Bin Cui

发表

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

M. Hayden, Xiangyin Kong, H. Eiberg, 2002, Nature Genetics.

Removal of Hsf4 leads to cataract development in mice through down-regulation of γS-crystallin and Bfsp expression

Xiangyin Kong, Xiaohe Shi, Bin Cui, 2009, BMC Molecular Biology.

Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Xiangyin Kong, Bin Cui, Yu Xia, 2009, American journal of human genetics.

Activation of paternally expressed imprinted genes in newly derived germline-competent mouse parthenogenetic embryonic stem cell lines

Guilai Shi, Yun Feng, Bin Cui, 2007, Cell Research.

Refinement of the locus for non-syndromic sensorineural deafness (DFN2)

Xiangyin Kong, Bin Cui, Landian Hu, 2004, Journal of Genetics.

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

Xiangyin Kong, L. Bu, Yiping Jin, 2003, Molecular vision.

Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.

Wei Huang, Jian Fei, Zhi-Min Yuan, 2009, American journal of human genetics.

Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22

Xiangyin Kong, L. Bu, Hai-ou Jiang, 2003, Journal of Human Genetics.

Removal of Hsf4 leads to cataract development in mice through down-regulation of γS-crystallin and Bfsp expression

Xiangyin Kong, Xiaohe Shi, Bin Cui, 2009, BMC Molecular Biology.