Search Results - "Valsoni, Sara"
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SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome
Published in Nature communications (08-12-2020)“…Hutchinson-Gilford progeria syndrome is a genetic disease caused by an aberrant form of Lamin A resulting in chromatin structure disruption, in particular by…”
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Identification of a retinoic acid-dependent haemogenic endothelial progenitor from human pluripotent stem cells
Published in Nature cell biology (01-05-2022)“…The generation of haematopoietic stem cells (HSCs) from human pluripotent stem cells (hPSCs) is a major goal for regenerative medicine. During embryonic…”
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Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines
Published in Skeletal muscle (08-12-2016)“…hTERT/cdk4 immortalized myogenic human cell lines represent an important tool for skeletal muscle research, being used as therapeutically pertinent models of…”
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Durable and efficient gene silencing in vivo by hit-and-run epigenome editing
Published in Nature (London) (14-03-2024)“…Permanent epigenetic silencing using programmable editors equipped with transcriptional repressors holds great promise for the treatment of human diseases 1 –…”
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Dysfunctional polycomb transcriptional repression contributes to lamin A/C-dependent muscular dystrophy
Published in The Journal of clinical investigation (01-05-2020)“…Lamin A is a component of the inner nuclear membrane that, together with epigenetic factors, organizes the genome in higher order structures required for…”
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DNA damage contributes to neurotoxic inflammation in Aicardi-Goutières syndrome astrocytes
Published in The Journal of experimental medicine (04-04-2022)“…Aberrant induction of type I IFN is a hallmark of the inherited encephalopathy Aicardi-Goutières syndrome (AGS), but the mechanisms triggering disease in the…”
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Altered peritumoral microRNA expression predicts head and neck cancer patients with a high risk of recurrence
Published in Modern pathology (01-10-2017)“…Head and neck squamous cell carcinoma is typically characterized by a high incidence of local recurrences. It has been extensively shown that mucosa from head…”
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PI3K Inhibitors Curtail MYC-Dependent Mutant p53 Gain-of-Function in Head and Neck Squamous Cell Carcinoma
Published in Clinical cancer research (15-06-2020)“…Mutation of gene is a hallmark of head and neck squamous cell carcinoma (HNSCC) not yet exploited therapeutically. mutation frequently leads to the synthesis…”
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In Vitro Selection of Engineered Transcriptional Repressors for Targeted Epigenetic Silencing
Published in Journal of visualized experiments (05-05-2023)“…Gene inactivation is instrumental to study gene function and represents a promising strategy for the treatment of a broad range of diseases. Among traditional…”
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CD32 captures committed haemogenic endothelial cells during human embryonic development
Published in Nature cell biology (01-05-2024)“…During embryonic development, blood cells emerge from specialized endothelial cells, named haemogenic endothelial cells (HECs). As HECs are rare and only…”
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Identification of a retinoic acid-dependent hemogenic endothelial progenitor from human pluripotent stem cells
Published in Nature cell biology (28-04-2022)Get full text
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A bioinformatics pipeline to uncover regulatory modules and their condition-specific regulators in human monocyte-to-macrophages differentiation and polarization
Published in Frontiers in immunology (2013)“…Abstract only…”
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