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Items: 1 to 20 of 42

1.

On the role of ephrinA2 in auditory function.

Ingham NJ, Steel KP, Drescher U.

Hear Res. 2017 Jul;350:11-16. doi: 10.1016/j.heares.2017.04.002. Epub 2017 Apr 5.

PMID:
28390777
2.

Oral Health Status Is Associated with Common Medical Comorbidities in Older Hospital Inpatients.

Ní Chróinín D, Montalto A, Jahromi S, Ingham N, Beveridge A, Foltyn P.

J Am Geriatr Soc. 2016 Aug;64(8):1696-700. doi: 10.1111/jgs.14247. Epub 2016 Aug 3.

PMID:
27487009
3.

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.

Ingham NJ, Carlisle F, Pearson S, Lewis MA, Buniello A, Chen J, Isaacson RL, Pass J, White JK, Dawson SJ, Steel KP.

Sci Rep. 2016 Jul 7;6:28964. doi: 10.1038/srep28964.

4.

Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.

Ebrahim S, Ingham NJ, Lewis MA, Rogers MJC, Cui R, Kachar B, Pass JC, Steel KP.

Cell Rep. 2016 May 3;15(5):935-943. doi: 10.1016/j.celrep.2016.03.081. Epub 2016 Apr 21.

5.

Enhancement of forward suppression begins in the ventral cochlear nucleus.

Ingham NJ, Itatani N, Bleeck S, Winter IM.

Brain Res. 2016 May 15;1639:13-27. doi: 10.1016/j.brainres.2016.02.043. Epub 2016 Mar 2.

6.

Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing.

Buniello A, Ingham NJ, Lewis MA, Huma AC, Martinez-Vega R, Varela-Nieto I, Vizcay-Barrena G, Fleck RA, Houston O, Bardhan T, Johnson SL, White JK, Yuan H, Marcotti W, Steel KP.

EMBO Mol Med. 2016 Mar 1;8(3):191-207. doi: 10.15252/emmm.201505523.

7.

Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

Chen J, Ingham N, Kelly J, Jadeja S, Goulding D, Pass J, Mahajan VB, Tsang SH, Nijnik A, Jackson IJ, White JK, Forge A, Jagger D, Steel KP.

PLoS Genet. 2014 Oct 30;10(10):e1004688. doi: 10.1371/journal.pgen.1004688. eCollection 2014 Oct.

8.

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.

Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA.

Hum Mol Genet. 2015 Feb 1;24(3):609-24. doi: 10.1093/hmg/ddu474. Epub 2014 Sep 12.

9.

Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.

Maguire S, Estabel J, Ingham N, Pearson S, Ryder E, Carragher DM, Walker N; Sanger MGP Slc25a21 Project Team, Bussell J, Chan WI, Keane TM, Adams DJ, Scudamore CL, Lelliott CJ, Ramírez-Solis R, Karp NA, Steel KP, White JK, Gerdin AK.

PLoS One. 2014 Mar 18;9(3):e91807. doi: 10.1371/journal.pone.0091807. eCollection 2014.

10.

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.

Simon MM, Greenaway S, White JK, Fuchs H, Gailus-Durner V, Wells S, Sorg T, Wong K, Bedu E, Cartwright EJ, Dacquin R, Djebali S, Estabel J, Graw J, Ingham NJ, Jackson IJ, Lengeling A, Mandillo S, Marvel J, Meziane H, Preitner F, Puk O, Roux M, Adams DJ, Atkins S, Ayadi A, Becker L, Blake A, Brooker D, Cater H, Champy MF, Combe R, Danecek P, di Fenza A, Gates H, Gerdin AK, Golini E, Hancock JM, Hans W, Hölter SM, Hough T, Jurdic P, Keane TM, Morgan H, Müller W, Neff F, Nicholson G, Pasche B, Roberson LA, Rozman J, Sanderson M, Santos L, Selloum M, Shannon C, Southwell A, Tocchini-Valentini GP, Vancollie VE, Westerberg H, Wurst W, Zi M, Yalcin B, Ramirez-Solis R, Steel KP, Mallon AM, de Angelis MH, Herault Y, Brown SD.

Genome Biol. 2013 Jul 31;14(7):R82. doi: 10.1186/gb-2013-14-7-r82.

11.

Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.

White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, Salisbury J, Clare S, Ingham NJ, Podrini C, Houghton R, Estabel J, Bottomley JR, Melvin DG, Sunter D, Adams NC; Sanger Institute Mouse Genetics Project, Tannahill D, Logan DW, Macarthur DG, Flint J, Mahajan VB, Tsang SH, Smyth I, Watt FM, Skarnes WC, Dougan G, Adams DJ, Ramirez-Solis R, Bradley A, Steel KP.

Cell. 2013 Jul 18;154(2):452-64. doi: 10.1016/j.cell.2013.06.022.

12.

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.

Proc Natl Acad Sci U S A. 2013 May 21;110(21):8720-5. doi: 10.1073/pnas.1219578110. Epub 2013 May 6.

13.

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.

PLoS One. 2013;8(3):e58156. doi: 10.1371/journal.pone.0058156. Epub 2013 Mar 13.

14.

Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome.

Basel-Vanagaite L, Dallapiccola B, Ramirez-Solis R, Segref A, Thiele H, Edwards A, Arends MJ, Miró X, White JK, Désir J, Abramowicz M, Dentici ML, Lepri F, Hofmann K, Har-Zahav A, Ryder E, Karp NA, Estabel J, Gerdin AK, Podrini C, Ingham NJ, Altmüller J, Nürnberg G, Frommolt P, Abdelhak S, Pasmanik-Chor M, Konen O, Kelley RI, Shohat M, Nürnberg P, Flint J, Steel KP, Hoppe T, Kubisch C, Adams DJ, Borck G.

Am J Hum Genet. 2012 Dec 7;91(6):998-1010. doi: 10.1016/j.ajhg.2012.10.011. Epub 2012 Nov 29.

15.

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.

Dis Model Mech. 2013 Mar;6(2):434-42. doi: 10.1242/dmm.010645. Epub 2012 Oct 12.

16.

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.

Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13775-80. doi: 10.1073/pnas.1204257109. Epub 2012 Aug 7.

17.

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.

PLoS One. 2012;7(2):e31433. doi: 10.1371/journal.pone.0031433. Epub 2012 Feb 14.

18.

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.

Genome Biol. 2011 Sep 21;12(9):R90. doi: 10.1186/gb-2011-12-9-r90.

19.

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.

Proc Natl Acad Sci U S A. 2011 Feb 8;108(6):2355-60. doi: 10.1073/pnas.1016646108. Epub 2011 Jan 18.

20.

Using the Auditory Brainstem Response (ABR) to Determine Sensitivity of Hearing in Mutant Mice.

Ingham NJ, Pearson S, Steel KP.

Curr Protoc Mouse Biol. 2011 Jun 1;1(2):279-87. doi: 10.1002/9780470942390.mo110059.

PMID:
26069055

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