Search Results - "Lasater, E A"

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    Nf1+/− mice have increased neointima formation via hyperactivation of a Gleevec sensitive molecular pathway by Lasater, Elisabeth A., Bessler, Waylan K., Mead, Laura E., Horn, Whitney E., Clapp, D. Wade, Conway, Simon J., Ingram, David A., Li, Fang

    Published in Human molecular genetics (01-08-2008)
    “…Neurofibromatosis type I (NF1) is a genetic disorder caused by mutations in the NF1 tumor suppressor gene. Neurofibromin is encoded by NF1 and functions as a…”
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    Journal Article
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    Genetic and cellular evidence of vascular inflammation in neurofibromin-deficient mice and humans by Lasater, Elisabeth A, Li, Fang, Bessler, Waylan K, Estes, Myka L, Vemula, Sasidhar, Hingtgen, Cynthia M, Dinauer, Mary C, Kapur, Reuben, Conway, Simon J, Ingram, Jr, David A

    Published in The Journal of clinical investigation (01-03-2010)
    “…Neurofibromatosis type 1 (NF1) results from mutations in the NF1 tumor suppressor gene, which encodes the protein neurofibromin. NF1 patients display diverse…”
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    Journal Article
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