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)
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP)
2004 L. Sangiorgio, B. Strumbo, M. L. Tenchini, M. Malcovati, S. Ronchi, T. Simonic
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
2007 C. Bozzao, V. Rimoldi, R. Asselta, M. Landau, R. Ghiotto, M.L. Tenchini, R. De Cristofaro, G. Castaman, S. Duga
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency
2005 G. Soldà, R. Asselta, R. Ghiotto, M. Malcovati, M.L. Tenchini, G. Castaman, S. Duga
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
2007 U. Albrecht, X. Yang, R. Asselta, V. Keitel, M.L. Tenchini, S. Ludwig, P.C. Heinrich, D. Häussinger, F. Schaper, J.G. Bode
Alternative splicing and nonsense-mediated decay in the F5 gene
2007 C. Dall’Osso, S. Duga, N. Locatelli, F. Peyvandi, M.L. Tenchini, R. Asselta
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia
2002 R. Asselta, S. Spena, S. Duga, F. Peyvandi, M. Malcovati, P.M. Mannucci, M.L. Tenchini
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein
2003 S. Duga, M.C. Montefusco, R. Asselta, M. Malcovati, F. Peyvandi, E. Santagostino, P.M. Mannucci, M.L. Tenchini
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population
2007 V. Bianchi, G. Maconi, S. Ardizzone, E. Colombo, E. Ferrara, A. Russo, M.L. Tenchini, G.B. Porro
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview
2004 R. Combi, L. Dalpra', M.L. Tenchini, L. Ferini-Strambi
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex
1997 T. Simonic, S. Duga, A. Negri, G. Tedeschi, M. Malcovati, M.L. Tenchini, S. Ronchi
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform
2006 R. Asselta, I. Guella, V. Rimoldi, M. Malcovati, M.L. Tenchini, S. Duga
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform
2007 I. Guella, R. Asselta, V. Rimoldi, M.L. Tenchini, S. Duga
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy
2009 R. Combi, D. Grioni, M. Contri, S. Redaelli, F. Redaelli, M.T. Bassi, D. Barisani, M.L. Lavitrano, G. Tredici, M.L. Tenchini, M. Bertolini, L. Dalprà
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
2003 M.C. Montefusco, S. Duga, R. Asselta, M. Malcovati, F. Peyvandi, E. Santagostino, P.M. Mannucci, M.L. Tenchini
Coagulation factor V
2004 S. Duga, R. Asselta, M.L. Tenchini
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions
2006 R. Asselta, C. Dall'Osso, S. Duga, M. Spreafico, R. Saxena, M.L. Tenchini
Coagulopatie ereditarie
2004 S. Duga, R. Asselta, E. Santagostino, F. Peyvandi, M.L.G. Tenchini, P.M. Mannucci
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy
2008 R. Combi, L. Ferini Strambi, M.L. Tenchini
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene
2004 S. Spena, S. Duga, R. Asselta, F. Peyvandi, C. Mahasandana, M. Malcovati, M.L. Tenchini
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene
2003 S. Spena, R. Asselta, S. Duga, M. Malcovati, F. Peyvandi, P.M. Mannucci, M.L. Tenchini