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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 2 |
2011 | 1 |
2013 | 2 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 609681
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A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.
Laryngoscope. 2014 Mar;124(3):E95-103. doi: 10.1002/lary.24361. Epub 2013 Dec 17.
Laryngoscope. 2014.
PMID: 23946138
Free PMC article.
SLITRK6 mutations cause myopia and deafness in humans and mice.
Tekin M, Chioza BA, Matsumoto Y, Diaz-Horta O, Cross HE, Duman D, Kokotas H, Moore-Barton HL, Sakoori K, Ota M, Odaka YS, Foster J 2nd, Cengiz FB, Tokgoz-Yilmaz S, Tekeli O, Grigoriadou M, Petersen MB, Sreekantan-Nair A, Gurtz K, Xia XJ, Pandya A, Patton MA, Young JI, Aruga J, Crosby AH.
Tekin M, et al.
J Clin Invest. 2013 May;123(5):2094-102. doi: 10.1172/JCI65853. Epub 2013 Apr 1.
J Clin Invest. 2013.
PMID: 23543054
Free PMC article.
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Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
Matsumoto Y, Katayama K, Okamoto T, Yamada K, Takashima N, Nagao S, Aruga J.
Matsumoto Y, et al.
PLoS One. 2011 Jan 26;6(1):e16497. doi: 10.1371/journal.pone.0016497.
PLoS One. 2011.
PMID: 21298075
Free PMC article.
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Human SLITRK family genes: genomic organization and expression profiling in normal brain and brain tumor tissue.
Aruga J, Yokota N, Mikoshiba K.
Aruga J, et al.
Gene. 2003 Oct 2;315:87-94. doi: 10.1016/s0378-1119(03)00715-7.
Gene. 2003.
PMID: 14557068
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Identification and characterization of Slitrk, a novel neuronal transmembrane protein family controlling neurite outgrowth.
Aruga J, Mikoshiba K.
Aruga J, et al.
Mol Cell Neurosci. 2003 Sep;24(1):117-29. doi: 10.1016/s1044-7431(03)00129-5.
Mol Cell Neurosci. 2003.
PMID: 14550773
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