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The -KTS splice variant of WT1 is essential for ovarian determination in mice.
Gregoire EP, De Cian MC, Migale R, Perea-Gomez A, Schaub S, Bellido-Carreras N, Stévant I, Mayère C, Neirijnck Y, Loubat A, Rivaud P, Sopena ML, Lachambre S, Linssen MM, Hohenstein P, Lovell-Badge R, Nef S, Chalmel F, Schedl A, Chaboissier MC. Gregoire EP, et al. Among authors: loubat a. Science. 2023 Nov 3;382(6670):600-606. doi: 10.1126/science.add8831. Epub 2023 Nov 2. Science. 2023. PMID: 37917714 Free PMC article.
Self-demixing of mRNA copies buffers mRNA:mRNA and mRNA:regulator stoichiometries.
Cardona AH, Ecsedi S, Khier M, Yi Z, Bahri A, Ouertani A, Valero F, Labrosse M, Rouquet S, Robert S, Loubat A, Adekunle D, Hubstenberger A. Cardona AH, et al. Among authors: loubat a. Cell. 2023 Sep 28;186(20):4310-4324.e23. doi: 10.1016/j.cell.2023.08.018. Epub 2023 Sep 12. Cell. 2023. PMID: 37703874
New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte Dehydration.
Allegrini B, Jedele S, David Nguyen L, Mignotet M, Rapetti-Mauss R, Etchebest C, Fenneteau O, Loubat A, Boutet A, Thomas C, Durin J, Petit A, Badens C, Garçon L, Da Costa L, Guizouarn H. Allegrini B, et al. Among authors: loubat a. Front Physiol. 2022 Aug 8;13:918620. doi: 10.3389/fphys.2022.918620. eCollection 2022. Front Physiol. 2022. PMID: 36003639 Free PMC article.
Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Runge K, Mathieu R, Bugeon S, Lafi S, Beurrier C, Sahu S, Schaller F, Loubat A, Herault L, Gaillard S, Pallesi-Pocachard E, Montheil A, Bosio A, Rosenfeld JA, Hudson E, Lindstrom K, Mercimek-Andrews S, Jeffries L, van Haeringen A, Vanakker O, Van Hecke A, Amrom D, Küry S, Ratner C, Jethva R, Gamble C, Jacq B, Fasano L, Santpere G, Lorente-Galdos B, Sestan N, Gelot A, Giacuzz S, Goebbels S, Represa A, Cardoso C, Cremer H, de Chevigny A. Runge K, et al. Among authors: loubat a. Mol Psychiatry. 2021 Dec;26(12):7852. doi: 10.1038/s41380-021-01234-7. Mol Psychiatry. 2021. PMID: 34282265 Free PMC article. No abstract available.
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Runge K, Mathieu R, Bugeon S, Lafi S, Beurrier C, Sahu S, Schaller F, Loubat A, Herault L, Gaillard S, Pallesi-Pocachard E, Montheil A, Bosio A, Rosenfeld JA, Hudson E, Lindstrom K, Mercimek-Andrews S, Jeffries L, van Haeringen A, Vanakker O, Van Hecke A, Amrom D, Küry S, Ratner C, Jethva R, Gamble C, Jacq B, Fasano L, Santpere G, Lorente-Galdos B, Sestan N, Gelot A, Giacuzz S, Goebbels S, Represa A, Cardoso C, Cremer H, de Chevigny A. Runge K, et al. Among authors: loubat a. Mol Psychiatry. 2021 Nov;26(11):6125-6148. doi: 10.1038/s41380-021-01179-x. Epub 2021 Jun 29. Mol Psychiatry. 2021. PMID: 34188164 Free PMC article.
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