| Year |
Citation |
Score |
| 2023 |
Lewis MA, Schulte J, Matthews L, Vaden KI, Steves CJ, Williams FMK, Schulte BA, Dubno JR, Steel KP. Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. Plos Genetics. 19: e1011058. PMID 38011198 DOI: 10.1371/journal.pgen.1011058 |
0.302 |
|
| 2023 |
Zhu W, Du W, Rameshbabu AP, Armstrong AM, Silver S, Kim Y, Wei W, Shu Y, Liu X, Lewis MA, Steel KP, Chen ZY. Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutation. Biorxiv : the Preprint Server For Biology. PMID 37961137 DOI: 10.1101/2023.10.26.564008 |
0.36 |
|
| 2023 |
Martelletti E, Ingham NJ, Steel KP. Reversal of an existing hearing loss by gene activation in mutant mice. Proceedings of the National Academy of Sciences of the United States of America. 120: e2307355120. PMID 37552762 DOI: 10.1073/pnas.2307355120 |
0.382 |
|
| 2023 |
Lachgar-Ruiz M, Morín M, Martelletti E, Ingham NJ, Preite L, Lewis MA, de Castro LSS, Steel KP, Moreno-Pelayo MÁ. Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants. Disease Models & Mechanisms. PMID 37165931 DOI: 10.1242/dmm.049757 |
0.354 |
|
| 2023 |
Lewis MA, Schulte J, Matthews L, Vaden KI, Steves CJ, Williams FMK, Schulte BA, Dubno JR, Steel KP. Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. Medrxiv : the Preprint Server For Health Sciences. PMID 37163093 DOI: 10.1101/2023.04.27.23289040 |
0.302 |
|
| 2023 |
Chiereghin C, Robusto M, Lewis MA, Caetano S, Massa V, Castorina P, Ambrosetti U, Steel KP, Duga S, Asselta R, Soldà G. In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear. Plos One. 18: e0273586. PMID 36689403 DOI: 10.1371/journal.pone.0273586 |
0.364 |
|
| 2022 |
Kochaj RM, Martelletti E, Ingham NJ, Buniello A, Sousa BC, Wakelam MJO, Lopez-Clavijo AF, Steel KP. The Effect of a Mutation on Hearing and Lipid Content of the Inner Ear. Cells. 11. PMID 36291074 DOI: 10.3390/cells11203206 |
0.391 |
|
| 2022 |
Bademci G, Lachgar-Ruiz M, Deokar M, Zafeer MF, Abad C, Yildirim Baylan M, Ingham NJ, Chen J, Sineni CJ, Vadgama N, Karakikes I, Guo S, Duman D, Singh N, Harlalka G, ... ... Steel KP, et al. Mutations in encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. Proceedings of the National Academy of Sciences of the United States of America. 119: e2204084119. PMID 35727972 DOI: 10.1073/pnas.2204084119 |
0.379 |
|
| 2022 |
Lewis MA, Ingham NJ, Chen J, Pearson S, Di Domenico F, Rekhi S, Allen R, Drake M, Willaert A, Rook V, Pass J, Keane T, Adams DJ, Tucker AS, White JK, ... Steel KP, et al. Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. Bmc Biology. 20: 67. PMID 35296311 DOI: 10.1186/s12915-022-01257-8 |
0.313 |
|
| 2022 |
Lorente-Cánovas B, Eckrich S, Lewis MA, Johnson SL, Marcotti W, Steel KP. Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells. Plos One. 17: e0261530. PMID 35235570 DOI: 10.1371/journal.pone.0261530 |
0.402 |
|
| 2022 |
Bryant D, Pauzuolyte V, Ingham NJ, Patel A, Pagarkar W, Anderson LA, Smith KE, Moulding DA, Leong YC, Jafree DJ, Long DA, Al-Yassin A, Steel KP, Jagger DJ, Forge A, et al. The timing of auditory sensory deficits in Norrie disease has implications for therapeutic intervention. Jci Insight. 7. PMID 35132964 DOI: 10.1172/jci.insight.148586 |
0.329 |
|
| 2021 |
Ingham NJ, Banafshe N, Panganiban C, Crunden JL, Chen J, Lewis MA, Steel KP. Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss. Plos One. 16: e0258158. PMID 34597341 DOI: 10.1371/journal.pone.0258158 |
0.405 |
|
| 2020 |
Lewis MA, Di Domenico F, Ingham NJ, Prosser HM, Steel KP. Hearing impairment due to mutations suggests both loss and gain of function effects. Disease Models & Mechanisms. PMID 33318051 DOI: 10.1242/dmm.047225 |
0.396 |
|
| 2020 |
Martelletti E, Ingham NJ, Houston O, Pass JC, Chen J, Marcotti W, Steel KP. Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice. Frontiers in Cellular Neuroscience. 14: 561857. PMID 33100973 DOI: 10.3389/fncel.2020.561857 |
0.402 |
|
| 2020 |
Ingham NJ, Rook V, Di Domenico F, James E, Lewis MA, Girotto G, Buniello A, Steel KP. Functional analysis of candidate genes from genome-wide association studies of hearing. Hearing Research. 387: 107879. PMID 31927188 DOI: 10.1016/j.heares.2019.107879 |
0.353 |
|
| 2019 |
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, ... ... Steel KP, et al. Mouse screen reveals multiple new genes underlying mouse and human hearing loss. Plos Biology. 17: e3000194. PMID 30973865 DOI: 10.1371/journal.pbio.3000194 |
0.327 |
|
| 2018 |
Schlüter T, Berger C, Rosengauer E, Fieth P, Krohs C, Ushakov K, Steel KP, Avraham KB, Hartmann A, Felmy F, Nothwang HG. miR-96 is required for normal development of the auditory hindbrain. Human Molecular Genetics. PMID 29325119 DOI: 10.1093/Hmg/Ddy007 |
0.302 |
|
| 2017 |
Bowl MR, Simon MM, Ingham NJ, Greenaway S, Santos L, Cater H, Taylor S, Mason J, Kurbatova N, Pearson S, Bower LR, Clary DA, Meziane H, Reilly P, Minowa O, ... ... Steel KP, et al. A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nature Communications. 8: 886. PMID 29026089 DOI: 10.1038/S41467-017-00595-4 |
0.341 |
|
| 2016 |
Ingham NJ, Carlisle F, Pearson S, Lewis MA, Buniello A, Chen J, Isaacson RL, Pass J, White JK, Dawson SJ, Steel KP. S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse. Scientific Reports. 6: 28964. PMID 27383011 DOI: 10.1038/srep28964 |
0.361 |
|
| 2016 |
Ebrahim S, Ingham NJ, Lewis MA, Rogers MJ, Cui R, Kachar B, Pass JC, Steel KP. Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia. Cell Reports. PMID 27117407 DOI: 10.1016/J.Celrep.2016.03.081 |
0.348 |
|
| 2016 |
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. Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing. Embo Molecular Medicine. PMID 26881968 DOI: 10.15252/emmm.201505523 |
0.313 |
|
| 2015 |
de Angelis MH, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, ... ... Steel KP, et al. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nature Genetics. PMID 26214591 DOI: 10.1038/Ng.3360 |
0.316 |
|
| 2015 |
Nyegaard M, Rendtorff ND, Nielsen MS, Corydon TJ, Demontis D, Starnawska A, Hedemand A, Buniello A, Niola F, Overgaard MT, Leal SM, Ahmad W, Wikman FP, Petersen KB, Crüger DG, ... ... Steel KP, et al. A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. Plos Genetics. 11: e1005386. PMID 26197441 DOI: 10.1371/journal.pgen.1005386 |
0.304 |
|
| 2015 |
Thoenes M, Zimmermann U, Ebermann I, Ptok M, Lewis MA, Thiele H, Morlot S, Hess MM, Gal A, Eisenberger T, Bergmann C, Nürnberg G, Nürnberg P, Steel KP, Knipper M, et al. OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet Journal of Rare Diseases. 10: 15. PMID 25759012 DOI: 10.1186/s13023-015-0238-5 |
0.339 |
|
| 2015 |
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. ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells. Human Molecular Genetics. 24: 609-24. PMID 25217574 DOI: 10.1093/Hmg/Ddu474 |
0.386 |
|
| 2014 |
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. Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss. Plos Genetics. 10: e1004688. PMID 25356849 DOI: 10.1371/Journal.Pgen.1004688 |
0.436 |
|
| 2014 |
Liakath-Ali K, Vancollie VE, Heath E, Smedley DP, Estabel J, Sunter D, Ditommaso T, White JK, Ramirez-Solis R, Smyth I, Steel KP, Watt FM. Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen. Nature Communications. 5: 3540. PMID 24721909 DOI: 10.1038/ncomms4540 |
0.303 |
|
| 2014 |
Maguire S, Estabel J, Ingham N, Pearson S, Ryder E, Carragher DM, Walker N, Bussell J, Chan WI, Keane TM, Adams DJ, Scudamore CL, Lelliott CJ, RamÃrez-Solis R, ... ... Steel KP, et al. Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene. Plos One. 9: e91807. PMID 24642684 DOI: 10.1371/Journal.Pone.0091807 |
0.379 |
|
| 2014 |
Chen J, Johnson SL, Lewis MA, Hilton JM, Huma A, Marcotti W, Steel KP. A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo. The European Journal of Neuroscience. 39: 744-56. PMID 24446963 DOI: 10.1111/ejn.12484 |
0.348 |
|
| 2013 |
Girotto G, Abdulhadi K, Buniello A, Vozzi D, Licastro D, d'Eustacchio A, Vuckovic D, Alkowari MK, Steel KP, Badii R, Gasparini P. Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. Plos One. 8: e80323. PMID 24312468 DOI: 10.1371/journal.pone.0080323 |
0.347 |
|
| 2013 |
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. Mcph1-deficient mice reveal a role for MCPH1 in otitis media. Plos One. 8: e58156. PMID 23516444 DOI: 10.1371/Journal.Pone.0058156 |
0.395 |
|
| 2013 |
Buniello A, Hardisty-Hughes RE, Pass JC, Bober E, Smith RJ, Steel KP. Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness. Plos One. 8: e56274. PMID 23457544 DOI: 10.1371/journal.pone.0056274 |
0.387 |
|
| 2013 |
Bosman EA, Estabel J, Ismail O, Podrini C, White JK, Steel KP. Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 44-53. PMID 23160729 DOI: 10.1007/s00335-012-9438-7 |
0.313 |
|
| 2013 |
Lorente-Cánovas B, Ingham N, Norgett EE, Golder ZJ, Karet Frankl FE, Steel KP. Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear. Disease Models & Mechanisms. 6: 434-42. PMID 23065636 DOI: 10.1242/dmm.010645 |
0.383 |
|
| 2012 |
Kuhn S, Ingham N, Pearson S, Gribble SM, Clayton S, Steel KP, Marcotti W. Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media. Plos One. 7: e31433. PMID 22348087 DOI: 10.1371/journal.pone.0031433 |
0.356 |
|
| 2011 |
Ingham NJ, Pearson S, Steel KP. Using the Auditory Brainstem Response (ABR) to Determine Sensitivity of Hearing in Mutant Mice. Current Protocols in Mouse Biology. 1: 279-87. PMID 26069055 DOI: 10.1002/9780470942390.mo110059 |
0.314 |
|
| 2011 |
Hilton JM, Lewis MA, Grati M, Ingham N, Pearson S, Laskowski RA, Adams DJ, Steel KP. Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice. Genome Biology. 12: R90. PMID 21936904 DOI: 10.1186/Gb-2011-12-9-R90 |
0.392 |
|
| 2011 |
Calvert JA, Dedos SG, Hawker K, Fleming M, Lewis MA, Steel KP. A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 290-305. PMID 21479780 DOI: 10.1007/s00335-011-9324-8 |
0.319 |
|
| 2010 |
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. 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. Human Molecular Genetics. 19: 4759-73. PMID 20858605 DOI: 10.1093/Hmg/Ddq402 |
0.409 |
|
| 2009 |
Bosman EA, Quint E, Fuchs H, Hrabé de Angelis M, Steel KP. Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome. Developmental Biology. 328: 285-96. PMID 19389353 DOI: 10.1016/j.ydbio.2009.01.030 |
0.419 |
|
| 2009 |
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. An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nature Genetics. 41: 614-8. PMID 19363478 DOI: 10.1038/ng.369 |
0.358 |
|
| 2009 |
Rzadzinska AK, Steel K. Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation Neuroscience. 158: 365-368. PMID 18996172 DOI: 10.1016/J.Neuroscience.2008.10.012 |
0.337 |
|
| 2008 |
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. The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. Plos Genetics. 4: e1000238. PMID 18974863 DOI: 10.1371/Journal.Pgen.1000238 |
0.398 |
|
| 2008 |
Hertzano R, Shalit E, Rzadzinska AK, Dror AA, Song L, Ron U, Tan JT, Shitrit AS, Fuchs H, Hasson T, Ben-Tal N, Sweeney HL, de Angelis MH, Steel KP, Avraham KB. A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. Plos Genetics. 4: e1000207. PMID 18833301 DOI: 10.1371/Journal.Pgen.1000207 |
0.346 |
|
| 2008 |
Prosser HM, Rzadzinska AK, Steel KP, Bradley A. Mosaic complementation demonstrates a regulatory role for myosin VIIa in actin dynamics of stereocilia. Molecular and Cellular Biology. 28: 1702-12. PMID 18160714 DOI: 10.1128/MCB.01282-07 |
0.355 |
|
| 2007 |
Mogensen MM, Rzadzinska A, Steel KP. The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development. Cell Motility and the Cytoskeleton. 64: 496-508. PMID 17326148 DOI: 10.1002/cm.20199 |
0.3 |
|
| 2007 |
Warren M, Wang W, Spiden S, Chen-Murchie D, Tannahill D, Steel KP, Bradley A. A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis. Genesis (New York, N.Y. : 2000). 45: 51-8. PMID 17216607 DOI: 10.1002/Dvg.20264 |
0.348 |
|
| 2006 |
Mashimo T, Erven AE, Spiden SL, Guénet JL, Steel KP. Two quantitative trait loci affecting progressive hearing loss in 101/H mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 841-50. PMID 16897347 DOI: 10.1007/s00335-004-2438-5 |
0.35 |
|
| 2006 |
Marcotti W, Erven A, Johnson SL, Steel KP, Kros CJ. Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea. The Journal of Physiology. 574: 677-98. PMID 16627570 DOI: 10.1113/jphysiol.2005.095661 |
0.407 |
|
| 2005 |
Bosman EA, Penn AC, Ambrose JC, Kettleborough R, Stemple DL, Steel KP. Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Human Molecular Genetics. 14: 3463-76. PMID 16207732 DOI: 10.1093/hmg/ddi375 |
0.324 |
|
| 2005 |
Hawker K, Fuchs H, Angelis MH, Steel KP. Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4. International Journal of Audiology. 44: 171-7. PMID 15916118 DOI: 10.1080/14992020500057434 |
0.356 |
|
| 2005 |
Kiernan AE, Pelling AL, Leung KKH, Tang ASP, Bell DM, Tease C, Lovell-Badge R, Steel KP, Cheah KSE. Sox2 is required for sensory organ development in the mammalian inner ear Nature. 434: 1031-1035. PMID 15846349 DOI: 10.1038/Nature03487 |
0.405 |
|
| 2004 |
Rhodes CR, Hertzano R, Fuchs H, Bell RE, de Angelis MH, Steel KP, Avraham KB. A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 686-97. PMID 15389316 DOI: 10.1007/S00335-004-2344-X |
0.407 |
|
| 2004 |
Pau H, Hawker K, Fuchs H, De Angelis MH, Steel KP. Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 25: 707-13. PMID 15353999 DOI: 10.1097/00129492-200409000-00010 |
0.315 |
|
| 2004 |
Ahituv N, Erven A, Fuchs H, Guy K, Ashery-Padan R, Williams T, de Angelis MH, Avraham KB, Steel KP. An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 424-32. PMID 15181535 DOI: 10.1007/S00335-004-2334-Z |
0.351 |
|
| 2004 |
Holme RH, Steel KP. Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation. Journal of the Association For Research in Otolaryngology : Jaro. 5: 66-79. PMID 14648237 DOI: 10.1007/s10162-003-4021-2 |
0.339 |
|
| 2003 |
Lillo C, Kitamoto J, Liu X, Quint E, Steel KP, Williams DS. Mouse models for Usher syndrome 1B. Advances in Experimental Medicine and Biology. 533: 143-50. PMID 15180258 DOI: 10.1007/978-1-4615-0067-4_18 |
0.376 |
|
| 2003 |
Rhodes CR, Parkinson N, Tsai H, Brooker D, Mansell S, Spurr N, Hunter AJ, Steel KP, Brown SD. The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon. Journal of Neurocytology. 32: 1143-54. PMID 15044845 DOI: 10.1023/B:NEUR.0000021908.98337.91 |
0.39 |
|
| 2003 |
Libby RT, Kitamoto J, Holme RH, Williams DS, Steel KP. Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration. Experimental Eye Research. 77: 731-9. PMID 14609561 DOI: 10.1016/J.Exer.2003.07.007 |
0.316 |
|
| 2003 |
Hardisty RE, Erven A, Logan K, Morse S, Guionaud S, Sancho-Oliver S, Hunter AJ, Brown SD, Steel KP. The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media. Journal of the Association For Research in Otolaryngology : Jaro. 4: 130-8. PMID 12943368 |
0.383 |
|
| 2003 |
Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, Rump A, Hardisty RE, Blanchard S, Coimbra RS, Perfettini I, Parkinson N, Mallon AM, Glenister P, Rogers MJ, ... ... Steel KP, et al. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nature Genetics. 34: 421-8. PMID 12833159 DOI: 10.1038/Ng1208 |
0.391 |
|
| 2003 |
Hulander M, Kiernan AE, Blomqvist SR, Carlsson P, Samuelsson EJ, Johansson BR, Steel KP, Enerbäck S. Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice. Development (Cambridge, England). 130: 2013-25. PMID 12642503 |
0.37 |
|
| 2002 |
Erven A, Skynner MJ, Okumura K, Takebayashi SI, Brown SDM, Steel KP, Allen ND. A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil European Journal of Neuroscience. 16: 1433-1441. PMID 12405956 DOI: 10.1046/j.1460-9568.2002.02213.x |
0.394 |
|
| 2002 |
Holme RH, Steel KP. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice. Hearing Research. 169: 13-23. PMID 12121736 DOI: 10.1016/s0378-5955(02)00334-9 |
0.41 |
|
| 2002 |
Kiernan AE, Erven A, Voegeling S, Peters J, Nolan P, Hunter J, Bacon Y, Steel KP, Brown SDM, Guénet JL. ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis Mammalian Genome. 13: 142-148. PMID 11919684 DOI: 10.1007/s0033501-2088-9 |
0.408 |
|
| 2002 |
Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nature Genetics. 30: 257-8. PMID 11850623 DOI: 10.1038/Ng848 |
0.379 |
|
| 2002 |
Kros CJ, Marcotti W, van Netten SM, Self TJ, Libby RT, Brown SD, Richardson GP, Steel KP. Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations. Nature Neuroscience. 5: 41-7. PMID 11753415 DOI: 10.1038/Nn784 |
0.396 |
|
| 1980 |
Bock GR, Steel K. Cochlear potentials in deafness and jerker mice Journal of the Acoustical Society of America. 67. DOI: 10.1121/1.2018460 |
0.375 |
|
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