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Mostrati risultati da 1 a 20 di 172
Titolo Data di pubblicazione Autori Tipo File Abstract
L-aspartate oxidase from Escherichia coli. I. Characterization of coenzyme binding and product inhibition 1996 M. MortarinoA. NegriG. TedeschiT. SimonicS. DugaS. Ronchi + Article (author) -
Physical mapping of connexin 32 (GJB1) and 43 (GJA1) genes to bovine chromosomes Xq22 and 9q15/16 by fluorescence in situ hybridization 1996 S. Duga + Article (author) -
Identification and spatial distribution of the mRNA encoding the gp49 component of the gilthead sea bream, Sparus aurata, egg envelope 1997 L. Del GiaccoS. DugaF. Cotelli + Article (author) -
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 1997 T. SimonicS. DugaA. NegriG. TedeschiM.L. TenchiniS. Ronchi + Article (author) -
Identification of a glucocorticoid response element in the human gamma chain fibrinogen promoter 1998 R. AsseltaS. Duga + Article (author) -
Analysis of the 16S rRNA gene sequence of the coryneform bacterium associated with hyperkeratotic dermatitis of athymic nude mice and development of a PCR-based detection assay 1998 S. DugaR. AsseltaE. Scanziani + Article (author) -
cDNA cloning of turtle prion protein 2000 T. SimonicS. DugaB. StrumboR. AsseltaF. CecilianiS. Ronchi 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 2001 R. AsseltaS. DugaS. SpenaF. PeyvandiM. MalcovatiP.M. MannucciM.L. Tenchini + Article (author) -
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 2001 M. MenegattiR. AsseltaS. DugaM. MalcovatiP. BucciarelliP.M. MannucciM.L. Tenchini Article (author) -
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 2001 S. DugaG. SoldàR. Asselta + Article (author) -
Rare coagulation deficiencies 2002 F. PeyvandiS. DugaP.M. Mannucci + Article (author) -
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 2002 S. SpenaS. DugaR. AsseltaM. MalcovatiF. PeyvandiM.L. Tenchini Article (author) -
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 2002 S. DugaR. AsseltaM. MalcovatiM.L. Tenchini + Article (author) -
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 2002 R. AsseltaS. SpenaS. DugaF. PeyvandiM. MalcovatiP.M. MannucciM.L. 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 2002 R. AsseltaS. DugaM. MalcovatiM.L. Tenchini + Article (author) -
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 2003 L. MonaldiniR. AsseltaM. MalcovatiM.L. TenchiniS. Duga Book Part (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 2003 S. DugaR. AsseltaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini + Article (author) -
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 2003 R. AsseltaS. DugaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini + Article (author) -
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 2003 S. SpenaR. AsseltaS. DugaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini Article (author) -
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 S. DugaR. AsseltaM. MalcovatiF. PeyvandiP.M. MannucciM.L. Tenchini + Article (author) -
Mostrati risultati da 1 a 20 di 172
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