Glycine Regulates Neural Stem Cell Proliferation During Development via Lnx1-Dependent Notch Signaling

di Bekri, Abdelhamid, Liao, Meijiang, Drapeau, Pierre
Pubblicato in Front Mol Neurosci (2019)

Synaptic Scaling and the Development of a Motor Network

di Knogler, Laura D., Liao, Meijiang, Drapeau, Pierre
Pubblicato in J Neurosci (2010)

Glycine receptors regulate interneuron differentiation during spinal network development

di McDearmid, Jonathan R., Liao, Meijiang, Drapeau, Pierre
Pubblicazione 2006

Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines

di Lissouba, Alexandra, Liao, Meijiang, Kabashi, Edor, Drapeau, Pierre
Pubblicato in Front Mol Neurosci (2018)

Individual knock out of glycine receptor alpha subunits identifies a specific requirement of glra1 for motor function in zebrafish

di Samarut, Eric, Chalopin, Domitille, Riché, Raphaëlle, Allard, Marc, Liao, Meijiang, Drapeau, Pierre
Pubblicato in PLoS One (2019)

FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis

di Kabashi, Edor, Bercier, Valérie, Lissouba, Alexandra, Liao, Meijiang, Brustein, Edna, Rouleau, Guy A., Drapeau, Pierre
Pubblicazione 2011

Homology Directed Knockin of Point Mutations in the Zebrafish tardbp and fus Genes in ALS Using the CRISPR/Cas9 System

di Armstrong, Gary Alan Barclay, Liao, Meijiang, You, Zhipeng, Lissouba, Alexandra, Chen, Brian Edwin, Drapeau, Pierre
Pubblicato in PLoS One (2016)

Neurogenic Role of the Depolarizing Chloride Gradient Revealed by Global Overexpression of KCC2 from the Onset of Development

di Reynolds, Annie, Brustein, Edna, Liao, Meijiang, Mercado, Adriana, Babilonia, Elisa, Mount, David B., Drapeau, Pierre
Pubblicato in J Neurosci (2008)

WNK1/HSN2 Mutation in Human Peripheral Neuropathy Deregulates KCC2 Expression and Posterior Lateral Line Development in Zebrafish (Danio rerio)

di Bercier, Valérie, Brustein, Edna, Liao, Meijiang, Dion, Patrick A., Lafrenière, Ronald G., Rouleau, Guy A., Drapeau, Pierre
Pubblicazione 2013

Phospholipids Induce Conformational Changes of SecA to Form Membrane-Specific Domains: AFM Structures and Implication on Protein-Conducting Channels

di You, Zhipeng, Liao, Meijiang, Zhang, Hao, Yang, Hsiuchin, Pan, Xijian, Houghton, John E., Sui, Sen-fang, Tai, Phang C.
Pubblicazione 2013

Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model

di Swaminathan, Amrutha, Bouffard, Marilou, Liao, Meijiang, Ryan, Sarah, Callister, Janis Bennion, Pickering-Brown, Stuart M, Armstrong, Gary Alan Barclay, Drapeau, Pierre
Pubblicato in Hum Mol Genet (2018)

Targeted knockout of GABA-A receptor gamma 2 subunit provokes transient light-induced reflex seizures in zebrafish larvae

di Liao, Meijiang, Kundap, Uday, Rosch, Richard E., Burrows, Dominic R. W., Meyer, Martin P., Ouled Amar Bencheikh, Bouchra, Cossette, Patrick, Samarut, Éric
Pubblicato in Dis Model Mech (2019)

Glycine decarboxylase deficiency–induced motor dysfunction in zebrafish is rescued by counterbalancing glycine synaptic level

di Riché, Raphaëlle, Liao, Meijiang, Pena, Izabella A., Leung, Kit-Yi, Lepage, Nathalie, Greene, Nicolas D.E., Sarafoglou, Kyriakie, Schimmenti, Lisa A., Drapeau, Pierre, Samarut, Éric
Pubblicato in JCI Insight (2018)

The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

di Bose, Poulomee, Tremblay, Elsa, Maios, Claudia, Narasimhan, Vijay, Armstrong, Gary A. B., Liao, Meijiang, Parker, J. Alex, Robitaille, Richard, Wen, Xiao Yan, Barden, Christopher, Drapeau, Pierre
Pubblicato in Neurotherapeutics (2019)

Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

di Patten, Shunmoogum A., Aggad, Dina, Martinez, Jose, Tremblay, Elsa, Petrillo, Janet, Armstrong, Gary A.B., La Fontaine, Alexandre, Maios, Claudia, Liao, Meijiang, Ciura, Sorana, Wen, Xiao-Yan, Rafuse, Victor, Ichida, Justin, Zinman, Lorne, Julien, Jean-Pierre, Kabashi, Edor, Robitaille, Richard, Korngut, Lawrence, Parker, J. Alexander, Drapeau, Pierre
Pubblicato in JCI Insight (2017)

Functional variants of POC5 identified in patients with idiopathic scoliosis

di Patten, Shunmoogum A., Margaritte-Jeannin, Patricia, Bernard, Jean-Claude, Alix, Eudeline, Labalme, Audrey, Besson, Alicia, Girard, Simon L., Fendri, Khaled, Fraisse, Nicolas, Biot, Bernard, Poizat, Coline, Campan-Fournier, Amandine, Abelin-Genevois, Kariman, Cunin, Vincent, Zaouter, Charlotte, Liao, Meijiang, Lamy, Raphaelle, Lesca, Gaetan, Menassa, Rita, Marcaillou, Charles, Letexier, Melanie, Sanlaville, Damien, Berard, Jerome, Rouleau, Guy A., Clerget-Darpoux, Françoise, Drapeau, Pierre, Moldovan, Florina, Edery, Patrick
Pubblicato in J Clin Invest (2015)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

di Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuck, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Pubblicato in Am J Hum Genet (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

di Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Pubblicato in Am J Hum Genet (2016)