STRANIERO, LETIZIA

STRANIERO, LETIZIA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Risultati 1 - 14 di 14 (tempo di esecuzione: 0.008 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ : Design, Synthesis, and Structure Activity Relationships 1-set-2017 V. StranieroC. ZanottoL. StranieroA. CasiraghiS. DugaA. RadaelliC. De Giuli MorghenE. Valoti 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) -
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 1-gen-2017 L. StranieroV. RimoldiM. SamaraniA. Di FonzoM. AureliG. SoldàS. DugaR. Asselta + Article (author) -
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay 1-gen-2015 E.M. ParaboschiL. Straniero + Article (author) -
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations 13-lug-2020 Edoardo MonfriniDario RonchiGiulia FrancoLetizia StranieroFederica ArientiStefano DugaGiacomo Pietro ComiNereo Bresolin + Article (author) -
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1 28-feb-2018 F. PischeddaL. StranieroN. TicozziC. TilocaS. Duga + 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) -
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 1-mar-2019 Monfrini, EdoardoStraniero, LetiziaBonato, SaraMonzio Compagnoni, GiacomoBordoni, AndreinaRinchetti, PaolaSilipigni, RosamariaRonchi, DarioCorti, StefaniaComi, Giacomo P.Bresolin, NereoDuga, StefanoDi Fonzo, Alessio + Article (author) -
A novel homozygous VPS11 variant may cause generalized dystonia 1-gen-2021 Monfrini, EdoardoCogiamanian, FilippoSalani, SabrinaStraniero, LetiziaCarsana, EmmaBorellini, LindaBiella, FabioBresolin, NereoCorti, StefaniaDuga, StefanoComi, Giacomo PAureli, Massimo + Article (author) -
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 1-giu-2022 Straniero, LetiziaRimoldi, ValeriaMonfrini, EdoardoAureli, MassimoDuga, StefanoAsselta, Rosanna + Article (author) -
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 1-gen-2015 STRANIERO, LETIZIA + Article (author) -
UNRAVELING THE MOLECULAR COMPLEXITY OF PARKINSON¿S DISEASE: FROM GENETIC RISK FACTORS TO MENDELIAN CAUSATIVE GENES 26-giu-2017 STRANIERO, LETIZIA Doctoral Thesis -
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis 1-dic-2016 Straniero, LetiziaSoldà, GiuliaColombo, Carla + Article (author) -
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 29-lug-2022 Lunghi, GiuliaCarsana, Emma VeronicaLoberto, NicolettaPrioni, SimonaMauri, LauraBassi, RosariaDuga, StefanoStraniero, LetiziaAsselta, RosannaFrattini, EmanueleFerrari, ElenaAureli, Massimo + Article (author) -