Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Woodling, Nathan S"'
Autor:
Simone, Roberto, Balendra, Rubika, Moens, Thomas G, Preza, Elisavet, Wilson, Katherine M, Heslegrave, Amanda, Woodling, Nathan S, Niccoli, Teresa, Gilbert‐Jaramillo, Javier, Abdelkarim, Samir, Clayton, Emma L, Clarke, Mica, Konrad, Marie‐Therese, Nicoll, Andrew J, Mitchell, Jamie S, Calvo, Andrea, Chio, Adriano, Houlden, Henry, Polke, James M, Ismail, Mohamed A, Stephens, Chad E, Vo, Tam, Farahat, Abdelbasset A, Wilson, W David, Boykin, David W, Zetterberg, Henrik, Partridge, Linda, Wray, Selina, Parkinson, Gary, Neidle, Stephen, Patani, Rickie, Fratta, Pietro, Isaacs, Adrian M
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 10, Iss 1, Pp 22-31 (2018)
EMBO Molecular Medicine, Vol 10, Iss 1, Pp 22-31 (2018)
Intronic GGGGCC repeat expansions in C9orf72 are the most common known cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), which are characterised by degeneration of cortical and motor neurons, respectively. Repeat expansi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6414c2407183893ea509c0981b6b29a8
http://hdl.handle.net/2318/1663027
http://hdl.handle.net/2318/1663027
Autor:
Mizielinska, Sarah, Ridler, Charlotte E., Balendra, Rubika, Thoeng, Annora, Woodling, Nathan S., Grässer, Friedrich A., Plagnol, Vincent, Lashley, Tammaryn, Partridge, Linda, Isaacs, Adrian M.
Publikováno v:
Acta Neuropathol Commun
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-11 (2017)
Mizielinska, S, Ridler, C E, Balendra, R, Thoeng, A, Woodling, N S, Grässer, F A, Plagnol, V, Lashley, T, Partridge, L & Isaacs, A M 2017, ' Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration ', Acta Neuropathologica Communications, vol. 5, no. 1, 29 . https://doi.org/10.1186/s40478-017-0432-x
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-11 (2017)
Mizielinska, S, Ridler, C E, Balendra, R, Thoeng, A, Woodling, N S, Grässer, F A, Plagnol, V, Lashley, T, Partridge, L & Isaacs, A M 2017, ' Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration ', Acta Neuropathologica Communications, vol. 5, no. 1, 29 . https://doi.org/10.1186/s40478-017-0432-x
Acta Neuropathologica Communications
An intronic GGGGCC expansion in C9orf72 is the most common known cause of both frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). The repeat expansion leads to the generation of sense and antisense repeat RNA aggregates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8cffffc8c9dbf8d06df8f513631ba9ec
https://hdl.handle.net/21.11116/0000-000B-4F59-A
https://hdl.handle.net/21.11116/0000-000B-4F59-A
Autor:
Simone, Roberto, Balendra, Rubika, Moens, Thomas G., Preza, Elisavet, Wilson, Katherine M., Heslegrave, Amanda, Woodling, Nathan S., Niccoli, Teresa, Gilbert‐Jaramillo, Javier, Abdelkarim, Samir, Clayton, Emma L., Clarke, Mica, Konrad, Marie‐Therese, Nicoll, Andrew J., Mitchell, Jamie S., Calvo, Andrea, Chio, Adriano, Houlden, Henry, Polke, James M., Ismail, Mohamed A.
Publikováno v:
EMBO Molecular Medicine; Jan2018, Vol. 10 Issue 1, p22-31, 10p
Akademický článek
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Autor:
Grant, Jacqueline L., Bou Ghosn, Eliver Eid, Axtell, Robert C., Herges, Katja, Kuipers, Hedwich F., Woodling, Nathan S., Andreasson, Katrin, Herzenberg, Leonard A., Herzenberg, Leonore A., Steinman, Lawrence
Publikováno v:
Science Translational Medicine; 8/1/2012, Vol. 4 Issue 145, preceding p1-12, 13p
Autor:
Grant, Jacqueline L., Ghosn, Eliver Eid Bou, Axtell, Robert C., Herges, Katja, Kuipers, Hedwich F., Woodling, Nathan S., Andreasson, Katrin, Herzenberg, Leonard A., Herzenberg, Leonore A., Steinman, Lawrence
Publikováno v:
Science Translational Medicine; August 2012, Vol. 4 Issue: 145 p145ra105-145ra105, 1p