Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sigrid, Aslaksen"'
Autor:
Hanna De Bruyn, Megan Johnson, Madelyn Moretti, Saleh Ahmed, Mircea Mujat, James D. Akula, Tomislav Glavan, Ivana Mihalek, Sigrid Aslaksen, Laurie L. Molday, Robert S. Molday, Bruce A. Berkowitz, Anne B. Fulton
Publikováno v:
Diagnostics, Vol 14, Iss 14, p 1545 (2024)
Stargardt disease (STGD1), associated with biallelic variants in the ABCA4 gene, is the most common heritable macular dystrophy and is currently untreatable. To identify potential treatment targets, we characterized surviving STGD1 photoreceptors. We
Externí odkaz:
https://doaj.org/article/fe319624f71648eeaee5f8a591cb1a63
Autor:
Alexander Hellesen, Sigrid Aslaksen, Lars Breivik, Ellen Christine Røyrvik, Øyvind Bruserud, Kine Edvardsen, Karl Albert Brokstad, Anette Susanne Bøe Wolff, Eystein Sverre Husebye, Eirik Bratland
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ObjectivesCD8+ T cells targeting 21-hydroxylase (21OH) are presumed to play a central role in the destruction of adrenocortical cells in autoimmune Addison’s disease (AAD). Earlier reports have suggested two immunodominant CD8+ T cell epitopes with
Externí odkaz:
https://doaj.org/article/5a9c0773ab494ceeb083fa4b8ce83735
Autor:
Sigrid Aslaksen, Paal Methlie, Magnus D. Vigeland, Dag E. Jøssang, Anette B. Wolff, Ying Sheng, Bergithe E. Oftedal, Beate Skinningsrud, Dag E. Undlien, Kaja K. Selmer, Eystein S. Husebye, Eirik Bratland
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Background: Underlying causes of adrenal insufficiency include congenital adrenal hyperplasia (CAH) and autoimmune adrenocortical destruction leading to autoimmune Addison's disease (AAD). Here, we report a patient with a homozygous stop-gain mutatio
Externí odkaz:
https://doaj.org/article/7eaf308ee3e9417f99d8ac950795f30c
Autor:
Sigrid Aslaksen, Anette B. Wolff, Magnus D. Vigeland, Lars Breivik, Ying Sheng, Bergithe E. Oftedal, Haydee Artaza, Beate Skinningsrud, Dag E. Undlien, Kaja K. Selmer, Eystein S. Husebye, Eirik Bratland
Publikováno v:
Journal of Translational Autoimmunity, Vol 1, Iss , Pp - (2019)
Autoimmune Addison's disease (AAD) is a classic organ-specific autoimmune disease characterized by an immune-mediated attack on the adrenal cortex. As most autoimmune diseases, AAD is believed to be caused by a combination of genetic and environmenta
Externí odkaz:
https://doaj.org/article/fa8fb395f5e3493b8d4b5373b55b768f
Autor:
Susanna, Croci, Mary Anna, Venneri, Stefania, Mantovani, Chiara, Fallerini, Elisa, Benetti, Nicola, Picchiotti, Federica, Campolo, Francesco, Imperatore, Maria, Palmieri, Sergio, Daga, Chiara, Gabbi, Francesca, Montagnani, Giada, Beligni, Ticiana D J, Farias, Miriam Lucia, Carriero, Laura, Di Sarno, Diana, Alaverdian, Sigrid, Aslaksen, Maria Vittoria, Cubellis, Ottavia, Spiga, Margherita, Baldassarri, Francesca, Fava, Paul J, Norman, Elisa, Frullanti, Andrea M, Isidori, Antonio, Amoroso, Francesca, Mari, Simone, Furini, Mario U, Mondelli, Gen-Covid Multicenter Study, Mario, Chiariello, Alessandra, Renieri, Ilaria, Meloni
Publikováno v:
Autophagy. 18(7)
The polymorphism L412F in TLR3 has been associated with several infectious diseases. However, the mechanism underlying this association is still unexplored. Here, we show that the L412F polymorphism in TLR3 is a marker of severity in COVID-19. This a
Autor:
Francesco Imperatore, Sergio Daga, Mary Anna Venneri, Laura Di Sarno, Maria Vittoria Cubellis, Francesca Montagnani, Sigrid Aslaksen, Alessandra Renieri, Paul Norman, Simone Furini, Stefania Mantovani, Mario Chiariello, Mario U. Mondelli, Giada Beligni, Gen-Covid Multicenter Study, Ilaria Meloni, Elisa Benetti, Ottavia Spiga, Federica Campolo, Margherita Baldassarri, Diana Alaverdian, Nicola Picchiotti, Francesca Fava, Chiara Fallerini, Andrea M. Isidori, Elisa Frullanti, Antonio Amoroso, Miriam Lucia Carriero, Francesca Mari, Maria Palmieri, Susanna Croci, Ticiana Della Justina Farias, C. Gabbi
The polymorphism L412F in TLR3 has been associated with several infectious diseases. However, the mechanism underlying this association is still unexplored. Here, we show that the L412F polymorphism in TLR3 is a marker of severity in COVID-19. This a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ece10eef00790bca320fa1a2bdd6c66
https://doi.org/10.1101/2021.03.23.21254158
https://doi.org/10.1101/2021.03.23.21254158
Autor:
Eirik Bratland, Eystein S. Husebye, Dag E. Undlien, Bergithe E. Oftedal, Sigrid Aslaksen, Kaja Kristine Selmer, Haydee Artaza, Magnus Dehli Vigeland, Ying Sheng, Lars Breivik, Anette S. B. Wolff, Beate Skinningsrud
Publikováno v:
Journal of Translational Autoimmunity
Journal of Translational Autoimmunity, Vol 1, Iss, Pp-(2019)
Journal of Translational Autoimmunity, Vol 1, Iss, Pp-(2019)
Autoimmune Addison's disease (AAD) is a classic organ-specific autoimmune disease characterized by an immune-mediated attack on the adrenal cortex. As most autoimmune diseases, AAD is believed to be caused by a combination of genetic and environmenta
Autor:
Hanne Roberg-Larsen, Steven Ray Wilson, Sigrid Aslaksen, Tore Vehus, Jo Waaler, Elsa Lundanes, Stefan Krauss
Publikováno v:
Scientific Reports
We have designed a versatile and sensitive liquid chromatographic (LC) system, featuring a monolithic trap column and a very narrow (10 μm ID) fused silica open tubular liquid chromatography (OTLC) separation column functionalized with C18-groups, f