Molecular organization and function of vertebrate septate-like junctions

Autor: Faivre-Sarrailh, Catherine

Publikováno v: In BBA - Biomembranes 1 May 2020 1862(5)

The Glycosylphosphatidyl Inositol-Anchored Adhesion Molecule F3/Contactin Is Required for Surface Transport of Paranodin/Contactin-Associated Protein (caspr)

Autor: Faivre-Sarrailh, Catherine, Gauthier, France, Denisenko-Nehrbass, Natalia, Le Bivic, André, Rougon, Geneviève, Girault, Jean-Antoine

Publikováno v: The Journal of Cell Biology, 2000 Apr . 149(2), 491-501.

Externí odkaz: https://www.jstor.org/stable/1619705

Pioneering Axons Regulate Neuronal Polarization in the Developing Cerebral Cortex

Autor: Namba, Takashi, Kibe, Yuji, Funahashi, Yasuhiro, Nakamuta, Shinichi, Takano, Tetsuya, Ueno, Takuji, Shimada, Akiko, Kozawa, Sachi, Okamoto, Mayumi, Shimoda, Yasushi, Oda, Kanako, Wada, Yoshino, Masuda, Tomoyuki, Sakakibara, Akira, Igarashi, Michihiro, Miyata, Takaki, Faivre-Sarrailh, Catherine, Takeuchi, Kosei, Kaibuchi, Kozo

Publikováno v: In Neuron 19 February 2014 81(4):814-829

GPI-anchored proteins at the node of Ranvier

Autor: Labasque, Marilyne, Faivre-Sarrailh, Catherine

Publikováno v: In FEBS Letters 2010 584(9):1787-1792

Fetal bovine serum impacts the observed N‐glycosylation defects in TMEM165 KO HEK cells

Autor: Climer, Leslie, Morelle, Willy, De Bettignies, Geoffroy, Krzewinski Recchi, Marie-Ange, Lupashin, Vladimir, Medina-Cano, Daniel, Ucuncu, Ekin, Nguyen, Lam Son, Nicouleau, Michael, Lipecka, Joanna, Bizot, Jean-Charles, Thiel, Christian, Lefort, Nathalie, Faivre-Sarrailh, Catherine, Colleaux, Laurence, Guerrera, Ida Chiara, Cantagrel, Vincent, Lebredonchel, Elodie, Garat, Anne, Legrand, Dominique, Decool, Valérie, Klein, André, Ouzzine, Mohamed, Gasnier, Bruno, Potelle, Sven, Groux‐Degroote, Sophie, Cogez, Virginie, Noel, Maxence, Portier, Lucie, Solórzano, Carlos, Dall'Olio, Fabio, Steenackers, Agata, Mortuaire, Marlène, Gonzalez‐Pisfil, Mariano, Henry, Mélanie, Heliot, Laurent, Harduin-Lepers, Anne, Berthe, Audrey, Zaffino, Marie, Muller, claire, Houdou, Marine, Schulz, Céline, Bost, Frédéric, De Fay, Elia, Mazerbourg, Sabine, Flament, Stéphane, Mouajjah, Dounia, Ashikov, Angel, Abu Bakar, Nurulamin, Wen, Xiao-Yan, Niemeijer, Marco, Rodrigues Pinto Osorio, Glentino, Brand-Arzamendi, Koroboshka, Hasadsri, Linda, Hansikova, Hana, Raymond, Kimiyo, Ondruskova, Nina, Simon, Marleen, Pfundt, Rolph, Timal, Sharita, Beumers, Roel, Smeets, Roel, Kersten, Marjan, Huijben, Karin, Linders, Peter, van den Bogaart, Geert, van Hijum, Sacha, Rodenburg, Richard, van den Heuvel, Lambertus, Van Spronsen, Francjan, Honzik, Tomas, van Scherpenzeel, Monique, Lefeber, Dirk, Mirjam, Wamelink, Han, Brunner, Helen, Mundy, Helen, Michelakakis, Peter, van Hasselt, Jiddeke, van de Kamp, Diego, Martinelli, Lars, Morkrid, Katja, Brocke Holmefjord, Jozef, Hertecant, Majid, Alfadhel, Kevin, Carpenter, Johann, te Water Naude, Delos, Maxime, Hellec, Charles, Fifre, Alexandre, Carpentier, Mathieu, Papy-Garcia, Dulce, Allain, Fabrice, Denys, Agnés, Gilormini, Pierre André, Lion, Cédric, Vicogne, Dorothée, Guerardel, Yann, Biot, Christophe, Witters, Peter, Breckpot, Jeroen, Preston, Graem, Morava, Eva, Rujano, Maria, Cannata Serio, Magda, Panasyuk, Ganna, Reunert, Janine, Hauser, Virginie, Park, Julien, Freisinger, Peter, Guida, Maria Clara, Maier, Esther, Wada, Yoshinao, Jäger, Stefanie, Krogan, Nevan, Kretz, Oliver, Nobre, Susana, Garcia, Paula, Quelhas, Dulce, Bird, Thomas, Raskind, Wendy, Schwake, Michael, Duvet, Sandrine, Marquardt, Thorsten, Simons, Matias, Blommaert, Eline, Péanne, Romain, Cherepanova, Natalia, Rymen, Daisy, Staels, Frederik, Jaeken, Jaak, Race, Valérie, Keldermans, Liesbeth, Souche, Erika, Corveleyn, Anniek, Sparkes, Rebecca, Bhattacharya, Kaustuv, Devalck, Christine, Schrijvers, Rik, Foulquier, Francois, Gilmore, Reid, Matthijs, Gert

Publikováno v: Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 2019, ⟨10.1002/jimd.12161⟩
Journal of Inherited Metabolic Disease, Springer Verlag, 2019, ⟨10.1002/jimd.12161⟩
Journal of Inherited Metabolic Disease, Springer Verlag, 2019, 214 (12), pp.201817815. ⟨10.1002/jimd.12161⟩

TMEM165 is involved in a rare genetic human disease named TMEM165‐CDG (congenital disorders of glycosylation). It is Golgi localized, highly conserved through evolution and belongs to the uncharacterized protein family 0016 (UPF0016). The use of is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc6c15a6e3ead5ae272f2f6a2e0ad76
https://hal.science/hal-02399421