Wu L - Search Results

1

Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read Sequencing.

Liu Y, Chen M, Liu J, Mao A, Teng Y, Yan H, Zhu H, Li Z, Liang D, Wu L. Liu Y, et al. Among authors: wu l. Clin Chem. 2022 Jul 3;68(7):927-939. doi: 10.1093/clinchem/hvac046. Clin Chem. 2022. PMID: 35714169

2

[Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)].

Liang DS, Wu LQ, Long ZG, Pan Q, Dai HP, Xia JH. Liang DS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):392-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15300643 Chinese.

3

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: wu l. J Radiat Res. 2004 Jun;45(2):281-9. doi: 10.1269/jrr.45.281. J Radiat Res. 2004. PMID: 15304972 Free article.

4

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: wu l. Cancer Gene Ther. 2004 Dec;11(12):790-6. doi: 10.1038/sj.cgt.7700728. Cancer Gene Ther. 2004. PMID: 15499380

5

[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.

6

Identification of the alternative promoters of the KChIP4 subfamily.

Deng XY, Cai F, Xia K, Pan Q, Long ZG, Wu LQ, Liang DS, Dai HP, Zhang ZH, Xia JH. Deng XY, et al. Acta Biochim Biophys Sin (Shanghai). 2005 Apr;37(4):241-7. doi: 10.1111/j.1745-7270.2005.00034.x. Acta Biochim Biophys Sin (Shanghai). 2005. PMID: 15806290

7

An improved mechanical technique for assisted hatching.

Lyu QF, Wu LQ, Li YP, Pan Q, Liu DE, Xia K, Liang DS, Cai F, Long ZG, Dai HP, Xia JH. Lyu QF, et al. Among authors: wu lq. Hum Reprod. 2005 Jun;20(6):1619-23. doi: 10.1093/humrep/deh809. Epub 2005 Apr 28. Hum Reprod. 2005. PMID: 15860502

8

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.

9

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. 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

10

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

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