المؤلفون: Rothwell, Simon, Amos, Christopher, Miller, Frederick, Rider, Lisa, Lundberg, Ingrid, Gregersen, Peter, Selva-O'Callaghan, Albert

المساهمون: Institut Català de la Salut, Rothwell S Centre for Genetics and Genomics Versus Arthritis, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. Amos CI Baylor College of Medicine, Houston, Texas. Miller FW, Rider LG Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, NIH, Bethesda, Maryland. Lundberg IE Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. Gregersen PK The Robert S. Boas Center for Genomics and Human Genetics, The Feinstein Institute, Manhasset, New York. Selva-O'Callaghan A Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Malalties autoimmunitàries - Aspectes genètics, Músculs - Malalties - Aspectes genètics, DISEASES::Immune System Diseases::Autoimmune Diseases, Other subheadings::Other subheadings::Other subheadings::/genetics, DISEASES::Musculoskeletal Diseases::Muscular Diseases::Myositis, PHENOMENA AND PROCESSES::Genetic Phenomena::Genotype::Genetic Predisposition to Disease, ENFERMEDADES::enfermedades del sistema inmune::enfermedades autoinmunes, Otros calificadores::Otros calificadores::Otros calificadores::/genética, ENFERMEDADES::enfermedades musculoesqueléticas::enfermedades musculares::miositis, FENÓMENOS Y PROCESOS::fenómenos genéticos::genotipo::predisposición genética a la enfermedad

وصف الملف: application/pdf

Relation: Arthritis & Rheumatology;75(6); https://doi.org/10.1002/art.42434; Rothwell S, Amos CI, Miller FW, Rider LG, Lundberg IE, Gregersen PK, et al. Identification of Novel Associations and Localization of Signals in Idiopathic Inflammatory Myopathies Using Genome-Wide Imputation. Arthritis Rheumatol. 2023 Jun;75(6):1021–7.; https://hdl.handle.net/11351/9719; 000951145400001

الاتاحة: https://hdl.handle.net/11351/9719
https://doi.org/10.1002/art.42434

المؤلفون: Remuzgo-Martínez, Sara, Atienza-Mateo, Belén, Ocejo‑Vinyals, J. Gonzalo, Genre, Fernanda, Pulito-Cueto, Verónica, Mora Cuesta, Víctor Manuel, Trallero Araguas, Ernesto, Selva O'Callaghan, Albert

المساهمون: Institut Català de la Salut, Remuzgo-Martínez S, Genre F, Pulito-Cueto V Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. Atienza-Mateo B Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. López Albo’ Post Residency Programme, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Rheumatology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Ocejo-Vinyals JG Department of Immunology, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Mora-Cuesta VM Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. Pneumology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Trallero-Araguas E Unitat de Reumatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Selva-O'Callaghan A Unitat de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Polimorfisme genètic, Pulmons - Malalties - Aspectes genètics, Malalties autoimmunitàries - Aspectes genètics, DISEASES::Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial, PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Diagnosis, Differential, ENFERMEDADES::enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales, FENÓMENOS Y PROCESOS::fenómenos genéticos::variación genética::polimorfismo genético::polimorfismo de nucleótido único, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::diagnóstico diferencial

وصف الملف: application/pdf

Relation: Scientific reports;11; https://doi.org/10.1038/s41598-021-01992-y; Remuzgo-Martínez S, Atienza-Mateo B, Ocejo-Vinyals JG, Genre F, Pulito-Cueto V, Mora-Cuesta VM, et al. Role of MUC1 rs4072037 polymorphism and serum KL-6 levels in patients with antisynthetase syndrome. Sci Rep. 2021 Nov 19;11:22574.; https://hdl.handle.net/11351/7603; 000720679400011

الاتاحة: https://hdl.handle.net/11351/7603
https://doi.org/10.1038/s41598-021-01992-y

المؤلفون: Rothwell, S., Amos, C. I., Miller, F. W., Rider, L. G., Lundberg, I. E., Gregersen, P. K., Vencovsky, J., Mchugh, N., Limaye, V., Selva-O'Callaghan, A., Hanna, M. G., Machado, P. M., Pachman, L. M., Reed, A. M., Molberg, Ø., Benveniste, O., Mathiesen, P., Radstake, T., Doria, A., De Bleecker, J. L., De Paepe, B., Maurer, B., Ollier, W. E., Padyukov, L., O'Hanlon, T. P., Lee, A., Wedderburn, L. R., Chinoy, H., Lamb, J. A.

المساهمون: Institut Català de la Salut, [Rothwell S] Centre for Genetics and Genomics Versus Arthritis, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. [Amos CI] Baylor College of Medicine, Houston, Texas. [Miller FW, Rider LG] Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, NIH, Bethesda, Maryland. [Lundberg IE] Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. [Gregersen PK] The Robert S. Boas Center for Genomics and Human Genetics, The Feinstein Institute, Manhasset, New York. [Selva-O'Callaghan A] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Rheumatology, Músculs - Malalties - Aspectes genètics, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Immunology, Malalties autoimmunitàries - Aspectes genètics, Immune System Diseases::Autoimmune Diseases [DISEASES], Other subheadings::Other subheadings::/genetics [Other subheadings], Genetic Phenomena::Genotype::Genetic Predisposition to Disease [PHENOMENA AND PROCESSES], enfermedades del sistema inmune::enfermedades autoinmunes [ENFERMEDADES], Immunology and Allergy, Musculoskeletal Diseases::Muscular Diseases::Myositis [DISEASES], enfermedades musculoesqueléticas::enfermedades musculares::miositis [ENFERMEDADES], fenómenos genéticos::genotipo::predisposición genética a la enfermedad [FENÓMENOS Y PROCESOS]

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9963c6ca7912cc631e5ff1d85cf563f
https://hdl.handle.net/11577/3476647

المؤلفون: Remuzgo Martínez, Sara, Atienza Mateo, Belén, Ocejo Vinyals, J. Gonzalo, Genre, Fernanda, Pulito Cueto, Verónica, Mora Cuesta, Víctor M., Iturbe Fernández, David, Lera Gómez, Leticia, Pérez Fernández, Raquel, Prieto Peña, Diana, Irure, Juan, Romero Bueno, Fredeswinda, Sanchez Pernaute, Olga, Alonso Moralejo, Rodrigo, Nuño, Laura, Bonilla, Gema, Vicente Rabaneda, Esther F., Grafia, Ignacio, Prieto González, Sergio, Narváez, Javier, Trallero Araguas, Ernesto, Selva O’Callaghan, Albert, Ortego Centeno, Norberto, Pérez Gómez, Nair, Mera, Antonio, Martínez Barrio, Julia, Moriano, Clara, Díez, Elvira, Calvo Alén, Jaime, Balsa, Alejandro, Ussetti, María Piedad, Laporta, Rosalía, Berastegui, Cristina, Solé, Amparo, Gualillo, Oreste, Cavagna, Lorenzo, Cifrián, José M., Renzoni, Elisabetta A., Castañeda, Santos, López Mejías, Raquel, González Gay, Miguel A., Spanish Biomarkers Of Antisynthetase Syndrome Consortium, Spanish Biomarkers Of Interstitial Lung Disease Consortium

المساهمون: Universidad de Cantabria, Institut Català de la Salut, [Remuzgo-Martínez S, Genre F, Pulito-Cueto V] Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. [Atienza-Mateo B] Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. López Albo’ Post Residency Programme, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Rheumatology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. [Ocejo-Vinyals JG] Department of Immunology, Hospital Universitario Marqués de Valdecilla, Santander, Spain. [Mora-Cuesta VM] Research Group on Genetic Epidemiology and Atherosclerosis in Systemic Diseases and in Metabolic Diseases of the Musculoskeletal System, IDIVAL, 39011 Santander, Spain. Pneumology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. [Trallero-Araguas E] Unitat de Reumatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Selva-O'Callaghan A] Unitat de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Sci Rep 11, 22574 (2021)
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Scientific Reports
Scientia
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Dipòsit Digital de la UB
Universidad de Barcelona

مصطلحات موضوعية: Male, Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial [DISEASES], Antisynthetase syndrome, Gastroenterology, Idiopathic pulmonary fibrosis, Genètica mèdica, 0302 clinical medicine, fenómenos genéticos::variación genética::polimorfismo genético::polimorfismo de nucleótido único [FENÓMENOS Y PROCESOS], Gene Frequency, Polymorphism (computer science), Genotype, Malalties autoimmunitàries - Aspectes genètics, diagnóstico::diagnóstico diferencial [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], 0303 health sciences, Multidisciplinary, Medical genetics, Fibrosi pulmonar, Middle Aged, respiratory system, 3. Good health, Up-Regulation, medicine.anatomical_structure, Phenotype, Biomarker (medicine), Medicine, Female, Adult, medicine.medical_specialty, Pulmons - Malalties - Aspectes genètics, Science, Polymorphism, Single Nucleotide, Article, Pulmonary fibrosis, Diagnosis, Differential, 03 medical and health sciences, Predictive Value of Tests, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Allele, Allele frequency, Genetic Association Studies, 030304 developmental biology, 030203 arthritis & rheumatology, Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [PHENOMENA AND PROCESSES], Lung, Myositis, business.industry, Polimorfisme genètic, Mucin-1, medicine.disease, Idiopathic Pulmonary Fibrosis, respiratory tract diseases, Cross-Sectional Studies, enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales [ENFERMEDADES], Spain, Case-Control Studies, Diagnosis::Diagnosis, Differential [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], business, Lung Diseases, Interstitial, Idiopathic inflammatory myopathies, Biomarkers

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42bde78093ff2241d784f67f28b13a2e
http://hdl.handle.net/10902/23299