New insight on the Xq28 association with systemic sclerosis

Autor: Maureen D. Mayes, Gabriela Riemekasten, Alexandre E. Voskuyl, V. Fonollosa, Jane Worthington, Madelon C. Vonk, Miguel A. González-Gay, Christopher P. Denton, José Luis Callejas-Rubio, Alexander Kreuter, Javier Martin, F. David Carmona, Annemie J. Schuerwegh, Jasper C A Broen, Patricia Carreira, Rajan Madhok, Timothy R D J Radstake, Paul G. Shiels, Lina-Marcela Diaz-Gallo, Frank C. Arnett, Jörg H W Distler, Carmen P. Simeon, Nicolas Hunzelmann, Jacob M van Laar, Torsten Witte, Filemon K. Tan, M. Carmen Cénit, Carmen Fonseca, Shervin Assassi, Ariane L. Herrick, Francisco Javier López-Longo

Publikováno v: Carmona, F D, Cenit, M C, Diaz-Gallo, L M, Broen, J C A, Simeon, C P, Carreira, P E, Callejas-Rubio, J L, Fonollosa, V, Lopez-Longo, F J, Gonzalez-Gay, M A, Hunzelmann, N, Riemekasten, G, Witte, T, Kreuter, A, Distler, J H W, Madhok, R, Shiels, P, van Laar, J M, Schuerwegh, A J, Vonk, M C, Voskuyl, A E, Fonseca, C, Denton, C P, Herrick, A, Worthington, J, Arnett, F C, Tan, F K, Assassi, S, Radstake, T R D J, Mayes, M D & Martin, J 2013, ' New insight on the Xq28 association with systemic sclerosis ', Annals of the Rheumatic Diseases, vol. 72, no. 12, pp. 2032-2038 . https://doi.org/10.1136/annrheumdis-2012-202742
Annals of the Rheumatic Diseases, 72, 12, pp. 2032-8
Annals of the Rheumatic Diseases, 72(12), 2032-2038. BMJ Publishing Group
Annals of the Rheumatic Diseases, 72, 2032-8

ObjectiveTo evaluate whether the systemic sclerosis (SSc)-associated IRAK1 non-synonymous single-nucleotide polymorphism rs1059702 is responsible for the Xq28 association with SSc or whether there are other independent signals in the nearby methyl-Cp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::878658de3daa7a65af224b40b6db94e5
https://doi.org/10.1136/annrheumdis-2012-202742

The genetics of celiac disease: A comprehensive review of clinical implications

Autor: M. Carmen Cénit, Romina Dieli-Crimi, Concepción Núñez

Publikováno v: Journal of autoimmunity. 64

Celiac disease (CD) is a complex immune-related disease with a very strong genetic component. Multiple genetic findings over the last decade have added to the already known MHC influence numerous genetic variants associated to CD susceptibility. Curr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db39f1425744a15e45b100261086a96c
https://pubmed.ncbi.nlm.nih.gov/26194613

DRB1*03:01 Haplotypes: Differential Contribution to Multiple Sclerosis Risk and Specific Association with the Presence of Intrathecal IgM Bands

Autor: José C. Álvarez-Cermeño, Luisa M. Villar, M. Carmen Cénit, Rafael Arroyo, Laura Leyva, Elena Urcelay, Concepción Núñez, Oscar Fernandez, Emilio G. de la Concha, María L. Cavanillas

Publikováno v: PLoS ONE, Vol 7, Iss 2, p e31018 (2012)
PLoS ONE

Journal Article; Research Support, Non-U.S. Gov't; BACKGROUND Multiple sclerosis (MS) is a multifactorial disease with a genetic basis. The strongest associations with the disease lie in the Human Leukocyte Antigen (HLA) region. However, except for t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b93ce1abf2f575492f23908263e6e71f
https://doi.org/10.1371/journal.pone.0031018

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.