Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis von Fossale, Elisa, Wolf, Pavlina, Espinola, Janice A, Lubicz-Nawrocka, Tanya, Teed, Allison M, Gao, Hanlin, Rigamonti, Dorotea, Cattaneo, Elena, MacDonald, Marcy E, Cotman, Susan L

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Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L, Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L, Johnson, Kevin A, Donahue, Leah-Rae, Teed, Allison M, Antonellis, Kristen, Bronson, Roderick T, Lerner, Terry J, MacDonald, Marcy E

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Cln3 Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L., Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L., Johnson, Kevin A., Donahue, Leah-Rae, Teed, Allison M., Antonellis, Kristen, Bronson, Roderick T., Lerner, Terry J., MacDonald, Marcy E.

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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum von Wheeler, Vanessa C, Lebel, Lori-Anne, Vrbanac, Vladimir, Teed, Allison, te Riele, Hein, MacDonald, Marcy E

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Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice von Fossale, Elisa, Wheeler, Vanessa C., Vrbanac, Vladimir, Lebel, Lori-Anne, Teed, Allison, Mysore, Jayalakshmi S., Gusella, James F., MacDonald, Marcy E., Persichetti, Francesca

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