Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Giulia Soldà

Showing results (11-20 of 69) with videos related to

Pageof 7
Sort By:
Cells|June 10, 2022
Role of Cytoskeletal Diaphanous-Related Formins in Hearing LossChiara Chiereghin, Michela Robusto, Valentina Massa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2012
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's diseaseIlaria Guella, Giulia Soldà, Roberto Cilia, et al.
Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Journal of Human Genetics|August 5, 2016
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosisLetizia Straniero, Giulia Soldà, Lucy Costantino, et al.
Human Molecular Genetics|December 20, 2018
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosisGiulia Cardamone, Elvezia M Paraboschi, Giulia Soldà, et al.
International Journal of Molecular Sciences|October 6, 2015
Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory GenesElvezia Maria Paraboschi, Giulia Cardamone, Valeria Rimoldi, et al.
Ebiomedicine|January 7, 2026
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severityClaudio Cappadona, Valeria Rimoldi, Francesca Tettamanzi, et al.
Thrombosis and Haemostasis|March 11, 2008
Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defectIlaria Guella, Giulia Soldà, Silvia Spena, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
Cells|June 10, 2022
Role of Cytoskeletal Diaphanous-Related Formins in Hearing LossChiara Chiereghin, Michela Robusto, Valentina Massa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2012
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's diseaseIlaria Guella, Giulia Soldà, Roberto Cilia, et al.
Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Journal of Human Genetics|August 5, 2016
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosisLetizia Straniero, Giulia Soldà, Lucy Costantino, et al.
Human Molecular Genetics|December 20, 2018
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosisGiulia Cardamone, Elvezia M Paraboschi, Giulia Soldà, et al.
International Journal of Molecular Sciences|October 6, 2015
Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory GenesElvezia Maria Paraboschi, Giulia Cardamone, Valeria Rimoldi, et al.
Ebiomedicine|January 7, 2026
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severityClaudio Cappadona, Valeria Rimoldi, Francesca Tettamanzi, et al.
Thrombosis and Haemostasis|March 11, 2008
Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defectIlaria Guella, Giulia Soldà, Silvia Spena, et al.
Pageof 7