Sfoglia per Autore
L-aspartate oxidase from Escherichia coli. I. Characterization of coenzyme binding and product inhibition
1996 M. Mortarino, A. Negri, G. Tedeschi, T. Simonic, S. Duga, H.G. Gassen, S. Ronchi
Physical mapping of connexin 32 (GJB1) and 43 (GJA1) genes to bovine chromosomes Xq22 and 9q15/16 by fluorescence in situ hybridization
1996 B. Castiglioni, L. Ferretti, M. L. Tenchini, A. Mezzelani, T. Simonic, S. Duga
Identification and spatial distribution of the mRNA encoding the gp49 component of the gilthead sea bream, Sparus aurata, egg envelope
1997 L. Del Giacco, C. Vanoni, D. Bonsignorio, S. Duga, G. Mosconi, A. Santucci, F. Cotelli
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex
1997 T. Simonic, S. Duga, A. Negri, G. Tedeschi, M. Malcovati, M.L. Tenchini, S. Ronchi
Identification of a glucocorticoid response element in the human gamma chain fibrinogen promoter
1998 R. Asselta, S. Duga, M. Modugno, M. Malcovati, M.L. Tenchini
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. Duga, A. Gobbi, R. Asselta, L. Crippa, M. L. Tenchini, T. Simonic, E. Scanziani
cDNA cloning of turtle prion protein
2000 T. Simonic, S. Duga, B. Strumbo, R. Asselta, F. Ceciliani, S. Ronchi
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
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein
2001 M. Menegatti, R. Asselta, S. Duga, M. Malcovati, P. Bucciarelli, P.M. Mannucci, M.L. Tenchini
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. Duga, G. Soldà, R. Asselta, M.T. Bonati, L. Dalprà, M. Malcovati, M.L. Tenchini
Rare coagulation deficiencies
2002 F. Peyvandi, S. Duga, S. Akhavan, P.M. Mannucci
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
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. Duga, R. Asselta, M.T. Bonati, M. Malcovati, L. Dalprà, A. Oldani, M. Zucconi, L. Ferini-Strambi, M.L. Tenchini
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
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
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations
2003 L. Monaldini, R. Asselta, M. Malcovati, M.L. Tenchini, S. Duga
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
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain
2003 R. Asselta, M.C. Montefusco, S. Duga, M. Malcovati, F. Peyvandi, P.M. Mannucci, 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
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
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