GUELLA, ILARIA

GUELLA, ILARIA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 20 di 37 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex 1-gen-2013 I. GuellaF. TorriF. Macciardi + 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) -
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) -
Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian population 1-ott-2011 I. GuellaS. DugaF. PeyvandiP.M. MannucciR. Asselta + Article (author) -
DNAJC12 and dopa-responsive nonprogressive parkinsonism 1-ott-2017 I. GuellaV. RimoldiA. Priori + Article (author) -
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population 1-nov-2010 I. GuellaR. AsseltaF. PeyvandiP.M. MannucciS. Duga + Article (author) -
Factor XI deficiency in Southern Iran: identification of a novel missense mutation 1-apr-2009 I. GuellaR. AsseltaF. Peyvandi + 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 a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 1-mar-2012 F. PeyvandiI. GuellaS. DugaR. Asselta + Article (author) -
Glucocerebrosidase mutations in primary parkinsonism 1-nov-2014 R. AsseltaV. RimoldiC. SiriI. GuellaG. SoldàS. Duga + Article (author) -
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 1-gen-2008 I. GuellaS. DugaR. Asselta + Conference Object -
Identification of the first alu-mediated large deletion involving the f5 gene in a compound heterozygous patient with severe factor v deficiency 1-ago-2011 I. GuellaE.M. ParaboschiR. AsseltaS. Duga + Article (author) -
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 1-gen-2006 R. AsseltaV. RimoldiI. GuellaM. MalcovatiM.L. TenchiniS. Duga Conference Object -
Molecular characterization of 9 genetic defects responsible for FV deficiency 1-lug-2009 E.M. ParaboschiI. GuellaS. DugaF. PeyvandiP.M. MannucciR. Asselta Article (author) -
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 11-mar-2010 R. AsseltaV. RimoldiI. GuellaG.SoldàF. PeyvandiS. Duga + Article (author) -
Molecular characterization of six novel mutations causing factor V deficiency 1-gen-2008 I. GuellaE.M. ParaboschiS. DugaF. PeyvandiP.M. MannucciR. Asselta + Article (author) -