Search Results - "Fathinajafabadi, Alihamze"

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    Reactive Glia-Derived Neuroinflammation: a Novel Hallmark in Lafora Progressive Myoclonus Epilepsy That Progresses with Age by Lahuerta, Marcos, Gonzalez, Daymé, Aguado, Carmen, Fathinajafabadi, Alihamze, García-Giménez, José Luis, Moreno-Estellés, Mireia, Romá-Mateo, Carlos, Knecht, Erwin, Pallardó, Federico V., Sanz, Pascual

    Published in Molecular neurobiology (01-03-2020)
    “…Lafora disease (LD) is a rare, fatal form of progressive myoclonus epilepsy. The molecular basis of this devastating disease is still poorly understood, and no…”
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    Journal Article
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    Eukaryotic Initiation Factor 5A2 localizes to actively translating ribosomes to promote cancer cell protrusions and invasive capacity by Martínez-Férriz, Arantxa, Gandía, Carolina, Pardo-Sánchez, José Miguel, Fathinajafabadi, Alihamze, Ferrando, Alejandro, Farràs, Rosa

    Published in Cell communication and signaling (13-03-2023)
    “…Eukaryotic Initiation Factor 5A (eIF-5A), an essential translation factor, is post-translationally activated by the polyamine spermidine. Two human genes…”
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    Journal Article
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    Ubiquitin-Regulated Cell Proliferation and Cancer by Pérez-Benavente, Beatriz, Nasresfahani, Alihamze Fathinajafabadi, Farràs, Rosa

    “…Ubiquitin ligases (E3) play a crucial role in the regulation of different cellular processes such as proliferation and differentiation via recognition,…”
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    CERKL, a retinal disease gene, encodes an mRNA-binding protein that localizes in compact and untranslated mRNPs associated with microtubules by Fathinajafabadi, Alihamze, Pérez-Jiménez, Eva, Riera, Marina, Knecht, Erwin, Gonzàlez-Duarte, Roser

    Published in PloS one (03-02-2014)
    “…The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its…”
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    Journal Article
  6. 6

    Ubiquitin-mediated mechanisms of translational control by Martínez-Férriz, Arantxa, Ferrando, Alejandro, Fathinajafabadi, Alihamze, Farràs, Rosa

    Published in Seminars in cell & developmental biology (01-12-2022)
    “…mRNAs translation to proteins constitutes an important step of cellular gene expression that is highly regulated in response to different extracellular stimuli…”
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  7. 7

    CERKL, a retinal disease gene,encodes an mRNA-biding protein that localizes in compact and unstranslated mRNPs associated to microtubules by Fathinajafabadi, Alihamze, Pérez-Jiménez, Eva, Riera, Marina, Knecht, Erwin, Gonzàlez-Duarte, Roser

    Published in PloS one (03-02-2014)
    “…The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its…”
    Get full text
    Journal Article
  8. 8

    CERKL, a Retinal Disease Gene, Encodes an mRNA-Binding Protein That Localizes in Compact and Untranslated mRNPs Associated with Microtubules: e87898 by Fathinajafabadi, Alihamze, Perez-Jimenez, Eva, Riera, Marina, Knecht, Erwin, Gonzalez-Duarte, Roser

    Published in PloS one (01-02-2014)
    “…The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its…”
    Get full text
    Journal Article