TALEN-Induced Double-Strand Break Repair of CTG Trinucleotide Repeats
Mosbach, Valentine, Poggi, Lucie, Viterbo, David, Charpentier, Marine, Richard, Guy-Franck
Published in Cell reports (Cambridge) (20.02.2018)
Published in Cell reports (Cambridge) (20.02.2018)
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Journal Article
Resection and repair of a Cas9 double-strand break at CTG trinucleotide repeats induces local and extensive chromosomal deletions
Mosbach, Valentine, Viterbo, David, Descorps-Declère, Stéphane, Poggi, Lucie, Vaysse-Zinkhöfer, Wilhelm, Richard, Guy-Franck
Published in PLoS genetics (16.07.2020)
Published in PLoS genetics (16.07.2020)
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Journal Article
Activated PI3Kinase Delta Syndrome—A Multifaceted Disease
Thouenon, Romane, Moreno-Corona, Nidia, Poggi, Lucie, Durandy, Anne, Kracker, Sven
Published in Frontiers in pediatrics (25.06.2021)
Published in Frontiers in pediatrics (25.06.2021)
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Journal Article
Time-resolved microfluidics unravels individual cellular fates during double-strand break repair
Vertti-Quintero, Nadia, Levien, Ethan, Poggi, Lucie, Amir, Ariel, Richard, Guy-Franck, Baroud, Charles N
Published in BMC biology (05.12.2022)
Published in BMC biology (05.12.2022)
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Journal Article
Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K Signaling
Moreno-Corona, Nidia, Chentout, Loïc, Poggi, Lucie, Thouenon, Romane, Masson, Cecile, Parisot, Melanie, Mouel, Lou Le, Picard, Capucine, André, Isabelle, Cavazzana, Marina, Perrin, Laurence, Durandy, Anne, Azarnoush, Saba, Kracker, Sven
Published in Frontiers in pediatrics (24.06.2021)
Published in Frontiers in pediatrics (24.06.2021)
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Journal Article
Alternative DNA Structures In Vivo : Molecular Evidence and Remaining Questions
Poggi, Lucie, Richard, Guy-Franck
Published in Microbiology and molecular biology reviews (17.02.2021)
Published in Microbiology and molecular biology reviews (17.02.2021)
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Journal Article
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency: A neomorphic variant in IRF4 alters transcriptional activity
Thouenon, Romane, Chentout, Loïc, Moreno-Corona, Nidia, Poggi, Lucie, Lombardi, Emilia Puig, Hoareau, Benedicte, Schmitt, Yohann, Lagresle-Peyrou, Chantal, Bustamante, Jacinta Cecilia, André, Isabelle, Cavazzana, Marina, Durandy, Anne, Casanova, Jean-Laurent, Galicier, Lionel, Fadlallah, Jehane, Fischer, Alain, Kracker, Sven
Published in The Journal of experimental medicine (05.06.2023)
Published in The Journal of experimental medicine (05.06.2023)
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Journal Article
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency
Thouenon, Romane, Chentout, Loïc, Moreno-Corona, Nidia, Poggi, Lucie, Lombardi, Emilia Puig, Hoareau, Benedicte, Schmitt, Yohann, Lagresle-Peyrou, Chantal, Bustamante, Jacinta, André, Isabelle, Cavazzana, Marina, Durandy, Anne, Casanova, Jean-Laurent, Galicier, Lionel, Fadlallah, Jehane, Fischer, Alain, Kracker, Sven
Published in The Journal of experimental medicine (05.06.2023)
Published in The Journal of experimental medicine (05.06.2023)
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Journal Article
Rescuing the cytolytic function of APDS1 patient T cells via TALEN-mediated PIK3CD gene correction
Poggi, Lucie, Chentout, Loïc, Lizot, Sabrina, Boyne, Alex, Juillerat, Alexandre, Moiani, Arianna, Luka, Marine, Carbone, Francesco, Ménager, Mickael, Cavazzana, Marina, Duchateau, Philippe, Valton, Julien, Kracker, Sven
Published in Molecular therapy. Methods & clinical development (14.12.2023)
Published in Molecular therapy. Methods & clinical development (14.12.2023)
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Journal Article
USE OF THE F359L MISSENSE IRF4 VARIANT FOR INCREASING THE STABILITY OF REGULATORY T CELLS
THOUENON, Romane, KRACKER, Sven, ZUBER, Julien, AYAS, Nicolas, CHARBONNIER, Soëli, POGGI, Lucie
Year of Publication 14.12.2023
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Year of Publication 14.12.2023
Patent
GENE THERAPY FOR THE TREATMENT OF ACTIVATED PI3KINASE DELTA SYNDROME TYPE 1 (APDS1)
JUILLERAT, Alexandre, VALTON, Julien, KRACKER, Sven, CAVAZZANA, Marina, DUCHATEAU, Philippe, BOYNE, Alex, POGGI, Lucie
Year of Publication 16.11.2023
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Year of Publication 16.11.2023
Patent
GENE THERAPY FOR THE TREATMENT OF ACTIVATED PI3KINASE DELTA SYNDROME TYPE 1 (APDS1)
JUILLERAT, Alexandre, VALTON, Julien, KRACKER, Sven, CAVAZZANA, Marina, DUCHATEAU, Philippe, BOYNE, Alex, POGGI, Lucie
Year of Publication 15.11.2023
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Year of Publication 15.11.2023
Patent
Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K Signaling
Moreno-Corona, Nidia, Chentout, Loïc, Poggi, Lucie, Thouenon, Romane, Masson, Cecile, Parisot, Melanie, Mouel, Lou Le, Picard, Capucine, André, Isabelle, Cavazzana, Marina, Perrin, Laurence, Durandy, Anne, Azarnoush, Saba, Kracker, Sven
Published in Frontiers in pediatrics (01.01.2021)
Published in Frontiers in pediatrics (01.01.2021)
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