Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vivianna Deerlin"'
Autor:
Orme, Tatiana, Hernandez, Dena, Ross, Owen, Kun-Rodrigues, Celia, Darwent, Lee, Shepherd, Claire, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence, Marder, Karen, Afina Lemstra, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Tammaryn Lashley, Holton, Janice, Yaroslau Compta, Vivianna Deerlin, Trojanowski, John, Geidy Serrano, Beach, Thomas, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pau Pastor, Tienari, Pentti, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad, Petersen, Ronald, Tanis Ferman, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel, Morris, John, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda, Stone, David, Dickson, Dennis, Hardy, John, Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Additional file 3: Table S3. Variants identified in the studied DLB cohort that have been previously reported in disease and have a gnomAD european allele count > 5. GnomAD NFE AC = gnomAD non-Finnish European allele count. GnomAD NFE AN = gno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324f16884865a94bc3d2b7f7e6da4710
Autor:
Orme, Tatiana, Hernandez, Dena, Ross, Owen, Kun-Rodrigues, Celia, Darwent, Lee, Shepherd, Claire, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence, Marder, Karen, Afina Lemstra, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Tammaryn Lashley, Holton, Janice, Yaroslau Compta, Vivianna Deerlin, Trojanowski, John, Geidy Serrano, Beach, Thomas, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pau Pastor, Tienari, Pentti, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad, Petersen, Ronald, Tanis Ferman, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel, Morris, John, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda, Stone, David, Dickson, Dennis, Hardy, John, Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Additional file 1: Table S1. Sources of samples. Research groups, clinical teams and brain banks where the DLB samples included in this study were collected from.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0467bf37074b320e901679c5e6b4f219
Autor:
Yousef, Ahmed, Robinson, John, Irwin, David, Byrne, Matthew, Kwong, Linda, Lee, Edward, Xu, Yan, Xie, Sharon, Rennert, Lior, EunRan Suh, Vivianna Deerlin, Grossman, Murray, Lee, Virginia, Trojanowski, John
Three observed Groups denoted by differences in NeuN and TDP-43 inclusions are seen in IF. Representative images in IF confirms the pattern of staining seen through IHC. In Group 1, NeuN staining remains high with little aggregation of pathology. Pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e3af228c55252392b1a3d54188ecb38
Autor:
Orme, Tatiana, Hernandez, Dena, Ross, Owen, Kun-Rodrigues, Celia, Darwent, Lee, Shepherd, Claire, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence, Marder, Karen, Afina Lemstra, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Tammaryn Lashley, Holton, Janice, Yaroslau Compta, Vivianna Deerlin, Trojanowski, John, Geidy Serrano, Beach, Thomas, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pau Pastor, Tienari, Pentti, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad, Petersen, Ronald, Tanis Ferman, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel, Morris, John, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda, Stone, David, Dickson, Dennis, Hardy, John, Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Additional file 2: Table S2. Neurodegenerative disease-causing genes and DLB risk genes analysed in this study. Genes known to cause neurodegenerative diseases are presented according to the mode of inheritance of the respective mendelian disease. Ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce87097f64bc630052862fe3ba3cd97b
Autor:
Orme, Tatiana, Hernandez, Dena, Ross, Owen, Kun-Rodrigues, Celia, Darwent, Lee, Shepherd, Claire, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence, Marder, Karen, Afina Lemstra, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Tammaryn Lashley, Holton, Janice, Yaroslau Compta, Vivianna Deerlin, Trojanowski, John, Geidy Serrano, Beach, Thomas, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pau Pastor, Tienari, Pentti, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad, Petersen, Ronald, Tanis Ferman, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel, Morris, John, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda, Stone, David, Dickson, Dennis, Hardy, John, Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Additional file 2: Table S2. Neurodegenerative disease-causing genes and DLB risk genes analysed in this study. Genes known to cause neurodegenerative diseases are presented according to the mode of inheritance of the respective mendelian disease. Ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::542405f7abe61b0a97fabf0263534807