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)  

Risultati 1 - 20 di 42 (tempo di esecuzione: 0.109 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Alternative splicing and nonsense-mediated decay in the F5 gene 1-gen-2007 S. DugaN. LocatelliF. PeyvandiM.L. TenchiniR. Asselta + 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) -
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 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 hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 1-gen-2008 R. AsseltaS. SpenaM. SpreaficoF. PeyvandiM.L. TenchiniS. Duga + Article (author) -
Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon 1-giu-2006 S. SpenaM.T. Tenchini + Article (author) -
CusMiBio : an opportunity for talented young people in biosciences 1-gen-2008 P. PlevaniM.L.G. TenchiniG. Viale + Book Part (author) -
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 1-gen-2003 L. MonaldiniR. AsseltaM. MalcovatiM.L. TenchiniS. Duga Book Part (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) -
Epilessia notturna del lobo frontale: non solo canalopatia! 1-gen-2005 M.L. Tenchini + Book Part (author) -
Epilessie idiopatiche e mutazioni nei geni per i canali del sodio 1-gen-2005 M.L. Tenchini + Book Part (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) -
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: 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) -