Presentation
Mégane Brusson received her Ph.D. in Genomes and Proteins in 2017 from Paris Diderot University. In Wassim El Nemer’s lab, she studied the role of JAK2V617F mutation and treatments by hydroxycarbamide and interferon-α on erythroid and endothelial abnormalities in Polycythemia Vera. From 2017-18, she was a lecturer at Versailles-Saint-Quentin-En-Yvelines University in Bernard Mignotte’s lab where she taught Genetics and studied the role of mitochondria in Rb-induced apoptosis in Drosophila. She joined the lab of Dr. Annarita Miccio in May 2018, where she developed a novel lentiviral vector, carrying gene addition and gene silencing functions, for gene therapy of β-hemoglobinopathies. Since 2020, she co-supervises the PhD project of Anne Chalumeau who aims to elaborate a universal genome editing approach for β-hemoglobinopathies using the prime editing technology. Finally, she is currently studying the gene expression signature at single cell level of erythroblast precursors from β-hemoglobinopathy patients to identify novel therapeutic targets.
Resources & publications
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Journal (source)Prog Mol Biol Transl Sci
Genome editing approaches to β-hemoglobinopathies.
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Journal (source)Nat Commun
Base-editing-mediated dissection of a γ-globin cis-regulatory element for the...
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Journal (source)Mol Ther Nucleic Acids
Novel lentiviral vectors for gene therapy of sickle cell disease combining ge...
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Journal (source)Stem Cells Transl Med
CRISPRthripsis: The Risk of CRISPR/Cas9-induced Chromothripsis in Gene Therapy.
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Journal (source)Mol Ther
Combination of lentiviral and genome editing technologies for the treatment o...
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Journal (source)Front Genome Ed
Base and Prime Editing Technologies for Blood Disorders.