Songbin Fu

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Genome Wide Identification

Polycystic Kidney Disease

Gene Expression

Top Venues

Molecular genetics & genomic medicine

Disease markers

Journal of cellular and molecular medicine

BMC medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Dong Wang, Siyu Hao, Hongjie He, Jian Zhang, Ge You, Xin Wu, Rui Zhang, Xiangning Meng, Xiaobo Cui, Jing Bai, Songbin Fu, Jingcui Yu
Contribution of PGAP3 co-amplified and co-overexpressed with ERBB2 at 17q12 involved poor prognosis in gastric cancer. Journal of cellular and molecular medicine (2023)
Yusi Wang, Xuguang Hao, Xueyuan Jia, Wei Ji, Shuai Yuan, Estelle Judith Abla Gnamey, Min Huang, Lidan Xu, Xuelong Zhang, Jing Bai, Wenjing Sun, Songbin Fu, Yong Liu, Jie Wu
A novel variant of GLI3, p.Asp1514Thrfs*5, is identified in a Chinese family affected by polydactyly. Molecular genetics & genomic medicine 10 (7) (2022)
Kexian Dong, Xiaogang Liu, Xueyuan Jia, Huanhuan Miao, Wei Ji, Jie Wu, Yun Huang, Lidan Xu, Xuelong Zhang, Hui Su, Guohua Ji, Peng Liu, Rongwei Guan, Jing Bai, Songbin Fu, Xianli Zhou, Wenjing Sun
Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease. Molecular genetics & genomic medicine 8 (11) (2020)
Tahir Zaib, Chunhui Zhang, Komal Saleem, Lidan Xu, Qian Qin, Yusi Wang, Wei Ji, Hanif Khan, Hanfei Yu, Siqi Zhu, Wei Gao, Yun Huang, Xueyuan Jia, Jie Wu, Hongtao Song, Yan-Qiao Zhang, Wenjing Sun, Songbin Fu
Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree. Disease markers 2020 (2020)
Komal Saleem, Qingbo Cui, Tahir Zaib, Siqi Zhu, Qian Qin, Yusi Wang, Jinxi Dam, Wei Ji, Peng Liu, Xueyuan Jia, Jie Wu, Jing Bai, Songbin Fu, Wenjing Sun
Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3. Disease markers 2020 (2020)
Xueyuan Jia, Rongwei Guan, Xiaobo Cui, Jing Zhu, Peng Liu, Ling Zhang, Dong Wang, Yang Zhang, Kexian Dong, Jie Wu, Wei Ji, Guohua Ji, Jing Bai, Jingcui Yu, Yang Yu, Wenjing Sun, Feng Zhang, Songbin Fu
Molecular structure and evolution mechanism of two populations of double minutes in human colorectal cancer cells. Journal of cellular and molecular medicine 24 (24) (2020)
Tahir Zaib, Wei Ji, Komal Saleem, Guangchen Nie, Chao Li, Lin Cao, Baijun Xu, Kexian Dong, Hanfei Yu, Xuguang Hao, Yan Xue, Shuhan Si, Xueyuan Jia, Jie Wu, Xuelong Zhang, Rongwei Guan, Guohua Ji, Jing Bai, Feng Chen, Yong Liu, Wenjing Sun, Songbin Fu
A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family. BMC medical genetics 20 (1) (2019)
Mengdi Cai, Huishu Zhang, Liqing Hou, Wei Gao, Ying Song, Xiaobo Cui, Chunxiang Li, Rongwei Guan, Jinfa Ma, Xu Wang, Yue Han, Yafan Lv, Feng Chen, Ping Wang, Xiangning Meng, Songbin Fu
Inhibiting homologous recombination decreases extrachromosomal amplification but has no effect on intrachromosomal amplification in methotrexate-resistant colon cancer cells. International journal of cancer 144 (5) (2018)