Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Fisher, Elizabeth MC"'
Autor:
Wiseman, Frances K, Pulford, Laura J, Barkus, Chris, Liao, Fan, Portelius, Erik, Webb, Robin, Chavez-Gutierrez, Lucia, Cleverley, Karen, Noy, Sue, Sheppard, Olivia, Collins, Toby, Powell, Caroline, Sarell, Claire J, Rickman, Matthew, Choong, Xun, Tosh, Justin L, Siganporia, Carlos, Whittaker, Heather T, Stewart, Floy, Szaruga, Maria, Murphy, Michael P, Blennow, Kaj, de Strooper, Bart, Zetterberg, Henrik, Bannerman, David, Holtzman, David M, Tybulewicz, Victor LJ, Fisher, Elizabeth MC
Down syndrome, caused by trisomy of chromosome 21, is the single most common risk factor for early-onset Alzheimer's disease. Worldwide approximately 6 million people have Down syndrome, and all these individuals will develop the hallmark amyloid pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1131::aed097e70c8597701ac6995eb6cd7b97
https://lirias.kuleuven.be/handle/123456789/628796
https://lirias.kuleuven.be/handle/123456789/628796
Autor:
Hafezparast, Majid, Ahmad-Annuar, Azlina, Wood, Nicholas W, Tabrizi, Sarah J, Fisher, Elizabeth MC
Publikováno v:
In Lancet Neurology 2002 1(4):215-224
Autor:
Tosh, Justin L, Rickman, Matthew, Rhymes, Ellie, Norona, Frances E, Clayton, Emma, Mucke, Lennart, Isaacs, Adrian M, Fisher, Elizabeth MC, Wiseman, Frances K
Background: Transgenic animal models are a widely used and powerful tool to investigate human disease and develop therapeutic interventions. Making a transgenic mouse involves random integration of exogenous DNA into the host genome that can have the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::491d7223917a22aab7d7d8d119c6894d
https://escholarship.org/uc/item/14m7d2sp
https://escholarship.org/uc/item/14m7d2sp
Autor:
Naert, Gaëlle, Ferré, Valentine, Keller, Emeline, Slender, Amy, Gibbins, Dorota, Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Maurice, Tangui, Fisher, Elizabeth Mc, Tybulewicz, Victor Lj
Publikováno v:
Journal of Psychopharmacology; Feb2018, Vol. 32 Issue 2, p174-190, 17p
Autor:
Urwin, Hazel, Josephs, Keith A, Rohrer, Jonathan D, Mackenzie, Ian R, Neumann, Manuela, Authier, Astrid, Seelaar, Harro, Van Swieten, John C, Brown, Jeremy M, Johannsen, Peter, Nielsen, Jorgen E, Holm, Ida E, FReJA Consortium, Dickson, Dennis W, Rademakers, Rosa, Graff-Radford, Neill R, Parisi, Joseph E, Petersen, Ronald C, Hatanpaa, Kimmo J, White, Charles L, Weiner, Myron F, Geser, Felix, Van Deerlin, Vivianna M, Trojanowski, John Q, Miller, Bruce L, Seeley, William W, van der Zee, Julie, Kumar-Singh, Samir, Engelborghs, Sebastiaan, De Deyn, Peter P, Van Broeckhoven, Christine, Bigio, Eileen H, Deng, Han-Xiang, Halliday, Glenda M, Kril, Jillian J, Munoz, David G, Mann, David M, Pickering-Brown, Stuart M, Doodeman, Valerie, Adamson, Gary, Ghazi-Noori, Shabnam, Fisher, Elizabeth MC, Holton, Janice L, Revesz, Tamas, Rossor, Martin N, Collinge, John, Mead, Simon, Isaacs, Adrian M
Publikováno v:
Acta neuropathologica, vol 120, iss 1
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-43)-negative frontotemporal lobar degeneration (FTLD) cases, and present here the first comprehensive analysis of these cases in terms of neuropatholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8b395737ebf0e015f571f4c6e22db85e
https://escholarship.org/uc/item/45v4c0cs
https://escholarship.org/uc/item/45v4c0cs
Autor:
Wells, Jack A, Holmes, Holly E, O'Callaghan, James M, Colgan, Niall, Ismail, Ozama, Fisher, Elizabeth MC, Siow, Bernard, Murray, Tracey K, Schwarz, Adam J, O'Neill, Michael J, Collins, Emily C, Lythgoe, Mark F
Publikováno v:
Journal of Cerebral Blood Flow & Metabolism; Mar2015, Vol. 35 Issue 3, p359-362, 4p
Autor:
van de Leemput, Joyce, Wavrant-De Vrièze, Fabienne, Rafferty, Ian, Bras, Jose M., Giunti, Paola, Fisher, Elizabeth MC, Hardy, John A., Singleton, Andrew B., Houlden, Henry
Publikováno v:
Movement Disorders; Apr2010, Vol. 25 Issue 6, p771-773, 3p
Autor:
Skibinski, Gaia, Parkinson, Nicholas J., Brown, Jeremy M., Chakrabarti, Lisa, Lloyd, Sarah L., Hummerich, Holger, Nielsen, Jørgen E., Hodges, John R., Spillantini, Maria Grazia, Thusgaard, Tove, Brandner, Sebastian, Brun, Arne, Rossor, Martin N., Gade, Anders, Johannsen, Peter, Sørensen, Sven Asger, Gydesen, Susanne, Fisher, Elizabeth MC, Collinge, John
Publikováno v:
Nature Genetics; Aug2005, Vol. 37 Issue 8, p806-808, 3p
Autor:
Granno, Simone, Nixon-Abell, Jonathon, Berwick, Daniel C, Tosh, Justin, Heaton, George, Almudimeegh, Sultan, Zenisha Nagda, Jean-Christophe Rain, Zanda, Manuela, Plagnol, Vincent, Tybulewicz, Victor LJ, Cleverley, Karen, Wiseman, Frances K, Fisher, Elizabeth MC, Harvey, Kirsten
Pathological mechanisms underlying Down syndrome (DS)/Trisomy 21, including dysregulation of essential signalling processes remain poorly understood. Combining bioinformatics with RNA and protein analysis, we identified downregulation of the Wnt/β-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3d2009273da740c88a0d932f72ba6b4
Autor:
Granno, Simone, Nixon-Abell, Jonathon, Berwick, Daniel C, Tosh, Justin, Heaton, George, Almudimeegh, Sultan, Zenisha Nagda, Jean-Christophe Rain, Zanda, Manuela, Plagnol, Vincent, Tybulewicz, Victor LJ, Cleverley, Karen, Wiseman, Frances K, Fisher, Elizabeth MC, Harvey, Kirsten
Pathological mechanisms underlying Down syndrome (DS)/Trisomy 21, including dysregulation of essential signalling processes remain poorly understood. Combining bioinformatics with RNA and protein analysis, we identified downregulation of the Wnt/β-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9602f8b1f7fb0a777956840a7fdd4647