Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Silvia Stringara"'
Autor:
Giacomo Borgonovo, Giuseppina Conteduca, Samuele Tardito, Silvia Stringara, Giorgio Carmignani, Gilberto Filaci, Federico Ivaldi, Alessia Parodi, Francesca Ferrera, Alchiede Simonato, Florinda Battaglia, Daniela Fenoglio, Paolo Traverso, Francesca Kalli, Simone Negrini
Publikováno v:
Cancer Immunology, Immunotherapy. 62:851-862
CD39 is an ectoenzyme, present on different immune cell subsets, which mediates immunosuppressive functions catalyzing ATP degradation. It is not known whether CD39 is expressed and implicated in the activity of CD8+ regulatory T lymphocytes (Treg).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a8376e3e53d1f374c5e0abaa01360f
https://doi.org/10.1007/s00262-013-1392-z
https://doi.org/10.1007/s00262-013-1392-z
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
https://doi.org/10.1038/labinvest.3700713
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
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
https://doi.org/10.1038/ng1870
Autor:
Santina Bruzzone, Silvia Stringara, Elena Zocchi, Giovanna Basile, Alessia Parodi, Daniela Fenoglio, Annalisa Salis, Gilberto Filaci, Laura Sturla, Elena Mannino, Floriana Fruscione, Florinda Battaglia, Francesca Kalli, Simone Negrini
The phytohormone abscisic acid (ABA) has been recently identified as an endogenous hormone in humans, regulating different cell functions, including inflammatory processes, insulin release and glucose uptake. Systemic sclerosis (SSc) is a chronic inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::796b17a601eb06d72afdd2de84f12e96
http://hdl.handle.net/11567/378327
http://hdl.handle.net/11567/378327
Autor:
Denise Cassandrini, Angelo Schenone, Roberta Biancheri, Fiore Manganelli, Marina Pedemonte, Lucio Santoro, Federico Zara, Silvia Stringara, Carlo Minetti, Emilia Bellone, Pasquale Striano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6f2018f9268afa62a3578b4a1e8b2a
http://hdl.handle.net/11567/314987
http://hdl.handle.net/11567/314987
Autor:
Andrea Rossi, Graziella Uziel, M.S. van der Knaap, Silvia Stringara, Stefania Assereto, Federico Zara, Carlo Minetti, R. Biancheri, Claudio Bruno, Stefania Gianotti, Laura Bordo, Paolo Tortori-Donati
Publikováno v:
Neuropediatrics. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcfe98430864a1f8f84a537caa0895c7
https://doi.org/10.1055/s-2006-943707
https://doi.org/10.1055/s-2006-943707
Autor:
Claudio Bruno, C. Savioli, Carlo Minetti, M. Marasini, Denise Cassandrini, C. Bellini, Silvia Stringara, D. Massocco
Publikováno v:
Neuropediatrics. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76c59b9ca77ed4f33cdf9b0de9a7f1c8
https://doi.org/10.1055/s-2006-943672
https://doi.org/10.1055/s-2006-943672
Autor:
Claudio Bruno, Gloria Bonuccelli, Michael P. Lisanti, Carlo Minetti, Roberta Biancheri, Federica Sotgia, Marina Pedemonte, Stefania Assereto, Monica Traverso, Federico Zara, Aldobrando Broccolini, Silvia Stringara
Publikováno v:
American journal of physiology. Cell physiology. 290(2)
In this report, we have developed a novel method to identify compounds that rescue the dystrophin-glycoprotein complex (DGC) in patients with Duchenne or Becker muscular dystrophy. Briefly, freshly isolated skeletal muscle biopsies (termed skeletal m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74bf417db1dfcd44510fc05ec78cba64
https://pubmed.ncbi.nlm.nih.gov/16192300
https://pubmed.ncbi.nlm.nih.gov/16192300
Autor:
S. Bonifacino, Silvia Stringara, Roberta Biancheri, Paolo Tortori-Donati, Andrea Rossi, Carlo Minetti
Publikováno v:
Neurology. 63(11)
Middle interhemispheric variant (MIH) of holoprosencephaly or syntelencephaly was described in 19931 as a fourth subtype of holoprosencephaly (HPE), in addition to the three classic types of alobar, semilobar, and lobar HPE.2 MIH consists of an abnor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::649e4a17885c949e3fdb0b931a5378df
https://pubmed.ncbi.nlm.nih.gov/15596788
https://pubmed.ncbi.nlm.nih.gov/15596788
Autor:
Claudio Bruno, Michael P. Lisanti, Antonio Frigeri, Silvia Stringara, Stefania Assereto, Paolo Broda, Elisabetta Gazzerro, Grazia Paola Nicchia, Maria Svelto, Carlo Minetti, Mauro Mastrototaro, Vincenzo Nigro
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Aquaporin-4 (AQP4) is the major water channel expressed in fast-twitch skeletal muscle fibers. AQP4 is reduced in Duchenne and Becker Muscular Dystrophies, but not in caveolinopathies, thus suggesting an interaction with dystrophin or with members of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe5330f7dc31ccb145df7efeb3c8575
http://www.scopus.com/inward/record.url?eid=2-s2.0-47749142452&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-47749142452&partnerID=MN8TOARS