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

著者: Di Nocera, P P, Casari, G
出版事項 1987

New protein functions in yeast chromosome VIII.

著者: Ouzounis, C., Bork, P., Casari, G., Sander, C.
出版事項 1995

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

著者: Siri, A, Carnemolla, B, Saginati, M, Leprini, A, Casari, G, Baralle, F, Zardi, L
出版事項 1991

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

著者: Caputi, M, Casari, G, Guenzi, S, Tagliabue, R, Sidoli, A, Melo, C A, Baralle, F E
出版事項 1994

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

著者: Auricchio, A., Brancolini, V., Casari, G., Milla, P. J., Smith, V. V., Devoto, M., Ballabio, A.
出版事項 1996

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

著者: Mastroianni, N., Bettinelli, A., Bianchetti, M., Colussi, G., De Fusco, M., Sereni, F., Ballabio, A., Casari, G.
出版事項 1996

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

著者: Bianchi, G, Tripodi, G, Casari, G, Salardi, S, Barber, B R, Garcia, R, Leoni, P, Torielli, L, Cusi, D, Ferrandi, M
出版事項 1994

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

著者: Musacchia, F., Ciolfi, A., Mutarelli, M., Bruselles, A., Castello, R., Pinelli, M., Basu, S., Banfi, S., Casari, G., Tartaglia, M., Nigro, V.
出版年 BMC Bioinformatics (2018)

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

著者: De Michele, G, De Fusco, M, Cavalcanti, F, Filla, A, Marconi, R, Volpe, G, Monticelli, A, Ballabio, A, Casari, G, Cocozza, S
出版事項 1998

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

著者: Scolari, F, Puzzer, D, Amoroso, A, Caridi, G, Ghiggeri, G M, Maiorca, R, Aridon, P, De Fusco, M, Ballabio, A, Casari, G
出版事項 1999

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

著者: Bassi, M, Bresolin, N, Tonelli, A, Nazos, K, Crippa, F, Baschirotto, C, Zucca, C, Bersano, A, Dolcetta, D, Boneschi, F, Barone, V, Casari, G
出版事項 2004