Canlyniadau Chwilio am Awdur

1

Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control gan Joffrey Mianné, Gemma Codner, Adam Caulder, Rachel Fell, Marie Hutchison, Ruairidh King, Michelle Stewart, Sara Wells, Lydia Teboul

Cyhoeddwyd 2017

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Revisão

2

Microhomologies are prevalent at Cas9-induced larger deletions gan Dominic D. G. Owens, Adam Caulder, Vincent Frontera, Joe Harman, Alasdair Allan, Akin Bucakci, Lucas Greder, Gemma Codner, Philip Hublitz, Peter J. McHugh, Lydia Teboul, Marella de Bruijn

Cyhoeddwyd 2019

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Artigo

3

Analysis of core circadian feedback loop in suprachiasmatic nucleus of <i>mCry1-luc</i> transgenic reporter mouse gan Elizabeth S. Maywood, Lesley Drynan, Johanna E. Chesham, Mathew D. Edwards, Hugues Dardente, Jean‐Michel Fustin, David G. Hazlerigg, John S. O’Neill, Gemma Codner, Nicola J. Smyllie, Marco Brancaccio, Michael H. Hastings

Cyhoeddwyd 2013

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Artigo

4

Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair gan Joffrey Mianné, Lauren Chessum, Saumya Kumar, Carlos Aguilar, Gemma Codner, Marie Hutchison, Andrew Parker, Ann‐Marie Mallon, Sara Wells, Michelle M. Simon, Lydia Teboul, Steve D. M. Brown, Michael R. Bowl

Cyhoeddwyd 2016

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Artigo

5

Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants gan Gemma Codner, Joffrey Mianné, Adam Caulder, Jorik Loeffler, Rachel Fell, Ruairidh King, Alasdair Allan, Matthew Mackenzie, Fran J. Pike, Christopher V. McCabe, Skevoulla Christou, Sam Joynson, Marie Hutchison, Michelle Stewart, Saumya Kumar, Michelle M. Simon, Loranne Agius, Quentin M. Anstee, Kirill E. Volynski, Dimitri M. Kullmann, Sara Wells, Lydia Teboul

Cyhoeddwyd 2018

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Artigo

6

An ultra-conserved poison exon in the Tra2b gene encoding a splicing activator is essential for male fertility and meiotic cell division gan Caroline Dalgliesh, Saad Aldalaqan, Christian Atallah, Andrew Best, Emma Scott, Ingrid Ehrmann, George Merces, Jonathan Mannion, Barbora Badurova, Raveen Sandher, Ylva Illing, Brunhilde Wirth, Sara Wells, Gemma Codner, Lydia Teboul, Graham R. Smith, A J Hedley, Mary Herbert, Dirk G. de Rooij, Colin Miles, Louise N. Reynard, David J. Elliott

Cyhoeddwyd 2025

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Artigo

7

Helios is a key transcriptional regulator of outer hair cell maturation gan Lauren Chessum, Maggie S. Matern, Michael C. Kelly, Stuart L. Johnson, Yoko Ogawa, Béatrice Milon, Mark McMurray, Elizabeth C. Driver, Andrew Parker, Yang Song, Gemma Codner, Christopher T. Esapa, Jack A. Prescott, Graham Trent, Sara Wells, Abigail K. Dragich, Gregory I. Frolenkov, Matthew W. Kelley, Walter Marcotti, Steve D. M. Brown, Ran Elkon, Michael R. Bowl, Ronna Hertzano

Cyhoeddwyd 2018

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Artigo

8

Mice with endogenous <scp>TDP</scp> ‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis gan Pietro Fratta, Prasanth Sivakumar, Jack Humphrey, Kitty Lo, Thomas C. Ricketts, Hugo M. De Oliveira, José Miguel Brito Armas, Bernadett Kalmár, Agnieszka M Ule, Yichao Yu, Nicol Birsa, Cristian Bodo, Toby Collins, Alexander E. Conicella, Alan Mejia Maza, Alessandro Marrero‐Gagliardi, Michelle Stewart, Joffrey Mianné, Silvia Corrochano, Warren Emmett, Gemma Codner, Michael J. Groves, Ryutaro Fukumura, Yoichi Gondo, Mark F. Lythgoe, Erwin Pauws, Emma Peskett, Philip Stanier, Lydia Teboul, Martina Hallegger, Andrea Calvo, Adriano Chió, Adrian M. Isaacs, Nicolas L. Fawzi, Eric T. Wang, David E. Housman, Francisco E. Baralle, Linda Greensmith, Emanuele Buratti, Vincent Plagnol, Elizabeth Fisher, Abraham Acevedo‐Arozena

Cyhoeddwyd 2018

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Artigo

9

Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium gan Terrence F. Meehan, Nathalie Conte, David B. West, Julius O.B. Jacobsen, Jeremy Mason, Jonathan Warren, Chao-Kung Chen, Ilinca Tudose, Mike Relac, Peter Matthews, Natasha A. Karp, Luís Santos, Tanja Fiegel, Natalie Ring, Henrik Westerberg, Simon Greenaway, Duncan Sneddon, Hugh W. Morgan, Gemma Codner, Michelle Stewart, James M. Brown, Neil Horner, Melissa Haendel, Nicole L. Washington, Chris Mungall, Corey L. Reynolds, Juan Gallegos, Valérie Gailus‐Durner, Tania Sorg, Guillaume Pavlovic, Lynette R Bower, Mark W. Moore, Iva Morse, Xiang Gao, Glauco P. Tocchini‐Valentini, Yuichi Obata, Soo Young Cho, Je Kyung Seong, John Seavitt, Arthur L. Beaudet, Mary E. Dickinson, Yann Hérault, Wolfgang Wurst, Martin Hrabě de Angelis, K. C. Kent Lloyd, Ann M Flenniken, Lauryl M. J. Nutter, Susan Newbigging, Colin McKerlie, Monica J. Justice, Stephen A. Murray, Karen L. Svenson, Robert E. Braun, Jacqueline K. White, Allan Bradley, Paul Flicek, Sara Wells, William C. Skarnes, David J. Adams, Helen Parkinson, Ann‐Marie Mallon, Steve D M Brown, Damian Smedley

Cyhoeddwyd 2017

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Artigo

10

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction gan Michael R. Bowl, Michelle M. Simon, Neil J. Ingham, Simon Greenaway, Luís Santos, Heather Cater, Sarah E. Taylor, Jeremy Mason, Natalja Kurbatova, Selina Pearson, Lynette Bower, Dave Clary, Hamid Méziane, Patrick T. Reilly, Osamu Minowa, Lois Kelsey, Sue Allen, Sharon Clementson-Mobbs, Gemma Codner, Martin Fray, Wendy Gardiner, Russell Joynson, Janet Kenyon, Jorik Loeffler, Barbara Nell, Andrew Parker, Deen Quwailid, Michelle Stewart, Alison Walling, Rumana Zaman, Chao-Kung Chen, Nathalie Conte, Peter Matthews, Mike Relac, Ilinca Tudose, Jonathan Warren, Elise Le Marchand, Amal El Amri, Leila El Fertak, Hamid Ennah, Dalila Ali-Hadji, Abdel Ayadi, Marie Wattenhofer‐Donzé, David Moulaert, Sylvie Jacquot, Philippe André, Marie‐Christine Birling, Guillaume Pavlovic, Valérie Lalanne, Aline Lux, Fabrice Riet, Christophe Mittelhaeuser, Raphaël Bour, Alain Guimond, Chaouki Bam’Hamed, Sophie Leblanc, Laurent Vasseur, Mohammed Selloum, Tania Sorg, Shinya Ayabe, Tamio Furuse, Hideki Kaneda, Kimio Kobayashi, Hiroshi Masuya, Ikuo Miura, Yuichi Obata, Tomohiro Suzuki, Masaru Tamura, Nobuhiko Tanaka, Ikuko Yamada, Atsushi Yoshiki, Zorana Berberovic, Mohammed Bubshait, Jorge Cabezas, Tracy Carroll, Greg Clark, Shannon Clarke, Amie Creighton, Ozge Danisment, Mohammad Eskandarian, Patricia Feugas, Marina Gertsenstein, Ruolin Guo, Jane Hunter, Elsa Jacob, Qing Lan, Valerie Laurin, Napoleon Law, Sue MacMaster, D. Craig Miller, Lily Morikawa, Susan Newbigging, Celeste Owen, Patricia Penton, Monica Pereira, Dawei Qu, Xueyuan Shang, Gillian Sleep, Khondoker Sohel, Sandra Tondat

Cyhoeddwyd 2017

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Artigo

11

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics gan Martin Hrabé de Angelis, George Nicholson, Mohammed Selloum, Jacqueline K. White, Hugh W. Morgan, Ramiro Ramírez‐Solis, Tania Sorg, Sara Wells, Helmut Fuchs, Martin Fray, David J. Adams, Niels C. Adams, Thure Adler, Juan Antonio Aguilar‐Pimentel, Dalila Ali-Hadji, Grégory Amann, Philippe André, Sarah Atkins, Aurélie Auburtin, Abdel Ayadi, Julien Becker, Lore Becker, Elodie Bedu, Raffi Bekeredjian, Marie‐Christine Birling, Andrew Blake, Joanna Bottomley, Michael R. Bowl, Véronique Brault, Dirk H. Busch, James Bussell, Julia Calzada‐Wack, Heather Cater, Marie‐France Champy, Philippe Charles, Claire Chevalier, Francesco Chiani, Gemma Codner, Roy Combe, Roger Cox, Emilie Dalloneau, André Dierich, Armida Di Fenza, Brendan Doe, Arnaud Duchon, Oliver Eickelberg, Chris Esapa, Lahcen El Fertak, Tanja Feigel, Irina Emelyanova, Jeanne Estabel, Jack Favor, Ann M. Flenniken, Alessia Gambadoro, Lillian Garrett, Hilary Gates, Anna-Karin Gerdin, Georgios V. Gkoutos, Simon Greenaway, Lisa Glasl, P Goetz, Isabelle Goncalves Da Cruz, Alexander Götz, Jochen Graw, Alain Guimond, Wolfgang Hans, Geoffrey G. Hicks, Sabine M. Hölter, Heinz Höfler, John M. Hancock, Robert Hoehndorf, Tertius Hough, Richard Houghton, Anja Hurt, Boris Ivandic, Hughes Jacobs, Sylvie Jacquot, Nora Jones, Natasha A. Karp, Hugo A. Katus, Sharon Kitchen, Tanja Klein‐Rodewald, Martin Klingenspor, Thomas Klopstock, Valérie Lalanne, Sophie Leblanc, Christoph Lengger, Elise Le Marchand, Tonia Ludwig, Aline Lux, Colin McKerlie, Holger Maier, Jean‐Louis Mandel, Susan Marschall, Manuel Mark, David Melvin, Hamid Méziane, Kateryna Micklich, Christophe Mittelhauser, Laurent Monassier

Cyhoeddwyd 2015

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Artigo

12

Prevalence of sexual dimorphism in mammalian phenotypic traits gan Natasha A. Karp, Jeremy Mason, Arthur L. Beaudet, Yoav Benjamini, Lynette Bower, Robert J. Braun, Steve D. M. Brown, Elissa J. Chesler, Mary E. Dickinson, Ann M. Flenniken, Helmut Fuchs, Martin Hrabě de Angelis, Xiang Gao, Shiying Guo, Simon Greenaway, Ruth Heller, Yann Hérault, Monica J. Justice, Natalja Kurbatova, Christopher J. Lelliott, K. C. Kent Lloyd, Ann‐Marie Mallon, Judith E. Mank, Hiroshi Masuya, Colin McKerlie, Terrence F. Meehan, Richard Mott, Stephen A. Murray, Helen Parkinson, Ramiro Ramírez‐Solis, Luís Santos, John R. Seavitt, Damian Smedley, Tania Sorg, Anneliese O. Speak, Karen P. Steel, Karen L. Svenson, Yuichi Obata, Tomohiro Suzuki, Masaru Tamura, Hideki Kaneda, Tamio Furuse, Kimio Kobayashi, Ikuo Miura, Ikuko Yamada, Nobuhiko Tanaka, Atsushi Yoshiki, Shinya Ayabe, David Clary, Heather Tolentino, Michael Schuchbauer, Todd Tolentino, J Aprile, Sheryl Pedroia, Lois Kelsey, Igor Vukobradovic, Zorana Berberovic, Celeste Owen, Dawei Qu, Ruolin Guo, Susan Newbigging, Lily Morikawa, Napoleon Law, Xueyuan Shang, Patricia Feugas, Yanchun Wang, Mohammad Eskandarian, Yingchun Zhu, Lauryl M. J. Nutter, Patricia Penton, Valerie Laurin, Shannon Clarke, Qing Lan, Khondoker Sohel, D. Craig Miller, Greg Clark, Jane Hunter, Jorge Cabezas, Mohammed Bubshait, Tracy Carroll, Sandra Tondat, S. MacMaster, Monica Pereira, Marina Gertsenstein, Ozge Danisment, Elsa Jacob, Amie Creighton, Gillian Sleep, James D. Clark, Lydia Teboul, Martin Fray, Adam Caulder, Jorik Loeffler, Gemma Codner, James Cleak, Sara Johnson, Zsombor Szoke-Kovacs, Adam Radage, Marina Maritati, Joffrey Mianné

Cyhoeddwyd 2017

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Artigo

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Identification of genetic elements in metabolism by high-throughput mouse phenotyping gan Jan Rozman, Birgit Rathkolb, Manuela A. Oestereicher, Christine Schütt, Aakash Chavan Ravindranath, Stefanie Leuchtenberger, Sapna Sharma, Martin Kistler, Monja Willershäuser, Robert Brommage, Terrence F. Meehan, Jeremy Mason, Hamed Haselimashhadi, Juan Antonio Aguilar‐Pimentel, Lore Becker, Irina Treise, Kristin Moreth, Lillian Garrett, Sabine M. Hölter, Annemarie Zimprich, Susan Marschall, Oana V. Amarie, Julia Calzada-Wack, Frauke Neff, Laura Brachthäuser, Christoph Lengger, Claudia Stoeger, Lilly Zapf, Yi‐Li Cho, Patricia da Silva‐Buttkus, Markus Kraiger, Philipp Mayer‐Kuckuk, Karen Kristine Gampe, Moya Wu, Nathalie Conte, Jonathan Warren, Chao-Kung Chen, Ilinca Tudose, Mike Relac, Peter Matthews, Heather Cater, Helen P. M. Natukunda, James Cleak, Lydia Teboul, Sharon Clementson-Mobbs, Zsombor Szoke-Kovacs, Alison P. Walling, Sara Johnson, Gemma Codner, Tanja Fiegel, Natalie Ring, Henrik Westerberg, Simon Greenaway, Duncan Sneddon, Hugh W. Morgan, Jorik Loeffler, Michelle Stewart, Ramiro Ramírez‐Solis, Allan Bradley, William C. Skarnes, Karen P. Steel, Simon A. Maguire, Joshua Dench, David Lafont, Valerie E. Vancollie, Selina Pearson, Amy S. Gates, Mark Sanderson, Carl Shannon, Lauren F. E. Anthony, Maksymilian T. Sumowski, Robbie S. B. McLaren, Brendan Doe, Hannah Wardle‐Jones, Mark Griffiths, Antonella Galli, Agnieszka Świątkowska, Christopher Isherwood, Anneliese O. Speak, Emma L. Cambridge, Heather Wilson, Susana Caetano, Anna Karin B. Maguire, David J. Adams, Joanna Bottomley, Edward J. Ryder, Diane Gleeson, Laurent Pouilly, Stéphane Rousseau, Aurélie Auburtin, Patrick T. Reilly, Abdel Ayadi, Mohammed Selloum, Joshua A. Wood, Dave Clary, Peter J. Havel, Todd Tolentino, Heather Tolentino, Mike Schuchbauer, Sheryl Pedroia

Cyhoeddwyd 2018

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Artigo

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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy gan Nadine Spielmann, Gregor Miller, Tudor I. Oprea, Chih‐Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy Mason, Violeta Muñoz‐Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik S. Westphal, Cordula M. Wolf, Agnes Görlach, Adrián Sanz‐Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Galter, Manuela A. Östereicher, Lilly Zapf, Philipp Mayer‐Kuckuk, Jan Rozman, Lydia Teboul, Rosie Bunton-Stasyshyn, Heather Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia Willett, Janine M. Wotton, Willson Roper, Audrey E. Christiansen, Christopher Ward, Jason D. Heaney, Corey L. Reynolds, Jan Procházka, Lynette Bower, David Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Méziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel W. Rayner, Juan Antonio Aguilar‐Pimentel, Lore Becker, Lillian Garrett, Sabine M. Hölter, Oana V. Amarie, Julia Calzada‐Wack, Tanja Klein‐Rodewald, Patricia da Silva‐Buttkus, Christoph Lengger, Claudia Stoeger, Raffaele Gerlini, Birgit Rathkolb, Daniela Mayr, John R. Seavitt, Angelina Gaspero, Jennie R. Green, Arturo Garza, Ritu Bohat, Leeyean Wong, Melissa L. McElwee, Sowmya Kalaga, Tara L. Rasmussen, Isabel Lorenzo, Denise G. Lanza, Rodney C. Samaco, Surabi Veeraragaven, Juan Gallegos, Petr Kašpárek, Silvia Petrezsélyová, Ruairidh King, Sara Johnson, James Cleak, Zsombor Szkoe-Kovacs, Gemma Codner, Matthew Mackenzie, Adam Caulder, Janet Kenyon, Wendy Gardiner, Hayley Phelps, Rhys Hancock, Claire Norris, Michayla Moore, Audrie Seluke, Rachel Urban, Coleen Kane, Leslie O. Goodwin, Kevin A. Peterson, Matthew Mckay

Cyhoeddwyd 2022

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Artigo

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A resource of targeted mutant mouse lines for 5,061 genes gan Marie‐Christine Birling, Atsushi Yoshiki, David J. Adams, Shinya Ayabe, Arthur L. Beaudet, Joanna Bottomley, Allan Bradley, Steve D. M. Brown, Antje Bürger, Wendy Bushell, Francesco Chiani, Hsian‐Jean Chin, Skevoulla Christou, Gemma Codner, Francesco J. DeMayo, Mary E. Dickinson, Brendan Doe, Leah Rae Donahue, Martin Fray, Alessia Gambadoro, Xiang Gao, Marina Gertsenstein, Alba Gomez-Segura, Leslie O. Goodwin, Jason D. Heaney, Yann Hérault, Martin Hrabé de Angelis, Si‐Tse Jiang, Monica J. Justice, Petr Kašpárek, Ruairidh King, Ralf Kühn, Ho Lee, Young Jae Lee, Zhiwei Liu, K. C. Kent Lloyd, Isabel Lorenzo, Ann‐Marie Mallon, Colin McKerlie, Terrence F. Meehan, Violeta Muñoz‐Fuentes, Stuart Newman, Lauryl M. J. Nutter, Goo Taeg Oh, Guillaume Pavlovic, Ramiro Ramírez‐Solis, Barry P. Rosen, Edward J. Ryder, Luís Santos, Joel Schick, John R. Seavitt, Radislav Sedláček, Claudia Seisenberger, Je Kyung Seong, William C. Skarnes, Tania Sorg, Karen P. Steel, Masaru Tamura, Glauco P. Tocchini‐Valentini, Chi‐Kuang Leo Wang, Hannah Wardle‐Jones, Marie Wattenhofer‐Donzé, Sara Wells, Michael V. Wiles, Brandon Willis, Joshua A. Wood, Wolfgang Wurst, Ying Xu, Juan Gallegos, Jennie R. Green, Ritu Bohat, Katie Zimmel, Monica Pereira, S. MacMaster, Sandra Tondat, Linda Wei, Tracy Carroll, Jorge Cabezas, Qing Fan-Lan, Elsa Jacob, Amie Creighton, Patricia Castellanos-Penton, Ozge Danisment, Shannon Clarke, Joanna Joeng, Deborah F. Kelly, Christine To, Rebekah van Bruggen, Valerie Gailus-Durner, Helmut Fuchs, Susan Marschall, Stefanie Dunst, Markus Romberger, Benjamin Rey, Sabine Fessele, Philipp Gormanns, Roland H. Friedel, Cornelia Kaloff, Andreas Hörlein, Sarah A. Teichmann

Cyhoeddwyd 2021

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Artigo

Canlyniadau Chwilio - Gemma Codner

Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control gan Joffrey Mianné, Gemma Codner, Adam Caulder, Rachel Fell, Marie Hutchison, Ruairidh King, Michelle Stewart, Sara Wells, Lydia Teboul

Microhomologies are prevalent at Cas9-induced larger deletions gan Dominic D. G. Owens, Adam Caulder, Vincent Frontera, Joe Harman, Alasdair Allan, Akin Bucakci, Lucas Greder, Gemma Codner, Philip Hublitz, Peter J. McHugh, Lydia Teboul, Marella de Bruijn

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