Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Nina A Daha"'
Autor:
Marcus Ronninger, Maria Seddighzadeh, Morten Christoph Eike, Darren Plant, Nina A Daha, Beate Skinningsrud, Jane Worthington, Tore K Kvien, Rene E M Toes, Benedicte A Lie, Lars Alfredsson, Leonid Padyukov
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32861 (2012)
HLA-DRB1 shared epitope (SE) alleles are the strongest genetic determinants for autoantibody positive rheumatoid arthritis (RA). One of the key regulators in expression of HLA class II receptors is MHC class II transactivator (CIITA). A variant of th
Externí odkaz:
https://doaj.org/article/8a36cd766198420392d7d345949bfe68
Autor:
Nina A. Daha, Monica van Eijck, Mattijs E. Numans, Johan Immerzeel, Margot W. M. de Waal, Marc Bruijnzeels, Ida Spelt
Publikováno v:
International Journal of Integrated Care; Vol 18: Annual Conference Supplement 2018; 395
Background: A major challenge in primary health care today, is the increase of frail elderly individuals in primary care practices. The current reactive approach leads to a rise of unplanned visits to the emergency room and after hours general practi
Publikováno v:
International Journal of Integrated Care; Vol 18: Annual Conference Supplement 2018; 394
Background: Costs of health care are rising, we enter the era of multimorbidity and the patient experiences are more important. With the ageing of the population and increased medical and technical possibilities forecasts show that resources for heal
Autor:
Harm-Jan Westra, Yonghong Li, René E. M. Toes, Twj Huizinga, Leendert A. Trouw, Nina A. Daha, Stefan Böhringer, Jeanine J. Houwing-Duistermaat, George N. Goulielmos, Gerrie Stoeken-Rijsbergen, E W N Levarht, Alexandra Zhernakova, Anja Roos, Fina A S Kurreeman, Willem Verduijn, Eli A. Stahl, Lude Franke
Publikováno v:
Clinical & Experimental Immunology; Vol 173
Clinical and Experimental Immunology, 173(1), 76-83. Wiley
Clinical and Experimental Immunology, 173(1), 76-83
Clinical & Experimental Immunology
Clinical and Experimental Immunology, 173(1), 76-83. Wiley
Clinical and Experimental Immunology, 173(1), 76-83
Clinical & Experimental Immunology
Rodent models for arthritis implicate a role for complement in disease development and progression. In humans, complement deposition has been observed in inflamed synovia of rheumatoid arthritis (RA) patients. In this study we analysed whether geneti
Autor:
Tore Saxne, M. K. Leijsma, Elisabet Lindqvist, Elisabeth Brouwer, Lude Franke, M. P. M. van der Linden, D. P. C. de Rooy, T. W. J. Huizinga, René E. M. Toes, Rachel Knevel, Nina A. Daha, Jeanine J. Houwing-Duistermaat, A. Krabben, A.H.M. van der Helm-van Mil, Harm-Jan Westra, Alexandra Zhernakova, S. Tsonaka, Anthony G. Wilson
Publikováno v:
ARTHRITIS AND RHEUMATISM, 65(3), 582-589. John Wiley and Sons Inc.
Arthritis & Rheumatism; Vol 65
Arthritis and Rheumatism, 65(3), 582-589
Arthritis & Rheumatism
Arthritis & Rheumatism; Vol 65
Arthritis and Rheumatism, 65(3), 582-589
Arthritis & Rheumatism
Objective Genetic factors account for an estimated 4558% of the variance in joint destruction in rheumatoid arthritis (RA). The serine proteinase granzyme B induces target cell apoptosis, and several in vitro studies suggest that granzyme B is involv
Autor:
Nina A. Daha, Jeanine J. Houwing-Duistermaat, Tore Saxne, B. P. C. Koeleman, T. W. J. Huizinga, Anthony G. Wilson, Elisabet Lindqvist, A. Zhernakoza, A. Krabben, Rachel Knevel, A.H.M. van der Helm-van Mil, M. P. M. van der Linden, M. D. Posthumus, L. van Toorn, René E. M. Toes, Elisabeth Brouwer, D. P. C. de Rooy, G. Stoeken, Roula Tsonaka
Publikováno v:
Annals of the Rheumatic Diseases; Vol 71
Annals of the Rheumatic Diseases, 71(10), 1651-1657
Annals of the Rheumatic Diseases, 71(10), 1651-1657. BMJ PUBLISHING GROUP
Annals of the Rheumatic Diseases, 71(10), 1651-1657
Annals of the Rheumatic Diseases, 71(10), 1651-1657. BMJ PUBLISHING GROUP
Background Interleukin (IL)-15 levels are increased in serum, synovium and bone marrow of patients with rheumatoid arthritis (RA). IL-15 influences both the innate and the adaptive immune response; its major role is activation and proliferation of T
Autor:
Tom W J Huizinga, Anthony G. Wilson, Dominique Baeten, Annette H M van der Helm-van Mil, Tore Saxne, Elisabeth Brouwer, S. Tsonaka, René E. M. Toes, Alexandra Zhernakova, Elisabet Lindqvist, Diederik P. C. de Rooy, Nataliya Yeremenko, M. K. Leijsma, Nina A. Daha, Jeanine J. Houwing-Duistermaat, A. Krabben, Rachel Knevel
Publikováno v:
Annals of the Rheumatic Diseases
Annals of the Rheumatic Diseases, 72(5), 769-775
Annals of the Rheumatic Diseases, 72(5), 769-775. BMJ PUBLISHING GROUP
Annals of the rheumatic diseases, 72(5), 769-775. BMJ Publishing Group
Annals of the Rheumatic Diseases; Vol 72
Annals of the Rheumatic Diseases, 72(5), 769-775
Annals of the Rheumatic Diseases, 72(5), 769-775. BMJ PUBLISHING GROUP
Annals of the rheumatic diseases, 72(5), 769-775. BMJ Publishing Group
Annals of the Rheumatic Diseases; Vol 72
Background Progression of joint destruction in rheumatoid arthritis (RA) is partly heritable; knowledge of genetic factors may increase our understanding of the mechanisms underlying joint destruction. The activity of the Wnt/beta-catenin pathway inf
Autor:
René E. M. Toes, Fina A S Kurreeman, Rute B. Marques, Nina A. Daha, Gerrie Stoeken-Rijsbergen, Tom W J Huizinga, Willem Verduijn
Publikováno v:
Arthritis & Rheumatism. 60:1255-1260
Objective Recent advances have led to novel identification of genetic polymorphisms that are associated with susceptibility to rheumatoid arthritis (RA). Currently, 5 loci (HLA, PTPN22, TRAF1/C5, TNFAIP3, and STAT4) have been consistently reported, w
Autor:
Xia Jiang, Henrik Källberg, Alejandro Balsa, Tore K Kvien, Paul I.W. de Bakker, Boel Brynedal, Nina A. Daha, Inge C. Olsen, Javier Gutierrez-Achury, René E. M. Toes, Bettina Kulle Andreassen, Fina A S Kurreeman, Javier Martín, Till Uhlig, Miguel A. González-Gay, Luis Rodriguez-Rodriguez, Marthe T. Maehlen, Benedicte A. Lie, Marte K. Viken, María Teruel, Lars Alfredsson, Alexandra Zhernakova
Publikováno v:
Annals of the Rheumatic Diseases, 74(4), 762-768. BMJ PUBLISHING GROUP
Annals of the Rheumatic Diseases, 74(4), 762-768
Annals of the Rheumatic Diseases, 74(4), 762. BMJ Publishing Group
Annals of the Rheumatic Diseases, 74(4), 762-768
Annals of the Rheumatic Diseases, 74(4), 762. BMJ Publishing Group
Objective Certain HLA-DRB1 alleles and single-nucleotide polymorphisms (SNPs) are associated with rheumatoid arthritis (RA). Our objective was to examine the combined effect of these associated variants, calculated as a cumulative genetic risk score
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b455b8067bc07cd4afbdc9466b7e9e6
https://doi.org/10.1136/annrheumdis-2013-204173
https://doi.org/10.1136/annrheumdis-2013-204173
Autor:
Leendert A. Trouw, Nina A. Daha, Joris J. M. Schonkeren, Rosanne A. van Schaarenburg, Daniëlle J. van Gijlswijk-Janssen, Carin A. Koelman, Cees van Kooten, Tom W J Huizinga, René E. M. Toes, E. W. Nivine Levarht, Anja Roos, Fina A S Kurreeman, Arjan C. Lankester, Margot R. Ernst-Kruis
Publikováno v:
Immunobiology, 220(3), 422-427
Introduction C1q deficiency is a rare genetic disorder that is strongly associated with development of systemic lupus erythematosus (SLE). Several mutations in the coding regions of the C1q genes have been described that result in stop-codons or othe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f97019218743f8635d6c2a81989eda
http://hdl.handle.net/1887/105996
http://hdl.handle.net/1887/105996