Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Rosella, Fulceri"'
Autor:
Pietro E. Lazzerini, Iacopo Bertolozzi, Francesco Finizola, Maurizio Acampa, Mariarita Natale, Francesca Vanni, Rosella Fulceri, Alessandra Gamberucci, Marco Rossi, Beatrice Giabbani, Michele Caselli, Ilaria Lamberti, Gabriele Cevenini, Franco Laghi-Pasini, Pier L. Capecchi
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Background: Torsades de pointes (TdP) is a life-threatening ventricular tachycardia occurring in long QT-syndrome patients. It usually develops when multiple QT-prolonging factors are concomitantly present, more frequently drugs and electrolyte imbal
Externí odkaz:
https://doaj.org/article/d96ba143a2d24f8b97d2ebd2090c8b4e
Autor:
Daniela Gentile, Pietro E. Lazzerini, Alessandra Gamberucci, Mariarita Natale, Enrico Selvi, Francesca Vanni, Alessandra Alì, Paolo Taddeucci, Silvia Del-Ry, Manuela Cabiati, Veronica Della-Latta, David J. Abraham, Maria A. Morales, Rosella Fulceri, Franco Laghi-Pasini, Pier L. Capecchi
Publikováno v:
Frontiers in Pharmacology, Vol 8 (2017)
Objectives: Systemic sclerosis (SSc) is a connective tissue disorder presenting fibrosis of the skin and internal organs, for which no effective treatments are currently available. Increasing evidence indicates that the P2X7 receptor (P2X7R), a nucle
Externí odkaz:
https://doaj.org/article/5b16d5004cd94d4389366910e179d482
Autor:
Éva Margittai, Marina Colombi, Pál Gróf, Bert Callewaert, Paul Coucke, Tamás Mészáros, Szilvia K. Nagy, Andy Willaert, Nicoletta Zoppi, Paola Marcolongo, Gábor Bánhegyi, Angiolo Benedetti, Csilla E. Németh, Rosella Fulceri, Marco Ritelli, Nicola Chiarelli, Alessandra Gamberucci
Publikováno v:
FEBS Letters. 590:1630-1640
Loss-of-function mutations in the gene encoding GLUT10 are responsible for arterial tortuosity syndrome (ATS), a rare connective tissue disorder. In this study GLUT10-mediated dehydroascorbic acid (DAA) transport was investigated, supposing its invol
Autor:
Franco Laghi-Pasini, Rosella Fulceri, Pietro Enea Lazzerini, Pier Leopoldo Capecchi, Iacopo Bertolozzi, Maurizio Acampa
Publikováno v:
Current pharmaceutical design. 24(3)
Polymyalgia rheumatica (PMR) represents the most common inflammatory rheumatic disease of the elderly. It is characterized by synovitis of proximal joints and extra-articular synovial structures, along with chronic high-grade systemic inflammation. P
Autor:
Elisa Costanzi, Giuliano Tomelleri, Valentina Polverino, Nila Volpi, Gabriele Siciliano, Luana Toniolo, Virginia Barone, Carlo Reggiani, Roberto Battistutta, Simone Spinozzi, Gaetano Vattemi, Enrico Pierantozzi, Daniela Rossi, Gianna Berti, Giulia Ricci, Vincenzo Sorrentino, Valeria Del Re, Alessandro Malandrini, Lucia Galli, Alessandra Gamberucci, Rosella Fulceri
Here, we report the identification of three novel missense mutations in the calsequestrin-1 (CASQ1) gene in four patients with tubular aggregate myopathy. These CASQ1 mutations affect conserved amino acids in position 44 (p.(Asp44Asn)), 103 (p.(Gly10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e0141d4d05286b0cb222620092cfff
http://hdl.handle.net/11577/3243665
http://hdl.handle.net/11577/3243665
Autor:
Andy Willaert, Rosella Fulceri, Gábor Bánhegyi, Tamás Hegedűs, Giulia Carini, Éva Margittai, Csilla E. Németh, Marina Colombi, Nicoletta Zoppi, Paola Marcolongo, Angiolo Benedetti, Marco Ritelli, András Szarka, Paul Coucke, Nicola Chiarelli, Bert Callewaert, Alessandra Gamberucci
Publikováno v:
International Journal of Molecular Sciences
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
International Journal of Molecular Sciences; Volume 18; Issue 8; Pages: 1820
International Journal of Molecular Sciences, Vol 18, Iss 8, p 1820 (2017)
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
International Journal of Molecular Sciences; Volume 18; Issue 8; Pages: 1820
International Journal of Molecular Sciences, Vol 18, Iss 8, p 1820 (2017)
GLUT10 belongs to a family of transporters that catalyze the uptake of sugars/polyols by facilitated diffusion. Loss-of-function mutations in the SLC2A10 gene encoding GLUT10 are responsible for arterial tortuosity syndrome (ATS). Since subcellular d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc67ebd7dadf9c4a03cb5506fb77e13c
http://hdl.handle.net/11379/494798
http://hdl.handle.net/11379/494798
Autor:
Balázs Legeza, Angelo Benedetti, Roberta Giunti, Christine Egger, Paola Marcolongo, Gábor Bánhegyi, Miklós Csala, Péter Szelényi, Zoltán Balázs, József Mandl, Silvia Senesi, Rosella Fulceri, Éva Kereszturi, Alex Odermatt
Publikováno v:
Endocrinology
Both fructose consumption and increased intracellular glucocorticoid activation have been implicated in the pathogenesis of the metabolic syndrome. Glucocorticoid activation by 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) depends on hexose-6-
Autor:
Vincenzo Sorrentino, Barbara Gava, Angelo Benedetti, Miklós Csala, Silvia Senesi, Beáta Lizák, Gábor Bánhegyi, Rosella Fulceri, Paola Marcolongo, Éva Margittai
Publikováno v:
Biochemical Pharmacology. 76:382-390
Preadipocyte differentiation is greatly affected by prereceptorial glucocorticoid activation catalyzed by 11β-hydroxysteroid dehydrogenase type 1 in the lumen of the endoplasmic reticulum. The role of the local NADPH pool in this process was investi