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pro vyhledávání: '"CALZONE R"'
Rosiglitazone is an effective insulin-sensitizer, however associated with bone loss mainly due to increased bone resorption and bone marrow adiposity. We investigated the effect of the co-administration of fish oil on rosiglitazone-induced bone loss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8d70778d2a68da32fea7432a767cf7c
https://doi.org/10.21203/rs.3.rs-126494/v1
https://doi.org/10.21203/rs.3.rs-126494/v1
Autor:
PAGANO G., ZATTERALE A., DEGAN P., D'ISCHIA, MARCO, KELLY F. J., PALLARDO F. V., CALZONE R., CASTELLO G., DUNSTER C., GIUDICE A., KILINC Y., LLORET A., MANINI, PAOLA, MASELLA R., VUTTARIELLO E., WARNAU M.
The hypothesis was tested that Werner syndrome (WS) phenotype might be associated with an in vivo prooxidant state. A set of redox-related endpoints were measured in three WS patients, two of their parents, and 99 controls within a study of some canc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7d34546e0bac1d343a8f99d541848c81
http://hdl.handle.net/11588/307238
http://hdl.handle.net/11588/307238
Autor:
Pagano G., Youssoufian H., Anak S. S., Brunk U. T., Calzone R., Clarke A. A., Degan P., Dunster C., Giudice A., Iaccarino M., Hirsch Kauffmann M., Kelly F. J., Lloret A., Malorni W., Manini P., Masella R., Nobili B., Pallardò F. V., Schweiger M., Vuttariello E., Youssoufian G., Zatterale A., D'ISCHIA, MARCO
Publikováno v:
BioEssays : news and reviews in molecular, cellular and developmental biology. 25(6)
Fanconi anaemia (FA) is a cancer-prone genetic disorder that is characterised by cytogenetic instability and redox abnormalities. Although rare subtypes of FA (B, D1 and D2) have been implicated in DNA repair through links with BRCA1 and BRCA2, such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da928d9196f76e8f310f9aa58c180b94
https://pubmed.ncbi.nlm.nih.gov/12766948
https://pubmed.ncbi.nlm.nih.gov/12766948
Autor:
Savino, M, Borriello, A, Dapolito, M, Criscuolo, M, DEL VECCHIO, M, Bianco, Am, DI PERNA, M, Calzone, R, Nobili, B, Zatterale, A, Zelante, L, Joenje, H, DELLA RAGIONE, F, Savoia, A.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::365a77b5a72e7da4500dfabe8a0b76aa
http://hdl.handle.net/11368/1701486
http://hdl.handle.net/11368/1701486
Autor:
Morelli, F, Peluso, G, Petillo, O, Giannattasio, A, Filosa, S, Motta, Cm, Tammaro, S, Zatterale, A, Calzone, R, Budillon, A, Cartenì, M, DE MARIA, S, Costanza, Mr, Nigro, A, Petrazzuolo, M, Buommino, E, Rizzo, M, Capasso, G, Baiano, S, Moscatiello, F, Ravagnan, G, Fuggetta, Mp, Tajana, Gianfranco, Stiuso, P, Metafora, Bm, Metafora, V, Metafora, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3666::95d7857f9e21405e087e2fae16c48706
http://hdl.handle.net/11386/1863965
http://hdl.handle.net/11386/1863965
PubMedID: 16036329 The hypothesis was tested that Werner syndrome (WS) phenotype might be associated with an in vivo prooxidant state. A set of redox-related endpoints were measured in three WS patients, two of their parents, and 99 controls within a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9491::dd78c10a004a5ea29d68a0e42930f342
https://hdl.handle.net/20.500.12605/16272
https://hdl.handle.net/20.500.12605/16272
Akademický článek
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Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fe3c6e3b7a609d8abe1c08b16dd9ceba
http://hdl.handle.net/11386/3097323
http://hdl.handle.net/11386/3097323