SOLDA', GIULIA MARIA EMILIA ANTONIETTA
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest
2018 M. Samarani, N. Loberto, G. Soldà, L. Straniero, R. Asselta, S. Duga, G. Lunghi, F.A. Zucca, L. Mauri, M.G. Ciampa, D. Schiumarini, R. Bassi, P. Giussani, E. Chiricozzi, A. Prinetti, M. Aureli, S. Sonnino
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs
2008 G. Soldà, D. Wilhelm, M.E. Dinger, T.R. Mercer, R.J. Taft, 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
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
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
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing
2009 A. Guffanti, M. Iacono, P. Pelucchi, N. Kim, G.M. Soldà, L.J. Croft, R.J. Taft, E. Rizzi, M. Askarian Amiri, R.J. Bonnal, M. Callari, F. Mignone, G. Pesole, G. Bertalot, L. Rossi Bernardi, A. Albertini, C. Lee, J.S. Mattick, I. Zucchi, G. De Bellis
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency
2005 G. Soldà, R. Asselta, R. Ghiotto, M. Malcovati, M.L. Tenchini, G. Castaman, S. Duga
Alpha3 and alpha5 neuronal nicotinic receptor subunit genes : a case of tail-to-tail overlap in humans
2005 G.M.E.A. Solda'
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes
2009 G. Soldà, I.V. Makunin, O.U. Sezerman, A. Corradin, G. Corti, A. Guffanti
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
Characterization of long noncoding RNAs associated with developmental genes in vertebrates
2008 P.P. Amaral, M.E. Dinger, T.R. Mercer, S.J. Bruce, M. Askarian Amiri, S.J. Wilkins, C. Neyt, G.M. Soldà, S.M. Sunkin, A.C. Perkins, J.S. Mattick
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms
2001 S. Duga, G. Soldà, R. Asselta, M.T. Bonati, L. Dalprà, M. Malcovati, M.L. Tenchini
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study
2018 M. Rossi, M. Meggendorfer, M. Zampini, M. Tettamanti, E. Riva, E. Saba, N. Manes, C. Milanesi, U. Marta, L. Morabito, E. Travaglino, C. Peano, G. Solda, R. Asselta, S. Duga, K. Malik, C.F. Selmi, E. Civilini, S. Mandelli, N. Bolli, G.S. Vassiliou, W. Kern, A. Santoro, U. Lucca, T. Haferlach, M. Giovanni Della Porta
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009 G. Solda’, E.M. Paraboschi, D. Gemmati, P. Zamboni, S. Duga, R. Asselta
Differential expression of microRNAs in peripheral blood mononuclear cells of multiple sclerosis patients
2009 E.M. Paraboschi, G. Soldà, D. Gemmati, G. Zeri, E. Orioli, P. Zamboni, S. Duga, R. Asselta
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript
2013 V. Rimoldi, G. Soldà, R. Asselta, S. Spena, C. Stuani, E. Buratti, S. Duga
Evolution, identification and expression of noncoding RNAs in animals
2006 J.S. Mattick, M. Pheasant, I.V. Makunin, E.A. Glazov, K.C. Pang, M.C. Frith, S. Stephen, L.J. Croft, M.J. Gagen, R.J. Taft, G. Soldà, S. Nahkuri, C. Simons, T. Mercer, S. Stanley
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
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
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene
2013 L. Costantino, D. Rusconi, G. Soldà, M. Seia, V. Paracchini, L. Porcaro, R. Asselta, C. Colombo, S. Duga