentary highlights the article by Wang et al that describes a preclinical model for targeting BRAF-mutant gliomas…”
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    Cooperativity between MAPK and PI3K signaling activation is required for glioblastoma pathogenesis by Vitucci, Mark, Karpinich, Natalie O, Bash, Ryan E, Werneke, Andrea M, Schmid, Ralf S, White, Kristen K, McNeill, Robert S, Huff, Byron, Wang, Sophie, Van Dyke, Terry, Miller, C Ryan

    Published in Neuro-oncology (Charlottesville, Va.) (01-10-2013)
    “…Glioblastoma (GBM) genomes feature recurrent genetic alterations that dysregulate core intracellular signaling pathways, including the G1/S cell cycle…”
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  11. 11

    Modeling astrocytoma pathogenesis in vitro and in vivo using cortical astrocytes or neural stem cells from conditional, genetically engineered mice by McNeill, Robert S, Schmid, Ralf S, Bash, Ryan E, Vitucci, Mark, White, Kristen K, Werneke, Andrea M, Constance, Brian H, Huff, Byron, Miller, C Ryan

    Published in Journal of visualized experiments (12-08-2014)
    “…Current astrocytoma models are limited in their ability to define the roles of oncogenic mutations in specific brain cell types during disease pathogenesis and…”
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  12. 12

    Influence of PI3K and MAPK Pathway Mutations on Response to Mono and Dual Treatment with Targeted Kinase Inhibitors by McNeill, Robert S, Canoutas, Demitra A, Bash, Ryan E, Schmid, Ralf S, Constance, Brian H, Johnson, Gary L, Miller, C. Ryan

    Published in The FASEB journal (01-04-2016)
    “…Abstract only Genetic heterogeneity and drug resistance has hindered the clinical development of targeted kinase inhibitors for treatment of glioblastoma, the…”
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    Journal Article
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