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	1.	Altering a histone H3K4 methylation pathway in glomerular podocytes promotes a chronic disease phenotype. [electronic resource] by Lefevre, Gaelle M Patel, Sanjeevkumar R Kim, Doyeob Tessarollo, Lino Dressler, Gregory R Producer: 20110307 In: PLoS genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mapping of long-range INS promoter interactions reveals a role for calcium-activated chloride channel ANO1 in insulin secretion. [electronic resource] by Xu, Zhixiong Lefevre, Gaelle M Gavrilova, Oksana Foster St Claire, Mark B Riddick, Gregory Felsenfeld, Gary Producer: 20150420 In: Proceedings of the National Academy of Sciences of the United States of America vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Human Argonaute 2 Is Tethered to Ribosomal RNA through MicroRNA Interactions. [electronic resource] by Atwood, Blake L Woolnough, Jessica L Lefevre, Gaelle M Saint Just Ribeiro, Mariana Felsenfeld, Gary Giles, Keith E Producer: 20170512 In: The Journal of biological chemistry vol. 291 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss. [electronic resource] by Dahmani, Malika Ammar-Khodja, Fatima Bonnet, Crystel Lefèvre, Gaelle M Hardelin, Jean-Pierre Ibrahim, Hassina Mallek, Zahia Petit, Christine Producer: 20160425 In: Orphanet journal of rare diseases vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. [electronic resource] by Verpy, Elisabeth Weil, Dominique Leibovici, Michel Goodyear, Richard J Hamard, Ghislaine Houdon, Carine Lefèvre, Gaelle M Hardelin, Jean-Pierre Richardson, Guy P Avan, Paul Petit, Christine Producer: 20081124 In: Nature vol. 456 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells. [electronic resource] by Michalski, Nicolas Michel, Vincent Caberlotto, Elisa Lefèvre, Gaelle M van Aken, Alexander F J Tinevez, Jean-Yves Bizard, Emilie Houbron, Christophe Weil, Dominique Hardelin, Jean-Pierre Richardson, Guy P Kros, Corné J Martin, Pascal Petit, Christine Producer: 20100108 In: Pflugers Archiv : European journal of physiology vol. 459 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. [electronic resource] by Bonnet, Crystel Riahi, Zied Chantot-Bastaraud, Sandra Smagghe, Luce Letexier, Mélanie Marcaillou, Charles Lefèvre, Gaëlle M Hardelin, Jean-Pierre El-Amraoui, Aziz Singh-Estivalet, Amrit Mohand-Saïd, Saddek Kohl, Susanne Kurtenbach, Anne Sliesoraityte, Ieva Zobor, Ditta Gherbi, Souad Testa, Francesco Simonelli, Francesca Banfi, Sandro Fakin, Ana Glavač, Damjan Jarc-Vidmar, Martina Zupan, Andrej Battelino, Saba Martorell Sampol, Loreto Claveria, Maria Antonia Catala Mora, Jaume Dad, Shzeena Møller, Lisbeth B Rodriguez Jorge, Jesus Hawlina, Marko Auricchio, Alberto Sahel, José-Alain Marlin, Sandrine Zrenner, Eberhart Audo, Isabelle Petit, Christine Producer: 20170711 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)