Gao X - Search Results

1

[Research progress on GSDME-mediated cell pyroptosis resulting in GSDME type hearing loss].

Peng L, Wang X, Wang W, Xu J, Gao X. Peng L, et al. Among authors: gao x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Oct 10;41(10):1271-1276. doi: 10.3760/cma.j.cn511374-20231004-00168. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 39344626 Review. Chinese.

2

Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.

Gao X, Huang SS, Qiu SW, Su Y, Wang WQ, Xu HY, Xu JC, Kang DY, Dai P, Yuan YY. Gao X, et al. J Med Genet. 2021 Jul;58(7):465-474. doi: 10.1136/jmedgenet-2020-106892. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737134

3

A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2.

Huang B, Liu Y, Gao X, Xu J, Dai P, Zhu Q, Yuan Y. Huang B, et al. Among authors: gao x. BMC Med Genet. 2017 Mar 24;18(1):36. doi: 10.1186/s12881-017-0396-5. BMC Med Genet. 2017. PMID: 28340560 Free PMC article.

4

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.

Gao X, Yuan YY, Lin QF, Xu JC, Wang WQ, Qiao YH, Kang DY, Bai D, Xin F, Huang SS, Qiu SW, Guan LP, Su Y, Wang GJ, Han MY, Jiang Y, Liu HK, Dai P. Gao X, et al. J Med Genet. 2018 May;55(5):298-306. doi: 10.1136/jmedgenet-2017-104954. Epub 2018 Feb 16. J Med Genet. 2018. PMID: 29453195 Free PMC article.

5

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.

Gao X, Xu JC, Wang WQ, Yuan YY, Bai D, Huang SS, Wang GJ, Su Y, Li J, Kang DY, Zhang MG, Lin X, Dai P. Gao X, et al. Biomed Res Int. 2018 Apr 4;2018:5370802. doi: 10.1155/2018/5370802. eCollection 2018. Biomed Res Int. 2018. PMID: 29850532 Free PMC article.

6

Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss.

Wang WQ, Gao X, Huang SS, Kang DY, Xu JC, Yang K, Han MY, Zhang X, Yang SY, Yuan YY, Dai P. Wang WQ, et al. Among authors: gao x. Front Genet. 2022 May 27;13:825082. doi: 10.3389/fgene.2022.825082. eCollection 2022. Front Genet. 2022. PMID: 35711932 Free PMC article.

7

A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4.

Yang K, Wang X, Wang WQ, Han MY, Hu LM, Kang DY, Yang JY, Liu M, Gao X, Yuan YY, Xu JC. Yang K, et al. Among authors: gao x. Mol Genet Genomic Med. 2023 Mar;11(3):e2103. doi: 10.1002/mgg3.2103. Epub 2022 Nov 14. Mol Genet Genomic Med. 2023. PMID: 36373990 Free PMC article. Review.

8

Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.

Yang JY, Wang WQ, Han MY, Huang SS, Wang GJ, Su Y, Xu JC, Fu Y, Kang DY, Yang K, Zhang X, Liu X, Gao X, Yuan YY, Dai P. Yang JY, et al. Among authors: gao x. BMC Med Genomics. 2022 Nov 18;15(1):241. doi: 10.1186/s12920-022-01368-9. BMC Med Genomics. 2022. PMID: 36401330 Free PMC article.

9

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment.

Gao X, Yuan YY, Wang GJ, Xu JC, Su Y, Lin X, Dai P. Gao X, et al. Biomed Res Int. 2017;2017:4707315. doi: 10.1155/2017/4707315. Epub 2017 Jan 29. Biomed Res Int. 2017. PMID: 28246597 Free PMC article.

10

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.

Gao X, Huang SS, Yuan YY, Xu JC, Gu P, Bai D, Kang DY, Han MY, Wang GJ, Zhang MG, Li J, Dai P. Gao X, et al. Neural Plast. 2017;2017:3192090. doi: 10.1155/2017/3192090. Epub 2017 Jun 13. Neural Plast. 2017. PMID: 28695016 Free PMC article.

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