Coordinate regulation of HOX genes in human hematopoietic cells.

par Magli, M C, Barba, P, Celetti, A, De Vita, G, Cillo, C, Boncinelli, E
Publié 1991

Two point mutations are responsible for G6PD polymorphism in Sardinia.

par De Vita, G, Alcalay, M, Sampietro, M, Cappelini, M D, Fiorelli, G, Toniolo, D
Publié 1989

Laparoscopic drainage of liver abscess: case report and literature review

par ROMANO, G., AGRUSA, A., FRAZZETTA, G., DE VITA, G., CHIANETTA, D., DI BUONO, G., AMATO, G., GULOTTA, G.
Publié 2013

Endoscopic sclerotherapy for hemostasis of acute esophageal variceal bleeding

par ROMANO, G., AGRUSA, A., AMATO, G., DE VITA, G., FRAZZETTA, G., CHIANETTA, D., SORCE, V., DI BUONO, G., GULOTTA, G.
Publié dans G Chir (2014)

Molecular heterogeneity of RET loss of function in Hirschsprung's disease.

par Carlomagno, F, De Vita, G, Berlingieri, M T, de Franciscis, V, Melillo, R M, Colantuoni, V, Kraus, M H, Di Fiore, P P, Fusco, A, Santoro, M
Publié 1996

Laparoscopic, three-port and SILS cholecystectomy: a retrospective study

par AGRUSA, A., ROMANO, G., CUCINELLA, G., COCORULLO, G., BONVENTRE, S., SALAMONE, G., DI BUONO, G., DE VITA, G., FRAZZETTA, G., CHIANETTA, D., SORCE, V., BELLANCA, G., GULOTTA, G.
Publié 2013

A potential pathogenetic mechanism for multiple endocrine neoplasia type 2 syndromes involves ret-induced impairment of terminal differentiation of neuroepithelial cells.

par Califano, D, D'Alessio, A, Colucci-D'Amato, G L, De Vita, G, Monaco, C, Santelli, G, Di Fiore, P P, Vecchio, G, Fusco, A, Santoro, M, de Franciscis, V
Publié 1996

DNAJC17 is localized in nuclear speckles and interacts with splicing machinery components

par Pascarella, A., Ferrandino, G., Credendino, S. C., Moccia, C., D’Angelo, F., Miranda, B., D’Ambrosio, C., Bielli, P., Spadaro, O., Ceccarelli, M., Scaloni, A., Sette, C., De Felice, M., De Vita, G., Amendola, E.
Publié dans Sci Rep (2018)