SOLDA', GIULIA MARIA EMILIA ANTONIETTA

SOLDA', GIULIA MARIA EMILIA ANTONIETTA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 20 di 58 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest 2018 Samarani, MauraLoberto, NicolettaSoldà, GiuliaStraniero, LetiziaAsselta, RosannaDuga, StefanoLunghi, GiuliaZucca, Fabio AMauri, LauraCiampa, Maria GraziaSchiumarini, DomitillaBassi, RosariaGiussani, PaolaChiricozzi, ElenaPrinetti, AlessandroAureli, MassimoSonnino, Sandro Article (author) -
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study 2018 Elena SabaSolda GiuliaRosanna AsseltaStefano DugaCarlo SelmiNiccolò Bolli + Article (author) -
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 2017 L. StranieroV. RimoldiM. SamaraniA. Di FonzoM. AureliG. SoldàS. DugaR. Asselta + Article (author) -
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis 2016 Straniero, LetiziaSoldà, GiuliaColombo, Carla + Article (author) -
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 2015 R. AsseltaG. SoldàM. MenegattiF. PeyvandiS. Duga + Article (author) -
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 2015 C. TilocaL. CorradoC. BertolinR. DEL BOD. CaliniG. LAURIA PINTERS.P. CortiG.M.E.A. Solda'S. DugaG.P. ComiN. TicozziA. RattiV. Silani + Article (author) -
Identification of novel NSHL-causing mutations by whole exome sequencing 2014 M. RobustoR. AsseltaS. CacciaU. AmbrosettiS. DugaG. Soldà + Conference Object -
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 2014 V. RimoldiL. StranieroR. AsseltaG. Soldà + Article (author) -
Improving mRNA 5' coding sequence determination in the mouse genome 2014 G. Soldà + Article (author) -
Identification of genetic factors associated with neural tube defects 2014 V. MassaG. SoldàL. AvaglianoG. BulfamanteA. MarozziF. CotelliA. PistocchiA. Gallina + Conference Object -
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome 2014 G. SoldàM. RobustoU. AmbrosettiR. AsseltaS. Duga + Conference Object -
Glucocerebrosidase mutations in primary parkinsonism 2014 R. AsseltaV. RimoldiC. SiriI. GuellaG. SoldàS. Duga + Article (author) -
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 2014 E.M. ParaboschiV. RimoldiG. SoldàE. SabaD. FornasariS. DugaR. Asselta + Article (author) -
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 2014 G. SoldaF. RomaE. Ginelli + Article (author) -
Role of miRNAs in neural tube development 2013 G. SoldàL. AvaglianoA. PistocchiA. GallinaG. BulfamanteV. Massa + Conference Object -
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript 2013 V. RimoldiG. SoldàR. AsseltaS. SpenaS. Duga + Article (author) -
In-depth study of breast cancer tumor promoting cell transcriptome using RNA-seq and microarrays 2013 G. Soldà + Conference Object -
Understanding genetic variation in the CFTR gene by next-generation sequencing 2013 G. SoldàC. ColomboR. AsseltaS. Duga + Conference Object -
No association of GBA mutations and multiple system atrophy 2013 R. AsseltaG. Soldà + Article (author) -
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 2013 L. CostantinoG. SoldàR. AsseltaC. ColomboS. Duga + Article (author) -