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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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2010 | 1 |
2012 | 1 |
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2019 | 1 |
2022 | 1 |
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PubMed (GeneRIF) for id: 57709
6 results
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Page 1
Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.
Sci Adv. 2022 Apr 8;8(14):eabk0942. doi: 10.1126/sciadv.abk0942. Epub 2022 Apr 8.
Sci Adv. 2022.
PMID: 35394837
Free PMC article.
Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy.
Guo LY, Zheng SL, Li J, Zhu Q, Duan WH, Zhang Y, Zhu YT, Hu M.
Guo LY, et al.
Ophthalmic Genet. 2019 Apr;40(2):118-123. doi: 10.1080/13816810.2019.1586964. Epub 2019 Mar 29.
Ophthalmic Genet. 2019.
PMID: 30924391
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Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa.
Sugahara M, Oishi M, Oishi A, Ogino K, Morooka S, Gotoh N, Kang I, Yoshimura N.
Sugahara M, et al.
Ophthalmic Genet. 2017 Jan-Feb;38(1):70-73. doi: 10.3109/13816810.2015.1136336. Epub 2016 Mar 30.
Ophthalmic Genet. 2017.
PMID: 27028480
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SLC7A14 linked to autosomal recessive retinitis pigmentosa.
Jin ZB, Huang XF, Lv JN, Xiang L, Li DQ, Chen J, Huang C, Wu J, Lu F, Qu J.
Jin ZB, et al.
Nat Commun. 2014 Mar 27;5:3517. doi: 10.1038/ncomms4517.
Nat Commun. 2014.
PMID: 24670872
Free PMC article.
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A chimera carrying the functional domain of the orphan protein SLC7A14 in the backbone of SLC7A2 mediates trans-stimulated arginine transport.
Jaenecke I, Boissel JP, Lemke M, Rupp J, Gasnier B, Closs EI.
Jaenecke I, et al.
J Biol Chem. 2012 Aug 31;287(36):30853-60. doi: 10.1074/jbc.M112.350322. Epub 2012 Jul 11.
J Biol Chem. 2012.
PMID: 22787143
Free PMC article.
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR.
Rose JE, et al.
Mol Med. 2010 Jul-Aug;16(7-8):247-53. doi: 10.2119/molmed.2009.00159. Epub 2010 Mar 17.
Mol Med. 2010.
PMID: 20379614
Free PMC article.
Clinical Trial.
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