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Author/Creator Codner, Gemma

1. An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation. Issue 17 (13th April 2022)

Authors:
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
Journal:
Human molecular genetics
Issue:
Volume 31:Issue 17(2022)
Page Start:
2951
Record Type:
Journal Article
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2. Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction. Issue 1 (December 2016)

Authors:
Codner, Gemma; Lindner, Loic; Caulder, Adam; Wattenhofer-Donzé, Marie; Radage, Adam; Mertz, Annelyse; Eisenmann, Benjamin; Mianné, Joffrey; Evans, Edward; Beechey, Colin; Fray, Martin; Birling, Marie-Christine; Hérault, Yann; Pavlovic, Guillaume; Teboul, Lydia
Journal:
BMC cell biology
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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3. Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2. Issue 10 (17th March 2021)

Authors:
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
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 10(2021)
Page Start:
880
Record Type:
Journal Article
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4. Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. Issue 1 (December 2016)

Authors:
Mianné, Joffrey; Chessum, Lauren; Kumar, Saumya; Aguilar, Carlos; Codner, Gemma; Hutchison, Marie; Parker, Andrew; Mallon, Ann-Marie; Wells, Sara; Simon, Michelle; Teboul, Lydia; Brown, Steve; Bowl, Michael
Journal:
Genome medicine
Issue:
Volume 8:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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5. Helios is a key transcriptional regulator of outer hair cell maturation. (29th November 2018)

Authors:
Chessum, Lauren; Matern, Maggie; Kelly, Michael; Johnson, Stuart; Ogawa, Yoko; Milon, Beatrice; McMurray, Mark; Driver, Elizabeth; Parker, Andrew; Song, Yang; Codner, Gemma; Esapa, Christopher; Prescott, Jack; Trent, Graham; Wells, Sara; Dragich, Abigail; Frolenkov, Gregory; Kelley, Matthew; Marc...
Journal:
Nature
Issue:
Volume 563:Number 7733(2018)
Page Start:
696
Record Type:
Journal Article
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6. Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. (15th May 2018)

Authors:
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, Mich...
Journal:
EMBO journal
Issue:
Volume 37:Number 11(2018)
Page Start:
n/a
Record Type:
Journal Article
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