Effects of FHIT gene on proliferation and apoptosis of osteosarcoma cells

por Xu, Zhengfeng, Wu, Jiajun, Cai, Pan, Zhou, Xiaoxiao, Yi, Cunguo, Wang, Bin
Publicado 2019

Pregnancy outcomes of rare autosomal trisomies results in non‐invasive prenatal screening: clinical follow‐up data from a single tertiary centre

por Lin, Ying, Hu, Ping, Li, Hang, Luo, Chunyu, Liang, Dong, Xu, Zhengfeng
Publicado 2022

Analyzing false‐negative results detected in low‐risk non‐invasive prenatal screening cases

por Lin, Ying, Liang, Dong, Wang, Yan, Li, Hang, Liu, An, Hu, Ping, Xu, Zhengfeng
Publicado 2020

Seasonal Dynamics of Soil Microbial Biomass C and N along an Elevational Gradient on the Eastern Tibetan Plateau, China

por Gou, Xiaolin, Tan, Bo, Wu, Fuzhong, Yang, Wanqin, Xu, Zhengfeng, Li, Zhiping, Zhang, Xitao
Publicado 2015

Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis

por MA, DINGYUAN, ZHANG, JINGJING, LUO, CHUNYU, LIN, YING, JI, XIUQING, HU, PING, XU, ZHENGFENG
Publicado 2016

Identifying Novel Copy Number Variants in Azoospermia Factor Regions and Evaluating Their Effects on Spermatogenic Impairment

por Zhou, Ran, Cheng, Jian, Ma, Dingyuan, Tan, Jianxin, Wang, Yuguo, Hu, Ping, Xu, Zhengfeng
Publicado 2019

Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing

por Zhou, Xiaoyan, Wang, Yan, Shao, Binbin, Wang, Chen, Hu, Ping, Qiao, Fengchang, Xu, Zhengfeng
Publicado 2020

Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome

por Qiao, Fengchang, Zhang, Cuiping, Wang, Yan, Liu, Gang, Shao, Binbin, Hu, Ping, Xu, Zhengfeng
Publicado 2021

Analysis of microbial differences in amniotic fluid between advanced and normal age pregnant women

por Wang, Ya, Luo, Chunyu, Cheng, Yiwei, Li, Li, Liang, Dong, Hu, Ping, Xu, Zhengfeng
Publicado 2021

Mesenchymal stem cell-derived exosomes carrying microRNA-150 suppresses the proliferation and migration of osteosarcoma cells via targeting IGF2BP1

por Xu, Zhengfeng, Zhou, Xiaoxiao, Wu, Jiajun, Cui, Xu, Wang, Minghui, Wang, Xiuhui, Gao, Zhenchao
Publicado 2020

Knockdown of lncRNA LINC00662 suppresses malignant behaviour of osteosarcoma cells via competition with miR-30b-3p to regulate ELK1 expression

por Wang, Bin, Xu, Zhengfeng, Wang, Xiuhui, Xia, Shengli, Cai, Pan, Wang, Minghui, Gao, Zhenchao
Publicado 2022

Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing

por Zhou, Ran, Jiao, Jiao, Wang, Yan, Meng, Lulu, Li, Yiming, Xu, Yiyun, Hu, Ping, Xu, Zhengfeng
Publicado 2023

Novel Missense Variants of ZFPM2/FOG2 Identified in Conotruncal Heart Defect Patients Do Not Impair Interaction with GATA4

por Zhang, Wenwen, Shen, Li, Deng, Zhantao, Ding, Yibing, Mo, Xuming, Xu, Zhengfeng, Gao, Qian, Yi, Long
Publicado 2014

A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation

por Hu, Ping, Meng, Lulu, Ma, Dingyuan, Qiao, Fengchang, Wang, Yan, Zhou, Jing, Yi, Long, Xu, Zhengfeng
Publicado 2015

Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing

por Ji, Xiuqing, Liang, Dong, Sun, Ruihong, Liu, Cuiyun, Ma, Dingyuan, Wang, Yan, Hu, Ping, Xu, Zhengfeng
Publicado 2015

A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencing

por Qiao, Fengchang, Wang, Chen, Luo, Chunyu, Wang, Yan, Shao, Binbin, Tan, Jianxin, Hu, Ping, Xu, Zhengfeng
Publicado 2019

Association between thyroid-stimulating hormone and maternal hemodynamics in hypertensive disorders of pregnancy: an observational study

por Liu, Yu, Gao, Bo, Zeng, Xin, Yang, Jing, Zhang, Lei, Xu, Ganwei, Jia, Ruizhe, Xu, Zhengfeng
Publicado 2019

Proline‐rich transmembrane protein 2 specifically binds to GluA1 but has no effect on AMPA receptor‐mediated synaptic transmission

por Feng, Hao‐Yang, Qiao, Fengchang, Tan, Jianxin, Zhang, Xiaozuo, Hu, Ping, Shi, Yun Stone, Xu, Zhengfeng
Publicado 2022

Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency

por Zhang, Jingjing, Ma, Dingyuan, Liu, Gang, Zeng, Huasha, Wang, Yuguo, Luo, Chunyu, Hu, Ping, Xu, Zhengfeng
Publicado 2022

11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four‐way balanced chromosomal translocation

por Zhang, Qinxin, Wang, Yan, Zhou, Jing, Zhou, Ran, Liu, An, Meng, Lulu, Ji, Xiuqing, Hu, Ping, Xu, Zhengfeng
Publicado 2023