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  1. Article

    Open Access

    The rs9953490 polymorphism of DAL-1 gene is associated with gastric cancer risk in the Han population in Northeast China

    DAL-1 gene was reported to inhibit proliferation, migration, invasion, and epithelial to mesenchymal transition (EMT) of gastric cancer (GC) cells in our previous study. The association between the genomic var...

    Hui Wang, Yuling Jiang, Lina Yu, Lidan Xu, Rongwei Guan, Mengdi Cai in BMC Gastroenterology (2021)

  2. Article

    Open Access

    A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

    Synpolydactyly type 1 (SPD1), also known as syndactyly type II, is an autosomal dominant limb deformity generally results in webbing of 3rd and 4th fingers, duplication of 4th or 5th toes. It is most commonly ...

    Tahir Zaib, Wei Ji, Komal Saleem, Guangchen Nie, Chao Li, Lin Cao in BMC Medical Genetics (2019)

  3. Article

    Open Access

    Association between sister chromatid exchange and double minute chromosomes in human tumor cells

    Double minute chromosomes (DMs) are the cytogenetic hallmark of extra-chromosomal genomic amplification. They can well represent the advanced stage of malignancy. However, the mechanisms of DM generation are s...

    Jie Xu, Peng Liu, **angning Meng, **g Bai, Songbin Fu in Molecular Cytogenetics (2015)

  4. Article

    Open Access

    Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract

    Congenital cataract is a Mendelian disorder that frequently causes blindness in infants. To date, various cataract-associated loci have been mapped; more than 30 genes have been identified by linkage analysis....

    Xueyuan Jia, Feng Zhang, **g Bai, Linghan Gao, Xuelong Zhang in BMC Medical Genetics (2013)

  5. No Access

    Article

    Identification of novel subregions of LOH in gastric cancer and analysis of the HIC1 and TOB1 tumor suppressor genes in these subregions

    Previously, we identified 3 overlap** regions showing loss of heterozygosity (LOH, R1–R3 from 11 to 30 cM) on chromosome 17 in 45 primary gastric cancers (GCs). The data indicated the presence of tumor suppress...

    **gcui Yu, Peng Liu, **aobo Cui, Yu Sui, Guohua Ji, Rongwei Guan in Molecules and Cells (2011)

  6. Article

    Open Access

    Comparison of the inhibitory effects of three transcriptional variants of CDKN2A in human lung cancer cell line A549

    The tumor suppressor gene CDKN2A generates at least three different transcriptional variants, each of which is thought to encode a tumor suppressor. However, the inhibitory activities of these variants have not y...

    Wei Zhang, **g Zhu, **g Bai, Hui Jiang in Journal of Experimental & Clinical Cancer … (2010)