MALCOVATI, MASSIMO

MALCOVATI, MASSIMO  

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 47 (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 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) -
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) -
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 -
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) -
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) -
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 1-gen-2006 L. MonaldiniR. AsseltaS. DugaF. PeyvandiM. MalcovatiM.L. Tenchini Article (author) -
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 1-gen-2002 S. SpenaS. DugaR. AsseltaM. MalcovatiF. PeyvandiM.L. Tenchini Article (author) -
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 1-gen-2001 R. AsseltaS. DugaS. SpenaF. PeyvandiM. MalcovatiP.M. MannucciM.L. Tenchini + Article (author) -
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 1-gen-2005 P. AlleviL. AnastasiaM.C. CantoneM. MalcovatiM.D.G. PoliM.L.G. Tenchini + Book (author) -
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria 1-gen-2005 P. AlleviL. AnastasiaM.C. CantoneM. MalcovatiM. PoliM.L. Tenchini + Book (author) -
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 1-gen-2005 P. AlleviL. AnastasiaM.C. CantoneM. MalcovatiM. PoliM.L. Tenchini + Book (author) -
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 1-gen-2005 S. DugaR. AsseltaM. MalcovatiM.L. Tenchini + Book Part (author) -
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 30-giu-2004 Massimo MalcovatiMaria Luisa Tenchini + Article (author) -
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 1-ago-2002 R. AsseltaS. DugaM. MalcovatiM.L. Tenchini + Article (author) -
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 1-gen-2005 R. AsseltaS. DugaM. MalcovatiM.L. Tenchini + Book Part (author) -
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 1-mag-2006 L. MonaldiniR. AsseltaS. DugaF. PeyvandiM. MalcovatiM.L. Tenchini + Article (author) -
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 1-gen-2005 L. MonaldiniS. DugaR. AsseltaM. MalcovatiM.L. Tenchini Book Part (author) -