Soldà G - Search Results

1

A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest.

Samarani M, Loberto N, Soldà 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. Samarani M, et al. Among authors: solda g. FASEB J. 2018 Oct;32(10):5685-5702. doi: 10.1096/fj.201701512RR. Epub 2018 May 10. FASEB J. 2018. PMID: 29746165 Free PMC article.

Our findings indicate the existence of a new molecular mechanism underlying cell damage triggered by lysosomal impairment.-Samarani, M., Loberto, N., Solda, G., Straniero, L., Asselta, R., Duga, S., Lunghi, G., Zucca, F. A., Mauri, L., Ciampa, M. G., S …

Our findings indicate the existence of a new molecular mechanism underlying cell damage triggered by lysosomal impairment.-Samarani, M., Lob …

2

Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect.

Guella I, Soldà G, Spena S, Asselta R, Ghiotto R, Tenchini ML, Castaman G, Duga S. Guella I, et al. Among authors: solda g. Thromb Haemost. 2008 Mar;99(3):523-30. doi: 10.1160/TH07-12-0723. Thromb Haemost. 2008. PMID: 18327400

3

Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA.

Asselta R, Rimoldi V, Guella I, Soldà G, De Cristofaro R, Peyvandi F, Duga S. Asselta R, et al. Among authors: solda g. Blood. 2010 Mar 11;115(10):2065-72. doi: 10.1182/blood-2009-09-245092. Epub 2009 Dec 30. Blood. 2010. PMID: 20042724 Free article.

4

A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.

Soldà G, Robusto M, Primignani P, Castorina P, Benzoni E, Cesarani A, Ambrosetti U, Asselta R, Duga S. Soldà G, et al. Hum Mol Genet. 2012 Feb 1;21(3):577-85. doi: 10.1093/hmg/ddr493. Epub 2011 Oct 28. Hum Mol Genet. 2012. PMID: 22038834 Free PMC article.

5

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population.

Trotta L, Guella I, Soldà G, Sironi F, Tesei S, Canesi M, Pezzoli G, Goldwurm S, Duga S, Asselta R. Trotta L, et al. Among authors: solda g. Parkinsonism Relat Disord. 2012 Mar;18(3):257-62. doi: 10.1016/j.parkreldis.2011.10.014. Epub 2011 Nov 21. Parkinsonism Relat Disord. 2012. PMID: 22104010 Free PMC article.

6

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients.

Paraboschi EM, Soldà G, Gemmati D, Orioli E, Zeri G, Benedetti MD, Salviati A, Barizzone N, Leone M, Duga S, Asselta R. Paraboschi EM, et al. Among authors: solda g. Int J Mol Sci. 2011;12(12):8695-712. doi: 10.3390/ijms12128695. Epub 2011 Dec 1. Int J Mol Sci. 2011. PMID: 22272099 Free PMC article.

7

Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene.

Costantino L, Rusconi D, Soldà G, Seia M, Paracchini V, Porcaro L, Asselta R, Colombo C, Duga S. Costantino L, et al. Among authors: solda g. Am J Respir Cell Mol Biol. 2013 May;48(5):619-25. doi: 10.1165/rcmb.2012-0371OC. Am J Respir Cell Mol Biol. 2013. PMID: 23349053

8

Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript.

Rimoldi V, Soldà G, Asselta R, Spena S, Stuani C, Buratti E, Duga S. Rimoldi V, et al. Among authors: solda g. PLoS One. 2013;8(3):e59333. doi: 10.1371/journal.pone.0059333. Epub 2013 Mar 22. PLoS One. 2013. PMID: 23533617 Free PMC article.

9

Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II.

Rimoldi V, Straniero L, Asselta R, Mauri L, Manfredini E, Penco S, Gesu GP, Del Longo A, Piozzi E, Soldà G, Primignani P. Rimoldi V, et al. Among authors: solda g. Gene. 2014 Mar 1;537(1):79-84. doi: 10.1016/j.gene.2013.11.102. Epub 2013 Dec 18. Gene. 2014. PMID: 24361966

10

Glucocerebrosidase mutations in primary parkinsonism.

Asselta R, Rimoldi V, Siri C, Cilia R, Guella I, Tesei S, Soldà G, Pezzoli G, Duga S, Goldwurm S. Asselta R, et al. Among authors: solda g. Parkinsonism Relat Disord. 2014 Nov;20(11):1215-20. doi: 10.1016/j.parkreldis.2014.09.003. Epub 2014 Sep 9. Parkinsonism Relat Disord. 2014. PMID: 25249066 Free PMC article.

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