The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia von Sanarico, A G, Ronchini, C, Croce, A, Memmi, E M, Cammarata, U A, De Antoni, A, Lavorgna, S, Divona, M, Giacò, L, Melloni, G E M, Brendolan, A, Simonetti, G, Martinelli, G, Mancuso, P, Bertolini, F, Coco, F Lo, Melino, G, Pelicci, P G, Bernassola, F

Volltext

The Cul4A–DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity von Malatesta, M, Peschiaroli, A, Memmi, E M, Zhang, J, Antonov, A, Green, D R, Barlev, N A, Garabadgiu, A V, Zhou, P, Melino, G, Bernassola, F

Volltext

Le poil est-il genré ? von Bromberger, Christian, Memmi, Dominique, Le Dû, Maï, Moisseeff, Marika

Volltext bestellen

Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel von Abriel, Hugues, Cabo, Candido, Wehrens, Xander H.T, Rivolta, Ilaria, Motoike, Howard K, Memmi, Mirella, Napolitano, Carlo, Priori, Silvia G, Kass, Robert S

Volltext

Unexpectedly high prevalence of structural genomic variations in the Long QT Syndrome: evidence for broader clinical uptake von Mazzanti, A, Memmi, M, Gambelli, P, Guarracino, A, Colombi, B, Nastoli, J, Trancuccio, A, Kukavica, D, Marino, M, Bloise, R, Napolitano, C, Priori, S G

Volltext

Implantable loop recorder monitoring in inherited cardiomyopathies: yield of clinically relevant arrhythmias von Trancuccio, A, Kukavica, D, Zvielli, G, Marino, M, Gambelli, P, Memmi, M, Bloise, R, Napolitano, C, Mazzanti, A, Priori, S G

Volltext

Natural History of Patients with Typical and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia von Trancuccio, A, Mazzanti, A, Kukavica, D, Giannini, G, Memmi, M, Gambelli, P, Bloise, R, Marino, M, Morini, M, Ortiz-Genga, M, Napolitano, C, Priori, S G

Volltext

Catecholaminergic polymorphic ventricular tachycardia: risk modulators in patients treated with beta-blockers von Kukavica, D, Mazzanti, A, Trancuccio, A, Giannini, G, Marino, M, Memmi, M, Gambelli, P, Bloise, R, Morini, M, Ortiz-Genga, M, Napolitano, C, Priori, S G

Volltext

Efficacy and safety of the ICD in patients with catecholaminergic polymorphic ventricular tachycardia von Mazzanti, A, Trancuccio, A, Kukavica, D, Marino, M, Giannini, G, Rossetti, L, Memmi, M, Bloise, R, Morini, M, Napolitano, C, Priori, S G

Volltext

Mutation site-specific risk profile in patients with Type 1 Long QT Syndrome von Trancuccio, A, Mazzanti, A, Kukavica, D, Marino, M, Monteforte, N, Bloise, R, Braghieri, L, Memmi, M, Morini, M, Napolitano, C, Priori, S.G

Volltext

Peopling of three Mediterranean Islands (Corsica, Sardinia, and Sicily) inferred by Y-chromosome biallelic variability von Francalacci, P., Morelli, L., Underhill, P.A., Lillie, A.S., Passarino, G., Useli, A., Madeddu, R., Paoli, G., Tofanelli, S., Calò, C.M., Ghiani, M.E., Varesi, L., Memmi, M., Vona, G., Lin, A.A., Oefner, P., Cavalli-Sforza, L.L.

Volltext

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death von Wehrens, Xander H.T., Lehnart, Stephan E., Huang, Fannie, Vest, John A., Reiken, Steven R., Mohler, Peter J., Sun, Jie, Guatimosim, Silvia, Song, Long-Sheng, Rosemblit, Nora, D'Armiento, Jeanine M., Napolitano, Carlo, Memmi, Mirella, Priori, Silvia G., Lederer, W.J., Marks, Andrew R.

Volltext

Role of CACNA1C variants in Brugada syndrome: clinical aspects and genetic testing strategies von Novelli, V, Memmi, M, Malovini, A, Mazzanti, A, Liu, N, Yanfei, R, Bongianino, R, Monteforte, N, Bloise, R, Morini, M, Napolitano, C, Priori, S.G

Volltext

Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region von Scozzari, R, Cruciani, F, Pangrazio, A, Santolamazza, P, Vona, G, Moral, P, Latini, V, Varesi, L, Memmi, M M, Romano, V, De Leo, G, Gennarelli, M, Jaruzelska, J, Villems, R, Parik, J, Macaulay, V, Torroni, A

Volltext

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia von PRIORI, Silvia G, NAPOLITANO, Carlo, TISO, Natascia, MEMMI, Mirella, VIGNATI, Gabriele, BLOISE, Raffaella, SORRENTINO, Vincenzo, DANIELI, Gian Antonio

Volltext

6081Efficacy and limitations of quinidine therapy in patients with Brugada Syndrome von Mazzanti, A, Tenuta, E, Marino, M, Pagan, E, Morini, M, Memmi, M, Curcio, A, Monteforte, N, Bloise, R, Napolitano, C, Bagnardi, V, Priori, S G

Volltext

Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia von PRIORI, Silvia G, NAPOLITANO, Carlo, CRUZ FILHO, Fernando E. S, VIGNATI, Gabriele, BENATAR, Abraham, DELOGU, Angelica, MEMMI, Mirella, COLOMBI, Barbara, DRAGO, Fabrizio, GASPARINI, Maurizio, DESIMONE, Luciano, COLTORTI, Fernando, BLOISE, Raffaella, KEEGAN, Roberto

Volltext

Le social à l’épreuve du dégoût von (†), Jean-François Boullier, Anchisi, Annick, Boisson, Marine Jeanne, Bonnet, Thomas, Castra, Michel, Chevandier, Christian, Constance, Jean, Dubois, Fanny, Jullien, Clémence, Lebeer, Guy, Memmi, Dominique, Michaud-Nérard, François, Morel, Sylvie, Pudal, Romain, Raveneau, Gilles, Schaub, Corinne, Taïeb, Emmanuel, Vigarello, Georges

Volltext

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia von Marks, Andrew R., Priori, Silvia, Memmi, Mirella, Kontula, Kimmo, Laitinen, Päivi J.

Volltext

Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes von Rivolta, I, Abriel, H, Tateyama, M, Liu, H, Memmi, M, Vardas, P, Napolitano, C, Priori, S G, Kass, R S

Volltext