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SOLDA', GIULIA MARIA EMILIA ANTONIETTA

SOLDA', GIULIA MARIA EMILIA ANTONIETTA  

Dipartimento Scienze Biomediche  

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Titolo Data di pubblicazione Autore(i) File
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 1-gen-2019 Cortesi, A; Pesant, M; Sinha, S; Marasca, F; Sala, E; Gregoretti, F; Antonelli, L; Oliva, G; Chiereghin, C; Solda', G; Bodega, B
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.
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
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
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 1-gen-2017 Cardamone, G; Paraboschi, Em; Rimoldi, V; Duga, S; Solda, G; Asselta, R
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.
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
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
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 1-gen-2015 Robusto, M; Fang, M; Asselta, R; Castorina, P; Previtali, Sc; Caccia, S; Benzoni, E; De Cristofaro, R; Yu, C; Cesarani, A; Liu, X; Li, W; Primignani, P; Ambrosetti, U; Xu, X; Duga, S; Solda', G.
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.
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 1-gen-2016 Solda, G; Caccia, S; Robusto, M; Chiereghin, C; Castorina, P; Ambrosetti, U; Duga, S; Asselta, R
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 1-gen-2018 Straniero, L; Rimoldi, V; Solda, G; Bellini, M; Biasucci, G; Asselta, R; Duga, S