IRIS

SOLDA', GIULIA MARIA EMILIA ANTONIETTA

SOLDA', GIULIA MARIA EMILIA ANTONIETTA  

Dipartimento Scienze Biomediche  

Mostra records
Risultati 1 - 20 di 85 (tempo di esecuzione: 0.026 secondi).
Titolo Data di pubblicazione Autore(i) File
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 1-gen-2018 Samarani, M; Loberto, N; Solda, G; Straniero, L; Asselta, R; Duga, S; Lunghi, G; Zucca, Fa; Mauri, L; Ciampa, Mg; Schiumarini, D; Bassi, R; Giussani, P; Chiricozzi, E; Prinetti, A; Aureli, M; Sonnino, S.
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 1-gen-2008 Soldà, G.; Wilhelm, D.; Dinger, M. E.; Mercer, T. R.; Taft, R. J.; Koopman, P.; Mattick, J. S.
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
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
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 1-gen-2012 Solda', G; Robusto, M; Primignani, P; Castorina, P; Benzoni, E; Cesarani, A; Ambrosetti, U; Asselta, R; Duga, S
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
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 1-gen-2009 Guffanti, A; Iacono, M; Pelucchi, P; Kim, N; Solda', G; Croft, Lj; Taft, Rj; Rizzi, E; Askarian-Amiri, M; Bonnal, Rj; Callari, M; Mignone, F; Pesole, G; Bertalot, G; Bernardi, Lr; Albertini, A; Lee, C; Mattick, Js; Zucchi, I; De Bellis, G
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 1-gen-2005 Solda, G; Asselta, R; Ghiotto, R; Tenchini, Ml; Castaman, G; 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.
Characterization of Long Noncoding RNAs Associated with Developmental Genes in Vertebrates 1-gen-2008 P. P., Amaral; M. E., Dinger; T. R., Mercer; S. J., Bruce; M., ASKARIAN-AMIRI; S. J., Wilkins; C., Neyt; Solda', G.; S. M., Sunkin; A. C., Perkins; J. S., Mattick
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
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 1-gen-2001 Duga, S; Solda, G; Asselta, R; Bonati, Mt; Dalpra, L; Malcovati, M; Tenchini, Ml
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 1-gen-2015 Asselta, R; Platè, M; Robusto, M; Borhany, M; Guella, I; Solda', G; Afrasiabi, A; Menegatti, M; Shamsi, T; Peyvandi, F; Duga, S
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 1-gen-2021 Rossi, Marianna; Meggendorfer, Manja; Zampini, Matteo; Tettamanti, Mauro; Riva, Emma; Travaglino, Erica; Bersanelli, Matteo; Mandelli, Sara; Galbussera, Alessia Antonella; Mosca, Ettore; Saba, Elena; Chiereghin, Chiara; Manes, Nicla; Milanesi, Chiara; Ubezio, Marta; Morabito, Lucio; Peano, Clelia; Soldà, Giulia; Asselta, Rosanna; Duga, Stefano; Selmi, Carlo; De Santis, Maria; Malik, Karolina; Maggioni, Giulia; Bicchieri, Maria Elena; Campagna, Alessia; Tentori, Cristina Astrid; Russo, Antonio; Civilini, Efrem; Allavena, Paola; Piazza, Rocco; Corrao, Giovanni; Sala, Claudia; Termanini, Alberto; Giordano, Laura; Detoma, Paolo; Malabaila, Aurelio; Sala, Luca; Rosso, Stefano; Zanetti, Roberto; Saitta, Claudia; Riva, Elena; Condorelli, Gianluigi; Passamonti, Francesco; Santoro, Armando; Sole, Francesc; Platzbecker, Uwe; Fenaux, Pierre; Bolli, Niccolo; Castellani, Gastone; Kern, Wolfgang; Vassiliou, George; Haferlach, Torsten; Lucca, Ugo; Della Porta, Matteo G
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 1-gen-2009 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
DNAJC12 and dopa-responsive nonprogressive parkinsonism 1-gen-2017 Straniero, L; Guella, I; Cilia, R; Parkkinen, L; Rimoldi, V; Young, A; Asselta, R; Solda', G; Sossi, V; Stoessl, Aj; Priori, A; Nishioka, K; Hattori, N; Follett, J; Rajput, A; Blau, N; Pezzoli, G; Farrer, Mj; Goldwurm, S; Rajput, Ah; Duga, S.
Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript 1-gen-2013 Rimoldi, V; Solda, G; Asselta, R; Spena, S; Stuani, C; Buratti, E; Duga, S
Evolution, identification and expression of noncoding RNAs in animals 1-gen-2006 PHEASANT M, MATTICK J. S; Makunin, I. V; Glazov, E. A; Pang, K. C; Frith, M. C; Stephen, S; Croft, L. J; Gagen, M. J; Taft, R. J; Solda', G.; Nahkuri, S; Simons, C; Mercer, T; Stanley, S
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.
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 1-gen-2013 Costantino, L.; Rusconi, D.; Solda', G.; Seia, M.; Paracchini, V.; Porcaro, L.; Asselta, R.; Colombo, C.; Duga, S.