Investigación de la Infección
Brigham and Women's Hospital
Boston, Estados UnidosPublicaciones en colaboración con investigadores/as de Brigham and Women's Hospital (9)
2017
-
The FASTK family of proteins: Emerging regulators of mitochondrial RNA biology
Nucleic Acids Research, Vol. 45, Núm. 19, pp. 10941-10947
2016
-
Deletion of FAST (Fas-activated serine/threonine phosphoprotein) ameliorates immune complex arthritis in mice
Modern Rheumatology, Vol. 26, Núm. 4, pp. 630-632
2015
-
A Mitochondria-Specific Isoform of FASTK Is Present In Mitochondrial RNA Granules and Regulates Gene Expression and Function
Cell Reports, Vol. 10, Núm. 7, pp. 1110-1121
2012
-
The translational repressor T-cell intracellular antigen-1 (TIA-1) is a key modulator of Th2 and Th17 responses driving pulmonary inflammation induced by exposure to house dust mite
Immunology Letters, Vol. 146, Núm. 1-2, pp. 8-14
2011
-
Rapid IgE desensitization is antigen specific and impairs early and late mast cell responses targeting FcεRI internalization
European Journal of Immunology, Vol. 41, Núm. 4, pp. 1004-1013
2010
-
Fas-activated serine/threonine phosphoprotein promotes immune-mediated pulmonary inflammation
Journal of Immunology, Vol. 184, Núm. 9, pp. 5325-5332
-
Fast kinase domain-containing protein 3 is a mitochondrial protein essential for cellular respiration
Biochemical and Biophysical Research Communications, Vol. 401, Núm. 3, pp. 440-446
2004
-
FAST is a survival protein that senses mitochondrial stress and modulates TIA-1-regulated changes in protein expression
Molecular and Cellular Biology, Vol. 24, Núm. 24, pp. 10718-10732
-
SAP increases FynT kinase activity and is required for phosphorylation of SLAM and Ly9
International Immunology, Vol. 16, Núm. 5, pp. 727-736