Noninvasive prenatal diagnosis of duchenne muscular dystrophy in five Chinese families based on relative mutation dosage approach

por Zhao, Ganye, Wang, Xiaofeng, Liu, Lina, Dai, Peng, Kong, Xiangdong
Publicado 2021

Analysis of L1CAM gene mutation and imaging appearance in three Chinese families with L1 syndrome: Three case reports

por Gao, Shanshan, Zhao, Xuechao, Zhao, Ganye, Dai, Peng, Kong, Xiangdong
Publicado 2022

Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China

por Zhao, Ganye, Dai, Peng, Wang, Conghui, Liu, Lina, Zhao, Xuechao, Kong, Xiangdong
Publicado 2022

Acetylation of FOXM1 is essential for its transactivation and tumor growth stimulation

por Lv, Cuicui, Zhao, Ganye, Sun, Xinpei, Wang, Pan, Xie, Nan, Luo, Jianyuan, Tong, Tanjun
Publicado 2016

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

por Zhao, Ganye, Dai, Peng, Gao, Shanshan, Zhao, Xuechao, Wang, Conghui, Liu, Lina, Kong, Xiangdong
Publicado 2019

Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique

por Zhao, Xuechao, Chen, Chen, Wei, Yanfu, Zhao, Ganye, Liu, Lina, Wang, Conghui, Zhang, Junjun, Kong, Xiangdong
Publicado 2019

Identification of four novel mutations in the COL4A5 gene identified in Chinese patients with X-linked Alport syndrome

por Zhao, Xuechao, Shang, Xueliang, Chen, Chen, Liu, Lina, Wang, Conghui, Zhao, Ganye, Zhang, Junjun, Kong, Xiangdong
Publicado 2020

A dPCR-NIPT assay for detections of trisomies 21, 18 and 13 in a single-tube reaction-could it replace serum biochemical tests as a primary maternal plasma screening tool?

por Dai, Peng, Yang, Yanfeng, Zhao, Ganye, Gu, Zhiqiang, Ren, Huanan, Hu, Shuang, Liu, Ning, Jiao, Weimeng, Li, Jinfang, Kong, Xiangdong
Publicado 2022

SIRT6 delays cellular senescence by promoting p27Kip1 ubiquitin-proteasome degradation

por Zhao, Ganye, Wang, Hui, Xu, Chenzhong, Wang, Pan, Chen, Jun, Wang, Pengfeng, Sun, Zhaomeng, Su, Yuanyuan, Wang, Zhao, Han, Limin, Tong, Tanjun
Publicado 2016

hnRNP A1 antagonizes cellular senescence and senescence‐associated secretory phenotype via regulation of SIRT1 mRNA stability

por Wang, Hui, Han, Limin, Zhao, Ganye, Shen, Hong, Wang, Pengfeng, Sun, Zhaomeng, Xu, Chenzhong, Su, Yuanyuan, Li, Guodong, Tong, Tanjun, Chen, Jun
Publicado 2016

Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review

por Zhu, Xiaofan, Lam, Doris Yuk Man, Chau, Matthew Hoi Kin, Xue, Shuwen, Dai, Peng, Zhao, Ganye, Cao, Ye, Cheung, Sunny Wai Hung, Kwok, Yvonne Ka Yin, Choy, Kwong Wai, Kong, Xiangdong, Leung, Tak Yeung
Publicado 2020