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	1.	Biochemical and NMR mapping of the interface between CREB-binding protein and ligand binding domains of nuclear receptor: beyond the LXXLL motif. [electronic resource] by Klein, Fabrice A C Atkinson, R Andrew Potier, Noelle Moras, Dino Cavarelli, Jean Producer: 20050418 In: The Journal of biological chemistry vol. 280 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Huntingtin affinity for partners is not changed by polyglutamine length: aggregation itself triggers aberrant interactions. [electronic resource] by Davranche, Aurélien Aviolat, Hubert Zeder-Lutz, Gabrielle Busso, Didier Altschuh, Danièle Trottier, Yvon Klein, Fabrice A C Producer: 20111011 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mammalian ataxin-2 modulates translation control at the pre-initiation complex via PI3K/mTOR and is induced by starvation. [electronic resource] by Lastres-Becker, Isabel Nonis, David Eich, Florian Klinkenberg, Michael Gorospe, Myriam Kötter, Peter Klein, Fabrice A C Kedersha, Nancy Auburger, Georg Producer: 20190128 In: Biochimica et biophysica acta vol. 1862 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Linear and extended: a common polyglutamine conformation recognized by the three antibodies MW1, 1C2 and 3B5H10. [electronic resource] by Klein, Fabrice A C Zeder-Lutz, Gabrielle Cousido-Siah, Alexandra Mitschler, André Katz, Aline Eberling, Pascal Mandel, Jean-Louis Podjarny, Alberto Trottier, Yvon Producer: 20140422 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pathogenic and non-pathogenic polyglutamine tracts have similar structural properties: towards a length-dependent toxicity gradient. [electronic resource] by Klein, Fabrice A C Pastore, Annalisa Masino, Laura Zeder-Lutz, Gabrielle Nierengarten, Hélène Oulad-Abdelghani, Mustapha Altschuh, Danièle Mandel, Jean-Louis Trottier, Yvon Producer: 20070920 In: Journal of molecular biology vol. 371 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	SynAggreg: A Multifunctional High-Throughput Technology for Precision Study of Amyloid Aggregation and Systematic Discovery of Synergistic Inhibitor Compounds. [electronic resource] by Aviolat, Hubert Nominé, Yves Gioria, Sophie Bonhoure, Anna Hoffmann, David Ruhlmann, Christine Nierengarten, Hélène Ruffenach, Frank Villa, Pascal Trottier, Yvon Klein, Fabrice A C Producer: 20190926 In: Journal of molecular biology vol. 430 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Structure of a single-chain Fv bound to the 17 N-terminal residues of huntingtin provides insights into pathogenic amyloid formation and suppression. [electronic resource] by De Genst, Erwin Chirgadze, Dimitri Y Klein, Fabrice A C Butler, David C Matak-Vinković, Dijana Trottier, Yvon Huston, James S Messer, Anne Dobson, Christopher M Producer: 20150723 In: Journal of molecular biology vol. 427 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Ataxin-7 is a subunit of GCN5 histone acetyltransferase-containing complexes. [electronic resource] by Helmlinger, Dominique Hardy, Sara Sasorith, Souphatta Klein, Fabrice Robert, Flavie Weber, Chantal Miguet, Laurent Potier, Noëlle Van-Dorsselaer, Alain Wurtz, Jean-Marie Mandel, Jean-Louis Tora, Làszlò Devys, Didier Producer: 20041222 In: Human molecular genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. [electronic resource] by Mallaret, Martial Synofzik, Matthis Lee, Jaeho Sagum, Cari A Mahajnah, Muhammad Sharkia, Rajech Drouot, Nathalie Renaud, Mathilde Klein, Fabrice A C Anheim, Mathieu Tranchant, Christine Mignot, Cyril Mandel, Jean-Louis Bedford, Mark Bauer, Peter Salih, Mustafa A Schüle, Rebecca Schöls, Ludger Aldaz, C Marcelo Koenig, Michel Producer: 20140411 In: Brain : a journal of neurology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy. [electronic resource] by Böhm, Johann Biancalana, Valérie Dechene, Elizabeth T Bitoun, Marc Pierson, Christopher R Schaefer, Elise Karasoy, Hatice Dempsey, Melissa A Klein, Fabrice Dondaine, Nicolas Kretz, Christine Haumesser, Nicolas Poirson, Claire Toussaint, Anne Greenleaf, Rebecca S Barger, Melissa A Mahoney, Lane J Kang, Peter B Zanoteli, Edmar Vissing, John Witting, Nanna Echaniz-Laguna, Andoni Wallgren-Pettersson, Carina Dowling, James Merlini, Luciano Oldfors, Anders Bomme Ousager, Lilian Melki, Judith Krause, Amanda Jern, Christina Oliveira, Acary S B Petit, Florence Jacquette, Aurélia Chaussenot, Annabelle Mowat, David Leheup, Bruno Cristofano, Michele Poza Aldea, Juan José Michel, Fabrice Furby, Alain Llona, Jose E Barcena Van Coster, Rudy Bertini, Enrico Urtizberea, Jon Andoni Drouin-Garraud, Valérie Béroud, Christophe Prudhon, Bernard Bedford, Melanie Mathews, Katherine Erby, Lori A H Smith, Stephen A Roggenbuck, Jennifer Crowe, Carol A Brennan Spitale, Allison Johal, Sheila C Amato, Anthony A Demmer, Laurie A Jonas, Jessica Darras, Basil T Bird, Thomas D Laurino, Mercy Welt, Selman I Trotter, Cynthia Guicheney, Pascale Das, Soma Mandel, Jean-Louis Beggs, Alan H Laporte, Jocelyn Producer: 20120906 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)