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Peptidergic Activation of Locomotor Pattern Generators in the Neonatal Spinal Cord.
Published in:
Journal of Neuroscience, 2003, v. 23, n. 31, p. 10154, doi. 10.1523/JNEUROSCI.23-31-10154.2003
By:
- Pearson, Selina A.;
- Mouihate, Abdeslam;
- Pittman, Quentin J.;
- Whelan, Patrick J.
Publication type:
Article
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Published in:
PLoS Biology, 2019, v. 17, n. 4, p. 1, doi. 10.1371/journal.pbio.3000194
By:
- Ingham, Neil J.;
- Pearson, Selina A.;
- Vancollie, Valerie E.;
- Rook, Victoria;
- Lewis, Morag A.;
- Chen, Jing;
- Buniello, Annalisa;
- Martelletti, Elisa;
- Preite, Lorenzo;
- Lam, Chi Chung;
- Weiss, Felix D.;
- Powis, Zӧe;
- Suwannarat, Pim;
- Lelliott, Christopher J.;
- Dawson, Sally J.;
- White, Jacqueline K.;
- Steel, Karen P.
Publication type:
Article
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Published in:
PLoS Biology, 2019, v. 17, n. 4, p. 1, doi. 10.1371/journal.pbio.3000194
By:
- Ingham, Neil J.;
- Pearson, Selina A.;
- Vancollie, Valerie E.;
- Rook, Victoria;
- Lewis, Morag A.;
- Chen, Jing;
- Buniello, Annalisa;
- Martelletti, Elisa;
- Preite, Lorenzo;
- Lam, Chi Chung;
- Weiss, Felix D.;
- Powis, Zӧe;
- Suwannarat, Pim;
- Lelliott, Christopher J.;
- Dawson, Sally J.;
- White, Jacqueline K.;
- Steel, Karen P.
Publication type:
Article
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
Published in:
BMC Biology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12915-022-01257-8
By:
- Lewis, Morag A.;
- Ingham, Neil J.;
- Chen, Jing;
- Pearson, Selina;
- Di Domenico, Francesca;
- Rekhi, Sohinder;
- Allen, Rochelle;
- Drake, Matthew;
- Willaert, Annelore;
- Rook, Victoria;
- Pass, Johanna;
- Keane, Thomas;
- Adams, David J.;
- Tucker, Abigail S.;
- White, Jacqueline K.;
- Steel, Karen P.
Publication type:
Article
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
Published in:
BMC Biology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12915-022-01257-8
By:
- Lewis, Morag A.;
- Ingham, Neil J.;
- Chen, Jing;
- Pearson, Selina;
- Di Domenico, Francesca;
- Rekhi, Sohinder;
- Allen, Rochelle;
- Drake, Matthew;
- Willaert, Annelore;
- Rook, Victoria;
- Pass, Johanna;
- Keane, Thomas;
- Adams, David J.;
- Tucker, Abigail S.;
- White, Jacqueline K.;
- Steel, Karen P.
Publication type:
Article
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.
Published in:
Scientific Reports, 2016, p. 28964, doi. 10.1038/srep28964
By:
- Ingham, Neil J.;
- Carlisle, Francesca;
- Pearson, Selina;
- Lewis, Morag A.;
- Buniello, Annalisa;
- Chen, Jing;
- Isaacson, Rivka L.;
- Pass, Johanna;
- White, Jacqueline K.;
- Dawson, Sally J.;
- Steel, Karen P.
Publication type:
Article
Targeting of <i>Slc25a21</i> Is Associated with Orofacial Defects and Otitis Media Due to Disrupted Expression of a Neighbouring Gene.
Published in:
PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091807
By:
- Maguire, Simon;
- Estabel, Jeanne;
- Ingham, Neil;
- Pearson, Selina;
- Ryder, Edward;
- Carragher, Damian M.;
- Walker, Nicolas;
- Bussell, James;
- Chan, Wai-In;
- Keane, Thomas M.;
- Adams, David J.;
- Scudamore, Cheryl L.;
- Lelliott, Christopher J.;
- Ramírez-Solis, Ramiro;
- Karp, Natasha A.;
- Steel, Karen P.;
- White, Jacqueline K.;
- Gerdin, Anna-Karin
Publication type:
Article
Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects.
Published in:
PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0051065
By:
- Steffes, Georg;
- Lorente-Cánovas, Beatriz;
- Pearson, Selina;
- Brooker, Rachael H.;
- Spiden, Sarah;
- Kiernan, Amy E.;
- Guénet, Jean-Louis;
- Steel, Karen P.
Publication type:
Article
Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media.
Published in:
PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031433
By:
- Kuhn, Stephanie;
- Ingham, Neil;
- Pearson, Selina;
- Gribble, Susan M.;
- Clayton, Stephen;
- Steel, Karen P.;
- Marcotti, Walter
Publication type:
Article
Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice.
Published in:
Genome Biology, 2011, v. 12, n. 9, p. 1, doi. 10.1186/gb-2011-12-9-r90
By:
- Hilton, Jennifer M.;
- Lewis, Morag A.;
- Grati, M'hamed;
- Ingham, Neil;
- Pearson, Selina;
- Laskowski, Roman A.;
- Adams, David J.;
- Steel, Karen P.
Publication type:
Article
Ecto‐5′‐nucleotidase (CD73) regulates peripheral chemoreceptor activity and cardiorespiratory responses to hypoxia.
Published in:
Journal of Physiology, 2018, v. 596, n. 15, p. 3137, doi. 10.1113/JP274498
By:
- Holmes, Andrew P.;
- Ray, Clare J.;
- Coney, Andrew M.;
- Kumar, Prem;
- Pearson, Selina A.
Publication type:
Article
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Published in:
Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00595-4
By:
- Bowl, Michael R.;
- Simon, Michelle M.;
- Ingham, Neil J.;
- Greenaway, Simon;
- Santos, Luis;
- Cater, Heather;
- Taylor, Sarah;
- Mason, Jeremy;
- Kurbatova, Natalja;
- Pearson, Selina;
- Bower, Lynette R.;
- Clary, Dave A.;
- Meziane, Hamid;
- Reilly, Patrick;
- Minowa, Osamu;
- Kelsey, Lois;
- Tocchini-Valentini, Glauco P.;
- Xiang Gao;
- Bradley, Allan;
- Skarnes, William C.
Publication type:
Article

Found: 12