Dai H - Search Results

1

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: dai h. 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

2

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: dai hp. 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

3

[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: dai hp. Zhonghua Fu Chan Ke Za Zhi. 2005 Sep;40(9):591-4. Zhonghua Fu Chan Ke Za Zhi. 2005. PMID: 16202311 Chinese.

4

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: dai h. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

5

A syndactyly type IV locus maps to 7q36.

Sato D, Liang D, Wu L, Pan Q, Xia K, Dai H, Wang H, Nishimura G, Yoshiura KI, Xia J, Niikawa N. Sato D, et al. Among authors: dai h. J Hum Genet. 2007;52(6):561-564. doi: 10.1007/s10038-007-0150-5. Epub 2007 May 3. J Hum Genet. 2007. PMID: 17476456

6

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. Tang BS, et al. Among authors: dai hp. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

7

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.

Tang BS, Zhao GH, Luo W, Xia K, Cai F, Pan Q, Zhang RX, Zhang FF, Liu XM, Chen B, Zhang C, Shen L, Jiang H, Long ZG, Dai HP. Tang BS, et al. Among authors: dai hp. Hum Genet. 2005 Feb;116(3):222-4. doi: 10.1007/s00439-004-1218-3. Epub 2004 Nov 23. Hum Genet. 2005. PMID: 15565283

8

[Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].

Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH. Liang DS, et al. Yi Chuan Xue Bao. 2005 Feb;32(2):124-9. Yi Chuan Xue Bao. 2005. PMID: 15759858 Review. Chinese.

9

Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells.

He LQ, Liu Y, Cai F, Tan ZP, Pan Q, Liang DS, Long ZG, Wu LQ, Huang LQ, Dai HP, Xia K, Xia JH, Zhang ZH. He LQ, et al. Acta Biochim Biophys Sin (Shanghai). 2005 Aug;37(8):547-54. doi: 10.1111/j.1745-7270.2005.00080.x. Acta Biochim Biophys Sin (Shanghai). 2005. PMID: 16077902 Free article.

10

A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector.

Liang Y, Liang DS, Xue ZG, Long ZG, Wu LQ, Pan Q, Hu YQ, Dai HP, Xia K, Xia JH. Liang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):493-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215933

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