Synaptic dysfunction in progranulin-deficient mice von Petkau, Terri L, Neal, Scott J, Milnerwood, Austen, Mew, Ada, Hill, Austin M, Orban, Paul, Gregg, Jenny, Lu, Ge, Feldman, Howard H, Mackenzie, Ian R.A, Raymond, Lynn A, Leavitt, Blair R

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Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis von Rademakers, Rosa, Stewart, Heather, Dejesus-Hernandez, Mariely, Krieger, Charles, Graff-Radford, Neill, Fabros, Marife, Briemberg, Hannah, Cashman, Neil, Eisen, Andrew, Mackenzie, Ian R.A.

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The neuropathology associated with repeat expansions in the C9ORF72 gene von Mackenzie, Ian R. A., Frick, Petra, Neumann, Manuela

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hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations von Mori, Kohji, Lammich, Sven, Mackenzie, Ian R. A., Forné, Ignasi, Zilow, Sonja, Kretzschmar, Hans, Edbauer, Dieter, Janssens, Jonathan, Kleinberger, Gernot, Cruts, Marc, Herms, Jochen, Neumann, Manuela, Van Broeckhoven, Christine, Arzberger, Thomas, Haass, Christian

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Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons von Wang, Wen-Yuan, Pan, Ling, Su, Susan C, Quinn, Emma J, Sasaki, Megumi, Jimenez, Jessica C, Mackenzie, Ian R A, Huang, Eric J, Tsai, Li-Huei

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Baylisascaris procyonis infection in elderly person, British Columbia, Canada von Hung, Tawny, Neafie, Ronald C, Mackenzie, Ian R A

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Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases von Chang, Andrew, Xiang, Xinyu, Wang, Jing, Lee, Carolyn, Arakhamia, Tamta, Simjanoska, Marija, Wang, Chi, Carlomagno, Yari, Zhang, Guoan, Dhingra, Shikhar, Thierry, Manon, Perneel, Jolien, Heeman, Bavo, Forgrave, Lauren M., DeTure, Michael, DeMarco, Mari L., Cook, Casey N., Rademakers, Rosa, Dickson, Dennis W., Petrucelli, Leonard, Stowell, Michael H.B., Mackenzie, Ian R.A., Fitzpatrick, Anthony W.P.

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Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway von Lin, Yen-Chen, Kumar, Meenakshi Sundaram, Ramesh, Nandini, Anderson, Eric N., Nguyen, Aivi T., Kim, Boram, Cheung, Simon, McDonough, Justin A., Skarnes, William C., Lopez-Gonzalez, Rodrigo, Landers, John E., Fawzi, Nicolas L., Mackenzie, Ian R. A., Lee, Edward B., Nickerson, Jeffrey A., Grunwald, David, Pandey, Udai B., Bosco, Daryl A.

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FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis von Mackenzie, Ian R.A, Neumann, Manuela

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Fused in Sarcoma Neuropathology in Neurodegenerative Disease von Mackenzie, Ian R A, Neumann, Manuela

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Early dipeptide repeat pathology in a frontotemporal dementia kindred with C9ORF72 mutation and intellectual disability von Proudfoot, Malcolm, Gutowski, Nick J., Edbauer, Dieter, Hilton, David A., Stephens, Mark, Rankin, Julia, Mackenzie, Ian R. A.

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Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects von Halliday, Glenda, Bigio, Eileen H., Cairns, Nigel J., Neumann, Manuela, Mackenzie, Ian R. A., Mann, David M. A.

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Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations von Neumann, Manuela, Valori, Chiara F., Ansorge, Olaf, Kretzschmar, Hans A., Munoz, David G., Kusaka, Hirofumi, Yokota, Osamu, Ishihara, Kenji, Ang, Lee-Cyn, Bilbao, Juan M., Mackenzie, Ian R. A.

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Progranulin: normal function and role in neurodegeneration von Eriksen, Jason L, Mackenzie, Ian R.A

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TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions von Cairns, Nigel J, Neumann, Manuela, Bigio, Eileen H, Holm, Ida E, Troost, Dirk, Hatanpaa, Kimmo J, Foong, Chan, White, Charles L, Schneider, Julie A, Kretzschmar, Hans A, Carter, Deborah, Taylor-Reinwald, Lisa, Paulsmeyer, Katherine, Strider, Jeffrey, Gitcho, Michael, Goate, Alison M, Morris, John C, Mishra, Manjari, Kwong, Linda K, Stieber, Anna, Xu, Yan, Forman, Mark S, Trojanowski, John Q, Lee, Virginia M.-Y, Mackenzie, Ian R.A

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FUS-Immunoreactive Intranuclear Inclusions in Neurodegenerative Disease von Woulfe, John, Gray, Douglas A., Mackenzie, Ian R.A.

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rs5848 polymorphism and serum progranulin level von Hsiung, Ging-Yuek R, Fok, Alice, Feldman, Howard H, Rademakers, Rosa, Mackenzie, Ian R.A

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FDG-PET in presymptomatic C9orf72 mutation carriers von Popuri, Karteek, Beg, Mirza Faisal, Lee, Hyunwoo, Balachandar, Rakesh, Wang, Lei, Sossi, Vesna, Jacova, Claudia, Baker, Matt, Shahinfard, Elham, Rademakers, Rosa, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R.

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Superficial Siderosis : A Potential Diagnostic Marker of Cerebral Amyloid Angiopathy in Alzheimer Disease von FELDMAN, Howard H, MAIA, Luis F, MACKENZIE, Ian R. A, FORSTER, Bruce B, MARTZKE, Jeff, WOOLFENDEN, Andrew

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Clinical phenotypes of Cerebral Amyloid Angiopathy von Maia, Luís F, Mackenzie, Ian R.A, Feldman, Howard H

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