Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marian Suarez-Gestal"'
Autor:
Elisa Alonso-Perez, Marian Suarez-Gestal, Manuel Calaza, Josep Ordi-Ros, Eva Balada, Marc Bijl, Chryssa Papasteriades, Patricia Carreira, Fotini N Skopouli, Torsten Witte, Emöke Endreffy, Maurizio Marchini, Sergio Migliaresi, Gian Domenico Sebastiani, Maria Jose Santos, Ana Suarez, Francisco J Blanco, Nadia Barizzone, Rudolf Pullmann, Sarka Ruzickova, Bernard R Lauwerys, Juan J Gomez-Reino, Antonio Gonzalez, European Consortium of SLE DNA Collections
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45356 (2012)
IntroductionSystemic Lupus Erythematosus (SLE) shows a spectrum of clinical manifestations that complicate its diagnosis, treatment and research. This variability is likely related with environmental exposures and genetic factors among which known SL
Externí odkaz:
https://doaj.org/article/d692975c5ef74c0bb689b2d428e6b30c
Autor:
Elisa Alonso-Perez, Marian Suarez-Gestal, Manuel Calaza, Torsten Witte, Chryssa Papasteriades, Maurizio Marchini, Sergio Migliaresi, Attila Kovacs, Josep Ordi-Ros, Marc Bijl, Maria Jose Santos, Sarka Ruzickova, Rudolf Pullmann, Patricia Carreira, Fotini N Skopouli, Sandra D'Alfonso, Gian Domenico Sebastiani, Ana Suarez, Francisco J Blanco, Juan J Gomez-Reino, Antonio Gonzalez, European Consortium of SLE DNA Collections
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e29033 (2011)
Systemic Lupus Erythematosus (SLE) is an autoimmune disease with a very varied spectrum of clinical manifestations that could be partly determined by genetic factors. We aimed to determine the relationship between prevalence of 11 clinical features a
Externí odkaz:
https://doaj.org/article/34af34c09cf743f4a1a00c4906574f32
Autor:
Juan J. Gomez-Reino, Elisa Alonso-Perez, Tony Kwan, Manuel Calaza, Antonio Gonzalez, Jacek Majewski, Marian Suarez-Gestal
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Arthritis Research & Therapy
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
instname
Arthritis Research & Therapy
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
Introduction Interferon regulatory factor 5 gene (IRF5) polymorphisms are strongly associated with several diseases, including systemic lupus erythematosus (SLE). The association includes risk and protective components. They could be due to combinati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68b48435facbfb6faf3326f9632a89fc
http://hdl.handle.net/10347/23036
http://hdl.handle.net/10347/23036
Autor:
Francisco J. Blanco, José Ramón Lamas, Benjamín Fernández-Gutiérrez, Juan D. Cañete, Manuel Calaza, Arturo Rodríguez de la Serna, José Luis Marenco, Rebeca Dieguez-Gonzalez, Juan J. Gomez-Reino, Luis Carreño, Eva Perez-Pampin, Marian Suarez-Gestal, Gabriel Herrero-Beaumont, Alejandro Balsa, Antonio Gonzalez, Javier Narváez, José L. Pablos, Ana M. Ortiz, F. Navarro, Rafael Cáliz
Publikováno v:
ARTHRITIS AND RHEUMATISM
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Objective. Rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) share some genetic factors such as HLA, PTPN22, STAT4, and 6q23. The aim of this study was to determine whether 9 other SLE genetic factors are also implicated in RA suscepti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::729e79faa60bfd4020d9227b2f06c474
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13147
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13147
Publikováno v:
Genes and immunity. 9(4)
This study aimed to test the functional effects of the PD1.3 single nucleotide polymorphism (SNP) (rs11568821), which were proposed based on its association to systemic lupus erythematosus (SLE) susceptibility and in electrophoretic mobility shift as
Autor:
Marian Suarez-Gestal, Bernard Lauwerys, Gian Domenico Sebastiani, Marc Bijl, Sergio Migliaresi, Fotini N. Skopouli, Rudolf Pullmann, Torsten Witte, Attila W. Kovács, Nadia Barrizone, Josep Ordi-Ros, Ana Suárez, Elisa Alonso-Perez, Patricia Carreira, Manuel Calaza, Juan J. Gomez-Reino, S Ruzickova, Francisco J. Blanco, Maria José Santos, Maurizio Marchini, C. Papasteriades, Antonio Gonzalez
Publikováno v:
Arthritis Research & Therapy
RUC. Repositorio da Universidade da Coruña
instname
Arthritis research & therapy, Vol. 16, no. 3, p. R128 [1-8] (2014)
RUO. Repositorio Institucional de la Universidad de Oviedo
RUC. Repositorio da Universidade da Coruña
instname
Arthritis research & therapy, Vol. 16, no. 3, p. R128 [1-8] (2014)
RUO. Repositorio Institucional de la Universidad de Oviedo
This work was supported by the Health Research Fund of the Instituto de Salud Carlos III (Spain) (grants 08/0744 and 11/01048) and by the RETICS Program (RD08/0075 and RD12/0009/0008), which that are partially financed by the European Regional Develo
Publikováno v:
The Journal of Rheumatology. 37:676.2-677
To the Editor: These are exciting times for the genetic investigation of systemic lupus erythematosus (SLE), characterized by the discovery of many reproducibly associated loci1. Further progress will require research in many different directions, in
Publikováno v:
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Arthritis Research & Therapy
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Universidad de Santiago de Compostela (USC)
Arthritis Research & Therapy
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Introduction We aimed to replicate the strong associations that a recent genome wide association study (GWAS) has found between 16 single nucleotide polymorphisms (SNPs) and response to anti-tumour necrosis factor (TNF) treatment in 89 patients with