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pro vyhledávání: '"Alexsson, Andrei"'
Autor:
Alexsson, Andrei
This thesis provides an in-depth analyze of expressed sequence tags (EST) that represent pieces of eukaryotic mRNA by using unsupervised hidden Markov model (HMM). ESTs are short nucleotide sequences that are used primarily for rapid identificationof
Externí odkaz:
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-69575
Autor:
Cai, Yixiao, Edin, Fredrik, Jin, Zhe, Alexsson, Andrei, Gudjonsson, Olafur, Liu, Wei, Rask-Andersen, Helge, Karlsson, Mikael, Li, Hao
Publikováno v:
In Acta Biomaterialia February 2016 31:211-220
Autor:
Abdulla, Maysaa1, Alexsson, Andrei2, Sundström, Christer1, Ladenvall, Claes2, Mansouri, Larry3, Lindskog, Cecilia4, Berglund, Mattias5, Cavelier, Lucia2, Enblad, Gunilla5, Hollander, Peter1, Amini, Rose-Marie1
Publikováno v:
Acta Oncologica. Apr2021, Vol. 60 Issue 4, p531-538. 8p. 2 Color Photographs, 2 Charts, 1 Graph.
Akademický článek
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Akademický článek
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Akademický článek
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Autor:
Thorlacius, Guðný Ella, Hultin-Rosenberg, Lina, Sandling, Johanna K., Bianchi, Matteo, Imgenberg-Kreuz, Juliana, Pucholt, Pascal, Theander, Elke, Kvarnström, Marika, Forsblad-D'elia, Helena, Bucher, Sara Magnusson, Norheim, Katrine B., Johnsen, Svein Joar Auglænd, Hammenfors, Daniel, Skarstein, Kathrine, Jonsson, Malin V., Baecklund, Eva, Aqrawi, Lara A., Jensen, Janicke Liaaen, Palm, Øyvind, Morris, Andrew P., Alexsson, Andrei, Backlin, Carin, Rönnblom, Lars, Vasaitis, Lilian, Eloranta, Maija Leena, Syvänen, Ann Christine, Mathioudaki, Argyri, Farias, Fabiana H.G., Meadows, Jennifer, Nordin, Jessika, Lindblad-Toh, Kerstin, Björk, Albin, Lundberg, Ingrid E., Sepúlveda, Jorge I.Ramírez, Wahren-Herlenius, Marie, Eriksson, Daniel, Eriksson, Per, Sjöwall, Christopher, Mandl, Thomas, Rantapaä¨-Dahlqvist, Solbritt, Brokstad, Karl A., Jonsson, Roland, Appel, Silke, Brun, Johan G., Norheim, Katrine Brække, Omdal, Roald, Aqrawi, Lara Adnan, Pielberg, Gerli Rosengren, Murén, Eva, Karlsson, Åsa, Andersson, Göran, Ahlgren, Kerstin M., Lobell, Anna, Söderkvist, Peter, Kämpe, Olle, Landegren, Nils, Meadows, Jennifer R.S., Lind, Lars, Nordmark, Gunnel
Publikováno v:
Thorlacius, G E, Hultin-Rosenberg, L, Sandling, J K, Bianchi, M, Imgenberg-Kreuz, J, Pucholt, P, Theander, E, Kvarnström, M, Forsblad-D'elia, H, Bucher, S M, Norheim, K B, Johnsen, S J A, Hammenfors, D, Skarstein, K, Jonsson, M V, Baecklund, E, Aqrawi, L A, Jensen, J L, Palm, Ø, Morris, A P, Alexsson, A, Pucholt, P, Backlin, C, Baecklund, E, Sandling, J K, Imgenberg-Kreuz, J, Rönnblom, L, Vasaitis, L, Eloranta, M L, Syvänen, A C, Mathioudaki, A, Farias, F H G, Meadows, J, Nordin, J, Hultin-Rosenberg, L, Bianchi, M, Lindblad-Toh, K, Björk, A, Thorlacius, G E, Lundberg, I E, Sepúlveda, J I R, Wahren-Herlenius, M, Kvarnström, M, Eriksson, D, Forsblad-D'elia, H, Eriksson, P, Sjöwall, C, Theander, E, Mandl, T, Rantapaä¨-Dahlqvist, S, Bucher, S M, Hammenfors, D, Brokstad, K A, Skarstein, K, Jonsson, R, Appel, S, Jonsson, M V, Brun, J G, Norheim, K B, Omdal, R, Johnsen, S J A, Palm, Ø, Jensen, J L, Aqrawi, L A, Lindblad-Toh, K, Pielberg, G R, Murén, E, Karlsson, Å, Andersson, G, Ahlgren, K M, Lobell, A, Rönnblom, L, Eloranta, M L, Söderkvist, P, Kämpe, O, Landegren, N, Meadows, J R S, Rantapaä¨-Dahlqvist, S, Mandl, T, Eriksson, P, Lind, L, Omdal, R, Jonsson, R, Lindblad-Toh, K, Rönnblom, L, Wahren-Herlenius, M & Nordmark, G 2021, ' Genetic and clinical basis for two distinct subtypes of primary Sjögren's syndrome ', Rheumatology (United Kingdom), vol. 60, no. 2, pp. 837-848 . https://doi.org/10.1093/rheumatology/keaa367
Objectives: Clinical presentation of primary Sjögren's syndrome (pSS) varies considerably. A shortage of evidence-based objective markers hinders efficient drug development and most clinical trials have failed to reach primary endpoints. Methods: We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3818::067068db6e99c5dc65cd946694c52921
https://doi.org/10.1093/rheumatology/keaa367
https://doi.org/10.1093/rheumatology/keaa367
Autor:
Matteo, Bianchi, Kozyrev, Sergey V., Notarnicola, Antonella, Rosenberg, Lina Hultin, Karlsson, Åsa, Pucholt, Pascal, Rothwell, Simon, Alexsson, Andrei, Sandling, Johanna K., Andersson, Anna Helena, Cooper, Robert G., Padyukov, Leonid, Tjarnlund, Anna, Dastmalchi, Maryam, Meadows, Jennifer R. S., Diederichsen, Louise Pyndt, Molberg, Øyvind, Chinoy, Hector, Lamb, Janine A., Rönnblom, Lars, Lindblad-Toh, Kerstin, Lundberg, Ingrid E
Publikováno v:
Matteo, Bianchi Kozyrev, Sergey V. Notarnicola, Antonella Rosenberg, Lina Hultin Karlsson, Åsa Pucholt, Pascal Rothwell, Simon Alexsson, Andrei Sandling, Johanna K. Andersson, Anna Helena Cooper, Robert G. Padyukov, Leonid Tjarnlund, Anna Dastmalchi, Maryam Meadows, Jennifer R. S. Diederichsen, Louise Pyndt Molberg, Øyvind Chinoy, Hector Lamb, Janine A. Rönnblom, Lars Lindblad-Toh, Kerstin Lundberg, Ingrid E . Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort. Arthritis & Rheumatology. 2021, 74(2), 342-352
Arthritis & Rheumatology
Arthritis & Rheumatology
Autor:
Sandling, Johanna K., Pucholt, Pascal, Hultin Rosenberg, Lina, Farias, Fabiana H.G., Kozyrev, Sergey V., Eloranta, Maija-Leena, Alexsson, Andrei, Bianchi, Matteo, Padyukov, Leonid, Bengtsson, Christine, Jonsson, Roland, Omdal, Roald, Lie, Benedicte Alexandra, Massarenti, Laura, Steffensen, Rudi, Jakobsen, Marianne A., Lillevang, Søren T., Lerang, Karoline, Molberg, Øyvind, Voss, Anne, Troldborg, Anne, Jacobsen, Søren, Syvänen, Ann-Christine, Jönsen, Andreas, Gunnarsson, Iva, Svenungsson, Elisabet, Rantapää-Dahlqvist, Solbritt, Bengtsson, Anders A., Sjöwall, Christopher, Leonard, Dag, Lindblad-Toh, Kerstin, Rönnblom, Lars
Externí odkaz:
https://hdl.handle.net/11250/2774944
Autor:
Bolin, Karin, Imgenberg-Kreuz, Juliana, Leonard, Dag, Sandling, Johanna K., Alexsson, Andrei, Pucholt, Pascal, Haarhaus, Malena Loberg, Almlöf, Jonas Carlsson, Nititham, Joanne, Jönsen, Andreas, Sjöwall, Christopher, Bengtsson, Anders A., Rantapää-Dahlqvist, Solbritt, Svenungsson, Elisabet, Gunnarsson, Iva, Syvänen, Ann Christine, Lerang, Karoline, Troldborg, Anne, Voss, Anne, Molberg, Øyvind, Jacobsen, Søren, Criswell, Lindsey, Rönnblom, Lars, Nordmark, Gunnel
Publikováno v:
Genes and Immunity
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, no. 3, pp. 194-202 . https://doi.org/10.1038/s41435-021-00142-8
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A-C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, no. 3, pp. 194-202 . https://doi.org/10.1038/s41435-021-00142-8
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, pp. 194–202 . https://doi.org/10.1038/s41435-021-00142-8
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, no. 3, pp. 194-202 . https://doi.org/10.1038/s41435-021-00142-8
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A-C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, no. 3, pp. 194-202 . https://doi.org/10.1038/s41435-021-00142-8
Bolin, K, Imgenberg-Kreuz, J, Leonard, D, Sandling, J K, Alexsson, A, Pucholt, P, Haarhaus, M L, Almlöf, J C, Nititham, J, Jönsen, A, Sjöwall, C, Bengtsson, A A, Rantapää-Dahlqvist, S, Svenungsson, E, Gunnarsson, I, Syvänen, A C, Lerang, K, Troldborg, A, Voss, A, Molberg, Ø, Jacobsen, S, Criswell, L, Rönnblom, L & Nordmark, G 2021, ' Variants in BANK1 are associated with lupus nephritis of European ancestry ', Genes and Immunity, vol. 22, pp. 194–202 . https://doi.org/10.1038/s41435-021-00142-8
The genetic background of lupus nephritis (LN) has not been completely elucidated. We performed a case-only study of 2886 SLE patients, including 947 (33%) with LN. Renal biopsies were available from 396 patients. The discovery cohort (Sweden, n = 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::694d2d3ea429256abb4782585df3f38b
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-177434
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-177434