STRANIERO, LETIZIA

STRANIERO, LETIZIA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 2022 Straniero L.Rimoldi V.Monfrini E.Aureli M.Duga S.Asselta R. + Article (author) -
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 2022 Lunghi, GiuliaCarsana, Emma VeronicaLoberto, NicolettaPrioni, SimonaMauri, LauraBassi, RosariaDuga, StefanoStraniero, LetiziaAsselta, RosannaFrattini, EmanueleFerrari, ElenaAureli, Massimo + Article (author) -
A novel homozygous VPS11 variant may cause generalized dystonia 2021 Monfrini, EdoardoCogiamanian, FilippoSalani, SabrinaStraniero, LetiziaCarsana, EmmaBorellini, LindaBiella, FabioBresolin, NereoCorti, StefaniaDuga, StefanoComi, Giacomo PAureli, Massimo + Article (author) -
Screening of LRP10 mutations in Parkinson's disease patients from Italy 2021 Straniero L.Monfrini E.Vizziello M.Rimoldi V.Corti S.Comi G. P.Duga S. + Article (author) -
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations 2020 Edoardo MonfriniDario RonchiGiulia FrancoLetizia StranieroFederica ArientiStefano DugaGiacomo Pietro ComiNereo Bresolin + Article (author) -
The SPID-GBA study: Sex distribution, penetrance, incidence, and dementia in GBA-PD 2020 Straniero L.Asselta R.Rimoldi V.Aureli M.Duga S. + Article (author) -
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 2019 Monfrini, EdoardoStraniero, LetiziaBonato, SaraMonzio Compagnoni, GiacomoBordoni, AndreinaRinchetti, PaolaSilipigni, RosamariaRonchi, DarioCorti, StefaniaComi, Giacomo P.Bresolin, NereoDuga, StefanoDi Fonzo, Alessio + Article (author) -
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest 2018 Samarani, MauraLoberto, NicolettaSoldà, GiuliaStraniero, LetiziaAsselta, RosannaDuga, StefanoLunghi, GiuliaZucca, Fabio AMauri, LauraCiampa, Maria GraziaSchiumarini, DomitillaBassi, RosariaGiussani, PaolaChiricozzi, ElenaPrinetti, AlessandroAureli, MassimoSonnino, Sandro Article (author) -
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1 2018 F. PischeddaL. StranieroN. TicozziC. TilocaS. Duga + Article (author) -
UNRAVELING THE MOLECULAR COMPLEXITY OF PARKINSON¿S DISEASE: FROM GENETIC RISK FACTORS TO MENDELIAN CAUSATIVE GENES 2017 STRANIERO, LETIZIA Doctoral Thesis -
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 2017 L. StranieroV. RimoldiM. SamaraniA. Di FonzoM. AureliG. SoldàS. DugaR. Asselta + Article (author) -
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ : Design, Synthesis, and Structure Activity Relationships 2017 V. StranieroC. ZanottoL. StranieroA. CasiraghiS. DugaA. RadaelliC. De Giuli MorghenE. Valoti Article (author) -
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis 2016 Straniero, LetiziaSoldà, GiuliaColombo, Carla + Article (author) -
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 2015 STRANIERO, LETIZIA + Article (author) -
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay 2015 E.M. ParaboschiL. Straniero + Article (author) -
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 2014 V. RimoldiL. StranieroR. AsseltaG. Soldà + Article (author) -