Jiang L - Search Results

1

Establishment of a risk index for early complications after trans-canal endoscopic ear surgery.

Jiang M, Cai X, Jiang L, Wu X, Jin Y, Wu L, Wu H, Liu C, Song J, Zhang S, Feng Y, He C, Mei L. Jiang M, et al. Among authors: jiang l. Am J Otolaryngol. 2022 May-Jun;43(3):103429. doi: 10.1016/j.amjoto.2022.103429. Epub 2022 Apr 5. Am J Otolaryngol. 2022. PMID: 35427935

2

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.

Chen H, Jiang L, Xie Z, Mei L, He C, Hu Z, Xia K, Feng Y. Chen H, et al. Among authors: jiang l. Biochem Biophys Res Commun. 2010 Jun 18;397(1):70-4. doi: 10.1016/j.bbrc.2010.05.066. Epub 2010 May 15. Biochem Biophys Res Commun. 2010. PMID: 20478267

3

[Tumorectomy by trans-oral approach of macrosis benign neoplasms in parapharyngeal space (reports of 6 cases)].

Zhang H, Feng Y, Jiang L. Zhang H, et al. Among authors: jiang l. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jun;24(12):556-8. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010. PMID: 20806862 Chinese.

4

[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].

Jiang L, Feng Y, Chen H, He C, Mei L. Jiang L, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jul;24(13):587-91. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010. PMID: 20842945 Chinese.

5

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.

Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Feng Y. Men M, et al. Among authors: jiang l. Acta Otolaryngol. 2011 Sep;131(9):970-5. doi: 10.3109/00016489.2011.575794. Epub 2011 Apr 19. Acta Otolaryngol. 2011. PMID: 21504270

6

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

Jiang L, Chen H, Jiang W, Hu Z, Mei L, Xue J, He C, Liu Y, Xia K, Feng Y. Jiang L, et al. Among authors: jiang w. Biochem Biophys Res Commun. 2011 May 20;408(4):620-4. doi: 10.1016/j.bbrc.2011.04.072. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531202

7

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.

Jiang L, Liu Y, Feng Y, Hu Z, Mei L, Long L, Chen H, Xue J, Xia K, He C. Jiang L, et al. Acta Otolaryngol. 2011 Oct;131(10):1061-8. doi: 10.3109/00016489.2011.591822. Epub 2011 Jun 8. Acta Otolaryngol. 2011. PMID: 21651318

8

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.

Zhang H, Chen H, Luo H, An J, Sun L, Mei L, He C, Jiang L, Jiang W, Xia K, Li JD, Feng Y. Zhang H, et al. Among authors: jiang w, jiang l. Hum Genet. 2012 Mar;131(3):491-503. doi: 10.1007/s00439-011-1098-2. Epub 2011 Oct 1. Hum Genet. 2012. PMID: 21965087

9

Novel multiplex primer extension and denaturing high-performance liquid chromatography for genotyping of the deafness gene mutations.

Men M, Xue J, Jiang L, Wang H, Pan Q, Feng Y. Men M, et al. Among authors: jiang l. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Nov;36(11):1079-84. doi: 10.3969/j.issn.1672-7347.2011.11.008. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 22169721

10

Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2.

Zhang H, Luo H, Chen H, Mei L, He C, Jiang L, Li JD, Feng Y. Zhang H, et al. Among authors: jiang l. FEBS Lett. 2012 Nov 30;586(23):4126-31. doi: 10.1016/j.febslet.2012.10.006. Epub 2012 Oct 23. FEBS Lett. 2012. PMID: 23098757 Free article.

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