Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Lupus Erythematosus, Systemic/genetics"'
Autor:
Sofie Vestergaard Fonager, Gudrun Winther, Thomas Rea Wittenborn, Lisbeth Jensen, Cecilia Fahlquist-Hagert, Lisbeth Ahm Hansen, Ernst-Martin Füchtbauer, Marina Romero-Ramos, Søren Egedal Degn
Publikováno v:
Fonager, S V, Winther, G, Wittenborn, T R, Jensen, L, Fahlquist-Hagert, C, Hansen, L A, Füchtbauer, E-M, Romero-Ramos, M & Degn, S E 2022, ' Increased maternofoetal transfer of antibodies in a murine model of systemic lupus erythematosus, but no immune activation and neuroimmune sequelae in offspring ', Journal of Neuroimmunology, vol. 370, 577927 . https://doi.org/10.1016/j.jneuroim.2022.577927
Maternally transferred autoantibodies can negatively impact the development and health of offspring, increasing the risk of neurodevelopmental disorders. We used embryo transfers to examine maternofoetal immune imprinting in the autoimmune BXSB/MpJ m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba039347c7a63e48b99862576184d6f7
https://pure.au.dk/portal/da/publications/increased-maternofoetal-transfer-of-antibodies-in-a-murine-model-of-systemic-lupus-erythematosus-but-no-immune-activation-and-neuroimmune-sequelae-in-offspring(5e13c1cc-0e1d-4d3c-9a81-c7c6d064d5ae).html
https://pure.au.dk/portal/da/publications/increased-maternofoetal-transfer-of-antibodies-in-a-murine-model-of-systemic-lupus-erythematosus-but-no-immune-activation-and-neuroimmune-sequelae-in-offspring(5e13c1cc-0e1d-4d3c-9a81-c7c6d064d5ae).html
Autor:
Ina Rudloff, Stefan J. White, Stuart Cantsilieris, Wendy Dankers, Melissa Northcott, Elena J. Tucker, James Harris, Qiang Cheng, Eric F Morand, Brendan E. Russ, Marcel F. Nold, Andrew E. J. Toh, Huapeng Fan, Sarah A. Jones
Publikováno v:
Scientific Reports
Scientific reports, 9(1). Nature Publishing Group
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific reports, 9(1). Nature Publishing Group
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Personalized medicine approaches are increasingly sought for diseases with a heritable component. Systemic lupus erythematosus (SLE) is the prototypic autoimmune disease resulting from loss of immunologic tolerance, but the genetic basis of SLE remai
Autor:
Charlotte Möller, Gregory J. Buchan, Francisco J. Schopfer, Rachel E. Rigby, Hiroyuki Arai, Jonathan J. Miner, Wei Qian, Anne L. Thielke, Camilla Gunderstofte, Martin R. Jakobsen, Jan Rehwinkel, Jessica Roos, Mona Motwani, Sonia R. Salvatore, Katherine A. Fitzgerald, Marie B. Iversen, Rongtuan Lin, Raphaela Goldbach-Mansky, Christian K. Holm, Michael Rühl, Kojiro Mukai, Thorsten J. Maier, Tomohiko Taguchi, Cathrine A. Miner, Andreas S. Jakobsen, Anne-Louise S. Hansen, Emari Ogawa, David Olagnier, Sidsel D. Andersen
Publikováno v:
Hansen, A L, Buchan, G J, Rühl, M, Mukai, K, Salvatore, S R, Ogawa, E, Andersen, S D, Iversen, M B, Thielke, A L, Gunderstofte, C, Motwani, M, Møller, C T, Jakobsen, A S, Fitzgerald, K A, Roos, J, Lin, R, Maier, T J, Goldbach-Mansky, R, Miner, C A, Qian, W, Miner, J J, Rigby, R E, Rehwinkel, J, Jakobsen, M R, Arai, H, Taguchi, T, Schopfer, F J, Olagnier, D & Holm, C K 2018, ' Nitro-fatty acids are formed in response to virus infection and are potent inhibitors of STING palmitoylation and signaling ', Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 33, pp. E7768-E7775 . https://doi.org/10.1073/pnas.1806239115
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance Several chronic inflammatory conditions have recently been shown to depend on abnormally high activity of the signaling protein stimulator of IFN genes (STING). These conditions include examples from systemic lupus erythematosus, Aicardi
Publikováno v:
Pediatric rheumatology online journal, vol. 14, no. 1, pp. 35
Defective regulation of type I interferon response is associated with severe inflammatory phenotypes and autoimmunity. Type I interferonopathies are a clinically heterogenic group of Mendelian diseases with a constitutive activation of this pathway t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1900::6259d649ae88c66ae8976fb1d7306c11
https://serval.unil.ch/notice/serval:BIB_F53B15A22E70
https://serval.unil.ch/notice/serval:BIB_F53B15A22E70
Autor:
B. L. Kotzin, Michael T. Falta, Trine N. Jørgensen, Johne Kappler, Pilippa Marrack, S. A. Flannery, Troy E. Metzger, Shozo Izui, Joshua M. Thurman
Publikováno v:
Genes and Immunity, Vol. 7, No 7 (2006) pp. 555-567
Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown etiology. Associations between viral infections and the onset of SLE have been suggested, and recent studies have provided evidence that type I interferons (IFNalpha/beta) might p
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 10, p e0186073 (2017)
PloS one, vol. 12, no. 10, pp. e0186073
PLoS ONE, Vol 12, Iss 10, p e0186073 (2017)
PloS one, vol. 12, no. 10, pp. e0186073
Genome-wide linkage analysis studies (GWAS) studies in systemic lupus erythematosus (SLE) identified the 1q23 region on human chromosome 1, containing the Signaling Lymphocytic Activation Molecule Family (SLAMF) cluster of genes, as a lupus susceptib
Autor:
Chenghui Huang, Susan Yung, Gongping Liang, Qianjin Lu, Rong Xiao, Tak Mao Chan, Ming Zhao, Yaping Li
Publikováno v:
Clinical and Developmental Immunology, Vol 2013 (2013)
Clinical and Developmental Immunology
Clinical and Developmental Immunology
The aberrant activity of CD4(+) T cells in patients with systemic lupus erythematosus (SLE) is associated with DNA hypomethylation of the regulatory regions in CD11a and CD70 genes. Our previous studies demonstrated that Gadd45a contributes to the de
Publikováno v:
European Journal of Immunology, Vol. 26, No 2 (1996) pp. 307-314
The expression of a transgene encoding the I-E alpha chain prevents a lupus-like autoimmune syndrome in BXSB mice. However, it had not been elucidated whether the E alpha d transgene-mediated protective effect results from I-E expression or from the
Publikováno v:
Journal of Clinical Investigation, Vol. 94, No 2 (1994) pp. 521-525
To investigate the specific contribution of select MHC class II genes on the development of murine lupus, H-2 congenic (NZB x BXSB)F1 hybrid mice bearing either H-2b/b, H-2d/b, or H-2d/d haplotypes were generated. We compared the clinical development
Autor:
John B. Harley, Yu-Lung Lau, Fei Lan Liu, Yuanjia Tang, Betty P. Tsao, Ji Yih Chen, Deh Ming Chang, Aya Kawasaki, Yee Ling Wu, Kenneth M. Kaufman, Xiaoxia Qian, Jennifer M. Grossman, Shunle Chen, C. Yung Yu, Bevra H. Hahn, Yasushi Kawaguchi, Joel M. Guthridge, Qiong Fu, Rita M. Cantor, Zhao Jian, Yeong Wook Song, So Young Bang, Yun Deng, Yoshinari Takasaki, Naoyuki Tsuchiya, Wanling Yang, Hwee Siew Howe, Nan Shen, Hiroshi Hashimoto, Sang Cheol Bae, Mo Yin Mok, Takayuki Sumida, Maida Wong
Systemic lupus erythematosus (SLE) is a multisystem, autoimmune disease that predominantly affects women. Previous findings that duplicated Toll-like receptor 7 (Tlr7) promotes lupus-like disease in male BXSB mice prompted us to evaluate TLR7 in huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8dc59c3a77351ad3be450bd5b3330aa
https://europepmc.org/articles/PMC2936646/
https://europepmc.org/articles/PMC2936646/