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Giulia Soldà

Research Profile

Chemicals & Drugs

Physiology

Post Transcriptional RNA Processing

Disorders

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Italy

Living Beings

Anatomy

COS Cells

Procedures

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Concepts & Ideas

Nucleic Acid Conformation

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Publications

TOP 3
Lucy Costantino; Rosanna Asselta; Carla Colombo; Valentina Paracchini; Luigi Porcaro; Damiana Rusconi; Manuela Seia; Giulia Soldà; Stefano Duga
Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene.
K Srulijes; Gregor Wenning; Ullrich Wüllner; R Asselta; P Barone; Daniela Berg; K Brockmann; Roberto Cilia; S Goldwurm; I Guella; A-K Hauser; Walter Maetzler; Wolfgang H Oertel; Werner Poewe; L Schols; C Schulte; Giulia Soldà; Thomas Gasser
No association of GBA mutations and multiple system atrophy.
Valeria Rimoldi; Giulia Soldà; Silvia Spena; Cristiana Stuani; Rosanna Asselta; Emanuele Buratti; Stefano Duga
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript.

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All Publications

2013: Lucy Costantino; Rosanna Asselta; Carla Colombo; Valentina Paracchini; Luigi Porcaro; Damiana Rusconi; Manuela Seia; Giulia Soldà; Stefano Duga
Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene.
American journal of respiratory cell and molecular biology 2013;48(5):619-25.
2013: K Srulijes; Gregor Wenning; Ullrich Wüllner; R Asselta; P Barone; Daniela Berg; K Brockmann; Roberto Cilia; S Goldwurm; I Guella; A-K Hauser; Walter Maetzler; Wolfgang H Oertel; Werner Poewe; L Schols; C Schulte; Giulia Soldà; Thomas Gasser
No association of GBA mutations and multiple system atrophy.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013;20(4):e61-2.
2013: Valeria Rimoldi; Giulia Soldà; Silvia Spena; Cristiana Stuani; Rosanna Asselta; Emanuele Buratti; Stefano Duga
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript.
PloS one 2013;8(3):e59333.
2012: Ilaria Guella; Gianni Pezzoli; Giulia Soldà; Rosanna Asselta; Roberto Cilia; Stefano Duga; Stefano Goldwurm
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2012;27(6):800-1.
2012: Luca Trotta; Margherita Canesi; Stefano Duga; Stefano Goldwurm; Ilaria Guella; Gianni Pezzoli; Francesca Sironi; Giulia Soldà; Silvana Tesei; Rosanna Asselta
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.
Parkinsonism & related disorders 2012;18(3):257-62.
2012: Giulia Soldà; Paola Primignani; Michela Robusto; Umberto Ambrosetti; Rosanna Asselta; Elena Benzoni; Pierangela Castorina; Antonio Cesarani; Stefano Duga
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
Human molecular genetics 2012;21(3):577-85.
2011: Tim R Mercer; Dagmar Wilhelm; Marcel Dinger; Giulia Soldà; Darren J Korbie; Evgeny A Glazov; Vy Truong; Maren Schwenke; Cas Simons; Klaus I Matthaei; Robert Saint; Peter Koopman; John S Mattick
Expression of distinct RNAs from 3' untranslated regions.
Nucleic acids research 2011;39(6):2393-403.
2011: Elvezia Maria Paraboschi; Alessandro Salviati; Giulia Soldà; Giulia Zeri; Nadia Barizzone; MD Benedetti; Stefano Duga; Donato Gemmati; Maurizio Leone; Elisa Orioli; Rosanna Asselta
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients.
International journal of molecular sciences 2011;12(12):8695-712.
2010: Rosanna Asselta; Valeria Rimoldi; Ilaria Guella; Giulia Soldà; Raimondo De Cristofaro; Flora Peyvandi; Stefano Duga
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA.
Blood 2010;115(10):2065-72.
2009: Giulia Soldà; Igor Makunin; Osman U Sezerman; Alberto Corradin; Giorgio Corti; Alessandro Guffanti
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes.
Briefings in bioinformatics 2009;10(5):475-89.
2008: Marcel Dinger; Paulo P Amaral; Tim R Mercer; Ken C Pang; Stephen J Bruce; brooke gardiner; Marjan E Askarian-Amiri; Kelin Ru; Giulia Soldà; Cas Simons; Susan M Sunkin; Mark L Crowe; Sean M Grimmond; Andrew C Perkins; John S Mattick
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation.
Genome research 2008;18(9):1433-45.
2008: Ilaria Guella; Giulia Soldà; Silvia Spena; Rosanna Asselta; Rossella Ghiotto; Maria Luisa Tenchini; Giancarlo Castaman; Stefano Duga
Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect.
Thrombosis and haemostasis 2008;99(3):523-30.
2008: Giulia Soldà; Mikita Suyama; Paride Pelucchi; Silvia Boi; Alessandro Guffanti; Ermanno Rizzi; Peer Bork; Maria Luisa Tenchini; Francesca D Ciccarelli
Non-random retention of protein-coding overlapping genes in Metazoa.
BMC genomics 2008;9():174.
2005: Giulia Soldà; Rosanna Asselta; Rossella Ghiotto; Maria Luisa Tenchini; Giancarlo Castaman; Stefano Duga
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency.
Haematologica 2005;90(12):1716-8.
2005: Giulia Soldà; Silvia Boi; Stefano Duga; Diego Fornasari; Roberta Benfante; Massimo Malcovati; Maria Luisa Tenchini
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs.
Gene 2005;345(2):155-64.
2001: Stefano Duga; Giulia Soldà; Rosanna Asselta; Maria Teresa Bonati; Leda Dalprà; Massimo Malcovati; Maria Luisa Tenchini
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms.
Journal of human genetics 2001;46(11):640-8.