1、Xu H, Wang P, You J, Zheng Y, Fu Y, Tang Q, Zhou L, Wei Z, Lin B, Shu Y, Zhu Y, Hu L, Kong X.#. Screening of Kozak-motif-located SNPs and analysis of their association with human diseases.. Biochem Biophys Res Commun.,2010;392(1):89-94.
2、Zhou L, Zhang Z, Zheng Y, Zhu Y, Wei Z, Xu H, Tang Q, Kong X#, Hu L.. SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell. . J Cell Mol Med.,2010;():-.
3、Xu H, Wang P, Fu Y, Zheng Y, Tang Q, Si L, You J, Zhang Z, Zhu Y, Zhou L, Wei Z, Lin B, Hu L, Kong X.#. Length of the ORF, position of the first AUG and the Kozak motif are important factors in potential dual-coding transcripts. . Cell Res.,2010;():-.
4、Cai Y, He J, Li X, Lu L, Yang X, Feng K, Lu W, Kong X. #. A novel computational approach to predict transcription factor DNA binding preference. . J Proteome Res.,2009;8(2):999-1003.
5、Shi X, Cui B, Wang Z, Weng L, Xu Z, Ma J, Xu G, Kong X#, Hu L.. Removal of Hsf4 leads to cataract development in mice through down-regulation of gamma S-crystallin and Bfsp expression.. BMC Mol Biol.,2009;10():-10
6、Wang ZQ, Si L, Tang Q, Lin D, Fu Z, Zhang J, Cui B, Zhu Y, Kong X#, Deng M, Xia Y, Xu H, Le W, Hu L, Kong X.. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.. Am J Hum Genet.,2009;84(5):672-7
7、Zhang Z, Xin D, Wang P, Zhou L, Hu L, Kong X#, Hurst LD.. Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay.. BMC Biol.,2009;7(1):-23
8、Yin S, Deng W, Zheng H, Zhang Z, Hu L, Kong X.#. Evidence that the nonsense-mediated mRNA decay pathway participates in X chromosome dosage compensation in mammals.. Biochem Biophys Res Commun.,2009;383(3):378-82.
9、Yin S, Deng W, Hu L, Kong X.#. The impact of nucleosome positioning on the organization of replication origins in eukaryotes. . Biochem Biophys Res Commun.,2009;385(3):363-8
10、Yin S, Wang P, Deng W, Zheng H, Hu L, Hurst LD, Kong X. #. Dosage compensation on the active X chromosome minimizes transcriptional noise of X-linked genes in mammals. . Genome Biol.,2009;10(7):-R74
11、Zhang Z, Zhou L, Wang P, Liu Y, Chen X, Hu L, Kong X.#. Divergence of exonic splicing elements after gene duplication and the impact on gene structures.. Genome Biol.,2009;10(11):-R120
12、Wang P, Yin S, Zhang Z, Xin D, Hu L, Kong X#, Hurst LD.. Evidence for common short natural trans sense-antisense pairing between transcripts from protein coding genes. . Genome Biol.,2008;9(12):-R169
13、Xin D, Hu L, Kong X.#. Alternative promoters influence alternative splicing at the genomic level.. PLoS ONE.,2008;3(6):-e2377
14、Shi Y, Shi X, Jin Y, Miao A, Bu L, He J, Jiang H, Lu Y, Kong X#, Hu L.. Mutation screening of HSF4 in 150 age-related cataract patients.. Mol Vis.,2008;14():1850-5
15、Zhang H, Zhang Q, Wang L, Chen H, Li Y, Cui T, Huang W, Zhang L, Yan F, Wang L, Xu Y, Hu L, Kong X. #. Association of IL4R gene polymorphisms with asthma in Chinese populations. . Hum Mutat.,2007;28(10):-1046
16、Lu Y, Yu Y, Zhu Z, Xu H, Ji J, Bu L, Liu B, Jiang H, Lin Y, Kong X#, Hu L.. Identification of a new target region by loss of heterozygosity at 5p15.33 in sporadic gastric carcinomas: genotype and phenotype related. . Cancer Lett.,2005;224(2):329-37
17、Zhu ZG, Yu YY, Zhang Y, Ji J, Zhang J, Liu BY, Chen XH, Lu Y, Jiang HS, Bu L, Hu LD, Kong XY.#. Germline mutational analysis of CDH1 and pathologic features in familial cancer syndrome with diffuse gastric cancer/breast cancer proband in a Chinese family. . Eur J Surg Oncol.,2004;30(5):531-5
18、Zheng G, Hu L, Huang W, Chen K, Zhang X, Yang S, Sun J, Jiang Y, Luo G, Kong X. #. CYLD mutation causes multiple familial trichoepithelioma in three Chinese families.. Hum Mutat.,2004;23(4):-400
19、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. #. Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract.. Nat Genet.,2002;31():276-278
20、Xiao S, Yu C, Chou X, Yuan W, Wang Y, Bu L, Fu G, Qian M, Yang J, Shi Y, Hu L, Han B, Wang Z, Huang W, Liu J, Chen Z, Zhao G, Kong X.#. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.. Nat Genet.,2001;27():201-204