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)
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
2007-09-01 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
2007-01-01 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
2002-08-01 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
2003-01-01 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
2007-03-01 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
2004-08-01 R. Combi, L. Dalpra', M.L. Tenchini, L. Ferini-Strambi
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex
1997-01-01 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
2006-01-01 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
2007-01-01 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
2009-01-01 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
2003-11-01 M.C. Montefusco, S. Duga, R. Asselta, M. Malcovati, F. Peyvandi, E. Santagostino, P.M. Mannucci, M.L. Tenchini
Coagulation factor V
2004-08-01 S. Duga, R. Asselta, M.L. Tenchini
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions
2006-12-01 R. Asselta, C. Dall'Osso, S. Duga, M. Spreafico, R. Saxena, M.L. Tenchini
Coagulopatie ereditarie
2004-01-01 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
2008-01-01 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
2004-11-01 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
2003-10-15 S. Spena, R. Asselta, S. Duga, M. Malcovati, F. Peyvandi, P.M. Mannucci, M.L. Tenchini
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran
2006-01-01 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, M. Malcovati, M.L. Tenchini
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites
2002-01-01 S. Spena, S. Duga, R. Asselta, M. Malcovati, F. Peyvandi, M.L. Tenchini
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs
2001-01-01 R. Asselta, S. Duga, S. Spena, E. Santagostino, F. Peyvandi, G. Piseddu, R. Targhetta, M. Malcovati, P.M. Mannucci, M.L. Tenchini