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The Journal of Infectious Diseases|April 6, 2013
Genotoxic signature in cord blood cells of newborns exposed in utero to a Zidovudine-based antiretroviral combinationIsabelle André-Schmutz, Liliane Dal-Cortivo, Emmanuelle Six, et al.Proceedings of the National Academy of Sciences of the United States of America|June 24, 2025
PIK3CA gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effectQuitterie Venot, Marina Firpion, Sophia Ladraa, et al.Science Translational Medicine|October 6, 2021
Alpelisib administration reduced lymphatic malformations in a mouse model and in patientsFlorence Delestre, Quitterie Venot, Charles Bayard, et al.Brain Communications|November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformationsSandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.Blood|October 4, 2013
A Mendelian predisposition to B-cell lymphoma caused by IL-10R deficiencyBénédicte Neven, Emilie Mamessier, Julie Bruneau, et al.Signal Transduction and Targeted Therapy|June 16, 2024
Targeted therapy for capillary-venous malformationsLola Zerbib, Sophia Ladraa, Antoine Fraissenon, et al.The Journal of Experimental Medicine|September 15, 2023
Hemifacial myohyperplasia is due to somatic muscular PIK3CA gain-of-function mutations and responds to pharmacological inhibitionCharles Bayard, Eleonora Segna, Maxime Taverne, et al.Blood Advances|October 20, 2023
High PDL1/PDL2 gene expression correlates with worse outcome in primary mediastinal large B-cell lymphomaVincent Camus, Pierre-Julien Viailly, Fanny Drieux, et al.The Journal of Allergy and Clinical Immunology|June 16, 2018
PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defectsAurélie Berland, Jérémie Rosain, Sophie Kaltenbach, et al.Proceedings of the National Academy of Sciences of the United States of America|February 21, 2023
Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafishDeepak Khatri, Audrey Putoux, Audric Cologne, et al.Pageof 4