SOLDA', GIULIA MARIA EMILIA ANTONIETTA
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
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
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
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
2017 L. Straniero, V. Rimoldi, M. Samarani, S. Goldwurm, A. Di Fonzo, R. Krüger, M. Deleidi, M. Aureli, G. Soldà, S. Duga, R. Asselta
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis
2016 L. Straniero, G. Soldà, L. Costantino, M. Seia, P. Melotti, C. Colombo, R. Asselta, S. Duga
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations
2015 V. Pensato, C. Tiloca, L. Corrado, C. Bertolin, V. Sardone, R. DEL BO, D. Calini, J. Mandrioli, G. LAURIA PINTER, L. Mazzini, G. Querin, M. Ceroni, R. Cantello, S.P. Corti, B. Castellotti, G.M.E.A. Solda', S. Duga, G.P. Comi, C. Cereda, G. Sorarù, S. D'Alfonso, F. Taroni, C.E. Shaw, J.E. Landers, N. Ticozzi, A. Ratti, C. Gellera, V. Silani
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
2015 R. Asselta, M. Platé, M. Robusto, M. Borhany, I. Guella, G. Soldà, A. Afrasiabi, M. Menegatti, T. Shamsi, F. Peyvandi, S. Duga
Identification of genetic factors associated with neural tube defects
2014 V. Massa, G. Soldà, L. Avagliano, G. Fazio, G. Cazzaniga, G. Bulfamante, A. Marozzi, F. Cotelli, A. Pistocchi, A. Gallina
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome
2014 G. Soldà, M. Robusto, P. Castorina, U. Ambrosetti, R. Asselta, S. Duga
Identification of novel NSHL-causing mutations by whole exome sequencing
2014 M. Robusto, C. Chiereghin, R. Asselta, P. Castorina, S. Caccia, E. Benzoni, M. Seia, U. Ambrosetti, S. Duga, G. Soldà
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
2014 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
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis
2014 V. Colangelo, S. François, G. Solda, R. Picco, F. Roma, E. Ginelli, R. Meneveri
Glucocerebrosidase mutations in primary parkinsonism
2014 R. Asselta, V. Rimoldi, C. Siri, R. Cilia, I. Guella, S. Tesei, G. Soldà, G. Pezzoli, S. Duga, S. Goldwurm
Improving mRNA 5' coding sequence determination in the mouse genome
2014 A. Piovesan, M. Caracausi, M.C. Pelleri, L. Vitale, S. Martini, C. Bassani, A. Gurioli, R. Casadei, G. Soldà, P. Strippoli
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II
2014 V. Rimoldi, L. Straniero, R. Asselta, L. Mauri, E. Manfredini, S. Penco, G.P. Gesu, A. Del Longo, E. Piozzi, G. Soldà, P. Primignani
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
No association of GBA mutations and multiple system atrophy
2013 K. Srulijes, A.K. Hauser, I. Guella, R. Asselta, K. Brockmann, C. Schulte, G. Soldà, R. Cilia, W. Maetzler, L. Schols, G.K. Wenning, W. Poewe, P. Barone, U. Wüllner, W. Oertel, D. Berg, S. Goldwurm, T. Gasser
Understanding genetic variation in the CFTR gene by next-generation sequencing
2013 L. Straniero, G. Soldà, L. Costantino, D. Rusconi, M. Seia, P. Melotti, C. Colombo, R. Asselta, S. Duga
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
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