Kong X - Search Results

1

Intact regulation of G1/S transition renders esophageal squamous cell carcinoma sensitive to PI3Kα inhibitors.

Zhang X, Wang Y, Zhang X, Shen Y, Yang K, Ma Q, Qiao Y, Shi J, Wang Y, Xu L, Yang B, Ge G, Hu L, Kong X, Yang C, Chen Y, Ding J, Meng L. Zhang X, et al. Among authors: kong x. Signal Transduct Target Ther. 2023 Apr 12;8(1):153. doi: 10.1038/s41392-023-01359-x. Signal Transduct Target Ther. 2023. PMID: 37041169 Free PMC article.

2

[New progress of serial analysis of gene expression].

Li J, Chen YG, Kong XY. Li J, et al. Among authors: kong xy. Sheng Wu Gong Cheng Xue Bao. 2001 Nov;17(6):613-6. Sheng Wu Gong Cheng Xue Bao. 2001. PMID: 11910750 Review. Chinese.

3

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

4

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: kong x. 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

5

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.

6

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: kong x. Hum Genet. 2003 Oct;113(5):382-6. doi: 10.1007/s00439-003-0989-2. Epub 2003 Aug 14. Hum Genet. 2003. PMID: 12920575

7

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: kong x. Genomics. 2003 Nov;82(5):575-9. doi: 10.1016/s0888-7543(03)00175-7. Genomics. 2003. PMID: 14559215

8

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: kong x. Mol Vis. 2003 Oct 24;9:579-83. Mol Vis. 2003. PMID: 14627959 Free article.

9

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

10

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. Among authors: kong x. 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

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