ASSELTA, ROSANNA

ASSELTA, ROSANNA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

Risultati 1 - 17 di 17 (tempo di esecuzione: 0.039 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Autosomal recessive deficiency of coagulation factors 1-gen-2001 F. PeyvandiR. AsseltaP.M. Mannucci Article (author) -
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study 1-nov-2018 Elena SabaSolda GiuliaRosanna AsseltaStefano DugaCarlo SelmiNiccolò Bolli + 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) -
Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055)) 1-feb-2022 Asselta R.Zhang J.Battezzati P. M.Casella G.Colli A.Cristoferi L.Lampertico P.Malinverno F.Mancuso C.Marra F.Massironi S.Miele L.O'Donnell S.Ronca V.Valenti L.Zuin M.Mori A.Tanaka T.Lotta L. A.Levi S.Bell A. + Article (author) -
Factor V deficiency 1-giu-2009 R. AsseltaF. Peyvandi Article (author) -
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 1-mar-2014 V. RimoldiL. StranieroR. AsseltaG. Soldà + Article (author) -
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 1-dic-2011 E.M. ParaboschiG. SoldàS. DugaR. Asselta + Article (author) -
Genetic background and risk of postpartum haemorrhage : results from an Italian cohort of 3219 women 1-nov-2014 F. FranchiR. AsseltaF. Peyvandi + Article (author) -
Genetica del comportamento 1-gen-2001 DEL GIACCO LucaASSELTA ROSANNASTRUMBO BICE Book (translator) -
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome 1-giu-2014 G. SoldàM. RobustoU. AmbrosettiR. AsseltaS. Duga + Conference Object -
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) -
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) -
Mutational screening and Zebrafish functional analysis of Gigyf2 as a Parkinson-disease gene 1-nov-2009 I. GuellaA. PistocchiR. AsseltaV. RimoldiA. GhilardiL. Del GiaccoS. Duga + Conference Object -
Newtonian to non-newtonian fluid transition of a model transient network 1-mag-2018 Nava, GiovanniParaboschi, Elvezia MariaAsselta, RosannaBellini, Tommaso + Article (author) -
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 1-lug-2020 Paraboschi, Elvezia MariaPeyvandi, FloraMenegatti, MarziaAsselta, RosannaDuga, Stefano + Article (author) -
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 9-mar-2022 Straniero, LetiziaRimoldi, ValeriaMonfrini, EdoardoAureli, MassimoDuga, StefanoAsselta, Rosanna + Article (author) -
Understanding genetic variation in the CFTR gene by next-generation sequencing 1-set-2013 G. SoldàC. ColomboR. AsseltaS. Duga + Conference Object -