Hu L - Search Results

1

Molecular analysis of PinX1 in medulloblastomas.

Chang Q, Pang JC, Li J, Hu L, Kong X, Ng HK. Chang Q, et al. Among authors: hu l. Int J Cancer. 2004 Mar 20;109(2):309-14. doi: 10.1002/ijc.11689. Int J Cancer. 2004. PMID: 14750185

2

Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.

Bu L, Jin Y, Shi Y, Chu R, Ban A, Eiberg H, Andres L, Jiang H, Zheng G, Qian M, Cui B, Xia Y, Liu J, Hu L, Zhao G, Hayden MR, Kong X. Bu L, et al. Among authors: hu l. Nat Genet. 2002 Jul;31(3):276-8. doi: 10.1038/ng921. Epub 2002 Jun 24. Nat Genet. 2002. PMID: 12089525

3

A high-resolution genetic and physical map of a mouse coat abnormality locus (Uncv).

Shi YZ, Wang DP, Hu LD, Zhao GP, Wang YZ, Kong XY, Li SR. Shi YZ, et al. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 May;35(5):397-402. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003. PMID: 12766798

4

Linkage analysis of the candidate genes of familial restless legs syndrome.

Li J, Hu LD, Wang WJ, Chen YG, Kong XY. Li J, et al. Yi Chuan Xue Bao. 2003 Apr;30(4):325-9. Yi Chuan Xue Bao. 2003. PMID: 12812056

5

Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22.

Zhong W, Cui B, Zhang Y, Jiang H, Wei S, Bu L, Zhao G, Hu L, Kong X. Zhong W, et al. Among authors: hu l. J Hum Genet. 2003;48(7):390-2. doi: 10.1007/s10038-003-0043-1. Epub 2003 Jun 28. J Hum Genet. 2003. PMID: 12838398

6

Mutation analysis of 20 SARS virus genome sequences: evidence for negative selection in replicase ORF1b and spike gene.

Hu LD, Zheng GY, Jiang HS, Xia Y, Zhang Y, Kong XY. Hu LD, et al. Acta Pharmacol Sin. 2003 Aug;24(8):741-5. Acta Pharmacol Sin. 2003. PMID: 12904271 Free article.

7

Novel mutations in the IRF6 gene for Van der Woude syndrome.

Wang X, Liu J, Zhang H, Xiao M, Li J, Yang C, Lin X, Wu Z, Hu L, Kong X. Wang X, et al. Among authors: hu l. Hum Genet. 2003 Oct;113(5):382-6. doi: 10.1007/s00439-003-0989-2. Epub 2003 Aug 14. Hum Genet. 2003. PMID: 12920575

8

A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family.

Yu C, Meng X, Zhang S, Zhao G, Hu L, Kong X. Yu C, et al. Among authors: hu l. Genomics. 2003 Nov;82(5):575-9. doi: 10.1016/s0888-7543(03)00175-7. Genomics. 2003. PMID: 14559215

9

A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.

Jiang H, Jin Y, Bu L, Zhang W, Liu J, Cui B, Kong X, Hu L. Jiang H, et al. Among authors: hu l. Mol Vis. 2003 Oct 24;9:579-83. Mol Vis. 2003. PMID: 14627959 Free article.

10

CYLD mutation causes multiple familial trichoepithelioma in three Chinese families.

Zheng G, Hu L, Huang W, Chen K, Zhang X, Yang S, Sun J, Jiang Y, Luo G, Kong X. Zheng G, et al. Among authors: hu l. Hum Mutat. 2004 Apr;23(4):400. doi: 10.1002/humu.9231. Hum Mutat. 2004. PMID: 15024746

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