Your search returned 10 results.

Results
	1.	FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man. [electronic resource] by Barak, Hila Huh, Sung-Ho Chen, Shuang Jeanpierre, Cécile Martinovic, Jelena Parisot, Mélanie Bole-Feysot, Christine Nitschké, Patrick Salomon, Rémi Antignac, Corinne Ornitz, David M Kopan, Raphael Producer: 20120831 In: Developmental cell vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development. [electronic resource] by Gacem, Nadjet Kavo, Anthula Zerad, Lisa Richard, Laurence Mathis, Stephane Kapur, Raj P Parisot, Melanie Amiel, Jeanne Dufour, Sylvie de la Grange, Pierre Pingault, Veronique Vallat, Jean Michel Bondurand, Nadege Producer: 20200402 In: Nature communications vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population. [electronic resource] by Megahed, Hisham Nicouleau, Michaël Barcia, Giulia Medina-Cano, Daniel Siquier-Pernet, Karine Bole-Feysot, Christine Parisot, Mélanie Masson, Cécile Nitschké, Patrick Rio, Marlène Bahi-Buisson, Nadia Desguerre, Isabelle Munnich, Arnold Boddaert, Nathalie Colleaux, Laurence Cantagrel, Vincent Producer: 20171107 In: Orphanet journal of rare diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation. [electronic resource] by Buchbinder, David Stinson, Jeffrey R Nugent, Diane J Heurtier, Lucie Suarez, Felipe Sukumar, Gauthaman Dalgard, Clifton L Masson, Cécile Parisot, Mélanie Zhang, Yu Matthews, Helen F Su, Helen C Durandy, Anne Fischer, Alain Kracker, Sven Snow, Andrew L Producer: 20151125 In: The Journal of allergy and clinical immunology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome. [electronic resource] by Charbit-Henrion, Fabienne Jeverica, Anja K Bègue, Bernadette Markelj, Gasper Parlato, Marianna Avčin, Simona Lucija Callebaut, Isabelle Bras, Marc Parisot, Mélanie Jazbec, Janez Homan, Matjaz Ihan, Alojz Rieux-Laucat, Frédéric Stolzenberg, Marie-Claude Ruemmele, Frank M Avčin, Tadej Cerf-Bensussan, Nadine Producer: 20180104 In: Journal of pediatric gastroenterology and nutrition vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1). [electronic resource] by Heurtier, Lucie Lamrini, Hicham Chentout, Loïc Deau, Marie-Céline Bouafia, Amine Rosain, Jérémie Plaza, Jean-Marc Parisot, Mélanie Dumont, Benoit Turpin, Delphine Merlin, Etienne Moshous, Despina Aladjidi, Nathalie Neven, Bénédicte Picard, Capucine Cavazzana, Marina Fischer, Alain Durandy, Anne Stephan, Jean-Louis Kracker, Sven Producer: 20180907 In: Haematologica vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. [electronic resource] by Jeanpierre, Cécile Macé, Guillaume Parisot, Mélanie Morinière, Vincent Pawtowsky, Audrey Benabou, Marion Martinovic, Jelena Amiel, Jeanne Attié-Bitach, Tania Delezoide, Anne-Lise Loget, Philippe Blanchet, Patricia Gaillard, Dominique Gonzales, Marie Carpentier, Wassila Nitschke, Patrick Tores, Frédéric Heidet, Laurence Antignac, Corinne Salomon, Rémi Producer: 20111025 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans. [electronic resource] by Humbert, Camille Silbermann, Flora Morar, Bharti Parisot, Mélanie Zarhrate, Mohammed Masson, Cécile Tores, Frédéric Blanchet, Patricia Perez, Marie-José Petrov, Yuliya Khau Van Kien, Philippe Roume, Joelle Leroy, Brigitte Gribouval, Olivier Kalaydjieva, Luba Heidet, Laurence Salomon, Rémi Antignac, Corinne Benmerah, Alexandre Saunier, Sophie Jeanpierre, Cécile Producer: 20140331 In: American journal of human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Low Prevalence of GSC Gene Mutations in a Large Cohort of Predominantly Caucasian Patients with Hidradenitis Suppurativa. [electronic resource] by Duchatelet, Sabine Miskinyte, Snaigune Delage, Maia Ungeheuer, Marie-Noëlle Lam, Thi Benhadou, Farida Del Marmol, Véronique Vossen, Allard R J V Prens, Errol P Cogrel, Olivier Beylot-Barry, Marie Girard, Céline Vidil, Julien Join-Lambert, Olivier Parisot, Mélanie Nitschké, Patrick Hanein, Sylvain Fraitag, Sylvie Van der Zee, Hessel H Bessis, Didier Damiani, Giovanni Altomare, Andrea Liao, Yi-Hua Nikolakis, Georgios Zouboulis, Christos C Nassif, Aude Hovnanian, Alain Producer: 20210405 In: The Journal of investigative dermatology vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Defects in t [electronic resource] by Arrondel, Christelle Missoury, Sophia Snoek, Rozemarijn Patat, Julie Menara, Giulia Collinet, Bruno Liger, Dominique Durand, Dominique Gribouval, Olivier Boyer, Olivia Buscara, Laurine Martin, Gaëlle Machuca, Eduardo Nevo, Fabien Lescop, Ewen Braun, Daniela A Boschat, Anne-Claire Sanquer, Sylvia Guerrera, Ida Chiara Revy, Patrick Parisot, Mélanie Masson, Cécile Boddaert, Nathalie Charbit, Marina Decramer, Stéphane Novo, Robert Macher, Marie-Alice Ranchin, Bruno Bacchetta, Justine Laurent, Audrey Collardeau-Frachon, Sophie van Eerde, Albertien M Hildebrandt, Friedhelm Magen, Daniella Antignac, Corinne van Tilbeurgh, Herman Mollet, Géraldine Producer: 20200107 In: Nature communications vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)