المؤلفون: Martínez-López, Javier, Kerick, Martin, Ortiz-Fernández, Lourdes, Acosta-Herrera, Marialbert, Márquez, Ana, Martín, Javier

مصطلحات موضوعية: SSc, low-frequency variant, seropositive immune-mediated diseases, Humans, Genetic Predisposition to Disease, Genome-Wide Association Study, Polymorphism, Single Nucleotide, Scleroderma, Systemic, Genotype, Autoimmune Diseases, Case-Control Studies, fms-Like Tyrosine Kinase 3

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/10668/19834Test; PMC9910569; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910569/pdfTest

الإتاحة: https://doi.org/10.1093/rheumatology/keac406Test
http://hdl.handle.net/10668/19834Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910569/pdfTest

المؤلفون: Ortiz-Fernández, Lourdes, Saruhan-Direskeneli, Güher, Alibaz-Oner, Fatma, Kaymaz-Tahra, Sema, Coit, Patrick, Kong, Xiufang, Kiprianos, Allan P, Maughan, Robert T, Aydin, Sibel Z, Aksu, Kenan, Keser, Gokhan, Kamali, Sevil, Inanc, Murat, Springer, Jason, Akar, Servet, Onen, Fatos, Akkoc, Nurullah, Khalidi, Nader A, Koening, Curry, Karadag, Omer, Kiraz, Sedat, Forbess, Lindsy, Langford, Carol A, McAlear, Carol A, Ozbalkan, Zeynep, Yavuz, Sule, Çetin, Gozde Yildirim, Alpay-Kanitez, Nilufer, Chung, Sharon, Ates, Askin, Karaaslan, Yasar, McKinnon-Maksimowicz, Kathleen, Monach, Paul A, Ozer, Hüseyin TE, Seyahi, Emire, Fresko, Izzet, Cefle, Ayse, Seo, Philip, Warrington, Kenneth J, Ozturk, Mehmet A, Ytterberg, Steven R, Cobankara, Veli, Onat, Ahmet Mesut, Duzgun, Nurşen, Bıcakcıgil, Muge, Yentür, Sibel P, Lally, Lindsay, Manfredi, Angelo A, Baldissera, Elena, Erken, Eren, Yazici, Ayten, Kısacık, Bünyamin, Kaşifoğlu, Timuçin, Dalkilic, Ediz, Cuthbertson, David, Pagnoux, Christian, Sreih, Antoine, Reales, Guillermo, Wallace, Chris, Wren, Jonathan D, Cunninghame-Graham, Deborah S, Vyse, Timothy J, Sun, Ying, Chen, Huiyong, Grayson, Peter C, Tombetti, Enrico, Jiang, Lindi, Mason, Justin C, Merkel, Peter A, Direskeneli, Haner, Sawalha, Amr H

مصطلحات موضوعية: GWAS, HLA, Takayasu arteritis, chromatin interaction, eQTL, epigenetic, genetic association, genetic risk scroe, vasculitis, Case-Control Studies, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Inflammatory Bowel Diseases, Male, Polymorphism, Single Nucleotide

وصف الملف: Print-Electronic; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/octet-stream

العلاقة: https://www.repository.cam.ac.uk/handle/1810/313440Test

الإتاحة: https://doi.org/10.17863/CAM.60547Test
https://www.repository.cam.ac.uk/handle/1810/313440Test

المؤلفون: Ortiz-Fernández, Lourdes, Carmona, Elio G, Kerick, Martin, Lyons, Paul, Carmona, Francisco David, López Mejías, Raquel, Khor, Chiea Chuen, Grayson, Peter C, Tombetti, Enrico, Jiang, Lindi, Direskeneli, Haner, Saruhan-Direskeneli, Guher, Callejas-Rubio, José-Luis, Vaglio, Augusto, Salvarani, Carlo, Hernández-Rodríguez, Jose, Cid, Maria Cinta, Morgan, Ann W, Merkel, Peter A, Burgner, David, Smith, Kenneth Gc, Gonzalez-Gay, Miguel Angel, Sawalha, Amr H, Martin, Javier, Marquez, Ana

المساهمون: Ortiz-Fernández, Lourdes [0000-0002-0247-4280], Carmona, Francisco David [0000-0002-1427-7639], Grayson, Peter C [0000-0002-8269-9438], Salvarani, Carlo [0000-0003-3708-3148], Hernández-Rodríguez, Jose [0000-0002-2357-2015], Cid, Maria Cinta [0000-0002-4730-0938], Gonzalez-Gay, Miguel Angel [0000-0002-7924-7406], Martin, Javier [0000-0002-2202-0622], Marquez, Ana [0000-0001-9913-7688], Apollo - University of Cambridge Repository, Ortiz-Fernandez L., Carmona E. G., Kerick M., Lyons P., Carmona F. D., Mejias R. L., Khor C. C., Grayson P. C., Tombetti E., Jiang L., et al.

مصطلحات موضوعية: Internal Diseases, Vasculitis, Immunology, Autoimmunity, SUSCEPTIBILITY, VARIANTS, Sağlık Bilimleri, İmmünoloji ve Romatoloji, İç Hastalıkları, Clinical Medicine (MED), General Biochemistry, Genetics and Molecular Biology, Immunology and Rheumatology, ACTIVATION, Genetic, Rheumatology, Health Sciences, Humans, Immunology and Allergy, Klinik Tıp (MED), CTLA-4 Antigen, Genetic Predisposition to Disease, Polymorphism, GENOME-WIDE ASSOCIATION, ROMATOLOJİ, Internal Medicine Sciences, Polymorphism, Genetic, Klinik Tıp, Systemic Vasculitis, Drug Repositioning, Dahili Tıp Bilimleri, CLINICAL MEDICINE, Tıp, Medicine, Romatoloji, Apoptosis Regulatory Proteins

وصف الملف: application/pdf; text/xml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cf053e3ff6df46f75171fa393cd0283Test
https://hdl.handle.net/10481/80813Test

المؤلفون: González-Serna, David, Ortiz-Fernández, Lourdes, Vargas, Sofía, García, Antonio, Raya, Enrique, Fernández-Gutierrez, Benjamín, López-Longo, Francisco Javier, Balsa, Alejandro, González-Álvaro, Isidoro, Narvaez, Javier, Gómez-Vaquero, Carmen, Sabio, José Mario, García-Portales, Rosa, González-Escribano, María Francisca, Tolosa, Carles, Carreira, Patricia, Kiemeney, Lambertus, Coenen, Marieke J H, Witte, Torsten, Schneider, Matthias, González-Gay, Miguel Ángel, Martín, Javier

مصطلحات موضوعية: Arthritis, Rheumatoid, B-Cell Activating Factor, Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Germany, Humans, INDEL Mutation, Lupus Erythematosus, Systemic, Netherlands, Polymorphism, Genetic, Spain

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/10668/12517Test; PMC5974315; https://www.nature.com/articles/s41598-018-26573-4.pdfTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974315/pdfTest

الإتاحة: https://doi.org/10.1038/s41598-018-26573-4Test
http://hdl.handle.net/10668/12517Test
https://www.nature.com/articles/s41598-018-26573-4.pdfTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974315/pdfTest

المؤلفون: Ortiz-Fernández, Lourdes, Carmona, Francisco David, López-Mejías, Raquel, González-Escribano, Maria Francisca, Lyons, Paul A, Morgan, Ann W, Sawalha, Amr H, Merkel, Peter A, Smith, Kenneth G C, González-Gay, Miguel A, Martín, Javier, Spanish GCA Study Group, UK GCA Consortium, Turkish Takayasu Study Group, Vasculitis Clinical Research Consortium, IgAV Study Group, AAV Study group

مصطلحات موضوعية: autoantibodies, outcomes research, systemic sclerosis, Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis, Case-Control Studies, Epigenesis, Genetic, Female, Genetic Loci, Genetic Predisposition to Disease, Giant Cell Arteritis, HLA-DQ Antigens, HLA-DQ beta-Chains, Humans, Jumonji Domain-Containing Histone Demethylases, Linkage Disequilibrium, Male, Phenotype, Polymorphism, Single Nucleotide, Protein Array Analysis, Systemic Vasculitis, Takayasu Arteritis

العلاقة: http://hdl.handle.net/10668/12055Test; PMC5849568; https://europepmc.org/articles/pmc5849568?pdf=renderTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849568/pdfTest

الإتاحة: https://doi.org/10.1136/annrheumdis-2017-212372Test
http://hdl.handle.net/10668/12055Test
https://europepmc.org/articles/pmc5849568?pdf=renderTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849568/pdfTest

المؤلفون: Burillo-Sanz, Sergio, Montes-Cano, Marco-Antonio, García-Lozano, José-Raúl, Ortiz-Fernández, Lourdes, Ortego-Centeno, Norberto, García-Hernández, Francisco-José, Espinosa, Gerard, Graña-Gil, Genaro, Sánchez-Bursón, Juan, Rosa Juliá, María, Solans, Roser, Blanco, Ricardo, Barnosi-Marín, Ana-Celia, Gómez De la Torre, Ricardo, Fanlo, Patricia, Rodríguez-Carballeira, Mónica, Rodríguez-Rodríguez, Luis, Camps, Teresa, Castañeda, Santos, Alegre-Sancho, Juan-Jose, Martín, Javier, González-Escribano, María Francisca

مصطلحات موضوعية: Adaptor Proteins, Signal Transducing, Adenosine Deaminase, Behcet Syndrome, Cytoskeletal Proteins, Female, Genetic Predisposition to Disease, High-Throughput Nucleotide Sequencing, Humans, Inflammasomes, Inflammation, Intercellular Signaling Peptides and Proteins, Male, Mutation, NLR Family, Pyrin Domain-Containing 3 Protein, Nod2 Signaling Adaptor Protein, Phosphotransferases (Alcohol Group Acceptor), Pyrin, Receptors, Tumor Necrosis Factor, Type I

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/10668/11513Test; PMC5559572; https://www.nature.com/articles/s41598-017-09164-7.pdfTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559572/pdfTest

الإتاحة: https://doi.org/10.1038/s41598-017-09164-7Test
http://hdl.handle.net/10668/11513Test
https://www.nature.com/articles/s41598-017-09164-7.pdfTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559572/pdfTest

المؤلفون: Ortiz-Fernández, Lourdes, Carmona, Francisco-David, Montes-Cano, Marco-Antonio, García-Lozano, José-Raúl, Conde-Jaldón, Marta, Ortego-Centeno, Norberto, Castillo, María Jesús, Espinosa, Gerard, Graña-Gil, Genaro, Sánchez-Bursón, Juan, Juliá, María Rosa, Solans, Roser, Blanco, Ricardo, Barnosi-Marín, Ana-Celia, Gómez de la Torre, Ricardo, Fanlo, Patricia, Rodríguez-Carballeira, Mónica, Rodríguez-Rodríguez, Luis, Camps, Teresa, Castañeda, Santos, Alegre-Sancho, Juan-Jose, Martín, Javier, González-Escribano, María Francisca

مصطلحات موضوعية: Alleles, Behcet Syndrome, Case-Control Studies, Contactins, Gene Frequency, Genetic Loci, Genetic Predisposition to Disease, HLA-A3 Antigen, HLA-B Antigens, HLA-B51 Antigen, Humans, Immunoassay, Interleukin-12 Subunit p35, Logistic Models, Microarray Analysis, Models, Molecular, Receptors, Interleukin, Spain

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/10668/10379Test; PMC4993481; https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0161305&type=printableTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993481/pdfTest

الإتاحة: https://doi.org/10.1371/journal.pone.0161305Test
http://hdl.handle.net/10668/10379Test
https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0161305&type=printableTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993481/pdfTest