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Cell
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September 4, 2012
A cornucopia of candidates for deafness
Morag A Lewis, Karen P Steel
Seminars in Cell & Developmental Biology
|
February 16, 2010
MicroRNAs in mouse development and disease
Morag A Lewis, Karen P Steel
Micropublication Biology
|
August 27, 2025
Genes underlying hereditary hearing impairment in humans and in mice
Morag A Lewis, Karen P Steel
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 1, 2024
Investigating the effects of a cryptic splice site in the En2 splice acceptor sequence used in the IKMC knockout-first alleles
Prerna Nair, Karen P Steel, Morag A Lewis
Gene Expression Patterns : GEP
|
March 27, 2012
Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti
Francesca A Carlisle, Karen P Steel, Morag A Lewis
Journal of the Association for Research in Otolaryngology : JARO
|
March 19, 2026
A Systematic Review of Genes Affecting Endocochlear Potential
Darcey A Kirwin, Morag A Lewis, Karen P Steel
BMC Biology
|
June 27, 2022
Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank
Morag A Lewis, Bradley A Schulte, Judy R Dubno, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2025
The importance of accurate phenotyping in large-scale analyses of common disorders such as hearing loss
Morag A Lewis, Bradley A Schulte, Judy R Dubno, et al.
Disease Models & Mechanisms
|
December 15, 2020
Hearing impairment due to <i>Mir183/96/182</i> mutations suggests both loss and gain of function effects
Morag A Lewis, Francesca Di Domenico, Neil J Ingham, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 12, 2011
A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice
Jennifer A Calvert, Skarlatos G Dedos, Kelvin Hawker, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Cell
|
September 4, 2012
A cornucopia of candidates for deafness
Morag A Lewis, Karen P Steel
Seminars in Cell & Developmental Biology
|
February 16, 2010
MicroRNAs in mouse development and disease
Morag A Lewis, Karen P Steel
Micropublication Biology
|
August 27, 2025
Genes underlying hereditary hearing impairment in humans and in mice
Morag A Lewis, Karen P Steel
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 1, 2024
Investigating the effects of a cryptic splice site in the En2 splice acceptor sequence used in the IKMC knockout-first alleles
Prerna Nair, Karen P Steel, Morag A Lewis
Gene Expression Patterns : GEP
|
March 27, 2012
Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti
Francesca A Carlisle, Karen P Steel, Morag A Lewis
Journal of the Association for Research in Otolaryngology : JARO
|
March 19, 2026
A Systematic Review of Genes Affecting Endocochlear Potential
Darcey A Kirwin, Morag A Lewis, Karen P Steel
BMC Biology
|
June 27, 2022
Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank
Morag A Lewis, Bradley A Schulte, Judy R Dubno, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2025
The importance of accurate phenotyping in large-scale analyses of common disorders such as hearing loss
Morag A Lewis, Bradley A Schulte, Judy R Dubno, et al.
Disease Models & Mechanisms
|
December 15, 2020
Hearing impairment due to <i>Mir183/96/182</i> mutations suggests both loss and gain of function effects
Morag A Lewis, Francesca Di Domenico, Neil J Ingham, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 12, 2011
A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice
Jennifer A Calvert, Skarlatos G Dedos, Kelvin Hawker, et al.
Page
of 4