C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies von Vatsavayai, Sarat C., Nana, Alissa L., Yokoyama, Jennifer S., Seeley, William W.

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Loss of TDP-43 function contributes to genomic instability in amyotrophic lateral sclerosis von Fang, Minggang, Deibler, Sara K, Nana, Alissa L, Vatsavayai, Sarat C, Banday, Shahid, Zhou, You, Almeida, Sandra, Weiss, Alexandra, Brown, Robert H, Seeley, William W, Gao, Fen-Biao, Green, Michael R

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Suppression of C9orf72 RNA repeat-induced neurotoxicity by the ALS-associated RNA-binding protein Zfp106 von Celona, Barbara, Dollen, John von, Vatsavayai, Sarat C, Kashima, Risa, Johnson, Jeffrey R, Tang, Amy A, Hata, Akiko, Miller, Bruce L, Huang, Eric J, Krogan, Nevan J, Seeley, William W, Black, Brian L

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TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A von Ma, X. Rosa, Prudencio, Mercedes, Koike, Yuka, Vatsavayai, Sarat C., Kim, Garam, Harbinski, Fred, Briner, Adam, Rodriguez, Caitlin M., Guo, Caiwei, Akiyama, Tetsuya, Schmidt, H. Broder, Cummings, Beryl B., Wyatt, David W., Kurylo, Katherine, Miller, Georgiana, Mekhoubad, Shila, Sallee, Nathan, Mekonnen, Gemechu, Ganser, Laura, Rubien, Jack D., Jansen-West, Karen, Cook, Casey N., Pickles, Sarah, Oskarsson, Björn, Graff-Radford, Neill R., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Dickson, Dennis W., Shorter, James, Myong, Sua, Green, Eric M., Seeley, William W., Petrucelli, Leonard, Gitler, Aaron D.

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Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementia von Vatsavayai, Sarat C, Yoon, Soo Jin, Gardner, Raquel C, Gendron, Tania F, Vargas, Jose Norberto S, Trujillo, Andrew, Pribadi, Mochtar, Phillips, Joanna J, Gaus, Stephanie E, Hixson, John D, Garcia, Paul A, Rabinovici, Gil D, Coppola, Giovanni, Geschwind, Daniel H, Petrucelli, Leonard, Miller, Bruce L, Seeley, William W

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Frontotemporal lobar degeneration targets brain regions linked to expression of recently evolved genes von Pasquini, Lorenzo, Pereira, Felipe L, Seddighi, Sahba, Zeng, Yi, Wei, Yongbin, Illán-Gala, Ignacio, Vatsavayai, Sarat C, Friedberg, Adit, Lee, Alex J, Brown, Jesse A, Spina, Salvatore, Grinberg, Lea T, Sirkis, Daniel W, Bonham, Luke W, Yokoyama, Jennifer S, Boxer, Adam L, Kramer, Joel H, Rosen, Howard J, Humphrey, Jack, Gitler, Aaron D, Miller, Bruce L, Pollard, Katherine S, Ward, Michael E, Seeley, William W

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Tuberous sclerosis complex is associated with a novel human tauopathy von Hwang, Ji-Hye L., Perloff, Olga S., Gaus, Stephanie E., Benitez, Camila, Alquezar, Carolina, Cosme, Celica Q., Nana, Alissa L., Vatsavayai, Sarat C., Ramos, Eliana M., Geschwind, Daniel H., Miller, Bruce L., Kao, Aimee W., Seeley, William W.

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C9orf72-specific phenomena associated with frontotemporal dementia and gastrointestinal symptoms in the absence of TDP-43 aggregation von Sampognaro, Paul J., Vatsavayai, Sarat C., Cosme, Celica G., Hwang, Ji-Hye L., Nolan, Amber, Huang, Eric J., Seeley, William W., De May, Mary G.

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Early development of aberrant synaptic plasticity in a mouse model of Huntington's disease von Milnerwood, Austen J., Cummings, Damian M., Dallérac, Glenn M., Brown, Jacki Y., Vatsavayai, Sarat C., Hirst, Mark C., Rezaie, Payam, Murphy, Kerry P.S.J.

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Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of huntington's disease von Cummings, Damian M., Milnerwood, Austen J., Dallérac, Glenn M., Waights, Verina, Brown, Jacki Y., Vatsavayai, Sarat C., Hirst, Mark C., Murphy, Kerry P.S.J.

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Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels von Dallérac, Glenn M., Levasseur, Grégoire, Vatsavayai, Sarat C., Milnerwood, Austen J., Cummings, Damian M., Kraev, Igor, Huetz, Chloé, Evans, Karen A., Walters, Steve W., Rezaie, Payam, Cho, Yoon, Hirst, Mark C., Murphy, Kerry P.S.J.

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Abnormal cortical synaptic plasticity in a mouse model of Huntington's disease von Cummings, Damian M, Milnerwood, Austen J, Dallérac, Glenn M, Vatsavayai, Sarat C, Hirst, Mark C, Murphy, Kerry P.S.J

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Progressive CAG expansion in the brain of a novel R6/1-89Q mouse model of Huntington's disease with delayed phenotypic onset von Vatsavayai, Sarat C, Dallérac, Glenn M, Milnerwood, Austen J, Cummings, Damian M, Rezaie, Payam, Murphy, Kerry P.S.J, Hirst, Mark C

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FTLD targets brain regions expressing recently evolved genes von Pasquini, Lorenzo, Pereira, Felipe L, Seddighi, Sahba, Zeng, Yi, Wei, Yongbin, Illán-Gala, Ignacio, Vatsavayai, Sarat C, Friedberg, Adit, Lee, Alex J, Brown, Jesse A, Spina, Salvatore, Grinberg, Lea T, Sirkis, Daniel W, Bonham, Luke W, Yokoyama, Jennifer S, Boxer, Adam L, Kramer, Joel H, Rosen, Howard J, Humphrey, Jack, Gitler, Aaron D, Miller, Bruce L, Pollard, Katherine S, Ward, Michael E, Seeley, William W, Universitat Autònoma de Barcelona

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C9orf72-specific phenomena associated with frontotemporal dementia and gastrointestinal symptoms in the absence of TDP-43 aggregation von Sampognaro, Paul J, Vatsavayai, Sarat C, Cosme, Celica G, Hwang, Ji-Hye L, Nolan, Amber, Huang, Eric J, Seeley, William W, De May, Mary G

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