Cargando…
Chimeric cells of maternal origin do not appear to be pathogenic in the juvenile idiopathic inflammatory myopathies or muscular dystrophy
INTRODUCTION: Microchimeric cells have been studied for over a decade, with conflicting reports on their presence and role in autoimmune and other inflammatory diseases. To determine whether microchimeric cells were pathogenic or mediating tissue repair in inflammatory myopathies, we phenotyped and...
Autores principales: | Artlett, Carol M., Sassi-Gaha, Sihem, Ramos, Ronald C., Miller, Frederick W., Rider, Lisa G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558637/ https://www.ncbi.nlm.nih.gov/pubmed/26338728 http://dx.doi.org/10.1186/s13075-015-0732-0 |
Ejemplares similares
-
The Clinical Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
por: Shah, Mona, et al.
Publicado: (2013) -
The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
por: Rider, Lisa G., et al.
Publicado: (2013) -
Mir-155 is overexpressed in systemic sclerosis fibroblasts and is required for NLRP3 inflammasome-mediated collagen synthesis during fibrosis
por: Artlett, Carol M., et al.
Publicado: (2017) -
Environmental factors preceding illness onset differ in phenotypes of the juvenile idiopathic inflammatory myopathies
por: Rider, Lisa G., et al.
Publicado: (2010) -
Targeting the unfolded protein response, XBP1, and the NLRP3 inflammasome in fibrosis and cancer
por: Overley-Adamson, Beth, et al.
Publicado: (2014)