He C - Search Results

1

A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development.

Wen J, Song J, Bai Y, Liu Y, Cai X, Mei L, Ma L, He C, Feng Y. Wen J, et al. Among authors: he c. Front Cell Dev Biol. 2021 Aug 6;9:720858. doi: 10.3389/fcell.2021.720858. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34426786 Free PMC article.

2

[An analysis of a large hereditary postlingually deaf families and detecting mutation of the deafness genes].

Feng Y, He Cf, Xiao J, Fang J, Zhao S, Tian X, Mei L, Xia K, Tang X. Feng Y, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2002 Jul;16(7):323-5. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 15510726 Chinese.

3

[Mutation analysis of gene CX31.1 in the hereditary hearing loss pedigrees].

Feng Y, He C, Xia K, Li Q, He D. Feng Y, et al. Among authors: he c, he d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005 Feb;19(4):178-9. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005. PMID: 15938215 Chinese.

4

[The prenatal diagnosis and early intervention of nonsyndromic hearing loss of connexin26 gene].

He C, Feng Y, Xia K, Mei L, He D. He C, et al. Among authors: he d. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Jul;20(13):579-81. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16981465 Chinese.

5

[The application of 3D reconstruction of CT scans for the observation of the cochlear implanted electrode location].

Liu H, Feng Y, Chen D, CaI X, He C. Liu H, et al. Among authors: he c. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Jul;20(13):597-9. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16981471 Chinese.

6

[Surgical approaches and related microsurgical anatomy about suprameatal approach: new surgical approach for cochlear implantation].

Liu H, Feng Y, Chen D, Mei L, He C, Cai X. Liu H, et al. Among authors: he c. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):447-9. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17650813 Chinese.

7

[Screening and identification interaction proteins of connexin 30].

He DH, Feng Y, Mei LY, He CF. He DH, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Sep;44(9):758-61. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 20079101 Chinese.

8

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: he c. 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

9

[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. Among authors: he c. 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.

10

[Inhibition of the expression of VEGF gene in nasopharyngeal carcinoma cells by microRNA].

Cai X, Wei W, Zhao S, Tang Y, He C, Wang C. Cai X, et al. Among authors: he c. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Aug;24(15):703-7. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010. PMID: 20942241 Chinese.

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