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	1.	The SWI/SNF protein BAF60b is ubiquitinated through a signalling process involving Rac GTPase and the RING finger protein Unkempt. [electronic resource] by Lorès, Patrick Visvikis, Orane Luna, Rosa Lemichez, Emmanuel Gacon, Gérard Producer: 20100416 In: The FEBS journal vol. 277 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Activated Rac1, but not the tumorigenic variant Rac1b, is ubiquitinated on Lys 147 through a JNK-regulated process. [electronic resource] by Visvikis, Orane Lorès, Patrick Boyer, Laurent Chardin, Pierre Lemichez, Emmanuel Gacon, Gérard Producer: 20080319 In: The FEBS journal vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	BAF60A mediates interactions between the microphthalmia-associated transcription factor and the BRG1-containing SWI/SNF complex during melanocyte differentiation. [electronic resource] by Aras, Shweta Saladi, Srinivas Vinod Basuroy, Tupa Marathe, Himangi G Lorès, Patrick de la Serna, Ivana L Producer: 20200505 In: Journal of cellular physiology vol. 234 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse. [electronic resource] by Lorès, Patrick Vernet, Nadège Kurosaki, Tomohiro Van de Putte, Tom Huylebroeck, Danny Hikida, Masaki Gacon, Gérard Touré, Aminata Producer: 20140326 In: Developmental biology vol. 386 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	In-vitro effects of Thymus munbyanus essential oil and thymol on human sperm motility and function. [electronic resource] by Chikhoune, Amirouche Stouvenel, Laurence Iguer-Ouada, Mokrane Hazzit, Mohamed Schmitt, Alain Lorès, Patrick Wolf, Jean Philippe Aissat, Kamel Auger, Jacques Vaiman, Daniel Touré, Aminata Producer: 20160617 In: Reproductive biomedicine online vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse. [electronic resource] by El Khouri, Elma Whitfield, Marjorie Stouvenel, Laurence Kini, Archana Riederer, Brigitte Lores, Patrick Roemermann, Dorothee di Stefano, Gabriella Drevet, Joël R Saez, Fabrice Seidler, Ursula Touré, Aminata Producer: 20191021 In: Molecular reproduction and development vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Escherichia coli producing CNF1 toxin hijacks Tollip to trigger Rac1-dependent cell invasion. [electronic resource] by Visvikis, Orane Boyer, Laurent Torrino, Stéphanie Doye, Anne Lemonnier, Marc Lorès, Patrick Rolando, Monica Flatau, Gilles Mettouchi, Amel Bouvard, Daniel Veiga, Esteban Gacon, Gérard Cossart, Pascale Lemichez, Emmanuel Producer: 20110714 In: Traffic (Copenhagen, Denmark) vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation. [electronic resource] by Rode, Baptiste Dirami, Thassadite Bakouh, Naziha Rizk-Rabin, Marthe Norez, Caroline Lhuillier, Pierre Lorès, Patrick Jollivet, Mathilde Melin, Patricia Zvetkova, Ilona Bienvenu, Thierry Becq, Frédéric Planelles, Gabrielle Edelman, Aleksander Gacon, Gérard Touré, Aminata Producer: 20120807 In: Human molecular genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction. [electronic resource] by Petre, Graciane Lorès, Patrick Sartelet, Hervé Truffot, Aurélie Poreau, Brice Brandeis, Sandrine Martinez, Guillaume Satre, Véronique Harbuz, Radu Ray, Pierre F Amblard, Florence Devillard, Françoise Vieville, Gaëlle Berger, Francois Jouk, Pierre-Simon Vaiman, Daniel Touré, Aminata Coutton, Charles Bidart, Marie Producer: 20191114 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse. [electronic resource] by Dong, Frederick N Amiri-Yekta, Amir Martinez, Guillaume Saut, Antoine Tek, Julie Stouvenel, Laurence Lorès, Patrick Karaouzène, Thomas Thierry-Mieg, Nicolas Satre, Véronique Brouillet, Sophie Daneshipour, Abbas Hosseini, Seyedeh Hanieh Bonhivers, Mélanie Gourabi, Hamid Dulioust, Emmanuel Arnoult, Christophe Touré, Aminata Ray, Pierre F Zhao, Haiqing Coutton, Charles Producer: 20181211 In: American journal of human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility. [electronic resource] by El Khouri, Elma Thomas, Lucie Jeanson, Ludovic Bequignon, Emilie Vallette, Benoit Duquesnoy, Philippe Montantin, Guy Copin, Bruno Dastot-Le Moal, Florence Blanchon, Sylvain Papon, Jean François Lorès, Patrick Yuan, Li Collot, Nathalie Tissier, Sylvie Faucon, Catherine Gacon, Gérard Patrat, Catherine Wolf, Jean Philippe Dulioust, Emmanuel Crestani, Bruno Escudier, Estelle Coste, André Legendre, Marie Touré, Aminata Amselem, Serge Producer: 20170509 In: American journal of human genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Corrigendum: Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. [electronic resource] by Lorès, Patrick Coutton, Charles Khouri, Elma El Stouvenel, Laurence Givelet, Maëlle Thomas, Lucie Rode, Baptiste Schmitt, Alain Louis, Bruno Sakheli, Zeinab Chaudhry, Marhaba Fernandez-Gonzales, Angeles Mitsialis, Alex Dacheux, Denis Wolf, Jean-Philippe Papon, Jean-François Gacon, Gérard Escudier, Estelle Arnoult, Christophe Bonhivers, Mélanie Savinov, Sergey N Amselem, Serge Ray, Pierre F Dulioust, Emmanuel Touré, Aminata Publication details: Human molecular genetics 03 2019 In: Human molecular genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. [electronic resource] by Lorès, Patrick Coutton, Charles El Khouri, Elma Stouvenel, Laurence Givelet, Maëlle Thomas, Lucie Rode, Baptiste Schmitt, Alain Louis, Bruno Sakheli, Zeinab Chaudhry, Marhaba Fernandez-Gonzales, Angeles Mitsialis, Alex Dacheux, Denis Wolf, Jean-Philippe Papon, Jean-François Gacon, Gérard Escudier, Estelle Arnoult, Christophe Bonhivers, Mélanie Savinov, Sergey N Amselem, Serge Ray, Pierre F Dulioust, Emmanuel Touré, Aminata Producer: 20190130 In: Human molecular genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility. [electronic resource] by Lorès, Patrick Dacheux, Denis Kherraf, Zine-Eddine Nsota Mbango, Jean-Fabrice Coutton, Charles Stouvenel, Laurence Ialy-Radio, Come Amiri-Yekta, Amir Whitfield, Marjorie Schmitt, Alain Cazin, Caroline Givelet, Maëlle Ferreux, Lucile Fourati Ben Mustapha, Selima Halouani, Lazhar Marrakchi, Ouafi Daneshipour, Abbas El Khouri, Elma Do Cruzeiro, Marcio Favier, Maryline Guillonneau, François Chaudhry, Marhaba Sakheli, Zeinab Wolf, Jean-Philippe Patrat, Catherine Gacon, Gérard Savinov, Sergey N Hosseini, Seyedeh Hanieh Robinson, Derrick R Zouari, Raoudha Ziyyat, Ahmed Arnoult, Christophe Dulioust, Emmanuel Bonhivers, Mélanie Ray, Pierre F Touré, Aminata Producer: 20200402 In: American journal of human genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human. [electronic resource] by Coutton, Charles Vargas, Alexandra S Amiri-Yekta, Amir Kherraf, Zine-Eddine Ben Mustapha, Selima Fourati Le Tanno, Pauline Wambergue-Legrand, Clémentine Karaouzène, Thomas Martinez, Guillaume Crouzy, Serge Daneshipour, Abbas Hosseini, Seyedeh Hanieh Mitchell, Valérie Halouani, Lazhar Marrakchi, Ouafi Makni, Mounir Latrous, Habib Kharouf, Mahmoud Deleuze, Jean-François Boland, Anne Hennebicq, Sylviane Satre, Véronique Jouk, Pierre-Simon Thierry-Mieg, Nicolas Conne, Beatrice Dacheux, Denis Landrein, Nicolas Schmitt, Alain Stouvenel, Laurence Lorès, Patrick El Khouri, Elma Bottari, Serge P Fauré, Julien Wolf, Jean-Philippe Pernet-Gallay, Karin Escoffier, Jessica Gourabi, Hamid Robinson, Derrick R Nef, Serge Dulioust, Emmanuel Zouari, Raoudha Bonhivers, Mélanie Touré, Aminata Arnoult, Christophe Ray, Pierre F Producer: 20180919 In: Nature communications vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)