Hu L - Search Results

1

Longitudinal immune profiling reveals dominant epitopes mediating long-term humoral immunity in COVID-19-convalescent individuals.

Li M, Liu J, Lu R, Zhang Y, Du M, Xing M, Wu Z, Kong X, Zhu Y, Zhou X, Hu L, Zhang C, Zhou D, Jin X. Li M, et al. Among authors: hu l. J Allergy Clin Immunol. 2022 Apr;149(4):1225-1241. doi: 10.1016/j.jaci.2022.01.005. Epub 2022 Jan 21. J Allergy Clin Immunol. 2022. PMID: 35074422 Free PMC article.

2

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

3

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

4

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.

5

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

6

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

7

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.

8

A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15.

Zhu Y, Zhang W, Huo Z, Zhang Y, Xia Y, Li B, Kong X, Hu L. Zhu Y, et al. Among authors: hu l. Hum Genet. 2007 Mar;121(1):113-23. doi: 10.1007/s00439-006-0283-1. Epub 2006 Oct 31. Hum Genet. 2007. PMID: 17075716

9

A single C to T transition in intron 5 of LMBR1 gene is associated with triphalangeal thumb-polysyndactyly syndrome in a Chinese family.

Wang ZQ, Tian SH, Shi YZ, Zhou PT, Wang ZY, Shu RZ, Hu L, Kong X. Wang ZQ, et al. Among authors: hu l. Biochem Biophys Res Commun. 2007 Apr 6;355(2):312-7. doi: 10.1016/j.bbrc.2007.01.129. Epub 2007 Feb 2. Biochem Biophys Res Commun. 2007. PMID: 17300748

10

Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus.

Zhou P, Wang Z, Zhang J, Hu L, Kong X. Zhou P, et al. Among authors: hu l. Mol Vis. 2008 May 30;14:1015-9. Mol Vis. 2008. PMID: 18523664 Free PMC article.

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