Showing 1 - 4 results of 4 for search 'Wertz, Mary H', query time: 0.02s Refine Results
  1. 1
    Genome-wide genetic screening in the mammalian CNS

    Genome-wide genetic screening in the mammalian CNS by Wertz, Mary H., Heiman, Myriam

    Published 2020
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    Book chapter
  2. 2
    Interleukin-6 deficiency exacerbates Huntington’s disease model phenotypes

    Interleukin-6 deficiency exacerbates Huntington’s disease model phenotypes by Wertz, Mary H., Pineda, S. Sebastian, Lee, Hyeseung, Kulicke, Ruth, Kellis, Manolis, Heiman, Myriam

    Published 2020
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    Article
  3. 3
    Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis

    Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis by Kong, Sek, Sahin, Mustafa, Krueger, Dilja, Collins, Christin D., Wertz, Mary H., Campbell, Malcolm G., Leech, Jarrett D., Bear, Mark, Kunkel, Louis M., Kohane, Isaac S.

    Published 2016
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    Article
  4. 4
    Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT Toxicity

    Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT Toxicity by Wertz, Mary H, Mitchem, Mollie R, Pineda, S Sebastian, Hachigian, Lea J, Lee, Hyeseung, Lau, Vanessa, Powers, Alex, Kulicke, Ruth, Madan, Gurrein K, Colic, Medina, Therrien, Martine, Vernon, Amanda, Beja-Glasser, Victoria F, Hegde, Mudra, Gao, Fan, Kellis, Manolis, Hart, Traver, Doench, John G, Heiman, Myriam

    Published 2021
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    Article

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