Alteration of Th17 and Treg cell subpopulations co-exist in patients affected with systemic sclerosis

Autor: Fenoglio, Daniela, Battaglia, Florinda, Parodi, Alessia, Stringara, Silvia, Negrini, Simone, Panico, Nicoletta, Rizzi, Marta, Kalli, Francesca, Conteduca, Giuseppina, Ghio, Massimo, De Palma, Raffaele, Indiveri, Francesco, Filaci, Gilberto

Publikováno v: In Clinical Immunology 2011 139(3):249-257

Acetylcholine synthesis and possible functions during sea urchin development

Autor: C Angelini, B Baccetti, P Piomboni, S Trombino, MG Aluigi, S Stringara, L Gallus, C Falugi

Publikováno v: European Journal of Histochemistry, Vol 48, Iss 3 (2009)

Cholinergic neurotransmitter system molecules were found to play a role during fertilisation and early cell cycles of a large number of invertebrate and vertebrate organisms. In this study, we investigated the presence and possible function of cholin

Externí odkaz: https://doaj.org/article/01d1f67fc7774d35bab539daaa3120fa

Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro

Autor: Sara Scapolan, Maria Anna Donati, Federico Zara, Marina Pedemonte, Elisabetta Gazzerro, Xiabo Wang, Monica Traverso, Stefania Assereto, Laura Giberti, Claudio Bruno, Federica Sotgia, Silvia Stringara, Roberta Biancheri, Carlo Minetti, Elisabetta Pasquini, Michael P. Lisanti

Publikováno v: Laboratory Investigation. 88:275-283

Caveolins are the principal protein components of caveolae, invaginations of the plasma membrane involved in cell signaling and trafficking. Caveolin-3 (Cav-3) is the muscle-specific isoform of the caveolin family and mutations in the CAV3 gene lead

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925563b9feb2a0b8a035a3250e08f08e
https://doi.org/10.1038/labinvest.3700713

Alteration of Th17 and Treg populations coexist in patients affected with systemic sclerosis

Autor: Battaglia F, Fenoglio D, Parodi A, Kalli F, Stringara S, Negrini S, Panico N, Rizzi M, Conteduca G, Ferrera F, Tardito S, Cortese M, Ghio M, Indiveri F, Filaci G., DE PALMA, Raffaele

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3977::d90a8113726899c98e0698938f2aef6c
http://hdl.handle.net/11591/322570

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract

Autor: Graziella Uziel, Marjo S. van der Knaap, Paolo Tortori-Donati, Andrea Rossi, Silvia Stringara, Federica Sotgia, Federico Zara, Angelo Schenone, Elisabetta Gazzerro, Stefania Gianotti, Carlo Minetti, Stefania Assereto, Laura Bordo, Roberta Biancheri, Claudio Bruno, Xiaobo Wang, Marina Pedemonte, Michael P. Lisanti

Publikováno v: Nature Genetics, 38(10), 1111-1113. Nature Publishing Group
Zara, F, Biancheri, R, Bruno, C, Bordo, L, Assereto, S, Gazzerro, E, Sotgia, F, Wang, X B, Gianotti, S, Stringara, S, Pedemonte, M, Uziel, G, Rossi, A, Schenone, A, Tortori-Donati, P, Van Der Knaap, M S, Lisanti, M P & Minetti, C 2006, ' Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract ', Nature Genetics, vol. 38, no. 10, pp. 1111-1113 . https://doi.org/10.1038/ng1870

We describe a new autosomal recessive white matter disorder ('hypomyelination and congenital cataract') characterized by hypomyelination of the central and peripheral nervous system, progressive neurological impairment and congenital cataract. We ide

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eee6c56e423f73d2bbf2bf50d5e1136
https://doi.org/10.1038/ng1870