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2016


121 publication(s):

Note: when necessary, only the first 5 authors are displayed.

Articles

81 - 
Ptbp1 and Exosc9 knockdowns trigger skin stability defects through different pathways
Maud Noiret, Stéphanie Mottier, Gaelle Angrand, Carole Gautier-Courteille, Hubert Lerivray et al.
Developmental Biology, 2016, 409 (2), pp.489-501.
DOI : https://doi.org/10.1016/j.ydbio.2015.11.002
Pubmed : 26546114
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82 - 
Amy2B copy number variation reveals starch diet adaptation in ancient European dogs
Morgane Ollivier, Anne Tresset, Fabiola Bastian, Laëtitia Lagoutte, Erik Axelsson et al.
Royal Society Open Science, 2016, 3 (11), pp.160449.
DOI : https://doi.org/10.1098/rsos.160449
Pubmed : 28018628
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83 - 
IgA Structure Variations Associate with Immune Stimulations and IgA Mesangial Deposition
Zéliha Oruc, Christelle Oblet, Ahmed Boumédiène, Anne Druilhe, Virginie Pascal et al.
Journal of the American Society of Nephrology, 2016, 27 (9), pp.2748-2761.
DOI : https://doi.org/10.1681/ASN.2015080911
Pubmed : 26825533
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84 - 
A glucose-starvation response regulates the diffusion of macromolecules
Ryan P. Joyner, Jeffrey H. Tang, Jonne Helenius, Elisa Dultz, Christiane Brune et al.
eLife, 2016, 5, pp.e09376. ⟨10.7554/eLife.09376⟩.
DOI : https://doi.org/10.7554/eLife.09376
Pubmed : 27003290
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85 - 
Protein folding activity of the ribosome: Key player in yeast prion propagation
Cecile P. Voisset, Marc Blondel, Flavie Soubigou, Justine Evrard, Phu Hai Nguyen et al.
Prion, 2016, 10 (sup1), pp.S24--S25.
DOI : https://doi.org/10.1080/19336896.2016.1163103
Pubmed : 27088809
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86 - 
Changes in Gene Expression and Estrogen Receptor Cistrome in Mouse Liver Upon Acute E2 Treatment
Gaëlle Palierne, Aurelie J Fabre, Romain Solinhac, Christine Le Peron, Stéphane Avner et al.
Molecular Endocrinology -Baltimore-, 2016, 30 (7), pp.709-732.
DOI : https://doi.org/10.1210/me.2015-1311
Pubmed : 27164166
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87 - 
Expanding the clinical spectrum of the "HDAC8-phenotype" - Implications for molecular diagnostics, counselling and risk prediction
Ilaria Parenti, Cristina Gervasini, Jelena Pozojevic, Kerstin S. Wendt, Erwan Watrin et al.
Clinical Genetics, 2016, 89 (5), pp.564-573.
DOI : https://doi.org/10.1111/cge.12717
Pubmed : 26671848
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88 - 
Broadening of cohesinopathies: Exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype
Ilaria Parenti, Cristina Gervasini, Jelena Pozojevic, Luitgard Graul-Neumann, Jacopo Azzollini et al.
Clinical Epigenetics, 2016, 89 (1), pp.74-81.
DOI : https://doi.org/10.1111/cge.12564
Pubmed : 25652421
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89 - 
Karyotype is not dead (yet)!
Laurent Pasquier, Mélanie Fradin, Elouan Chérot, Dominique Martin-Coignard, Estelle Colin et al.
European Journal of Medical Genetics, 2016, 59 (1), pp.11-15.
DOI : https://doi.org/10.1016/j.ejmg.2015.11.016
Pubmed : 26691665
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90 - 
A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
Jocelyn Plassais, Laetitia Lagoutte, Solenne Correard, Manon Paradis, Eric Guaguère et al.
PLoS Genetics, 2016, 12 (12), pp.e1006482.
DOI : https://doi.org/10.1371/journal.pgen.1006482
Pubmed : 28033318
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