Trophic activity of a naturally occurring truncated isoform of the P2X7 receptor von Adinolfi, Elena, Cirillo, Maria, Woltersdorf, Ronja, Falzoni, Simonetta, Chiozzi, Paola, Pellegatti, Patrizia, Callegari, Maria Giulia, Sandonà, Doriana, Markwardt, Fritz, Schmalzing, Günther, Di Virgilio, Francesco

Volltext

Different outcome of sarcoglycan missense mutation between human and mouse von Henriques, Sara F, Patissier, Cécile, Bourg, Nathalie, Fecchio, Chiara, Sandona, Doriana, Marsolier, Justine, Richard, Isabelle

Volltext

Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly von Fornetti, Ersilia, Testa, Stefano, De Paolis, Francesca, Fuoco, Claudia, Bernardini, Sergio, Pozo Devoto, Victorio, Stokin, Gorazd Bernard, Giannitelli, Sara Maria, Rainer, Alberto, Bigot, Anne, Zoccali, Carmine, Baldi, Jacopo, Sandonà, Doriana, Rizzi, Roberto, Bearzi, Claudia, Forte, Giancarlo, Cannata, Stefano, Gargioli, Cesare

Volltext

Expression and characterization of Edg‐1 receptors in rat cardiomyocytes von Nakajima, Nobuko, Cavalli, Amy L., Biral, Donatella, Glembotski, Christopher C., McDonough, Patrick M., Ho, Peter D., Betto, Romeo, Sandoná, Doriana, Palade, Philip T., Dettbarn, Christine A., Klepper, Robert E., Sabbadini, Roger A.

Volltext

The Novel Skeletal Muscle Sarcoplasmic Reticulum JP-45 Protein von Anderson, Ayuk A., Treves, Susan, Biral, Donatella, Betto, Romeo, Sandonà, Doriana, Ronjat, Michel, Zorzato, Francesco

Volltext

The novel skeletal muscle sarcoplasmic reticulum JP-45 protein. Molecular cloning, tissue distribution, developmental expression, and interaction with alpha 1.1 subunit of the volt... von Anderson, Ayuk A, Treves, Susan, Biral, Donatella, Betto, Romeo, Sandonà, Doriana, Ronjat, Michel, Zorzato, Francesco

Volltext

Expression and characterization of Edg-1 receptors in rat cardiomyocytes: calcium deregulation in response to sphingosine 1-phosphate von Nakajima, N, Cavalli, A L, Biral, D, Glembotski, C C, McDonough, P M, Ho, P D, Betto, R, Sandoná, D, Palade, P T, Dettbarn, C A, Klepper, R E, Sabbadini, R A

Volltext

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho° transformants von Tiranti, Valeria, Munaro, Monica, Sandonà, Doriana, Lamantea, Eleonora, Rimoldi, Marco, DiDonato, Stefano, Bisson, Roberto, Zeviani, Massimo

Volltext

A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's Syndrome von Munaro, Monica, Tiranti, Valeria, Sandonà, Doriana, Lamantea, Eleonora, Uziel, Graziella, Bisson, Roberto, Zeviani, Massimo

Volltext