Use of Zebrafish Models to Boost Research in Rare Genetic Diseases

por Crouzier, Lucie, Richard, Elodie M., Sourbron, Jo, Lagae, Lieven, Maurice, Tangui, Delprat, Benjamin
Publicado 2021

Sigma-1 Receptor Is Critical for Mitochondrial Activity and Unfolded Protein Response in Larval Zebrafish

por Crouzier, Lucie, Denus, Morgane, Richard, Elodie M., Tavernier, Amarande, Diez, Camille, Cubedo, Nicolas, Maurice, Tangui, Delprat, Benjamin
Publicado 2021

Loss of Pde6a Induces Rod Outer Segment Shrinkage and Visual Alterations in pde6a(Q70X) Mutant Zebrafish, a Relevant Model of Retinal Dystrophy

por Crouzier, Lucie, Diez, Camille, Richard, Elodie M., Cubedo, Nicolas, Barbereau, Clément, Rossel, Mireille, Delaunay, Thomas, Maurice, Tangui, Delprat, Benjamin
Publicado 2021

NCS1 overexpression restored mitochondrial activity and behavioral alterations in a zebrafish model of Wolfram syndrome

por Crouzier, Lucie, Richard, Elodie M., Diez, Camille, Denus, Morgane, Peyrel, Amandine, Alzaeem, Hala, Cubedo, Nicolas, Delaunay, Thomas, Maurice, Tangui, Delprat, Benjamin
Publicado 2022

An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans

por Jaworek, Thomas J., Richard, Elodie M., Ivanova, Anna A., Giese, Arnaud P. J., Choo, Daniel I., Khan, Shaheen N., Riazuddin, Sheikh, Kahn, Richard A., Riazuddin, Saima
Publicado 2013

Morphological, behavioral and cellular analyses revealed different phenotypes in Wolfram syndrome wfs1a and wfs1b zebrafish mutant lines

por Crouzier, Lucie, Richard, Elodie M, Diez, Camille, Alzaeem, Hala, Denus, Morgane, Cubedo, Nicolas, Delaunay, Thomas, Glendenning, Emily, Baxendale, Sarah, Liévens, Jean-Charles, Whitfield, Tanya T, Maurice, Tangui, Delprat, Benjamin
Publicado 2022

Wfs1(E864K) knock-in mice illuminate the fundamental role of Wfs1 in endocochlear potential production

por Richard, Elodie M., Brun, Emilie, Korchagina, Julia, Crouzier, Lucie, Affortit, Corentin, Alves, Stacy, Cazevieille, Chantal, Mausset-Bonnefont, Anne-Laure, Lenoir, Marc, Puel, Jean-Luc, Maurice, Tangui, Thiry, Marc, Wang, Jing, Delprat, Benjamin
Publicado 2023

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

por Simon, Mariella, Richard, Elodie M., Wang, Xinjian, Shahzad, Mohsin, Huang, Vincent H., Qaiser, Tanveer A., Potluri, Prasanth, Mahl, Sarah E., Davila, Antonio, Nazli, Sabiha, Hancock, Saege, Yu, Margret, Gargus, Jay, Chang, Richard, Al-sheqaih, Nada, Newman, William G., Abdenur, Jose, Starr, Arnold, Hegde, Rashmi, Dorn, Thomas, Busch, Anke, Park, Eddie, Wu, Jie, Schwenzer, Hagen, Flierl, Adrian, Florentz, Catherine, Sissler, Marie, Khan, Shaheen N., Li, Ronghua, Guan, Min-Xin, Friedman, Thomas B., Wu, Doris K., Procaccio, Vincent, Riazuddin, Sheikh, Wallace, Douglas C., Ahmed, Zubair M., Huang, Taosheng, Riazuddin, Saima
Publicado 2015