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Derniers dépôts
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Mojdeh Dormishian, Gulen Turkeri, K. Urayama, Thu Lan Nguyen, Mounia Boulberdaa, et al.. Prokineticin receptor-1 is a new regulator of endothelial insulin uptake and capillary formation to control insulin sensitivity and cardiovascular and kidney functions. Journal of the American Heart Association, 2013, 2 (5), Non spécifié. ⟨10.1161/JAHA.113.000411⟩. ⟨hal-03404074⟩
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Yannick-Noël Anno, Evelyne Myslinski, Richard Patryk Ngondo-Mbongo, Alain Krol, Olivier Poch, et al.. Genome-wide evidence for an essential role of the human Staf/ZNF143 transcription factor in bidirectional transcription.. Nucleic Acids Research, 2010, epub ahead of print. ⟨10.1093/nar/gkq1301⟩. ⟨hal-00561392⟩
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Aileen Bar, Virginie Marchand, Georges Khoury, Natacha Dreumont, Annie Mougin, et al.. Structural and functional analysis of the Rous Sarcoma virus negative regulator of splicing and demonstration of its activation by the 9G8 SR protein. Nucleic Acids Research, 2011, 39 (8), pp.3388-3403. ⟨10.1093/nar/gkq1114⟩. ⟨hal-02270591⟩
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Benjamin Albert, Isabelle Léger-Silvestre, Christophe Normand, Martin K Ostermaier, Jorge Pérez-Fernández, et al.. RNA polymerase I-specific subunits promote polymerase clustering to enhance the rRNA gene transcription cycle.. Journal of Cell Biology, 2011, 192 (2), pp.277-93. ⟨10.1083/jcb.201006040⟩. ⟨hal-00667459⟩
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Mohamed Mlih, Lionel Host, S. Martin, Nathalie Niederhoffer, Laurent Monassier, et al.. The Src Homology and Collagen A (ShcA) adaptor protein is required for the spatial organization of the costamere/Z-disk network during heart development. Journal of Biological Chemistry, 2015, 290 (4), pp.2419-2430. ⟨10.1074/jbc.M114.597377⟩. ⟨hal-01111660⟩
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Emmanuel Moutier, Tao Ye, Mohamed-Amin Choukrallah, Sylvia Urban, Judit Osz, et al.. Retinoic acid receptors recognise the mouse genome through binding elements with diverse spacing and topology.. Journal of Biological Chemistry, 2012, 287 (31), pp.26328-26341. ⟨10.1074/jbc.M112.361790⟩. ⟨hal-00720090⟩
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U. Kristensen, Alexey Epanchintsev, Marc-Alexander Rauschendorf, Vincent Laugel, Tinna Stevnsner, et al.. Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress. Proceedings of the National Academy of Sciences of the United States of America, 2013, 110 (25), pp.E2261-E2270. ⟨10.1073/pnas.1220071110⟩. ⟨hal-03542283⟩
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Chantal Sellier, Fernande Freyermuth, Ricardos Tabet, Tuan Tran, Fang He, et al.. Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome. Cell Reports, 2013, 3 (3), pp.869-880. ⟨10.1016/j.celrep.2013.02.004⟩. ⟨hal-03339569⟩
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Christel Depienne, Caroline Nava, Boris Keren, Solveig Heide, Agnès Rastetter, et al.. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU. Human Genetics, 2017, 136 (4), pp.463-479. ⟨10.1007/s00439-017-1772-0⟩. ⟨hal-01502135⟩
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Viorica Chelban, Henriette Aksnes, Reza Maroofian, Lauren C Lamonica, Luis Seabra, et al.. Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. Nature Communications, 2024, 15 (1), pp.2269. ⟨10.1038/s41467-024-46354-0⟩. ⟨hal-04905283⟩
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Majid Pahlevan Kakhki, Antonino Giordano, Chiara Starvaggi Cucuzza, Tejaswi Venkata S. Badam, Samudyata Samudyata, et al.. A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis. Nature Communications, 2024, 15 (1), pp.6419. ⟨10.1038/s41467-024-50794-z⟩. ⟨hal-04896573⟩
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