Zobrazeno 1 - 10
of 67
pro vyhledávání: '"G Pontarelli"'
Autor:
G, Orlando, A, Chiavaroli, C, Ferrante, L, Recinella, S, Leone, L, Brunetti, S C, Di Simone, L, Menghini, M, Petrucci, G, Zengin, F, Cesaroni, G, Pontarelli, L, Cindolo, F, Neri
Publikováno v:
European review for medical and pharmacological sciences. 25(7)
Fluxonorm® is a dietary supplement that includes water-soluble extracts of Solidago virga-aurea, Phyllantus niruri, Epilobium angustifolium, Peumus boldus and Ononis spinosa. The aim of the present study was to evaluate the tolerability and efficacy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6b9c16fea49b1babf3404572f2f0bf3
https://pubmed.ncbi.nlm.nih.gov/33877671
https://pubmed.ncbi.nlm.nih.gov/33877671
Autor:
Stefania Montagnani, E Gionti, G Pontarelli, V Alaia, Saverio Francesco Retta, Alessandro Arcucci, Guido Tarone
Publikováno v:
Biochimie. 85:483-492
Chondrocytes have been shown to express both in vivo and in vitro a number of integrins of the beta1-, beta3- and beta5-subfamilies (Biorheology 37 (2000) 109). Normal and v-Src-transformed chick epiphyseal chondrocytes (CEC) display different adhesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8cdaf3cfc75a792d718d837ed559fa3
https://doi.org/10.1016/s0300-9084(03)00075-0
https://doi.org/10.1016/s0300-9084(03)00075-0
Autor:
PISANI, ANTONIO, VILLANI, GUGLIELMO ROSARIO DOMENI, DI NATALE, PAOLA, C. Porto, I. De Maggio, R. Russo, G. Pontarelli, B. Visciano, B. Cianciaruso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::8ec34751a96c4b8a0f8baacacf3976c0
http://hdl.handle.net/11588/404016
http://hdl.handle.net/11588/404016
Autor:
VILLANI, GUGLIELMO ROSARIO DOMENI, GROSSO, MICHELA, DI NATALE, PAOLA, G. Pontarelli, A. Chierchia, R. Sessa, M. Sibilio, G. Parenti
Mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome) is a lysosomal disease due to the deficiency of arylsulfatase B (ARSB). In the absence of this enzyme, the stepwise degradation of the glycosaminoglycan (GAG) dermatan sulfate is blocked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::7e4db545ee5d3eb75e8ab6218017775c
http://hdl.handle.net/11588/476264
http://hdl.handle.net/11588/476264
Autor:
VILLANI, GUGLIELMO ROSARIO DOMENI, GROSSO, MICHELA, DI NATALE, PAOLA, V. Carcassa, G. Pontarelli, G. Sersale, R. Parini, R. Tomanin, M. Scarpa, M. Sibilio, G. Parenti, R. Barone, A. Fiumara
Mucopolysaccharidosis type VI is a lysosomal storage disease in which deficient activity of the enzyme N-acetylgalactosamine 4-sulfatase (arylsulfatase B, ASB) impairs the stepwise degradation of the glycosaminoglycan (GAG) dermatan sulfate resulting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::2bec0e72255b661843603320b6588050
http://hdl.handle.net/11588/476280
http://hdl.handle.net/11588/476280
Publikováno v:
Human genetics. 119(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e6c0aad727ce9e3324c59d10676fd35
https://pubmed.ncbi.nlm.nih.gov/17128482
https://pubmed.ncbi.nlm.nih.gov/17128482