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Page 1
Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.
J Vestib Res. 2016;25(5-6):211-8. doi: 10.3233/VES-160569.
J Vestib Res. 2016.
PMID: 26890422
Review.
Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss.
Jin Z, Zhu Q, Lu Y, Cheng J, Yuan H, Han D.
Jin Z, et al.
Acta Otolaryngol. 2022 May;142(5):448-453. doi: 10.1080/00016489.2019.1597984. Epub 2022 May 31.
Acta Otolaryngol. 2022.
PMID: 35640035
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The epigenetically-regulated miR-34a targeting c-SRC suppresses RAF/MEK/ERK signaling pathway in K-562 cells.
Yang Y, Ding L, Guo ZK, Zheng XL, Wang LS, Sun HY, Jin ZG, Wang HX.
Yang Y, et al. Among authors: jin zg.
Leuk Res. 2017 Apr;55:91-96. doi: 10.1016/j.leukres.2017.01.020. Epub 2017 Jan 22.
Leuk Res. 2017.
PMID: 28157629
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Radiotherapeutic treatment of a fighter pilot with nasopharyngeal carcinoma.
Xu XR, Wang BR, Zhang Y, Jin ZG.
Xu XR, et al. Among authors: jin zg.
Aviat Space Environ Med. 2014 Oct;85(10):1056-60. doi: 10.3357/ASEM.3901.2014.
Aviat Space Environ Med. 2014.
PMID: 25245907
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