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2016

International refereed journal articles

31 - 

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).

 

32 - 

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

 

33 - 

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

 

34 - 

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

 

35 - 

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

 

36 - 

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

 

37 - 

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

 

38 - 

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

 

39 - 

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

 

40 - 

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