Ingham NJ - Search Results

1

Mouse screen reveals multiple new genes underlying mouse and human hearing loss.

Ingham NJ, Pearson SA, Vancollie VE, Rook V, Lewis MA, Chen J, Buniello A, Martelletti E, Preite L, Lam CC, Weiss FD, Powis Z, Suwannarat P, Lelliott CJ, Dawson SJ, White JK, Steel KP. Ingham NJ, et al. PLoS Biol. 2019 Apr 11;17(4):e3000194. doi: 10.1371/journal.pbio.3000194. eCollection 2019 Apr. PLoS Biol. 2019. PMID: 30973865 Free PMC article.

2

The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.

Spiden SL, Bortolozzi M, Di Leva F, de Angelis MH, Fuchs H, Lim D, Ortolano S, Ingham NJ, Brini M, Carafoli E, Mammano F, Steel KP. Spiden SL, et al. Among authors: ingham nj. PLoS Genet. 2008 Oct;4(10):e1000238. doi: 10.1371/journal.pgen.1000238. Epub 2008 Oct 31. PLoS Genet. 2008. PMID: 18974863 Free PMC article.

3

The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.

Schütz M, Scimemi P, Majumder P, De Siati RD, Crispino G, Rodriguez L, Bortolozzi M, Santarelli R, Seydel A, Sonntag S, Ingham N, Steel KP, Willecke K, Mammano F. Schütz M, et al. Hum Mol Genet. 2010 Dec 15;19(24):4759-73. doi: 10.1093/hmg/ddq402. Epub 2010 Sep 21. Hum Mol Genet. 2010. PMID: 20858605 Free PMC article.

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. 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

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. Genome Biol. 2011 Sep 21;12(9):R90. doi: 10.1186/gb-2011-12-9-r90. Genome Biol. 2011. PMID: 21936904 Free PMC article.

6

Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media.

Kuhn S, Ingham N, Pearson S, Gribble SM, Clayton S, Steel KP, Marcotti W. Kuhn S, et al. PLoS One. 2012;7(2):e31433. doi: 10.1371/journal.pone.0031433. Epub 2012 Feb 14. PLoS One. 2012. PMID: 22348087 Free PMC article.

7

Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype.

Norgett EE, Golder ZJ, Lorente-Cánovas B, Ingham N, Steel KP, Karet Frankl FE. Norgett EE, et al. Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13775-80. doi: 10.1073/pnas.1204257109. Epub 2012 Aug 7. Proc Natl Acad Sci U S A. 2012. PMID: 22872862 Free PMC article.

8

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear.

Lorente-Cánovas B, Ingham N, Norgett EE, Golder ZJ, Karet Frankl FE, Steel KP. Lorente-Cánovas B, et al. Dis Model Mech. 2013 Mar;6(2):434-42. doi: 10.1242/dmm.010645. Epub 2012 Oct 12. Dis Model Mech. 2013. PMID: 23065636 Free PMC article.

9

Mcph1-deficient mice reveal a role for MCPH1 in otitis media.

Chen J, Ingham N, Clare S, Raisen C, Vancollie VE, Ismail O, McIntyre RE, Tsang SH, Mahajan VB, Dougan G, Adams DJ, White JK, Steel KP. Chen J, et al. PLoS One. 2013;8(3):e58156. doi: 10.1371/journal.pone.0058156. Epub 2013 Mar 13. PLoS One. 2013. PMID: 23516444 Free PMC article.

10

Presynaptic maturation in auditory hair cells requires a critical period of sensory-independent spiking activity.

Johnson SL, Kuhn S, Franz C, Ingham N, Furness DN, Knipper M, Steel KP, Adelman JP, Holley MC, Marcotti W. Johnson SL, et al. Proc Natl Acad Sci U S A. 2013 May 21;110(21):8720-5. doi: 10.1073/pnas.1219578110. Epub 2013 May 6. Proc Natl Acad Sci U S A. 2013. PMID: 23650376 Free PMC article.

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