검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation Terrinoni A, Codispoti A, Serra V, Didona B, Bruno E, Nistico R, Giustizieri M, Alessandrini M, Campione E, Melina G Biochemical and Biophysical Research Communications, 394(4), 909, 2010 |
| 2 |
Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss Terrinoni A, Codispoti A, Serra V, Bruno E, Didona B, Paradisi M, Nistico S, Campione E, Napolitano B, Diluvio L, Melino G Biochemical and Biophysical Research Communications, 395(1), 25, 2010 |
| 3 |
Scotin: A new p63 target gene expressed during epidermal differentiation Zocchi L, Bourdon JC, Codispoti A, Knight R, Lane DP, Melino G, Terrinoni A Biochemical and Biophysical Research Communications, 367(2), 271, 2008 |
| 4 |
p73 induces apoptosis by different mechanisms Ramadan S, Terrinoni A, Catani MV, Sayan AE, Knight RA, Mueller M, Krammer PH, Melino G, Candi E Biochemical and Biophysical Research Communications, 331(3), 713, 2005 |
| 5 |
p63 and p73 transactivate differentiation gene promoters in human keratinocytes De Laurenzi V, Rossi A, Terrinoni A, Barcaroli D, Levrero M, Costanzo A, Knight RA, Guerrieri P, Melino G Biochemical and Biophysical Research Communications, 273(1), 342, 2000 |