Multiclass Sparse Bayesian Regression for fMRI-Based Prediction

Por Michel, Vincent, Eger, Evelyn, Keribin, Christine, Thirion, Bertrand
Publicado em 2011

Coupling of the mechanotransduction machinery and F-actin polymerization in the cochlear hair bundles

Por Caberlotto, Elisa, Michel, Vincent, de Monvel, Jacques Boutet, Petit, Christine
Publicado em 2011

Total variation regularization for fMRI-based prediction of behavior

Por Michel, Vincent, Gramfort, Alexandre, Varoquaux, Gaël, Eger, Evelyn, Thirion, Bertrand
Publicado em 2011

Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

Por Bahloul, Amel, Michel, Vincent, Hardelin, Jean-Pierre, Nouaille, Sylvie, Hoos, Sylviane, Houdusse, Anne, England, Patrick, Petit, Christine
Publicado em 2010

Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

Por Cohen-Salmon, Martine, Ott, Thomas, Michel, Vincent, Hardelin, Jean-Pierre, Perfettini, Isabelle, Eybalin, Michel, Wu, Tao, Marcus, Daniel C., Wangemann, Philine, Willecke, Klaus, Petit, Christine
Publicado em 2002

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth

Por Lelli, Andrea, Michel, Vincent, Boutet de Monvel, Jacques, Cortese, Matteo, Bosch-Grau, Montserrat, Aghaie, Asadollah, Perfettini, Isabelle, Dupont, Typhaine, Avan, Paul, El-Amraoui, Aziz, Petit, Christine
Publicado no J Cell Biol (2016)

Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells

Por Bahloul, Amel, Simmler, Marie-Christine, Michel, Vincent, Leibovici, Michel, Perfettini, Isabelle, Roux, Isabelle, Weil, Dominique, Nouaille, Sylvie, Zuo, Jian, Zadro, Cristina, Licastro, Danilo, Gasparini, Paolo, Avan, Paul, Hardelin, Jean-Pierre, Petit, Christine
Publicado em 2009

An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells

Por Kamiya, Kazusaku, Michel, Vincent, Giraudet, Fabrice, Riederer, Brigitte, Foucher, Isabelle, Papal, Samantha, Perfettini, Isabelle, Le Gal, Sébastien, Verpy, Elisabeth, Xia, Weiliang, Seidler, Ursula, Georgescu, Maria-Magdalena, Avan, Paul, El-Amraoui, Aziz, Petit, Christine
Publicado em 2014

The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells

Por Pepermans, Elise, Michel, Vincent, Goodyear, Richard, Bonnet, Crystel, Abdi, Samia, Dupont, Typhaine, Gherbi, Souad, Holder, Muriel, Makrelouf, Mohamed, Hardelin, Jean-Pierre, Marlin, Sandrine, Zenati, Akila, Richardson, Guy, Avan, Paul, Bahloul, Amel, Petit, Christine
Publicado em 2014

Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

Por 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
Publicado em 2009

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

Por Caberlotto, Elisa, Michel, Vincent, Foucher, Isabelle, Bahloul, Amel, Goodyear, Richard J., Pepermans, Elise, Michalski, Nicolas, Perfettini, Isabelle, Alegria-Prévot, Olinda, Chardenoux, Sébastien, Do Cruzeiro, Marcio, Hardelin, Jean-Pierre, Richardson, Guy P., Avan, Paul, Weil, Dominique, Petit, Christine
Publicado em 2011

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

Por Sahly, Iman, Dufour, Eric, Schietroma, Cataldo, Michel, Vincent, Bahloul, Amel, Perfettini, Isabelle, Pepermans, Elise, Estivalet, Amrit, Carette, Diane, Aghaie, Asadollah, Ebermann, Inga, Lelli, Andrea, Iribarne, Maria, Hardelin, Jean-Pierre, Weil, Dominique, Sahel, José-Alain, El-Amraoui, Aziz, Petit, Christine
Publicado em 2012

Human adenylate kinase 2 deficiency causes a profound haematopoietic defect associated with sensorineural deafness

Por Lagresle-Peyrou, Chantal, Six, Emmanuelle M., Picard, Capucine, Rieux-Laucat, Frédéric, Michel, Vincent, Ditadi, Andrea, Chappedelaine, Corinne Demerens-de, Morillon, Estelle, Valensi, Françoise, Simon-Stoos, Karen L., Mullikin, James C., Noroski, Lenora M., Besse, Céline, Wulffraat, Nicolas M., Ferster, Alina, Abecasis, Manuel M., Calvo, Fabien, Petit, Christine, Candotti, Fabio, Abel, Laurent, Fischer, Alain, Cavazzana-Calvo, Marina
Publicado em 2008

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

Por Potter, Paul K., Bowl, Michael R., Jeyarajan, Prashanthini, Wisby, Laura, Blease, Andrew, Goldsworthy, Michelle E., Simon, Michelle M., Greenaway, Simon, Michel, Vincent, Barnard, Alun, Aguilar, Carlos, Agnew, Thomas, Banks, Gareth, Blake, Andrew, Chessum, Lauren, Dorning, Joanne, Falcone, Sara, Goosey, Laurence, Harris, Shelley, Haynes, Andy, Heise, Ines, Hillier, Rosie, Hough, Tertius, Hoslin, Angela, Hutchison, Marie, King, Ruairidh, Kumar, Saumya, Lad, Heena V., Law, Gemma, MacLaren, Robert E., Morse, Susan, Nicol, Thomas, Parker, Andrew, Pickford, Karen, Sethi, Siddharth, Starbuck, Becky, Stelma, Femke, Cheeseman, Michael, Cross, Sally H., Foster, Russell G., Jackson, Ian J., Peirson, Stuart N., Thakker, Rajesh V., Vincent, Tonia, Scudamore, Cheryl, Wells, Sara, El-Amraoui, Aziz, Petit, Christine, Acevedo-Arozena, Abraham, Nolan, Patrick M., Cox, Roger, Mallon, Anne-Marie, Brown, Steve D. M.
Publicado no Nat Commun (2016)