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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2016 | 1 |
2017 | 1 |
2018 | 1 |
2019 | 1 |
2022 | 1 |
2024 | 0 |
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Page 1
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
BMC Biol. 2022 Mar 17;20(1):67. doi: 10.1186/s12915-022-01257-8.
BMC Biol. 2022.
PMID: 35296311
Free PMC article.
miR-96 is required for normal development of the auditory hindbrain.
Schlüter T, Berger C, Rosengauer E, Fieth P, Krohs C, Ushakov K, Steel KP, Avraham KB, Hartmann AK, Felmy F, Nothwang HG.
Schlüter T, et al.
Hum Mol Genet. 2018 Mar 1;27(5):860-874. doi: 10.1093/hmg/ddy007.
Hum Mol Genet. 2018.
PMID: 29325119
Item in Clipboard
On the role of ephrinA2 in auditory function.
Ingham NJ, Steel KP, Drescher U.
Ingham NJ, et al.
Hear Res. 2017 Jul;350:11-16. doi: 10.1016/j.heares.2017.04.002. Epub 2017 Apr 5.
Hear Res. 2017.
PMID: 28390777
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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.
Ingham NJ, et al.
Sci Rep. 2016 Jul 7;6:28964. doi: 10.1038/srep28964.
Sci Rep. 2016.
PMID: 27383011
Free PMC article.
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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.
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