TENCHINI, MARIA LUISA GIUDITTA

TENCHINI, MARIA LUISA GIUDITTA  

DIPARTIMENTO DI BIOLOGIA E GENETICA PER LE SCIENZE MEDICHE (attivo dal 01/11/1983 al 26/04/2012)  

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Risultati 1 - 20 di 86 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 1-gen-2004 L. SangiorgioB. StrumboM. L. TenchiniM. MalcovatiS. RonchiT. Simonic Article (author) -
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) -
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 1-gen-2005 G. SoldàR. AsseltaM. MalcovatiM.L. TenchiniS. Duga + Article (author) -
Activation of NF-kappaB by IL-1beta blocks IL-6-induced sustained STAT3 activation and STAT3-dependent gene expression of the human gamma-fibrinogen gene 1-set-2007 R. AsseltaM.L. Tenchini + Article (author) -
Alternative splicing and nonsense-mediated decay in the F5 gene 1-gen-2007 S. DugaN. LocatelliF. PeyvandiM.L. TenchiniR. Asselta + Article (author) -
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 1-ago-2002 R. AsseltaS. SpenaS. DugaF. PeyvandiM. MalcovatiP.M. MannucciM.L. Tenchini Article (author) -
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 1-gen-2003 S. DugaR. AsseltaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini + Article (author) -
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population 1-mar-2007 V. BianchiG. MaconiS. ArdizzoneM.L. TenchiniG. B. Porro + Article (author) -
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview 1-ago-2004 M.L. Tenchini + Article (author) -
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 1-gen-1997 T. SimonicS. DugaA. NegriG. TedeschiM.L. TenchiniS. Ronchi + Article (author) -
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) -
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 1-gen-2009 M.L. Tenchini + Article (author) -
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V : broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations 1-nov-2003 S. DugaR. AsseltaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini + Article (author) -
Coagulation factor V 1-ago-2004 S. DugaR. AsseltaM.L. Tenchini Article (author) -
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 1-dic-2006 R. AsseltaS. DugaM. SpreaficoM.L. Tenchini + Article (author) -
Coagulopatie ereditarie 1-gen-2004 S. DugaR. AsseltaF. PeyvandiM.L.G. TenchiniP.M. Mannucci + Book Part (author) -
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy 1-gen-2008 M.L. Tenchini + Article (author) -
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 1-nov-2004 S. SpenaS. DugaR. AsseltaF. PeyvandiM. MalcovatiM.L. Tenchini + Article (author) -
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 15-ott-2003 S. SpenaR. AsseltaS. DugaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini Article (author) -