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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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2000 | 1 |
2005 | 1 |
2011 | 1 |
2023 | 1 |
2024 | 0 |
PubMed (cited) for id: 611123
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A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans.
Hum Mol Genet. 2023 Feb 19;32(5):720-731. doi: 10.1093/hmg/ddac223.
Hum Mol Genet. 2023.
PMID: 36048850
Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.
Jiang L, Liu Y, Feng Y, Hu Z, Mei L, Long L, Chen H, Xue J, Xia K, He C.
Jiang L, et al.
Acta Otolaryngol. 2011 Oct;131(10):1061-8. doi: 10.3109/00016489.2011.591822. Epub 2011 Jun 8.
Acta Otolaryngol. 2011.
PMID: 21651318
Item in Clipboard
Characterization of a novel Eph receptor tyrosine kinase, EphA10, expressed in testis.
Aasheim HC, Patzke S, Hjorthaug HS, Finne EF.
Aasheim HC, et al.
Biochim Biophys Acta. 2005 May 25;1723(1-3):1-7. doi: 10.1016/j.bbagen.2005.01.011. Epub 2005 Feb 16.
Biochim Biophys Acta. 2005.
PMID: 15777695
Review.
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The protein tyrosine kinase family of the human genome.
Robinson DR, Wu YM, Lin SF.
Robinson DR, et al.
Oncogene. 2000 Nov 20;19(49):5548-57. doi: 10.1038/sj.onc.1203957.
Oncogene. 2000.
PMID: 11114734
Review.
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