Browsing by Author "Venturi, Veronica"

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  • CoDysAn: A telemedicine tool to improve awareness and diagnosis for patients with congenital dyserythropoietic anemia
    Tornador Antolin, Cristian, 1979-; Sánchez Prados, Edgar; Cadenas, Beatriz; Russo, Roberta; Venturi, Veronica; Andolfo, Immacolata; Hernández Rodriguez, Ines; Iolascon, Achille; Sánchez, Mayka (Frontiers, 2019)
    Congenital Dyserythropoietic Anemia (CDA) is a heterogeneous group of hematological disorders characterized by chronic hyporegenerative anemia and distinct morphological abnormalities of erythroid precursors in the bone ...
  • Distinct recruitment of human eIF4E isoforms to processing bodies and stress granules
    Frydryskova, Klara; Masek, Tomas; Borcin, Katerina; Mrvova, Silvia; Venturi, Veronica; Pospíšek, Martin (BioMed Central, 2016)
    Background: Eukaryotic translation initiation factor 4E (eIF4E) plays a pivotal role in the control of cap-dependent translation initiation, modulates the fate of specific mRNAs, occurs in processing bodies (PBs) and is ...
  • Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levels.
    Rué, Laura; Bañez Coronel, Mónica; Creus-Muncunill, Jordi; Giralt, Albert; Alcalá-Vida, Rafael; Mentxaka, Gartze; Kagerbauer, Birgit; Zomeño-Abellán, M. Teresa; Aranda, Zeus; Venturi, Veronica; Pérez-Navarro, Esther; Estivill, Xavier, 1955-; Martí, Eulàlia (American Society for Clinical Investigation, 2016)
    Huntington's disease (HD) is a polyglutamine disorder caused by a CAG expansion in the Huntingtin (HTT) gene exon 1. This expansion encodes a mutant protein whose abnormal function is traditionally associated with HD ...

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