Gong S - Search Results

1

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.

Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX. Shen Z, et al. Among authors: gong s. J Transl Med. 2011 Jan 4;9:4. doi: 10.1186/1479-5876-9-4. J Transl Med. 2011. PMID: 21205314 Free PMC article.

2

[Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].

Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX. Zhang T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):367-73. doi: 10.3760/cma.j.issn.1003-9406.2011.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811972 Chinese.

3

[Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].

Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX. Gong SS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):382-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875491 Chinese.

4

Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.

Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX. Tang X, et al. Among authors: gong s. Mol Genet Metab. 2010 May;100(1):57-64. doi: 10.1016/j.ymgme.2010.01.008. Epub 2010 Jan 25. Mol Genet Metab. 2010. PMID: 20153673

5

Contribution of the tRNA^Ile 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.

Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX. Meng F, et al. Among authors: gong s. J Biol Chem. 2018 Mar 2;293(9):3321-3334. doi: 10.1074/jbc.RA117.000530. Epub 2018 Jan 18. J Biol Chem. 2018. PMID: 29348176 Free PMC article.

6

Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA^His mutation.

Gong S, Wang X, Meng F, Cui L, Yi Q, Zhao Q, Cang X, Cai Z, Mo JQ, Liang Y, Guan MX. Gong S, et al. J Biol Chem. 2020 Jan 24;295(4):940-954. doi: 10.1074/jbc.RA119.010998. Epub 2019 Dec 9. J Biol Chem. 2020. PMID: 31819004 Free PMC article.

7

A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.

Gong S, Peng Y, Jiang P, Wang M, Fan M, Wang X, Zhou H, Li H, Yan Q, Huang T, Guan MX. Gong S, et al. Nucleic Acids Res. 2014 Jul;42(12):8039-48. doi: 10.1093/nar/gku466. Epub 2014 Jun 11. Nucleic Acids Res. 2014. PMID: 24920829 Free PMC article.

8

Steering the Absorption Configuration of Intermediates over Pd-Based Electrocatalysts toward Efficient and Stable CO₂ Reduction.

Wei S, Xu Y, Song T, Dai H, Li F, Gao X, Zhai Y, Gong S, Li R, Zhang X, Chan K. Wei S, et al. Among authors: gong s. J Am Chem Soc. 2025 Jan 24. doi: 10.1021/jacs.4c14253. Online ahead of print. J Am Chem Soc. 2025. PMID: 39854612

9

The Incidence and Clinical Characteristics of COVID-19 in Children With IBD During the Omicron Wave: A Single-Center Experience in China.

Li R, Chen PY, Li HW, Ren L, Cheng Y, Liu LY, Wei LJ, Zeng ZH, Xu WF, Gong ST, Geng LL. Li R, et al. Among authors: gong st. Gastroenterol Res Pract. 2025 Jan 16;2025:1868214. doi: 10.1155/grp/1868214. eCollection 2025. Gastroenterol Res Pract. 2025. PMID: 39850808 Free PMC article.

10

Bioinformatic identification of important roles of COL1A1 and TNFRSF12A in cartilage injury and osteoporosis.

Liu M, Gong S, Sheng X, Zhang Z, Wang X. Liu M, et al. Among authors: gong s. J Int Soc Sports Nutr. 2025 Dec;22(1):2454641. doi: 10.1080/15502783.2025.2454641. Epub 2025 Jan 23. J Int Soc Sports Nutr. 2025. PMID: 39847474 Free article.

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