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Last submissions
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Agnès Dubois, Loris Vincenti, Almira Chervova, Maxim Greenberg, Sandrine Vandormael-Pournin, et al.. H3K9 tri-methylation at Nanog times differentiation commitment and enables the acquisition of primitive endoderm fate. Development (Cambridge, England), 2022, 149 (17), pp.dev201074. ⟨10.1242/dev.201074⟩. ⟨pasteur-03796516v2⟩
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Rémi Duclaux-Loras, Corinne Lebreton, Jérémy Berthelet, Fabienne Charbit-Henrion, Ophélie Nicolle, et al.. UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking. Journal of Clinical Investigation, 2022, 132 (10), ⟨10.1172/JCI154997⟩. ⟨hal-03756921⟩
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Rafael Galupa, Christel Picard, Nicolas Servant, Elphège P Nora, Yinxiu Zhan, et al.. Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication. Development (Cambridge, England), 2022, 149 (9), pp.dev200568. ⟨10.1242/dev.200568⟩. ⟨hal-03746685⟩
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Sébastien Küry, Frédéric Ebstein, Alice Mollé, Thomas Besnard, Ming-Kang Lee, et al.. Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder. American Journal of Human Genetics, 2022, 109 (2), pp.361-372. ⟨10.1016/j.ajhg.2021.12.011⟩. ⟨hal-03661178⟩