GRAZIOLI, PAOLO

GRAZIOLI, PAOLO  

Dipartimento di Scienze della Salute  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency 2023 Oleari, RobertoLettieri, AntonellaManzini, StefanoPaganoni, AlyssaGrazioli, PaoloBusnelli, MarcoAmoruso, FedericaVezzoli, ValeriaMassa, ValentinaCariboni, Anna + Article (author) -
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies 2022 Di Fede, ElisabettaGrazioli, PaoloColombo, Elisa AdeleAncona, SilviaPriori, AlbertoGervasini, CristinaMassa, Valentina + Article (author) -
KMT2A : umbrella gene for multiple diseases 2022 Castiglioni, SilviaDi Fede, ElisabettaBernardelli, ClaraLettieri, AntonellaParodi, ChiaraGrazioli, PaoloColombo, Elisa AdeleAncona, SilviaOttaviano, EmerenzianaBorghi, ElisaMassa, ValentinaGhelma, FilippoVignoli, AglaiaLesma, ElenaGervasini, Cristina + Article (author) -
IN VITRO AND IN VIVO MODELLING OF CORNELIA DE LANGE SYNDROME CAUSATIVE MUTATIONS: WNT ACTIVATION AS A POSSIBLE THERAPEUTIC APPROACH 2021 GRAZIOLI, PAOLO Doctoral Thesis -
Insights into the role of the microbiota and of short-chain fatty acids in Rubinstein–Taybi syndrome 2021 Di Fede E.Ottaviano E.Grazioli P.Ceccarani C.Galeone A.Parodi C.Colombo E. A.Bassanini G.Milani D.Verduci E.Vaccari T.Massa V.Borghi E.Gervasini C. + Article (author) -
Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome 2021 Grazioli P.Parodi C.Bottai D.Di Fede E.Zulueta A.Avagliano L.Tenconi R.Adami R.Vaccari T.Gervasini C.Massa V. + Article (author) -
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies 2021 Parodi, ChiaraDi Fede, ElisabettaPeron, AngelaViganò, IlariaGrazioli, PaoloCastiglioni, SilviaGervasini, CristinaVignoli, AglaiaMassa, Valentina + Article (author) -
Chromatinopathies: a focus on Cornelia de Lange Syndrome 2020 Avagliano, LauraParenti, IlariaGrazioli, PaoloDi Fede, ElisabettaParodi, ChiaraMariani, MilenaGervasini, CristinaMassa, Valentina + Article (author) -
Microbial colonization during early phases of amphibian life 2019 G. BassaniniF. Di RenzoV. MassaC. CeccaraniP. GrazioliR. BacchettaE. OttavianoE. MenegolaE. Borghi Conference Object -
Modeling Cornelia de Lange Syndrome in vitro and in vivo reveals a role for cohesin complex in neuronal survival and differentiation 2019 Daniele BottaiMarco SpreaficoAnna PistocchiRaffaella AdamiPaolo GrazioliAdriana CanuSilvia RigamontiChiara ParodiFranco CotelliValentina Massa + Article (author) -
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes 2019 Grazioli, PaoloVaccari, ThomasMassa, Valentina + Article (author) -
Dynamic acetylation profile during mammalian neurulation 2019 Massa, ValentinaAvagliano, LauraGrazioli, PaoloParodi, ChiaraBulfamante, Gaetano + Article (author) -
Drosophila melanogaster as a model to study WNT pathway alteration in Cornelia de Lange Syndrome 2018 Paolo GrazioliCristina GervasiniThomas VaccariValentina Massa + Conference Object -
Modulating the WNT pathway in Drosophila models of Cornelia de Lange Syndrome 2018 P. GrazioliT. VaccariV. Massa Conference Object -
Cornelia de Lange Syndrome: different models and strategies to study the disease 2018 Grazioli PaoloBottai DanielePistocchi AnnaVaccari ThomasMassa Valentina + Conference Object -
Lithium as a positive modulator of defective WNT pathway in Cornelia de Lange Syndrome models 2018 Chiara ParodiPaolo GrazioliDaniele BottaiElisabetta Di FedeThomas VaccariCristina GervasiniValentina Massa Conference Object -
Rings and bricks : Expression of cohesin components is dynamic during development and adult life 2018 P. GrazioliG. CazzanigaL. LarizzaV. Massa + Article (author) -
Modulating the WNT pathway in Drosophila models of Cornelia de Lange Syndrome 2017 P. GrazioliC. GervasiniT. VaccariV. Massa + Conference Object -
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome 2017 L. AvaglianoP. GrazioliMARIANI, MILENAG.P. BulfamanteV. Massa + Article (author) -