SESTINI, SILVIA

SESTINI, SILVIA  

DPT. BIOLOGIA MOLECOLARE (attivo dal 01/01/1900 al 31/10/2012)  

Mostra records
Risultati 1 - 9 di 9 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) File Abstract
11β-hydroxysteroid dehydrogenase expression in first trimester human trophoblasts 1-gen-1998 Arcuri, Felice; Sestini, Silvia; Ricci, Luana; Bracci, Luisa; Carducci, Antonietta; Manzoni, Francesca; Cardone, Concetta; Cintorino, Marcella -
Enzyme activities and dimensional parameters in human red blood cells of different density: an insight into the ageing process 1-gen-1989 Pescaglini, Monica; Cevenini, Gabriele; Rocchigiani, Marina; Micheli, Vanna; Sestini, Silvia -
[Evaluation of NAD glycohydrolase in leukocytes from peripheral blood and broncho-alveolar lavage in man]. 1-gen-1986 Sestini, Silvia; Sestini, Piersante; A., Collodoro; F., Sparnacci; Micheli, Vanna; C., Ricci -
In vitro toxicity evaluation of silver soldering, electrical resistance, and laser welding of orthodontic wires. 1-gen-2006 Sestini, Silvia; Notarantonio, L; Cerboni, B; Alessandrini, C; Fimiani, Michele; Nannelli, Pietro; Pelagalli, A; Giorgetti, R. -
METABOLITE AND PROTEIN PATTERNS IN PLASMA OF LESCH-NYHAN SYNDROME PATIENTS 1-gen-2004 Santucci, Annalisa; Iacomelli, Gabriella; Paffetti, Alessandro; Sestini, Silvia; Cerboni, Barbara; Pompucci, Giuseppe; Micheli, Vanna -
Poly(ADP-ribose) polymerase activity in systemic lupus erythematosus and systemic sclerosis. 1-gen-2009 Cerboni, B; Morozzi, Gabriella; Galeazzi, Mauro; Bellisai, F; Micheli, Vanna; Pompucci, G; Sestini, Silvia -
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 1-gen-2000 Arcuri, F.; Sestini, S.; Ricci, C.; Runci, Y.; Carducci, A.; Ricci, L.; Cintorino, M. -
RSK2 enzymatic assay as a second level diagnostic tool in Coffin-Lowry syndrome. 1-gen-2007 Micheli, Vanna; Sestini, Silvia; Parri, V; Fichera, M; Romano, C; Ariani, Francesca; Longo, I; Mari, Francesca; Bruttini, M; Renieri, Alessandra; Meloni, I. -
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on ‘black bone disease’ in Italy 1-gen-2016 Nemethova, Martina; Radvanszky, Jan; Kadasi, Ludevit; Ascher, David B; Pires, Douglas E. V; Blundell, Tom L; Porfirio, Berardino; Mannoni, Alessandro; Santucci, Annalisa; Milucci, Lia; Sestini, Silvia; Biolcati, Gianfranco; Sorge, Fiammetta; Aurizi, Caterina; Aquaron, Robert; Alsbou, Mohammed; Marques Lourenço, Charles; Ramadevi, Kanakasabapathi; Ranganath, Lakshminarayan R; Gallagher, James A; van Kan, Christa; Hall, Anthony K; Olsson, Birgitta; Sireau, Nicolas; Ayoob, Hana; Timmis, Oliver G; Le Quan Sang, Kim Hanh; Genovese, Federica; Imrich, Richard; Rovensky, Jozef; Srinivasaraghavan, Rangan; Bharadwaj, Shruthi K; Spiegel, Ronen; Zatkova, Andrea -