Lewis MA - Search Results

1

Two new mouse alleles of Ocm and Slc26a5.

Lachgar-Ruiz M, Ingham NJ, Martelletti E, Chen J, James E, Panganiban C, Lewis MA, Steel KP. Lachgar-Ruiz M, et al. Among authors: lewis ma. Hear Res. 2024 Oct;452:109109. doi: 10.1016/j.heares.2024.109109. Epub 2024 Sep 1. Hear Res. 2024. PMID: 39241555 Free article.

2

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.

Lewis MA, Quint E, Glazier AM, Fuchs H, De Angelis MH, Langford C, van Dongen S, Abreu-Goodger C, Piipari M, Redshaw N, Dalmay T, Moreno-Pelayo MA, Enright AJ, Steel KP. Lewis MA, et al. Nat Genet. 2009 May;41(5):614-8. doi: 10.1038/ng.369. Epub 2009 Apr 12. Nat Genet. 2009. PMID: 19363478 Free PMC article.

3

MicroRNAs in mouse development and disease.

Lewis MA, Steel KP. Lewis MA, et al. Semin Cell Dev Biol. 2010 Sep;21(7):774-80. doi: 10.1016/j.semcdb.2010.02.004. Epub 2010 Feb 10. Semin Cell Dev Biol. 2010. PMID: 20152923 Free PMC article. Review.

4

miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cells.

Kuhn S, Johnson SL, Furness DN, Chen J, Ingham N, Hilton JM, Steffes G, Lewis MA, Zampini V, Hackney CM, Masetto S, Holley MC, Steel KP, Marcotti W. Kuhn S, et al. Among authors: lewis ma. Proc Natl Acad Sci U S A. 2011 Feb 8;108(6):2355-60. doi: 10.1073/pnas.1016646108. Epub 2011 Jan 18. Proc Natl Acad Sci U S A. 2011. PMID: 21245307 Free PMC article.

5

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice.

Calvert JA, Dedos SG, Hawker K, Fleming M, Lewis MA, Steel KP. Calvert JA, et al. Among authors: lewis ma. Mamm Genome. 2011 Jun;22(5-6):290-305. doi: 10.1007/s00335-011-9324-8. Epub 2011 Apr 10. Mamm Genome. 2011. PMID: 21479780 Free PMC article.

6

Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice.

Hilton JM, Lewis MA, Grati M, Ingham N, Pearson S, Laskowski RA, Adams DJ, Steel KP. Hilton JM, et al. Among authors: lewis ma. Genome Biol. 2011 Sep 21;12(9):R90. doi: 10.1186/gb-2011-12-9-r90. Genome Biol. 2011. PMID: 21936904 Free PMC article.

7

Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti.

Carlisle FA, Steel KP, Lewis MA. Carlisle FA, et al. Among authors: lewis ma. Gene Expr Patterns. 2012 May-Jun;12(5-6):172-9. doi: 10.1016/j.gep.2012.03.001. Epub 2012 Mar 16. Gene Expr Patterns. 2012. PMID: 22446089 Free PMC article.

8

A cornucopia of candidates for deafness.

Lewis MA, Steel KP. Lewis MA, et al. Cell. 2012 Aug 31;150(5):879-81. doi: 10.1016/j.cell.2012.08.007. Cell. 2012. PMID: 22939617 Free article.

9

Pitpnm1 is expressed in hair cells during development but is not required for hearing.

Carlisle FA, Pearson S, Steel KP, Lewis MA. Carlisle FA, et al. Among authors: lewis ma. Neuroscience. 2013 Sep 17;248:620-5. doi: 10.1016/j.neuroscience.2013.06.045. Epub 2013 Jun 29. Neuroscience. 2013. PMID: 23820044 Free PMC article.

10

A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo.

Chen J, Johnson SL, Lewis MA, Hilton JM, Huma A, Marcotti W, Steel KP. Chen J, et al. Among authors: lewis ma. Eur J Neurosci. 2014 Mar;39(5):744-56. doi: 10.1111/ejn.12484. Epub 2014 Jan 22. Eur J Neurosci. 2014. PMID: 24446963 Free PMC article.

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