Related polypeptides are encoded by Drosophila F elements, I factors, and mammalian L1 sequences.

por Di Nocera, P P, Casari, G
Publicado 1987

New protein functions in yeast chromosome VIII.

por Ouzounis, C., Bork, P., Casari, G., Sander, C.
Publicado 1995

Human tenascin: primary structure, pre-mRNA splicing patterns and localization of the epitopes recognized by two monoclonal antibodies.

por Siri, A, Carnemolla, B, Saginati, M, Leprini, A, Casari, G, Baralle, F, Zardi, L
Publicado 1991

A novel bipartite splicing enhancer modulates the differential processing of the human fibronectin EDA exon.

por Caputi, M, Casari, G, Guenzi, S, Tagliabue, R, Sidoli, A, Melo, C A, Baralle, F E
Publicado 1994

The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28.

por Auricchio, A., Brancolini, V., Casari, G., Milla, P. J., Smith, V. V., Devoto, M., Ballabio, A.
Publicado 1996

Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome.

por Mastroianni, N., Bettinelli, A., Bianchetti, M., Colussi, G., De Fusco, M., Sereni, F., Ballabio, A., Casari, G.
Publicado 1996

Two point mutations within the adducin genes are involved in blood pressure variation.

por Bianchi, G, Tripodi, G, Casari, G, Salardi, S, Barber, B R, Garcia, R, Leoni, P, Torielli, L, Cusi, D, Ferrandi, M
Publicado 1994

VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

por Musacchia, F., Ciolfi, A., Mutarelli, M., Bruselles, A., Castello, R., Pinelli, M., Basu, S., Banfi, S., Casari, G., Tartaglia, M., Nigro, V.
Publicado en BMC Bioinformatics (2018)

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

por De Michele, G, De Fusco, M, Cavalcanti, F, Filla, A, Marconi, R, Volpe, G, Monticelli, A, Ballabio, A, Casari, G, Cocozza, S
Publicado 1998

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

por Scolari, F, Puzzer, D, Amoroso, A, Caridi, G, Ghiggeri, G M, Maiorca, R, Aridon, P, De Fusco, M, Ballabio, A, Casari, G
Publicado 1999

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

por Bassi, M, Bresolin, N, Tonelli, A, Nazos, K, Crippa, F, Baschirotto, C, Zucca, C, Bersano, A, Dolcetta, D, Boneschi, F, Barone, V, Casari, G
Publicado 2004