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Neil J Ingham

Showing results (31-40 of 41) with videos related to

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Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
American Journal of Human Genetics|December 4, 2012
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndromeLina Basel-Vanagaite, Bruno Dallapiccola, Ramiro Ramirez-Solis, et al.
Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Biology|August 2, 2013
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strainsMichelle M Simon, Simon Greenaway, Jacqueline K White, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cellsEva L Morozko, Ayako Nishio, Neil J Ingham, et al.
BMC Biology|March 17, 2022
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programmeMorag A Lewis, Neil J Ingham, Jing Chen, et al.
EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
American Journal of Human Genetics|December 4, 2012
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndromeLina Basel-Vanagaite, Bruno Dallapiccola, Ramiro Ramirez-Solis, et al.
Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Biology|August 2, 2013
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strainsMichelle M Simon, Simon Greenaway, Jacqueline K White, et al.
Pageof 5