Search Results - Knopp, S.J

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  1. 1
    Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X

    Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X by Bissonnette, J.M, Schaevitz, L.R, Knopp, S.J, Zhou, Z

    Published in Neuroscience
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  2. 2
    Acute intermittent hypoxia-induced expression of brain-derived neurotrophic factor is disrupted in the brainstem of methyl-CpG-binding protein 2 null mice

    Acute intermittent hypoxia-induced expression of brain-derived neurotrophic factor is disrupted in the brainstem of methyl-CpG-binding protein 2 null mice by Vermehren-Schmaedick, A, Jenkins, V.K, Knopp, S.J, Balkowiec, A, Bissonnette, J.M

    Published in Neuroscience
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    O.20 A mouse model that recapitulates features of facioscapulohumeral muscular dystrophy

    O.20 A mouse model that recapitulates features of facioscapulohumeral muscular dystrophy by Krom, Y.D, den Hamer, B, Snider, L, Knopp, P, Zammit, P.S, Tapscott, S.J, van der Maarel, S.M

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