Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Monica Castrichini"'
Autor:
Nabil El-Sherif, Marie Wahren-Herlenius, Pietro Enea Lazzerini, Zhengfeng Zhou, Craig T. January, Mohamed Boutjdir, Mohamed Chahine, Franco Laghi-Pasini, Ujala Srivastava, Monica Castrichini, M. Mahmood Hussain, Xian-Cheng Jiang, Frank Fabris, Eric A. Sobie, Zhiqiang Li, Yuankun Yue, Pier Leopoldo Capecchi, Yongxia Qu, Krupa Shah
Publikováno v:
Circulation. 132:230-240
Background— Emerging clinical evidence demonstrates high prevalence of QTc prolongation and complex ventricular arrhythmias in patients with anti-Ro antibody (anti-Ro Ab)–positive autoimmune diseases. We tested the hypothesis that anti-Ro Abs tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15023049935f2fdc4b921aaeae8fb0a7
https://doi.org/10.1161/circulationaha.115.009800
https://doi.org/10.1161/circulationaha.115.009800
The purinergic P2×7 receptor is expressed on monocytes in Behçet's disease and is modulated by TNF-α
Autor:
Enrico Selvi, Cinzia Montilli, Elena Gianchecchi, Pietro Enea Lazzerini, Mariarita Natale, Rossella Franceschini, Stefania Zimbone, Franco Laghi-Pasini, Gianluca Ricci, Antonio Moramarco, Pier Leopoldo Capecchi, Monica Castrichini, Mauro Galeazzi, Alessandra Gamberucci, Mohamed Hammoud, Luca Cantarini
Publikováno v:
European Journal of Immunology. 44:227-238
The P2×7 receptor (P2×7r) is expressed in innate immune cells (e.g. monocyte/macrophages), playing a key role in IL-1β release. Since innate immune activation and IL-1β release seem to be implicated in Behcet's disease (BD), a systemic immune-inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6997c6a3c2e8d951bcf6703e64d46fc
https://doi.org/10.1002/eji.201343353
https://doi.org/10.1002/eji.201343353
Autor:
Thomas Braulke, Marisa Encarnação, Monica Castrichini, Katrin Kollmann, Sven Müller-Loennies, Stephan Tiede, Sandra Pohl, Nicole Muschol, Kurt Ullrich, Katrin Marschner
Publikováno v:
Journal of Biological Chemistry. 285:23936-23944
GlcNAc-1-phosphotransferase is a Golgi-resident 540-kDa complex of three subunits, alpha(2)beta(2)gamma(2), that catalyze the first step in the formation of the mannose 6-phosphate (M6P) recognition marker on lysosomal enzymes. Anti-M6P antibody anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daac1a6b5bb9edc17a122d19497361d7
https://doi.org/10.1074/jbc.m110.129684
https://doi.org/10.1074/jbc.m110.129684
Autor:
E. Balistreri, Elena Gianchecchi, Mauro Galeazzi, Stefania Zimbone, Pietro Enea Lazzerini, Franco Laghi-Pasini, Cinzia Montilli, Pier Leopoldo Capecchi, Estrella Garcia-Gonzalez, Monica Castrichini, Gianluca Ricci, Mariarita Natale, Enrico Selvi
Systemic sclerosis (SSc) is a connective tissue disease characterised by exaggerated collagen deposition in the skin and visceral organs. Adenosine A2A receptor stimulation (A2Ar) promotes dermal fibrosis, while the cannabinoid system modulates fibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ddd3792c7a841ef19dbaa8d0b420d1f
http://hdl.handle.net/11365/39664
http://hdl.handle.net/11365/39664
Autor:
Sven Müller-Loennies, Nicole Muschol, Thomas Braulke, Sandra Pohl, Marisa Encarnação, Monica Castrichini
Publikováno v:
American journal of medical genetics. Part A. (1)
Mucolipidosis type III gamma (MLIII, pseudo-Hurler polydystrophy) is a rare autosomal recessive disorder where the activity of the multimeric GlcNAc-1–phosphotransferase is reduced and formation of the mannose 6-phosphate (M6P) recognition marker o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77260e49aa054be4745dbdda3565d0e1
https://pubmed.ncbi.nlm.nih.gov/20034096
https://pubmed.ncbi.nlm.nih.gov/20034096