RIMOLDI, VALERIA

RIMOLDI, VALERIA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 53 (tempo di esecuzione: 0.002 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 1-dic-2007 V. RimoldiR. AsseltaM.L. TenchiniS. Duga + Article (author) -
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency 1-set-2009 S. SpenaR. AsseltaS. CacciaV. RimoldiF. PeyvandiS. Duga + Article (author) -
Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease 1-gen-2009 I. GuellaV. RimoldiR. AsseltaM. FrancoliniF. PeyvandiP.M. MannucciS. Duga + Article (author) -
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation FXI isoform 1-gen-2008 V. RimoldiI. GuellaR. AsseltaF. PeyvandiP.M. MannucciS. Duga + Conference Object -
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 1-gen-2006 R. AsseltaI. GuellaV. RimoldiM. MalcovatiM.L. TenchiniS. Duga Conference Object -
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform 1-gen-2007 I. GuellaR. AsseltaV. RimoldiM.L. TenchiniS. Duga Article (author) -
Characterization of the genetic basis of FXI deficiency in fourteen unrelated patients 1-gen-2009 V. RimoldiI. GuellaS. SpenaF. PeyvandiR. AsseltaP.M. MannucciS. Duga + Article (author) -
Characterization of the genetic basis of FXI deficiency in two Turkish patients 1-gen-2010 V. RimoldiS. Duga + Article (author) -
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 1-gen-2022 Mantovani, AlbertoZanella, AlbertoBandera, AlessandraCherubini, AlessandroProtti, AlessandroAghemo, AlessioLleo, AnaGori, AndreaFracanzani, Anna LudovicaRuello, AntonellaPesenti, AntonioHu, CinziaPaccapelo, CinziaCappadona, ClaudioGalimberti, DanielaScarpini, ElioParaboschi, Elvezia MariaMartinelli-Boneschi, FilippoPeyvandi, FloraBlasi, FrancescoMalvestiti, FrancescoGrasselli, GiacomoCostantino, GiorgioBaselli, GuidoTerranova, LeonardoCarrabba, MariaMiozzo, MonicaMontano, NicolaPreatoni, PaolettaBonfanti, PaoloGualtierotti, RobertaPelusi, SerenaBosari, SilvanoAliberti, StefanoRimoldi, ValeriaDuga, StefanoAsselta, RosannaValenti, Luca + Article (author) -
DNAJC12 and dopa-responsive nonprogressive parkinsonism 1-ott-2017 I. GuellaV. RimoldiA. Priori + Article (author) -
Dowregulation of the oxytocin receptor after ligand binding 1-gen-2005 S. SerticV. Rimoldi + 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) -
Effects of cholesterol manipulation on the signaling of the human oxytocin receptor 1-ott-2006 A. ReversiV. RimoldiBRAMBILLASCA, SILVIA + Article (author) -
Evidence of Liquid Crystal–Assisted Abiotic Ligation of Nucleic Acids 1-gen-2015 T.P. FracciaG. ZanchettaV. RimoldiT. Bellini + Article (author) -
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 1-lug-2017 Paraboschi, Elvezia MariaRimoldi, ValeriaMenegatti, MarziaPeyvandi, Flora + Article (author) -
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction 1-gen-2008 I. GuellaV. RimoldiR. AsseltaM. FrancoliniF. PeyvandiP.M. MannucciS. 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) -
Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema) 7-mar-2009 M. CicardiA. ZanichelliC. SuffrittiL. MaggioniS. CacciaR. RussoZHI, YUXIANGS. DugaR. AsseltaV. RimoldiG. Castellano + Conference Object -
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 23-ott-2011 S. CacciaV. RimoldiR. AsseltaG.M. SoldàR. RussoS. DugaM. Cicardi + Conference Object -