ASSELTA, ROSANNA

ASSELTA, ROSANNA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 20 di 167 (tempo di esecuzione: 0.004 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A functional variant in ERAP1 predisposes to multiple sclerosis 1-gen-2012 D. GalimbertiC. FenoglioM. BiasinR. AsseltaE. ScarpiniG.P. ComiN. BresolinM.S. Clerici + Article (author) -
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest 1-ott-2018 Samarani, MauraLoberto, NicolettaSoldà, GiuliaStraniero, LetiziaAsselta, RosannaDuga, StefanoLunghi, GiuliaZucca, Fabio AMauri, LauraCiampa, Maria GraziaSchiumarini, DomitillaBassi, RosariaGiussani, PaolaChiricozzi, ElenaPrinetti, AlessandroAureli, MassimoSonnino, Sandro Article (author) -
A new exon in the 5' untranslated region of the connexin32 gene 1-gen-1999 S. DugaR. AsseltaL. Del Giacco + Article (author) -
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 1-ott-2011 M. RobustoR. AsseltaA. CesaraniU. AmbrosettiS. DugaG. Soldà + Conference Object -
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 1-dic-2007 V. RimoldiR. AsseltaM.L. TenchiniS. Duga + Article (author) -
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family 1-mar-2009 I. GuellaR. Asselta + Article (author) -
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 1-gen-2011 G.M. SoldàM. RobustoR. AsseltaU. AmbrosettiS. Duga + Conference Object -
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 1-nov-2011 M. RobustoG. SoldàA. CesaraniU. AmbrosettiR. AsseltaS. Duga + Conference Object -
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) -
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 1-gen-2013 M. MenegattiR. AsseltaF. Peyvandi + Article (author) -
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 1-gen-2013 M. MenegattiR. AsseltaF. Peyvandi + Article (author) -
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 1-gen-2020 Benetti E.Asselta R.Furini S.Seri M.Nigro V.Tartaglia M.Sara A.Palmieri M.D'Alessandro M.Feri M.Scala R.Donati A.D'Arminio Monforte A.Merlini E.Rusconi S.Siano M.Gabrieli A.Riva A.Parisi S. G.Magro P.Carella M.Meloni I.Mandala M.Fiorentino G.Menatti E.Baratti S.Pinto A. M. + Article (author) -
Activation of NF-kappaB by IL-1beta blocks IL-6-induced sustained STAT3 activation and STAT3-dependent gene expression of the human gamma-fibrinogen gene 1-set-2007 R. AsseltaM.L. Tenchini + Article (author) -
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality 1-dic-2021 Duga S.Asselta R.Valenti L. + Article (author) -
Alternative splicing and nonsense-mediated decay in the F5 gene 1-gen-2007 S. DugaN. LocatelliF. PeyvandiM.L. TenchiniR. Asselta + Article (author) -
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs 1-set-2021 Asselta R.Battezzati P. M.Cristoferi L.Lampertico P.Malinverno F.Mancuso C.Marra F.Massironi S.O'Donnell S.Ronca V.Valenti L.Zuin M. + Article (author) -
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis 11-giu-2019 Menegatti M.Asselta R.Duga S.Payvandi F. + 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) -
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 1-ago-1998 S. DugaR. AsseltaE. Scanziani + Article (author) -
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency 1-set-2009 S. SpenaR. AsseltaS. CacciaV. RimoldiF. PeyvandiS. Duga + Article (author) -