SOLDA', GIULIA MARIA EMILIA ANTONIETTA
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing
2011-10-01 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
2011-01-01 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
2011-11-01 M. Robusto, G. Soldà, P. Primignani, P. Castorina, E. Benzoni, A. Cesarani, U. Ambrosetti, R. Asselta, S. Duga
Alpha3 and alpha5 neuronal nicotinic receptor subunit genes : a case of tail-to-tail overlap in humans
2005-01-10 G.M.E.A. Solda'
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes
2009-09-01 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
2012-01-01 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
2008-01-01 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
2001-01-01 S. Duga, G. Soldà, R. Asselta, M.T. Bonati, L. Dalprà, M. Malcovati, M.L. Tenchini
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
2015-03-01 R. Asselta, M. Platé, M. Robusto, M. Borhany, I. Guella, G. Soldà, A. Afrasiabi, M. Menegatti, T. Shamsi, F. Peyvandi, S. Duga
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study
2018-11-01 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
2009-10-01 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
2009-11-01 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
2013-01-01 V. Rimoldi, G. Soldà, R. Asselta, S. Spena, C. Stuani, E. Buratti, S. Duga
Evolution, identification and expression of noncoding RNAs in animals
2006-01-01 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
2012-06-01 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
2011-03-01 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
2013-05-01 L. Costantino, D. Rusconi, G. Soldà, M. Seia, V. Paracchini, L. Porcaro, R. Asselta, C. Colombo, S. Duga
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II
2014-03-01 V. Rimoldi, L. Straniero, R. Asselta, L. Mauri, E. Manfredini, S. Penco, G.P. Gesu, A. Del Longo, E. Piozzi, G. Soldà, P. Primignani
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
2014-12-20 E.M. Paraboschi, V. Rimoldi, G. Soldà, T. Tabaglio, C. Dall'Osso, E. Saba, M. Vigliano, A. Salviati, M. Leone, M.D. Benedetti, D. Fornasari, J. Saarela, P.L. De Jager, N.A. Patsopoulos, S. D'Alfonso, D. Gemmati, S. Duga, R. Asselta
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
2017-01-01 L. Straniero, V. Rimoldi, M. Samarani, S. Goldwurm, A. Di Fonzo, R. Krüger, M. Deleidi, M. Aureli, G. Soldà, S. Duga, R. Asselta