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Mostrati risultati da 21 a 40 di 91
Titolo Data di pubblicazione Autore(i) File
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 1-gen-2009 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 1-gen-2009 Solda', G; Makunin, Iv; Sezerman, Ou; Corradin, A; Corti, G; Guffanti, A.
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 1-gen-2010 Asselta, R; Rimoldi, V; Guella, I; Solda, G; De Cristofaro, R; Peyvandi, F; Duga, S.
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 1-gen-2010 Soldà, G; Oldoni, F; Asselta, R; Primignani, P; Castorina, P; Radaelli, C; Coviello, D; Duga, S
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 1-gen-2010 Guella, I; Trotta, L; Asselta, R; Solda', G; Zini, M; Zecchinelli, A; Pezzoli, G; Goldwurm, S; Duga, S
The double-faced association of the PRKCA gene with multiple sclerosis 1-gen-2010 Paraboschi, E; Solda', G; Rimoldi, V; Dall’Osso, C; Anelli, G; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S; Asselta, R
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 1-gen-2010 Asselta, R.; Rimoldi, V.; Guella, I.; De Cristofaro, R.; Peyvandi, F.; Duga, S.; Soldà, G. M.
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 1-gen-2011 Robusto, M; Zhang, J; Solda', Giulia; Asselta, Rosanna; Zhang, Q; Liang, J; Liu, X; Primignani, P; Castorina, P; Ambrosetti, U; Yin, Y; Wang, J; Yang, H; Wang, J; Duga, Stefano
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 1-gen-2011 Solda', Giulia; Zhang, J; Asselta, Rosanna; Robusto, M; Zhang, Q; Liang, J; Liu, X; Primignani, P; Castorina, P; Ambrosetti, U; Yin, Y; Wang, J; Yang, H; Wang, J; Duga, Stefano
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 1-gen-2011 Robusto, M; Asselta, Rosanna; Primignani, P; Castorina, P; Benzoni, E; Cesarani, A; Ambrosetti, U; Duga, Stefano; Solda', Giulia
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 1-gen-2011 Guella, I; Solda', Giulia; Cilia, R; Pezzoli, G; Asselta, Rosanna; Goldwurm, S; Duga, Stefano
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-microRNA processing to its mature forms 1-gen-2011 Robusto, M; Asselta, Rosanna; Duga, Stefano; Solda', Giulia
MiR-634: a new player in the pathogenesis of multiple sclerosis? 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 1-gen-2011 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 1-gen-2011 Caccia, S; Rimoldi, V; Asselta, Rosanna; Solda', Giulia; Bonanni, E; Russo, R; Duga, Stefano; Cicardi, M
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 1-gen-2011 Solda', Giulia; Robusto, M; Asselta, Rosanna; Primignani, P; Coviello, D; Castorina, P; Ambrosetti, U; Duga, Stefano
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 1-gen-2011 Mercer, Tr; Wilhelm, D; Dinger, Me; Solda', G; Korbie, Dj; Glazov, Ea; Truong, V; Schwenke, M; Simons, C; Matthaei, Ki; Saint, R; Koopman, P; Mattick, Js.
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 1-gen-2011 Paraboschi, E.; Solda', G.; Gemmati, D.; Orioli, E.; Zeri, G.; Benedetti, D.; Salviati, A.; Barizzone, N.; Leone, M.; Duga, S.; Asselta, R.
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 1-gen-2012 Guella, I; Solda', G; Cilia, R; Pezzoli, G; Asselta, R; Goldwurm, S; Duga, S
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