Phospholipases and fatty acid signalling in exocytosis

Por Darios, Frédéric, Connell, Emma, Davletov, Bazbek
Publicado em 2007

Promiscuous interaction of SNAP-25 with all plasma membrane syntaxins in a neuroendocrine cell

Por Bajohrs, Mark, Darios, Frédéric, Peak-Chew, Sew-Yeu, Davletov, Bazbek
Publicado em 2005

α-Synuclein sequesters arachidonic acid to modulate SNARE-mediated exocytosis

Por Darios, Frédéric, Ruipérez, Violeta, López, Inmaculada, Villanueva, Jose, Gutierrez, Luis M, Davletov, Bazbek
Publicado em 2010

Binary polypeptide system for permanent and oriented protein immobilization

Por Ferrari, Enrico, Darios, Frédéric, Zhang, Fan, Niranjan, Dhevahi, Bailes, Julian, Soloviev, Mikhail, Davletov, Bazbek
Publicado em 2010

Mechanism of arachidonic acid action on syntaxin–Munc18

Por Connell, Emma, Darios, Frédéric, Broersen, Kerensa, Gatsby, Naomi, Peak-Chew, Sew-Yeu, Rickman, Colin, Davletov, Bazbek
Publicado em 2007

VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission

Por Raingo, Jesica, Khvotchev, Mikhail, Liu, Pei, Darios, Frederic, Li, Ying C., Ramirez, Denise M.O., Adachi, Megumi, Lemieux, Philippe, Toth, Katalin, Davletov, Bazbek, Kavalali, Ege T.
Publicado em 2012

SNARE tagging allows stepwise assembly of a multimodular medicinal toxin

Por Darios, Frédéric, Niranjan, Dhevahi, Ferrari, Enrico, Zhang, Fan, Soloviev, Mikhail, Rummel, Andreas, Bigalke, Hans, Suckling, Jason, Ushkaryov, Yuri, Naumenko, Nikolay, Shakirzyanova, Anastasia, Giniatullin, Rashid, Maywood, Elizabeth, Hastings, Michael, Binz, Thomas, Davletov, Bazbek
Publicado em 2010

Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration

Por Branchu, Julien, Boutry, Maxime, Sourd, Laura, Depp, Marine, Leone, Céline, Corriger, Alexandrine, Vallucci, Maeva, Esteves, Typhaine, Matusiak, Raphaël, Dumont, Magali, Muriel, Marie-Paule, Santorelli, Filippo M., Brice, Alexis, El Hachimi, Khalid Hamid, Stevanin, Giovanni, Darios, Frédéric
Publicado no Neurobiol Dis (2017)

Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease

Por Hirst, Jennifer, Edgar, James R., Esteves, Typhaine, Darios, Frédéric, Madeo, Marianna, Chang, Jaerak, Roda, Ricardo H., Dürr, Alexandra, Anheim, Mathieu, Gellera, Cinzia, Li, Jun, Züchner, Stephan, Mariotti, Caterina, Stevanin, Giovanni, Blackstone, Craig, Kruer, Michael C., Robinson, Margaret S.
Publicado no Hum Mol Genet (2015)

Sphingosine Facilitates SNARE Complex Assembly and Activates Synaptic Vesicle Exocytosis

Por Darios, Frédéric, Wasser, Catherine, Shakirzyanova, Anastasia, Giniatullin, Artur, Goodman, Kerry, Munoz-Bravo, Jose L., Raingo, Jesica, Jorgačevski, Jernej, Kreft, Marko, Zorec, Robert, Rosa, Juliana M., Gandia, Luis, Gutiérrez, Luis M., Binz, Thomas, Giniatullin, Rashid, Kavalali, Ege T., Davletov, Bazbek
Publicado em 2009

Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia

Por Esteves, Typhaine, Durr, Alexandra, Mundwiller, Emeline, Loureiro, José L., Boutry, Maxime, Gonzalez, Michael A., Gauthier, Julie, El-Hachimi, Khalid H., Depienne, Christel, Muriel, Marie-Paule, Acosta Lebrigio, Rafael F., Gaussen, Marion, Noreau, Anne, Speziani, Fiorella, Dionne-Laporte, Alexandre, Deleuze, Jean-François, Dion, Patrick, Coutinho, Paula, Rouleau, Guy A., Zuchner, Stephan, Brice, Alexis, Stevanin, Giovanni, Darios, Frédéric
Publicado em 2014

Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia

Por Boukhris, Amir, Schule, Rebecca, Loureiro, José L., Lourenço, Charles Marques, Mundwiller, Emeline, Gonzalez, Michael A., Charles, Perrine, Gauthier, Julie, Rekik, Imen, Acosta Lebrigio, Rafael F., Gaussen, Marion, Speziani, Fiorella, Ferbert, Andreas, Feki, Imed, Caballero-Oteyza, Andrés, Dionne-Laporte, Alexandre, Amri, Mohamed, Noreau, Anne, Forlani, Sylvie, Cruz, Vitor T., Mochel, Fanny, Coutinho, Paula, Dion, Patrick, Mhiri, Chokri, Schols, Ludger, Pouget, Jean, Darios, Frédéric, Rouleau, Guy A., Marques, Wilson, Brice, Alexis, Durr, Alexandra, Zuchner, Stephan, Stevanin, Giovanni
Publicado em 2013

Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia

Por Coutelier, Marie, Goizet, Cyril, Durr, Alexandra, Habarou, Florence, Morais, Sara, Dionne-Laporte, Alexandre, Tao, Feifei, Konop, Juliette, Stoll, Marion, Charles, Perrine, Jacoupy, Maxime, Matusiak, Raphaël, Alonso, Isabel, Tallaksen, Chantal, Mairey, Mathilde, Kennerson, Marina, Gaussen, Marion, Schule, Rebecca, Janin, Maxime, Morice-Picard, Fanny, Durand, Christelle M., Depienne, Christel, Calvas, Patrick, Coutinho, Paula, Saudubray, Jean-Marie, Rouleau, Guy, Brice, Alexis, Nicholson, Garth, Darios, Frédéric, Loureiro, José L., Zuchner, Stephan, Ottolenghi, Chris, Mochel, Fanny, Stevanin, Giovanni
Publicado no Brain (2015)

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Por Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni
Publicado em 2012

Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan

Por Elsayed, Liena E O, Mohammed, Inaam N, Hamed, Ahlam A A, Elseed, Maha A, Johnson, Adam, Mairey, Mathilde, Mohamed, Hassab Elrasoul S A, Idris, Mohamed N, Salih, Mustafa A M, El-sadig, Sarah M, Koko, Mahmoud E, Mohamed, Ashraf Y O, Raymond, Laure, Coutelier, Marie, Darios, Frédéric, Siddig, Rayan A, Ahmed, Ahmed K M A, Babai, Arwa M A, Malik, Hiba M O, Omer, Zulfa M B M, Mohamed, Eman O E, Eltahir, Hanan B, Magboul, Nasr Aldin A, Bushara, Elfatih E, Elnour, Abdelrahman, Rahim, Salah M Abdel, Alattaya, Abdelmoneim, Elbashir, Mustafa I, Ibrahim, Muntaser E, Durr, Alexandra, Audhya, Anjon, Brice, Alexis, Ahmed, Ammar E, Stevanin, Giovanni
Publicado no Eur J Hum Genet (2017)