Screening and validation of genome-edited animals

por Bunton-Stasyshyn, Rosie K, Codner, Gemma F, Teboul, Lydia
Publicado 2021

The guanine nucleotide exchange factor, Spata13, influences social behaviour and nocturnal activity

por Bourbia, Nora, Chandler, Paige, Codner, Gemma, Banks, Gareth, Nolan, Patrick M.
Publicado 2019

MON-539 Mice Harboring a Germline Heterozygous AP2S1 Mutation, Arg15Leu, Are a Model for Familial Hypocalciuric Hypercalcemia Type 3 (FHH3)

por Hannan, Fadil, Stokes, Victoria, Gorvin, Caroline, Hough, Tertius, Codner, Gemma, Stewart, Michelle, Wells, Sara, Teboul, Lydia, Thakker, Rajesh
Publicado 2019

Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight

por Livermore, Catherine, Warr, Nick, Chalon, Nicolas, Siggers, Pam, Mianné, Joffrey, Codner, Gemma, Teboul, Lydia, Wells, Sara, Greenfield, Andy
Publicado 2019

Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing

por Newton, Sherylanne, Kong, Fanbo, Carlton, Adam J., Aguilar, Carlos, Parker, Andrew, Codner, Gemma F., Teboul, Lydia, Wells, Sara, Brown, Steve D. M., Marcotti, Walter, Bowl, Michael R.
Publicado 2022

An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1(Y446C/Y446C) mutation

por Hu, Yalan, Lauffer, Peter, Stewart, Michelle, Codner, Gemma, Mayerl, Steffen, Heuer, Heike, Ng, Lily, Forrest, Douglas, van Trotsenburg, Paul, Jongejan, Aldo, Fliers, Eric, Hennekam, Raoul, Boelen, Anita
Publicado 2022

Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2

por Hannan, Fadil M, Stevenson, Mark, Bayliss, Asha L, Stokes, Victoria J, Stewart, Michelle, Kooblall, Kreepa G, Gorvin, Caroline M, Codner, Gemma, Teboul, Lydia, Wells, Sara, Thakker, Rajesh V
Publicado 2021

Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair

por Mianné, Joffrey, Chessum, Lauren, Kumar, Saumya, Aguilar, Carlos, Codner, Gemma, Hutchison, Marie, Parker, Andrew, Mallon, Ann-Marie, Wells, Sara, Simon, Michelle M., Teboul, Lydia, Brown, Steve D. M., Bowl, Michael R.
Publicado 2016

Microhomologies are prevalent at Cas9-induced larger deletions

por Owens, Dominic D G, Caulder, Adam, Frontera, Vincent, Harman, Joe R, Allan, Alasdair J, Bucakci, Akin, Greder, Lucas, Codner, Gemma F, Hublitz, Philip, McHugh, Peter J, Teboul, Lydia, de Bruijn, Marella F T R
Publicado 2019

Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction

por Codner, Gemma F., Lindner, Loic, Caulder, Adam, Wattenhofer-Donzé, Marie, Radage, Adam, Mertz, Annelyse, Eisenmann, Benjamin, Mianné, Joffrey, Evans, Edward P., Beechey, Colin V., Fray, Martin D., Birling, Marie-Christine, Hérault, Yann, Pavlovic, Guillaume, Teboul, Lydia
Publicado 2016

Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants

por Codner, Gemma F., Mianné, Joffrey, Caulder, Adam, Loeffler, Jorik, Fell, Rachel, King, Ruairidh, Allan, Alasdair J., Mackenzie, Matthew, Pike, Fran J., McCabe, Christopher V., Christou, Skevoulla, Joynson, Sam, Hutchison, Marie, Stewart, Michelle E., Kumar, Saumya, Simon, Michelle M., Agius, Loranne, Anstee, Quentin M., Volynski, Kirill E., Kullmann, Dimitri M., Wells, Sara, Teboul, Lydia
Publicado 2018

Ikzf2/helios is a key transcriptional regulator of outer hair cell maturation

por Chessum, Lauren, Matern, Maggie S, Kelly, Michael C, Johnson, Stuart L, Ogawa, Yoko, Milon, Beatrice, McMurray, Mark, Driver, Elizabeth C, Parker, Andrew, Song, Yang, Codner, Gemma, Esapa, Christopher T, Prescott, Jack, Trent, Graham, Wells, Sara, Dragich, Abigail K, Frolenkov, Gregory I., Kelley, Matthew W, Marcotti, Walter, Brown, Steve DM, Elkon, Ran, Bowl, Michael R, Hertzano, Ronna
Publicado 2018

Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration

por Joyce, Peter I., Fratta, Pietro, Landman, Allison S., Mcgoldrick, Philip, Wackerhage, Henning, Groves, Michael, Busam, Bharani Shiva, Galino, Jorge, Corrochano, Silvia, Beskina, Olga A., Esapa, Christopher, Ryder, Edward, Carter, Sarah, Stewart, Michelle, Codner, Gemma, Hilton, Helen, Teboul, Lydia, Tucker, Jennifer, Lionikas, Arimantas, Estabel, Jeanne, Ramirez-Solis, Ramiro, White, Jacqueline K., Brandner, Sebastian, Plagnol, Vincent, Bennet, David L. H., Abramov, Andrey Y., Greensmith, Linda, Fisher, Elizabeth M. C., Acevedo-Arozena, Abraham
Publicado 2016

Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function

por Dunbar, Lucy A, Patni, Pranav, Aguilar, Carlos, Mburu, Philomena, Corns, Laura, Wells, Helena RR, Delmaghani, Sedigheh, Parker, Andrew, Johnson, Stuart, Williams, Debbie, Esapa, Christopher T, Simon, Michelle M, Chessum, Lauren, Newton, Sherylanne, Dorning, Joanne, Jeyarajan, Prashanthini, Morse, Susan, Lelli, Andrea, Codner, Gemma F, Peineau, Thibault, Gopal, Suhasini R, Alagramam, Kumar N, Hertzano, Ronna, Dulon, Didier, Wells, Sara, Williams, Frances M, Petit, Christine, Dawson, Sally J, Brown, Steve DM, Marcotti, Walter, El‐Amraoui, Aziz, Bowl, Michael R
Publicado 2019

Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models

por Devoy, Anny, Price, Georgia, De Giorgio, Francesca, Bunton-Stasyshyn, Rosie, Thompson, David, Gasco, Samanta, Allan, Alasdair, Codner, Gemma F., Nair, Remya R., Tibbit, Charlotte, McLeod, Ross, Ali, Zeinab, Noda, Judith, Marrero-Gagliardi, Alessandro, Brito-Armas, José M., Williams, Chloe, Öztürk, Muhammet M., Simon, Michelle, O'Neill, Edward, Bryce-Smith, Sam, Harrison, Jackie, Atkins, Gemma, Corrochano, Silvia, Stewart, Michelle, Gilthorpe, Jonathan D., Teboul, Lydia, Acevedo-Arozena, Abraham, Fisher, Elizabeth M.C., Cunningham, Thomas J.
Publicado 2021

Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models

por Devoy, Anny, Price, Georgia, De Giorgio, Francesca, Bunton-Stasyshyn, Rosie, Thompson, David, Gasco, Samanta, Allan, Alasdair, Codner, Gemma F., Nair, Remya R., Tibbit, Charlotte, McLeod, Ross, Ali, Zeinab, Noda, Judith, Marrero-Gagliardi, Alessandro, Brito-Armas, José M., Williams, Chloe, Öztürk, Muhammet M., Simon, Michelle, O’Neill, Edward, Bryce-Smith, Sam, Harrison, Jackie, Atkins, Gemma, Corrochano, Silvia, Stewart, Michelle, Gilthorpe, Jonathan D., Teboul, Lydia, Acevedo-Arozena, Abraham, Fisher, Elizabeth M.C., Cunningham, Thomas J.
Publicado 2022

Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

por Fratta, Pietro, Sivakumar, Prasanth, Humphrey, Jack, Lo, Kitty, Ricketts, Thomas, Oliveira, Hugo, Brito‐Armas, Jose M, Kalmar, Bernadett, Ule, Agnieszka, Yu, Yichao, Birsa, Nicol, Bodo, Cristian, Collins, Toby, Conicella, Alexander E, Mejia Maza, Alan, Marrero‐Gagliardi, Alessandro, Stewart, Michelle, Mianne, Joffrey, Corrochano, Silvia, Emmett, Warren, Codner, Gemma, Groves, Michael, Fukumura, Ryutaro, Gondo, Yoichi, Lythgoe, Mark, Pauws, Erwin, Peskett, Emma, Stanier, Philip, Teboul, Lydia, Hallegger, Martina, Calvo, Andrea, Chiò, Adriano, Isaacs, Adrian M, Fawzi, Nicolas L, Wang, Eric, Housman, David E, Baralle, Francisco, Greensmith, Linda, Buratti, Emanuele, Plagnol, Vincent, Fisher, Elizabeth MC, Acevedo‐Arozena, Abraham
Publicado 2018

Disease Model Discovery from 3,328 Gene Knockouts by The International Mouse Phenotyping Consortium

por Meehan, Terrence F., Conte, Nathalie, West, David B., Jacobsen, Julius O., Mason, Jeremy, Warren, Jonathan, Chen, Chao-Kung, Tudose, Ilinca, Relac, Mike, Matthews, Peter, Karp, Natasha, Santos, Luis, Fiegel, Tanja, Ring, Natalie, Westerberg, Henrik, Greenaway, Simon, Sneddon, Duncan, Morgan, Hugh, Codner, Gemma F, Stewart, Michelle E, Brown, James, Horner, Neil, Haendel, Melissa, Washington, Nicole, Mungall, Christopher J., Reynolds, Corey L, Gallegos, Juan, Gailus-Durner, Valerie, Sorg, Tania, Pavlovic, Guillaume, Bower, Lynette R, Moore, Mark, Morse, Iva, Gao, Xiang, Tocchini-Valentini, Glauco P, Obata, Yuichi, Cho, Soo Young, Seong, Je Kyung, Seavitt, John, Beaudet, Arthur L., Dickinson, Mary E., Herault, Yann, Wurst, Wolfgang, de Angelis, Martin Hrabe, Lloyd, K.C. Kent, Flenniken, Ann M, Nutter, Lauryl MJ, Newbigging, Susan, McKerlie, Colin, Justice, Monica J., Murray, Stephen A., Svenson, Karen L., Braun, Robert E., White, Jacqueline K., Bradley, Allan, Flicek, Paul, Wells, Sara, Skarnes, William C., Adams, David J., Parkinson, Helen, Mallon, Ann-Marie, Brown, Steve D.M., Smedley, Damian
Publicado 2017

Analysis of mammalian gene function through broad based phenotypic screens across a consortium of mouse clinics

por de Angelis, Martin Hrabě, Nicholson, George, Selloum, Mohammed, White, Jacqui, Morgan, Hugh, Ramirez-Solis, Ramiro, Sorg, Tania, Wells, Sara, Fuchs, Helmut, Fray, Martin, Adams, David J, Adams, Niels C, Adler, Thure, Aguilar-Pimentel, Antonio, Ali-Hadji, Dalila, Amann, Gregory, André, Philippe, Atkins, Sarah, Auburtin, Aurelie, Ayadi, Abdel, Becker, Julien, Becker, Lore, Bedu, Elodie, Bekeredjian, Raffi, Birling, Marie-Christine, Blake, Andrew, Bottomley, Joanna, Bowl, Mike, Brault, Véronique, Busch, Dirk H, Bussell, James N, Calzada-Wack, Julia, Cater, Heather, Champy, Marie-France, Charles, Philippe, Chevalier, Claire, Chiani, Francesco, Codner, Gemma F, Combe, Roy, Cox, Roger, Dalloneau, Emilie, Dierich, André, Di Fenza, Armida, Doe, Brendan, Duchon, Arnaud, Eickelberg, Oliver, Esapa, Chris T, El Fertak, Lahcen, Feigel, Tanja, Emelyanova, Irina, Estabel, Jeanne, Favor, Jack, Flenniken, Ann, Gambadoro, Alessia, Garrett, Lilian, Gates, Hilary, Gerdin, Anna-Karin, Gkoutos, George, Greenaway, Simon, Glasl, Lisa, Goetz, Patrice, Da Cruz, Isabelle Goncalves, Götz, Alexander, Graw, Jochen, Guimond, Alain, Hans, Wolfgang, Hicks, Geoff, Hölter, Sabine M, Höfler, Heinz, Hancock, John M, Hoehndorf, Robert, Hough, Tertius, Houghton, Richard, Hurt, Anja, Ivandic, Boris, Jacobs, Hughes, Jacquot, Sylvie, Jones, Nora, Karp, Natasha A, Katus, Hugo A, Kitchen, Sharon, Klein-Rodewald, Tanja, Klingenspor, Martin, Klopstock, Thomas, Lalanne, Valerie, Leblanc, Sophie, Lengger, Christoph, le Marchand, Elise, Ludwig, Tonia, Lux, Aline, McKerlie, Colin, Maier, Holger, Mandel, Jean-Louis, Marschall, Susan, Mark, Manuel, Melvin, David G, Meziane, Hamid, Micklich, Kateryna, Mittelhauser, Christophe, Monassier, Laurent, Moulaert, David, Muller, Stéphanie, Naton, Beatrix, Neff, Frauke, Nolan, Patrick M, Nutter, Lauryl MJ, Ollert, Markus, Pavlovic, Guillaume, Pellegata, Natalia S, Peter, Emilie, Petit-Demoulière, Benoit, Pickard, Amanda, Podrini, Christine, Potter, Paul, Pouilly, Laurent, Puk, Oliver, Richardson, David, Rousseau, Stephane, Quintanilla-Fend, Leticia, Quwailid, Mohamed M, Racz, Ildiko, Rathkolb, Birgit, Riet, Fabrice, Rossant, Janet, Roux, Michel, Rozman, Jan, Ryder, Ed, Salisbury, Jennifer, Santos, Luis, Schäble, Karl-Heinz, Schiller, Evelyn, Schrewe, Anja, Schulz, Holger, Steinkamp, Ralf, Simon, Michelle, Stewart, Michelle, Stöger, Claudia, Stöger, Tobias, Sun, Minxuan, Sunter, David, Teboul, Lydia, Tilly, Isabelle, Tocchini-Valentini, Glauco P, Tost, Monica, Treise, Irina, Vasseur, Laurent, Velot, Emilie, Vogt-Weisenhorn, Daniela, Wagner, Christelle, Walling, Alison, Weber, Bruno, Wendling, Olivia, Westerberg, Henrik, Willershäuser, Monja, Wolf, Eckhard, Wolter, Anne, Wood, Joe, Wurst, Wolfgang, Yildirim, Ali Önder, Zeh, Ramona, Zimmer, Andreas, Zimprich, Annemarie, Holmes, Chris, Steel, Karen P, Herault, Yann, Gailus-Durner, Valérie, Mallon, Ann-Marie, Brown, Steve DM
Publicado 2015