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: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 1-ott-2011 M. RobustoR. AsseltaA. CesaraniU. AmbrosettiS. DugaG. Soldà + Conference Object -
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 1-gen-2011 G.M. SoldàM. RobustoR. AsseltaU. AmbrosettiS. Duga + Conference Object -
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 1-nov-2011 M. RobustoG. SoldàA. CesaraniU. AmbrosettiR. AsseltaS. Duga + Conference Object -
Alpha3 and alpha5 neuronal nicotinic receptor subunit genes : a case of tail-to-tail overlap in humans 10-gen-2005 G.M.E.A. Solda' Doctoral Thesis -
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes 1-set-2009 G. Soldà + Article (author) -
Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease 1-gen-2012 I. GuellaG. SoldàR. AsseltaS. Duga + Article (author) -
Characterization of long noncoding RNAs associated with developmental genes in vertebrates 1-gen-2008 G.M. Soldà + Conference Object -
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 S. DugaG. SoldàR. Asselta + Article (author) -
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 1-mar-2015 R. AsseltaG. SoldàM. MenegattiF. PeyvandiS. Duga + Article (author) -
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study 1-nov-2018 Elena SabaSolda GiuliaRosanna AsseltaStefano DugaCarlo SelmiNiccolò Bolli + Article (author) -
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 1-ott-2009 G. Solda’E.M. ParaboschiS. DugaR. Asselta + Conference Object -
Differential expression of microRNAs in peripheral blood mononuclear cells of multiple sclerosis patients 1-nov-2009 E.M. ParaboschiG. SoldàS. DugaR. Asselta + Conference Object -
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 V. RimoldiG. SoldàR. AsseltaS. SpenaS. Duga + Article (author) -
Evolution, identification and expression of noncoding RNAs in animals 1-gen-2006 G. Soldà + Conference Object -
Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian population 1-giu-2012 M. RobustoR. AsseltaS. CacciaU. AmbrosettiS. DugaG. Soldà + Conference Object -
Expression of distinct RNAs from 3' untranslated regions 1-mar-2011 G. Solda + Article (author) -
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 1-mag-2013 L. CostantinoG. SoldàR. AsseltaC. ColomboS. Duga + Article (author) -
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 1-mar-2014 V. RimoldiL. StranieroR. AsseltaG. Soldà + Article (author) -
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 20-dic-2014 E.M. ParaboschiV. RimoldiG. SoldàE. SabaD. FornasariS. DugaR. Asselta + Article (author) -
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 1-gen-2017 L. StranieroV. RimoldiM. SamaraniA. Di FonzoM. AureliG. SoldàS. DugaR. Asselta + Article (author) -