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

Por Bekri, Abdelhamid, Liao, Meijiang, Drapeau, Pierre
Publicado no Front Mol Neurosci (2019)

Synaptic Scaling and the Development of a Motor Network

Por Knogler, Laura D., Liao, Meijiang, Drapeau, Pierre
Publicado no J Neurosci (2010)

Glycine receptors regulate interneuron differentiation during spinal network development

Por McDearmid, Jonathan R., Liao, Meijiang, Drapeau, Pierre
Publicado em 2006

Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines

Por Lissouba, Alexandra, Liao, Meijiang, Kabashi, Edor, Drapeau, Pierre
Publicado no Front Mol Neurosci (2018)

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

Por Samarut, Eric, Chalopin, Domitille, Riché, Raphaëlle, Allard, Marc, Liao, Meijiang, Drapeau, Pierre
Publicado no PLoS One (2019)

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

Por Kabashi, Edor, Bercier, Valérie, Lissouba, Alexandra, Liao, Meijiang, Brustein, Edna, Rouleau, Guy A., Drapeau, Pierre
Publicado em 2011

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

Por Armstrong, Gary Alan Barclay, Liao, Meijiang, You, Zhipeng, Lissouba, Alexandra, Chen, Brian Edwin, Drapeau, Pierre
Publicado no PLoS One (2016)

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

Por Reynolds, Annie, Brustein, Edna, Liao, Meijiang, Mercado, Adriana, Babilonia, Elisa, Mount, David B., Drapeau, Pierre
Publicado no J Neurosci (2008)

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

Por Bercier, Valérie, Brustein, Edna, Liao, Meijiang, Dion, Patrick A., Lafrenière, Ronald G., Rouleau, Guy A., Drapeau, Pierre
Publicado em 2013

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

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

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

Por Swaminathan, Amrutha, Bouffard, Marilou, Liao, Meijiang, Ryan, Sarah, Callister, Janis Bennion, Pickering-Brown, Stuart M, Armstrong, Gary Alan Barclay, Drapeau, Pierre
Publicado no Hum Mol Genet (2018)

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

Por Liao, Meijiang, Kundap, Uday, Rosch, Richard E., Burrows, Dominic R. W., Meyer, Martin P., Ouled Amar Bencheikh, Bouchra, Cossette, Patrick, Samarut, Éric
Publicado no Dis Model Mech (2019)

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

Por 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
Publicado no JCI Insight (2018)

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

Por 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
Publicado no Neurotherapeutics (2019)

Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

Por 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
Publicado no JCI Insight (2017)

Functional variants of POC5 identified in patients with idiopathic scoliosis

Por 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
Publicado no J Clin Invest (2015)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por 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
Publicado no Am J Hum Genet (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por 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
Publicado no Am J Hum Genet (2016)