Zobrazeno 91 - 100
of 1 024
pro vyhledávání: '"Kockum I"'
Autor:
Beecham, AH, Patsopoulos, NA, Xifara, DK, Davis, MF, Kemppinen, A, Cotsapas, C, Shah, TS, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli-Boneschi, F, Taylor, B, Harbo, HF, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, JR, Hintzen, R, Barcellos, LF, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, HB, Baker, A, Band, G, Baranzini, SE, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, TMC, Blackburn, H, Bomfim, IL, Brambilla, P, Broadley, S, Brochet, B, Brundin, L, Buck, D, Butzkueven, H, Caillier, SJ, Camu, W, Carpentier, W, Cavalla, P, Celius, EG, Coman, I, Comi, G, Corrado, L, Cosemans, L, Cournu-Rebeix, I, Cree, BAC, Cusi, D, Damotte, V, Defer, G, Delgado, SR, Deloukas, P, Di Sapio, A, Dilthey, AT, Donnelly, P, Dubois, B, Duddy, M, Edkins, S, Elovaara, I, Esposito, F, Evangelou, N, Fiddes, B, Field, J, Franke, A
Publikováno v:
Beecham, AH; Patsopoulos, NA; Xifara, DK; Davis, MF; Kemppinen, A; Cotsapas, C; et al.(2013). Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics, 45(11), 1353-1362. doi: 10.1038/ng.2770. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/0tz6x2q0
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 potentially associated regions (P < 1.0 × 10 -4). In a replication phase,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::3cbd226ce07622c6ab0f1afe7e90bad2
http://www.escholarship.org/uc/item/0tz6x2q0
http://www.escholarship.org/uc/item/0tz6x2q0
Autor:
Mero, I., Gustavsen, M.W., Sã¦ther, H.S., Flã¥m, S.T., Berg-Hansen, P., Sã¸ndergaard, H.B., Jensen, P.E.H., Berge, T., Bjã¸lgerud, A., Muggerud, A., Aarseth, J.H., International Multiple Sclerosis Genetics Consortium, Myhr, K., Celius, E.G., Sellebjerg, F., Hillert, J., Alfredsson, L., Olsson, T., Oturai, A.B., Kockum, I., Lie, B.A., Andreassen, B.K., Harbo, Collaborators: Barcellos L, H.F., Booth, D., Comabella, M., Compston, A., D'Alfonso, S., De Jager, P., Fontaine, B., Goris, A., Hafler, D., Haines, J., Harbo, H., Hauser, S., Hawkins, C., Hemmer, B., Ivinson, A., Martin, R., Martinelli Boneschi, F., Mccauley, J., Oksenberg, J., Oturai, A., Patsopoulos, N., Pericak-Vance, M., Saarela, J., Sawcer, S., Spurkland, A., Stewart, G., Zipp, F.
Publikováno v:
Mero, I-L, Gustavsen, M W, Sæther, H S, Flåm, S T, Berg-Hansen, P, Søndergaard, H B, Jensen, P E H, Berge, T, Bjølgerud, A, Muggerud, A, Aarseth, J H, Myhr, K-M, Celius, E G, Sellebjerg, F, Hillert, J, Alfredsson, L, Olsson, T, Oturai, A B, Kockum, I, Lie, B A, Andreassen, B K, Harbo, H F & Consortium, I M S G 2013, ' Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles ', P L o S One, vol. 8, no. 3, e58352 . https://doi.org/10.1371/journal.pone.0058352
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e58352 (2013)
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e58352 (2013)
The presence of oligoclonal bands (OCB) in cerebrospinal fluid (CSF) is a typical finding in multiple sclerosis (MS). We applied data from Norwegian, Swedish and Danish (i.e. Scandinavian) MS patients from a genome-wide association study (GWAS) to se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d39f98fe6da95a91c0739cf0773bf02
https://curis.ku.dk/portal/da/publications/oligoclonal-band-status-in-scandinavian-multiple-sclerosis-patients-is-associated-with-specific-genetic-risk-alleles(073c4a0e-ed1b-4645-9875-d51237b80cc5).html
https://curis.ku.dk/portal/da/publications/oligoclonal-band-status-in-scandinavian-multiple-sclerosis-patients-is-associated-with-specific-genetic-risk-alleles(073c4a0e-ed1b-4645-9875-d51237b80cc5).html
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Barrizzone, N., Leone, M. A., Esposito, F., Lucenti, A., Harbo, H. F., Goris, A., Kockum, I., Oturai, A. B., Celius, E. G., Mero, I. L., Dubois, B., Olsson, T., Søndergaard, H. B., Cusi, D., Lupoli, S., Guerini, F., Galimberti, D., Salvetti, Marco, Liberatore, G., Martinelli, V., Naldi, P., Myhr, K. M., Bergamaschi, R., Comi, G., Martinelli Boneschi, F., D'Alfonso, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0070bfec55bdf446ab85b17881d8bae3
http://hdl.handle.net/11573/504621
http://hdl.handle.net/11573/504621
Autor:
Sawcer, S, Hellenthal, G, Pirinen, M, Spencer, CCA, Patsopoulos, NA, Moutsianas, L, Dilthey, A, Su, Z, Freeman, C, Hunt, SE, Edkins, S, Gray, E, Booth, DR, Potter, SC, Goris, A, Band, G, Oturai, AB, Strange, A, Saarela, J, Bellenguez, C, Fontaine, B, Gillman, M, Hemmer, B, Gwilliam, R, Zipp, F, Jayakumar, A, Martin, R, Leslie, S, Hawkins, S, Giannoulatou, E, D'Alfonso, S, Blackburn, H, Boneschi, FM, Liddle, J, Harbo, HF, Perez, ML, Spurkland, A, Waller, MJ, Mycko, MP, Ricketts, M, Comabella, M, Hammond, N, Kockum, I, McCann, OT, Ban, M, Whittaker, P, Kemppinen, A, Weston, P, Hawkins, C, Widaa, S, Zajicek, J, Dronov, S, Robertson, N, Bumpstead, SJ, Barcellos, LF, Ravindrarajah, R, Abraham, R, Alfredsson, L, Ardlie, K, Aubin, C, Baker, A, Baker, K, Baranzini, SE, Bergamaschi, L, Bergamaschi, R, Bernstein, A, Berthele, A, Boggild, M, Bradfield, JP, Brassat, D, Broadley, SA, Buck, D, Butzkueven, H, Capra, R, Carroll, WM, Cavalla, P, Celius, EG, Cepok, S, Chiavacci, R, Clerget-Darpoux, F, Clysters, K, Comi, G, Cossburn, M, Cournu-Rebeix, I, Cox, MB, Cozen, W, Cree, BAC, Cross, AH, Cusi, D, Daly, MJ
Publikováno v:
Sawcer, S; Hellenthal, G; Pirinen, M; Spencer, CCA; Patsopoulos, NA; Moutsianas, L; et al.(2011). Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature, 476(7359), 214-219. doi: 10.1038/nature10251. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5x17t6tz
Multiple sclerosis is a common disease of the central nervous system in which the interplay between inflammatory and neurodegenerative processes typically results in intermittent neurological disturbance followed by progressive accumulation of disabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::90cde6ee4de0a9db52db4164ba38c288
http://www.escholarship.org/uc/item/5x17t6tz
http://www.escholarship.org/uc/item/5x17t6tz
Autor:
Leppa, International Multiple Sclerosis Genetics Consortium V., Surakka, I., Tienari, P. J., Elovaara, I., Compston, A., Sawcer, S., Robertson, N., De Jager, P. L., Aubin, C., Hafler, D. A., Oturai, A. B., Sondergaard, H. B., Sellebjerg, F., Sorensen, P. S., Hemmer, B., Cepok, S., Winkelmann, J., Wichmann, H. E., Comabella, M., Bustamante, M. F., Montalban, X., Olsson, T., Kockum, I., Hillert, J., Alfredsson, L., Goris, A., Dubois, B., Mero, I. L., Smestad, C., Celius, E. G., Harbo, H. F., D'Alfonso, S., Bergamaschi, L., Leone, M., Ristori, Giovanni, Kappos, L., Hauser, S. L., Cournu Rebeix, I., Fontaine, B., Boonen, S., Polman, C., Palotie, A., Peltonen, L., Saarela, J.
Publikováno v:
Leppa, V, Surakka, I, Tienari, P J, Elovaara, I, Compston, A, Sawcer, S, Robertson, N, de Jager, P L, Aubin, C, Hafler, D A, Bang Oturai, A, Bach Søndergaard, H, Sellebjerg, F, Sørensen, P S, Hemmer, B, Cepok, S, Winkelmann, J, Wichmann, H-E, Bustamente, M F, Montalban, X, Olsson, T, Kockum, I, Hillert, J, Alfredsson, L, Goris, A, Dubois, B, Mero, I-L, Smestad, C, Celius, E G, Harbo, H F, D'Alfonso, S, Bergamaschi, L, Leone, M, Ristori, G, Kappos, L, Hauser, D L, Cornu-Rebeix, I, Fontaine, B, Boonen, S, Polman, C H, Palotie, A, Peltonen, L & Saarela, J 2011, ' The Genetic Association of Variants in CD6, TNFRSF1A and IRF8 to Multiple Sclerosis: A Multicenter Case-Control Study ', PLoS ONE, vol. 6, no. 4, e18813 . https://doi.org/10.1371/journal.pone.0018813
PLoS
PLoS ONE, 6(4):e18813. Public Library of Science
PLoS ONE, Vol 6, Iss 4, p e18813 (2011)
PLoS ONE
PLoS ONE 6:e18813 (2011)
PLoS
PLoS ONE, 6(4):e18813. Public Library of Science
PLoS ONE, Vol 6, Iss 4, p e18813 (2011)
PLoS ONE
PLoS ONE 6:e18813 (2011)
Background In the recently published meta-analysis of multiple sclerosis genome-wide association studies De Jager et al. identified three single nucleotide polymorphisms associated to MS: rs17824933 (CD6), rs1800693 (TNFRSF1A) and rs17445836 (61.5 kb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336591664e0acd7a628309e927acab61
https://research.vumc.nl/ws/files/880683/283097.pdf
https://research.vumc.nl/ws/files/880683/283097.pdf
Autor:
Ekelund, E., Bradley, M., Weidinger, S., Jovanovic, D.L., Johansson, C., Lindgren, C.M., Todorova, A., Jakob, T., Illig, T., von Mutius, E., Braun-Fahrlander, C., Doekes, G., Riedler, T., Scheynius, A., Pershagen, G., Kockum, I., Kere, J., Risk Assessment of Toxic and Immunomodulatory Agents, Dep IRAS
Publikováno v:
Acta Dermato-Venereologica, 89(2), 115. Society for the Publication of Acta Dermato-Venereologica
Eczema is often associated with development of allergic asthma. The Neuropeptide S Receptor 1 (NPSR1) gene has previously been associated with asthma and elevated serum IgE levels. The aim of this study was to investigate a potential association betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::cfd34236848fcb39f549551eafe2f82d
https://dspace.library.uu.nl/handle/1874/39276
https://dspace.library.uu.nl/handle/1874/39276
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.