Feng Y - Search Results

1

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.

Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K. Xia J, et al. Among authors: feng y. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

2

The combination of suicide gene therapy and radiation enhances the killing of nasopharyngeal carcinoma xenographs.

Xia J, Xia K, Feng Y, Tang A, Tang Y, Wu L, Liang D, Cai F, Pan Q, Long Z, Dai H, Zhang Y, Zhao S, Chen Z. Xia J, et al. Among authors: feng y. J Radiat Res. 2004 Jun;45(2):281-9. doi: 10.1269/jrr.45.281. J Radiat Res. 2004. PMID: 15304972 Free article.

3

A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinoma.

Xia K, Liang D, Tang A, Feng Y, Zhang J, Pan Q, Long Z, Dai H, Cai F, Wu L, Zhao S, Chen Z, Xia J. Xia K, et al. Among authors: feng y. Cancer Gene Ther. 2004 Dec;11(12):790-6. doi: 10.1038/sj.cgt.7700728. Cancer Gene Ther. 2004. PMID: 15499380

4

[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.

5

[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. 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.

6

Molecular analysis of SLC26A4 gene in a Chinese deafness family.

Hu H, Liang DS, Wu LQ, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Among authors: feng y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):376-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086271

7

[Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation].

Hu H, Wu LQ, Liang DS, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Among authors: feng y. Zhonghua Fu Chan Ke Za Zhi. 2005 Sep;40(9):591-4. Zhonghua Fu Chan Ke Za Zhi. 2005. PMID: 16202311 Chinese.

8

Combined radiation and suicide gene therapy for Nasopharyngeal Carcinoma: in vitro and in vivo models.

Tang A, Zhang J, Tang Y, Feng Y, Wu L, Pan Q, Long Z, Dai H, Zhao S, Liu T, Chen Z, Xia K, Xia J. Tang A, et al. Among authors: feng y. Acta Biochim Pol. 2005 Nov 6. Online ahead of print. Acta Biochim Pol. 2005. PMID: 16273130

9

[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: feng y. 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.

10

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.

Hu H, Wu L, Feng Y, Pan Q, Long Z, Li J, Dai H, Xia K, Liang D, Niikawa N, Xia J. Hu H, et al. Among authors: feng y. J Hum Genet. 2007;52(6):492-497. doi: 10.1007/s10038-007-0139-0. Epub 2007 Apr 19. J Hum Genet. 2007. PMID: 17443271

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