Sfoglia per Autore
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA
2010 R. Asselta, V. Rimoldi, I. Guella, G.Soldà, R. De Cristofaro, F. Peyvandi, S. Duga
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population
2010 I. Guella, L.C. Trotta, R. Asselta, G.M. Soldà, M. Zini, A. Zecchinelli, G. Pezzoli, S. Goldwurm, S. Duga
The double-faced association of the PRKCA gene with multiple sclerosis
2010 E.M. Paraboschi, G. Soldà, V. Rimoldi, C. Dall’Osso, G.M. Anelli, D. Gemmati, P. Zamboni, A. Salviati, M. Benedetti, S. D’Alfonso, S. Duga, R. Asselta
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population
2010 G.M. Soldà, F. Oldoni, R. Asselta, P. Primignani, P. Castorina, C. Radaelli, D. Coviello, S. Duga
Response: Further thoughts on the "phantom" delta6/7 FXI isoform
2010 R. Asselta, V. Rimoldi, I. Guella, G.M. Soldà, R. De Cristofaro, F. Peyvandi, S. Duga
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families
2011 G.M. Soldà, J. Zhang, R. Asselta, M. Robusto, Q. Zhang, J. Liang, X. Liu, P. Primignani, P. Castorina, U. Ambrosetti, Y. Yin, J. Wang, H. Yang, J. Wang, S. Duga
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss
2011 G.M. Soldà, M. Robusto, R. Asselta, P. Primignani, D. Coviello, P. Castorina, U. Ambrosetti, S. Duga
Expression of distinct RNAs from 3' untranslated regions
2011 T. Mercer, D. Wilhelm, M. Dinger, G. Solda, D. Korbie, E. Glazov, V. Truong, M. Schwenke, C. Simons, K. Matthaei, R. Saint, P. Koopman, J.S. Mattick
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing
2011 M. Robusto, R. Asselta, P. Primignani, P. Castorina, E. Benzoni, A. Cesarani, U. Ambrosetti, S. Duga, G. Soldà
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema)
2011 S. Caccia, V. Rimoldi, R. Asselta, G.M. Soldà, E. Bonanni, R. Russo, S. Duga, M. Cicardi
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss
2011 M. Robusto, J. Zhang, G. Soldà, R. Asselta, Q. Zhang, J. Liang, X. Liu, P. Primignani, P. Castorina, U. Ambrosetti, Y. Yin, J. Wang, H. Yang, J. Wang, S. Duga
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing
2011 M. Robusto, G. Soldà, P. Primignani, P. Castorina, E. Benzoni, A. Cesarani, U. Ambrosetti, R. Asselta, S. Duga
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
2011 E.M. Paraboschi, G. Soldà, D. Gemmati, E. Orioli, G. Zeri, D. Benedetti, A. Salviati, N. Barizzone, M. Leone, S. Duga, R. Asselta
Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
2012 I. Guella, G. Soldà, R. Cilia, G. Pezzoli, R. Asselta, S. Duga, S. Goldwurm
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
2012 L. Trotta, I. Guella, G. Soldà, F. Sironi, S. Tesei, M. Canesi, G. Pezzoli, S. Goldwurm, S. Duga, R. Asselta
Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian population
2012 M. Robusto, J. Zhang, R. Asselta, J. Liang, X. Liu, P. Primignani, P. Castorina, S. Caccia, U. Ambrosetti, Y. Yin, J. Wang, S. Duga, G. Soldà
Identification by exome sequencing and functional characterization of novel deafness-causing mutations in PRPS1
2012 M. Robusto, R. Asselta, S. Lancellotti, P. Primignani, P. Castorina, S. Caccia, U. Ambrosetti, S. Duga, G. Soldà
Identification of novel deafness-causing variants in the tmprss3 gene by whole-exome sequencing
2012 M. Robusto, R. Asselta, A. Ghilardi, P. Castorina, E. Benzoni, P. Primignani, U. Ambrosetti, L. Del Giacco, S. Caccia, S. Duga, G. Soldà
Role of miRNAs in neural tube development
2013 G. Soldà, L. Avagliano, G. Fazio, A. Pistocchi, A. Gallina, G. Cazzaniga, G. Bulfamante, V. Massa
In-depth study of breast cancer tumor promoting cell transcriptome using RNA-seq and microarrays
2013 M. Callari, G. Merilino, A. Guffanti, A. Felsani, E. Fina, R. Villa, E. Brini, G. Soldà, A. Moles, V. Cappelletti
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