ROSATI, JESSICA

ROSATI, JESSICA  

DIPARTIMENTO DI INFORMATICA, SISTEMISTICA E COMUNICAZIONE  

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Titolo Tipologia Data di pubblicazione Autori File
Generation and characterization of a patient-derived iPSC line, CSSi022-A (15666), with a pathogenic MFN2 mutation causing Charcot-Marie-Tooth disease type 2A 01 - Articolo su rivista 2025 Giovenale, Angela Maria GiadaTomaselli, SilviaRuotolo, GiorgiaVulcano, EdvigeFerrari, DanielaRosati, Jessica +
INTERROGATING ALS SIGNATURE IN EARLY NEURAL PROGENITOR CELLS: A DIFFERENT PERSPECTIVE 02 - Intervento a convegno 2025 Vulcano EdvigePerciballi ElisaLombardi IvanBovio FedericaMatilde ForcellaRosati JessicaFusi PaolaVescovi Angelo LuigiFerrari Daniela +
INTERROGATING ALS SIGNATURE IN HUMAN INDUCED NEURAL STEM CELLS 02 - Intervento a convegno 2025 Vulcano EdvigePerciballi ElisaLombardi IvanBovio FedericaMatilde ForcellaRosati JessicaFusi PaolaVescovi Angelo LuigiFerrari Daniela +
Investigating Primary Cilium Defects in Joubert Syndrome via iPSC-Derived Neural Stem Cells 02 - Intervento a convegno 2025 Ruotolo, GRosati, J +
Lysosomal Dysfunction in Amyotrophic Lateral Sclerosis: A Familial Case Linked to the p.G376D TARDBP Mutation 01 - Articolo su rivista 2025 Ruotolo, GiorgiaRosati, Jessica +
Mitochondrial and energy metabolism dysfunctions are hallmarks of TDP-43G376D fibroblasts from members of an Amyotrophic Lateral Sclerosis family 01 - Articolo su rivista 2025 Perciballi E.Bovio F.Ferro S.Forcella M.Rosati J.Innocenti M.Lombardi I.Vulcano E.Ruotolo G.Mercurio S.Vescovi A. L.Fusi P.Ferrari D. +
Neurogenesis in Smith-Magenis Syndrome: When Brain Development and Lipid Metabolism Go Awry 02 - Intervento a convegno 2025 Giovenale, AMGRosati, J. +
Production and characterization of different cellular models for studying ALS 02 - Intervento a convegno 2025 Ruotolo, GRosati, J
SMITH-MAGENIS SYNDROME: WHEN BRAIN DEVELOPMENT AND LIPID METALOMISM GO AWRY 02 - Intervento a convegno 2025 Giovenale AMGRosati J. +
A Look at Neurogenesis in Smith-Magenis Syndrome: What Goes Wrong? 02 - Intervento a convegno 2024 GIOVENALE, AMGRosati j. +
Exploring the metabolic signature of ALS patients-derived cells 02 - Intervento a convegno 2024 Vulcano EdvigePerciballi ElisaLombardi IvanBovio FedericaMatilde ForcellaRosati JessicaFusi PaolaVescovi Angelo LuigiFerrari Daniela +
Exploring the metabolic signature of Amyotrophic Lateral Sclerosis patients-derived cells 02 - Intervento a convegno 2024 Vulcano EdvigePerciballi ElisaFerro SaraLombardi IvanBovio FedericaMatilde ForcellaRosati JessicaFusi PaolaVescovi Angelo LuigiFerrari Daniela +
Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene 01 - Articolo su rivista 2024 Ruotolo, G.Ferrari, D.Lombardi, I.Vescovi, A. L.Rosati, J. +
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region 01 - Articolo su rivista 2024 Giovenale A. M. G.Vulcano E.Ferrari D.Rosati J. +
Uncovering primary cilium defects in Joubert Syndrome using iPSCs derived-Neural Stem Cells 02 - Intervento a convegno 2024 Ruotolo, GFerrari, DVescovi, ALRosati, J. +
Uno sguardo alla neurogenesi nella sindrome di Smith-Maghenis 02 - Intervento a convegno 2024 Giovenale, AMGRosati, j. +
Corrigendum: Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview 99 - Altro 2023 Giovenale, Angela Maria GiadaRuotolo, GiorgiaVescovi, Angelo LuigiRosati, Jessica +
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3 01 - Articolo su rivista 2022 Giovenale, Angela Maria GiadaVescovi, Angelo LuigiRosati, Jessica +
Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein 01 - Articolo su rivista 2022 Perciballi, ElisaRuotolo, GiorgiaFerrari, DanielaLombardi, IvanLuigi Vescovi, AngeloRosati, Jessica +
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease 01 - Articolo su rivista 2018 Rosati, JessicaFerrari, DanielaVescovi, Angelo Luigi +