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Open Access Repository.
2016
121 publication(s):Note: when necessary, only the first 15 authors are displayed.International refereed journal articles
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RNA sequencing analysis of Celf1 mouse mutants identifies a cohort of abnormally expressed lens development regulators
- Archana D. Siddam, Deepti Anand, Luc Paillard, Salil Anil Lachke
- Investigative Ophthalmology & Visual Science, 2016, 57 (12).
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Wild-type VHL Clear Cell Renal Cell Carcinomas Are a Distinct Clinical and Histologic Entity: A 10-Year Follow-up
- Julien Dagher, Solene-Florence Kammerer-Jacquet, Angélique Brunot, Adélaide Pladys, Jean-Jacques Patard, Karim Bensalah, Christophe Perrin, Gregory Verhoest, Jean Mosser, Alexandra Lespagnol, Cécile Vigneau, Frédéric Dugay, Marc-Antoine Belaud-Rotureau, Nathalie Rioux-Leclercq
- European Urology Focus, 2016, 1 (3), pp.284-290.
- DOI : https://doi.org/10.1016/j.euf.2015.06.001
- Pubmed : 28723401
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Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis
- L. Davignon, C. Chauveau, C. Julien, C. Dill, L. Duband-Goulet, E. Cabet, B. Buendia, A. Lilienbaum, J. Rendu, M. Minot, A. Guichet, V. Allamand, N. Vadrot, J. Faure, S. Odent et al.
- Neuromuscular Disorders, 2016, 26 (suppl 2), pp.S118--S119.
- DOI : https://doi.org/10.1016/j.nmd.2016.06.121
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The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease
- Laurianne Davignon, Claire Chauveau, Cédric Julien, Corinne Dill, Isabelle Duband-Goulet, Eva Cabet, Brigitte Buendia, Alain Lilienbaum, John Rendu, Marie-Christine Minot, Agnès Guichet, Valérie Allamand, Nathalie Vadrot, Julien Fauré, Sylvie Odent et al.
- Human Molecular Genetics, 2016, 25 (8), pp.1559--1573.
- DOI : https://doi.org/10.1093/hmg/ddw033
- Pubmed : 27008887
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Rationally rewiring the connectivity of the XylR/Pu regulatory node of the m-xylene degradation pathway in Pseudomonas putida
- Aitor De Las Heras, Esteban Martínez-García, Maria Rosa Domingo-Sananes, Sofia Fraile, Víctor De Lorenzo
- Integrative biology, 2016, 8 (4), pp.571-576.
- DOI : https://doi.org/10.1039/c5ib00310e
- Pubmed : 26961967
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Flexibility vs. robustness in cell cycle regulation of timing of M-phase entry in Xenopus laevis embryo cell-free extract
- Mateusz Debowski, Mohammed El Dika, Jacek Malejczyk, Robert Zdanowski, Claude Prigent, Jean-Pierre Tassan, Malgorzata Kloc, Miroslaw Lachowicz, Jacek Z. Kubiak
- International Journal of Developmental Biology, 2016, 60 (7-9), pp.305--314.
- DOI : https://doi.org/10.1387/ijdb.160134jk
- Pubmed : 27759157
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Single Wavelength Excitation Dual Color Flim for Multiplexing Genetically Encoded FRET Biosensors
- Claire Demeautis, François Sipieter, Julien Roul, Catherine Chapuis, Sergi Padilla-Parra, Franck Riquet, Marc Tramier
- Biophysical Journal, 2016, 110 (3), pp.518a.
- DOI : https://doi.org/10.1016/j.bpj.2015.11.2771
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An improved non-denaturing method for the purification of spiralin, the main membrane lipoprotein of the pathogenic bacteria Spiroplasma melliferum
- Yann Desfougeres, Jean-Michel Poitou, Henri Wróblewski, Laure Beven
- Journal of Chromatography B - Analytical Technologies in the Biomedical and Life Sciences, 2016, 1036-1037, pp.149-156.
- DOI : https://doi.org/10.1016/j.jchromb.2016.10.012
- Pubmed : 27760404
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Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway
- Christèle Dubourg, Wilfrid Carré, Houda Hamdi-Rozé, Charlotte Mouden, Joëlle Roume, Benmansour Abdelmajid, Daniel Amram, Clarisse Baumann, Nicolas Chassaing, Christine Coubes, Laurence Faivre-Olivier, Emmanuelle Ginglinger, Marie Gonzales, Annie Levy-Mozziconacci, Sally-Ann Lynch et al.
- Human Mutation, 2016, 37 (12), pp.1329-1339.
- DOI : https://doi.org/10.1002/humu.23038
- Pubmed : 27363716
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Large national series of patients with Xq28 duplication involving MECP2: Delineation of brain MRI abnormalities in 30 affected patients
- Salima El Chehadeh, Laurence Faivre, Anne-Laure Mosca-Boidron, Valérie Malan, Jeanne Amiel, Mathilde Nizon, Renaud Touraine, Fabienne Prieur, Laurent Pasquier, Patrick Callier, Mathilde Lefebvre, Nathalie Marle, Christèle Dubourg, Sophie Julia, Catherine Sarret et al.
- American Journal of Medical Genetics Part A, 2016, 170 (1), pp.116-129.
- DOI : https://doi.org/10.1002/ajmg.a.37384
- Pubmed : 26420639
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