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Resultats globals: 4 registres trobats en 0.03 segons.
Articles, 4 registres trobats
Articles 4 registres trobats  
1.
10 p, 1.3 MB Coordinated local RNA overexpression of complement induced by interferon gamma in myositis / Casal-Dominguez, Maria (Johns Hopkins University School of Medicine) ; Pinal-Fernandez, Iago (Johns Hopkins University School of Medicine) ; Pak, Katherine (National Institute of Arthritis and Musculoskeletal and Skin Diseases) ; Muñoz-Braceras, Sandra (National Institute of Arthritis and Musculoskeletal and Skin Diseases) ; Milisenda, Jose C. (Hospital Clínic i Provincial de Barcelona) ; Torres-Ruiz, Jiram (Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán) ; Dell'Orso, Stefania (National Institute of Arthritis and Musculoskeletal and Skin Diseases) ; Naz, Faiza (National Institute of Arthritis and Musculoskeletal and Skin Diseases) ; Gutierrez-Cruz, Gustavo (National Institute of Arthritis and Musculoskeletal and Skin Diseases) ; Duque-Jaimez, Yaiza (Hospital Clínic i Provincial de Barcelona) ; Matas-Garcia, Ana (Hospital Clínic i Provincial de Barcelona) ; Valls-Roca, Laura (Hospital Clínic i Provincial de Barcelona) ; Garrabou, Glòria (Hospital Clínic i Provincial de Barcelona) ; Trallero-Araguas, Ernesto (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Walitt, Brian (National Institute of Neurological Disorders and Stroke) ; Christopher-Stine, Lisa (Johns Hopkins University School of Medicine) ; Lloyd, Thomas E. (Johns Hopkins University School of Medicine) ; Paik, Julie J. (Johns Hopkins University School of Medicine) ; Albayda, Jemima (Johns Hopkins University School of Medicine) ; Corse, Andrea (Johns Hopkins University School of Medicine) ; Grau, Josep Maria (Hospital Clínic i Provincial de Barcelona) ; Selva O'Callaghan, Albert (Universitat Autònoma de Barcelona) ; Mammen, Andrew L. (Johns Hopkins University School of Medicine)
Complement proteins are deposited in the muscles of patients with myositis. However, the local expression and regulation of complement genes within myositis muscle have not been well characterized. In this study, bulk RNA sequencing (RNAseq) analyses of muscle biopsy specimens revealed that complement genes are locally overexpressed and correlate with markers of myositis disease activity, including the expression of interferon-gamma (IFN γ)-induced genes. [...]
2023 - 10.1038/s41598-023-28838-z
Scientific reports, Vol. 13 (february 2023)  
Registre complet - Creative Commons
2.
17 p, 648.0 KB Role of autoantibodies in the diagnosis and prognosis of interstitial lung disease in autoimmune rheumatic disorders / Kuwana, Masataka (Nippon Medical School Graduate School of Medicine) ; Gil-Vila, Albert (Hospital Universitari Vall d'Hebron) ; Selva O'Callaghan, Albert (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona
Interstitial lung disease (ILD) has been recognized as a frequent manifestation associated with a substantial morbidity and mortality burden in patients with autoimmune rheumatic disorders. Serum autoantibodies are considered good biomarkers for identifying several subsets or specific phenotypes of ILD involvement in these patients. [...]
2021 - 10.1177/1759720X211032457
Therapeutic Advances in Musculoskeletal Disease, Vol. 13 (july 2021)  
Registre complet - Creative Commons
3.
11 p, 754.8 KB Worldwide population distribution of the common LCE3C-LCE3B deletion associated with psoriasis and other autoimmune disorders / Bassaganyas, Laia (Centre de Regulació Genòmica) ; Riveira Muñoz, Eva (Institut Germans Trias i Pujol. Institut de Recerca de la Sida IrsiCaixa) ; García Aragonés, Manel (Centre de Regulació Genòmica) ; González, Juan Ramón (Institut Hospital del Mar d'Investigacions Mèdiques) ; Cáceres Aguilar, Mario (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Armengol, Lluís (Centre de Regulació Genòmica) ; Estivill, Xavier (Centre de Regulació Genòmica)
Background: there is increasing evidence of the importance of copy number variants (CNV) in genetic diversity among individuals and populations, as well as in some common genetic diseases. We previously characterized a common 32-kb insertion/deletion variant of the PSORS4 locus at chromosome 1q21 that harbours the LCE3C and LCE3B genes. [...]
2013 - 10.1186/1471-2164-14-261
BMC genomics, Vol. 14 (2013) , art. 261  
Registre complet - Creative Commons
4.
16 p, 13.5 MB Anti-neurofascin-155 IgG4 antibodies prevent paranodal complex formation in vivo / Manso, Constance (Aix-Marseille Université) ; Querol, Luis (Institut d'Investigació Biomèdica Sant Pau) ; Lleixà, Cinta (Institut d'Investigació Biomèdica Sant Pau) ; Poncelet, Mallory (Université de Montpellier. Hopital Gui de Chauliac) ; Mekaouche, Mourad (Aix-Marseille Université) ; Vallat, Jean-Michel (National Reference Center for "rare peripheral neuropathies" (Limoges, França)) ; Illa, Isabel (Institut d'Investigació Biomèdica Sant Pau) ; Devaux, Jérôme (Université de Montpellier. Hopital Gui de Chauliac)
Neurofascin-155 (Nfasc155) is an essential glial cell adhesion molecule expressed in paranodal septate-like junctions of peripheral and central myelinated axons. The genetic deletion of Nfasc155 results in the loss of septate-like junctions and in conduction slowing. [...]
2019 - 10.1172/JCI124694
The journal of clinical investigation, Vol. 129 Núm. 6 (march 2019) , p. 2222-2236  
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