MALCOVATI, MASSIMO
MALCOVATI, MASSIMO
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 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
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
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
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
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
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran
2006 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 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 R. Asselta, S. Duga, S. Spena, E. Santagostino, F. Peyvandi, G. Piseddu, R. Targhetta, M. Malcovati, P.M. Mannucci, M.L. Tenchini
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria
2005 P. Allevi, L. Anastasia, M.C. Cantone, M. Malcovati, A.M. Paganoni, M.D.G. Poli, M.L.G. Tenchini
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria
2005 P. Allevi, L. Anastasia, M.C. Cantone, M. Malcovati, A.M. Paganoni, M. Poli, M.L. Tenchini
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica
2005 P. Allevi, L. Anastasia, M.C. Cantone, M. Malcovati, A.M. Paganoni, M. Poli, M.L. Tenchini
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione
2005 S. Duga, C. Bozzao, R. Asselta, R. Ghiotto, M. Malcovati, M.L. Tenchini, G. Castaman
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy
2004 Romina Combi, Leda Dalprà, Massimo Malcovati, Alessandro Oldani, Maria Luisa Tenchini, Luigi Ferini-Strambi
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families
2002 M.T. Bonati, R. Combi, R. Asselta, S. Duga, M. Malcovati, A. Oldani, M. Zucconi, L. Ferini Strambi, L. Dalprà, M.L. Tenchini
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation
2005 C. Dall’Osso, R. Asselta, S. Duga, M. Malcovati, M.L. Tenchini
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene
2006 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, K. Ghosh, M. Malcovati, M.L. Tenchini
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene
2005 L. Monaldini, S. Duga, R. Asselta, M. Malcovati, M.L. Tenchini