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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function.
Published in:
EMBO Molecular Medicine, 2019, v. 11, n. 9, p. N.PAG, doi. 10.15252/emmm.201910288
By:
- 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
Publication type:
Article
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
Published in:
Nature Communications, 2016, v. 7, n. 8, p. 12444, doi. 10.1038/ncomms12444
By:
- Potter, Paul K.;
- Bowl, Michael R.;
- Jeyarajan, Prashanthini;
- Wisby, Laura;
- Blease, Andrew;
- Goldsworthy, Michelle E.;
- Simon, Michelle M.;
- Greenaway, Simon;
- Michel, Vincent;
- Barnard, Alun;
- Aguilar, Carlos;
- Agnew, Thomas;
- Banks, Gareth;
- Blake, Andrew;
- Chessum, Lauren;
- Dorning, Joanne;
- Falcone, Sara;
- Goosey, Laurence;
- Harris, Shelley;
- Haynes, Andy
Publication type:
Article
epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 4, p. 584, doi. 10.1093/hmg/ddy370
By:
- Finelli, Mattéa J;
- Aprile, Davide;
- Castroflorio, Enrico;
- Jeans, Alexander;
- Moschetta, Matteo;
- Chessum, Lauren;
- Degiacomi, Matteo T;
- Grasegger, Julia;
- Lupien-Meilleur, Alexis;
- Bassett, Andrew;
- Rossignol, Elsa;
- Campeau, Philippe M;
- Bowl, Michael R;
- Benfenati, Fabio;
- Fassio, Anna;
- Oliver, Peter L
Publication type:
Article
Functional analysis of a novel ENU-induced PHD finger 11 ( Phf11) mouse mutant.
Published in:
Mammalian Genome, 2014, v. 25, n. 11/12, p. 573, doi. 10.1007/s00335-014-9535-x
By:
- Zhang, Youming;
- Dean, Charlotte;
- Chessum, Lauren;
- Nguyen, Dao;
- Stewart, Michelle;
- Taylor, Martin;
- Cookson, William;
- Moffatt, Miriam
Publication type:
Article
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
Published in:
Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0273-4
By:
- 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.
Publication type:
Article
Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.
Published in:
Journal of Neuroscience, 2016, v. 36, n. 1, p. 222, doi. 10.1523/JNEUROSCI.1808-15.2016
By:
- Carrott, Leanne;
- Bowl, Michael R.;
- Aguilar, Carlos;
- Johnson, Stuart L.;
- Chessum, Lauren;
- West, Melissa;
- Morse, Susan;
- Dorning, Joanne;
- Smart, Elizabeth;
- Hardisty-Hughes, Rachel;
- Ball, Greg;
- Parker, Andrew;
- Barnard, Alun R.;
- MacLaren, Robert E.;
- Wells, Sara;
- Marcotti, Walter;
- Brown, Steve D. M.
Publication type:
Article

Found: 6

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

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons.

Functional analysis of a novel ENU-induced PHD finger 11 ( Phf11) mouse mutant.

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

Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.