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

per Di Nocera, P P, Casari, G
Publicat 1987

New protein functions in yeast chromosome VIII.

per Ouzounis, C., Bork, P., Casari, G., Sander, C.
Publicat 1995

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

per Siri, A, Carnemolla, B, Saginati, M, Leprini, A, Casari, G, Baralle, F, Zardi, L
Publicat 1991

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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