Hu LD - Search Results

1

Adaptive resistance to PI3Kα-selective inhibitor CYH33 is mediated by genomic and transcriptomic alterations in ESCC cells.

Wang YX, Zhang X, Ma QY, Hu LD, Zhang X, Wang Y, Xu L, Yang CH, Tan C, Kong XY, Ding J, Meng LH. Wang YX, et al. Among authors: hu ld. Cell Death Dis. 2021 Jan 14;12(1):85. doi: 10.1038/s41419-020-03370-4. Cell Death Dis. 2021. PMID: 33446653 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. Among authors: hu ld. 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. 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. 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. 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. Mol Vis. 2003 Oct 24;9:579-83. Mol Vis. 2003. PMID: 14627959 Free article.

8

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. Hum Mutat. 2004 Apr;23(4):400. doi: 10.1002/humu.9231. Hum Mutat. 2004. PMID: 15024746

9

Identification of a new target region by loss of heterozygosity at 5p15.33 in sporadic gastric carcinomas: genotype and phenotype related.

Lu Y, Yu Y, Zhu Z, Xu H, Ji J, Bu L, Liu B, Jiang H, Lin Y, Kong X, Hu L. Lu Y, et al. Cancer Lett. 2005 Jun 28;224(2):329-37. doi: 10.1016/j.canlet.2004.11.057. Epub 2005 Jan 26. Cancer Lett. 2005. PMID: 15914283

10

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. Hum Genet. 2007 Mar;121(1):113-23. doi: 10.1007/s00439-006-0283-1. Epub 2006 Oct 31. Hum Genet. 2007. PMID: 17075716

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