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	1.	Defective prolactin signaling impairs pancreatic β-cell development during the perinatal period. [electronic resource] by Auffret, Julien Freemark, Michael Carré, Nadège Mathieu, Yves Tourrel-Cuzin, Cécile Lombès, Marc Movassat, Jamileh Binart, Nadine Producer: 20140123 In: American journal of physiology. Endocrinology and metabolism vol. 305 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Membrane responses induced by oligogalacturonides in suspension-cultured tobacco cells. [electronic resource] by Mathieu, Yves Armen, Kurkdjian Xia, Hua Guern, Jean Koller, Alan Spiro, Mark D O'Neill, Malcolm Albersheim, Peter Darvill, Alan Publication details: The Plant journal : for cell and molecular biology Nov 1991 In: The Plant journal : for cell and molecular biology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Comparing targeted exome and whole exome approaches for genetic diagnosis of neuromuscular disorders. [electronic resource] by Gorokhova, Svetlana Cerino, Mathieu Mathieu, Yves Courrier, Sébastien Desvignes, Jean-Pierre Salgado, David Béroud, Christophe Krahn, Martin Bartoli, Marc Producer: 20160407 In: Applied & translational genomics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	In Vitro studies of non poly alanine PHOX2B mutations argue against a loss-of-function mechanism for congenital central hypoventilation. [electronic resource] by Trochet, Delphine Mathieu, Yves Pontual, Loïc de Savarirayan, Ravi Munnich, Arnold Brunet, Jean-François Lyonnet, Stanislas Goridis, Christo Amiel, Jeanne Producer: 20090410 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Contributions of PHOX2B in the pathogenesis of Hirschsprung disease. [electronic resource] by Fernández, Raquel María Mathieu, Yves Luzón-Toro, Berta Núñez-Torres, Rocío González-Meneses, Antonio Antiñolo, Guillermo Amiel, Jeanne Borrego, Salud Producer: 20130802 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse). [electronic resource] by Trochet, Delphine de Pontual, Loïc Estêvao, Maria Helena Mathieu, Yves Munnich, Arnold Feingold, J Goridis, Christo Lyonnet, Stanislas Amiel, Jeanne Producer: 20080821 In: Human mutation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Wnt glycoproteins regulate the expression of FoxN1, the gene defective in nude mice. [electronic resource] by Balciunaite, Gina Keller, Marcel P Balciunaite, Egle Piali, Luca Zuklys, Saulius Mathieu, Yves D Gill, Jason Boyd, Richard Sussman, Daniel J Holländer, Georg A Producer: 20021204 In: Nature immunology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells. [electronic resource] by Barthélémy, Florian Blouin, Cédric Wein, Nicolas Mouly, Vincent Courrier, Sébastien Dionnet, Eugénie Kergourlay, Virginie Mathieu, Yves Garcia, Luis Butler-Browne, Gillian Lamaze, Christophe Lévy, Nicolas Krahn, Martin Bartoli, Marc Publication details: Journal of neuromuscular diseases Sep 2015 In: Journal of neuromuscular diseases vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing. [electronic resource] by Sevy, Amandine Cerino, Mathieu Gorokhova, Svetlana Dionnet, Eugénie Mathieu, Yves Verschueren, Annie Franques, Jérôme Maues de Paula, André Figarella-Branger, Dominique Lagarde, Arnaud Desvignes, Jean Pierre Béroud, Christophe Attarian, Shahram Levy, Nicolas Bartoli, Marc Krahn, Martin Campana-Salort, Emmanuelle Pouget, Jean Producer: 20160627 In: Journal of neurology, neurosurgery, and psychiatry vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome. [electronic resource] by de Pontual, Loïc Mathieu, Yves Golzio, Christelle Rio, Marlène Malan, Valérie Boddaert, Nathalie Soufflet, Christine Picard, Capucine Durandy, Anne Dobbie, Angus Heron, Delphine Isidor, Bertrand Motte, Jacques Newburry-Ecob, Ruth Pasquier, Laurent Tardieu, Marc Viot, Géraldine Jaubert, Francis Munnich, Arnold Colleaux, Laurence Vekemans, Michel Etchevers, Heather Lyonnet, Stanislas Amiel, Jeanne Producer: 20090706 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)