Zobrazeno 1 - 10
of 12
pro vyhledávání: '"E. V. Avvedimento"'
Autor:
PERRINO, CINZIA, ESPOSITO, GIOVANNI, RAPACCIUOLO, ANTONIO, CHIARIELLO, MASSIMO, R. Guerriero, A. Feliciello, A. Scognamiglio, E. Capasso, A. Del Gatto, M. Saviano, E. V. Avvedimento
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::42081a2c99aebe9ab0bbe60a6d41207d
http://hdl.handle.net/11588/340188
http://hdl.handle.net/11588/340188
Publikováno v:
Journal of molecular biology. 308(2)
cAMP-dependent protein kinase is targeted to discrete subcellular locations by a family of specific anchor proteins (A-kinase anchor proteins, AKAPs). Localization recruits protein kinase A (PKA) holoenzyme close to its substrate/effector proteins, d
Autor:
Antonio Feliciello, Adriana Gallo, Massimo Chiariello, Giancarlo Troncone, E. V. Avvedimento, Ciro Indolfi, Luigi Cavuto, Daniele Torella, Giovanna Allevato, Carmela Coppola, Eugenio Stabile, Emilio Di Lorenzo, Cinzia Perrino
Publikováno v:
Scopus-Elsevier
Abstract —cAMP-dependent protein kinase is anchored to discrete cellular compartments by a family of proteins, the A-kinase anchor proteins (AKAPs). We have investigated in vivo and in vitro the biological effects of the expression of a prototypic
Autor:
B, Quaresima, C, Grandinetti, F, Baudi, P, Tassone, V, Barbieri, S, Conforti, E V, Avvedimento, F, Costanzo, S, Venuta
Publikováno v:
Human mutation. 12(6)
Hereditary nonpolyposis colon cancer results from heritable defects in the MLH1, MSH2, PMS1 and PMS2 genes, which encode proteins involved in the mismatch repair process. In this work we report the identification of two novel germline mutations in th
Autor:
Antonio Leccia, E. V. Avvedimento, Antonio Pisani, Alaide Chieffo, A. Coppola, E. Di Lorenzo, Giovanni Esposito, Massimo Chiariello, Antonio Rapacciuolo, Ciro Indolfi
Publikováno v:
ResearcherID
The mitogen-activated protein kinase kinase (MAPKK) is a protein downstream ras which is rapidly activated in cells stimulated with various extracellular signals. These proteins are believed to play a pivotal role in integrating and transmitting tran
Autor:
B, Di Jeso, A, Feliciello, F, Pacifico, A, Iannelli, F, D'Armiento, D, Liguoro, P, Giuliano, G, Ferulano, E V, Avvedimento
Publikováno v:
Cell growthdifferentiation : the molecular biology journal of the American Association for Cancer Research. 6(10)
Differentiated thyroid cells expressing polyoma Middle-T became transformed and tumorigenic when injected into syngenic animals. The expression of thyroglobulin was greatly reduced and no longer responsive to thyrotropin (TSH) and to cAMP. Inhibition
Autor:
A, Rapacciuolo, C, Indolfi, E, Di Lorenzo, G, Esposito, E, Stabile, A M, Stingone, E V, Avvedimento, M, Condorelli, M, Chiariello
Publikováno v:
Cardiologia (Rome, Italy). 39(12)
Accumulation and proliferation of vascular smooth muscle cells are associated with atherosclerosis and hypertension. Proliferation of smooth muscle cells constitutes a major pathological event responsible for long-term failure of coronary and periphe
Publikováno v:
The Journal of biological chemistry. 269(26)
AG--A transition at -78 base pairs from the transcription start site of the apolipoprotein A-I (apoA-I) gene has been associated with increased apoA-I serum levels in humans. We report here that this mutation (G--A) increases significantly (5-7-fold)
Publikováno v:
The Journal of biological chemistry. 265(22)
The 3500-base pair region located immediately upstream of the transcriptional start site of the human pro-alpha 2(I) collagen gene contains all the sequences necessary for cell-specific transcription. In transient expression assays, the pro-alpha 2(I
Autor:
Salvatore Venuta, Francesco Costanzo, Vito Barbieri, Cristina Grandinetti, E. V. Avvedimento, Barbara Quaresima, Francesco Baudi, Pierfrancesco Tassone, Serafino Conforti
Publikováno v:
Human Mutation. 12:433-433
Hereditary nonpolyposis colon cancer results from heritable defects in the MLH1, MSH2, PMS1 and PMS2 genes, which encode proteins involved in the mismatch repair process. In this work we report the identification of two novel germline mutations in th