Efficient Gene Transfection into Mammalian Cells Mediated by Cross-linked Polyethylenimine

por Dong, Wei, Li, Shufeng, Jin, Guanghui, Sun, Qiming, Ma, Dingyuan, Hua, Zichun
Publicado 2007

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

por Li, Yahong, Ma, Dingyuan, Sun, Yun, Meng, Lulu, Wang, Yanyun, Jiang, Tao
Publicado 2018

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

Miltirone induces cell death in hepatocellular carcinoma cell through GSDME-dependent pyroptosis

por Zhang, Xiaowei, Zhang, Ping, An, Lin, Sun, Ningyuan, Peng, Liying, Tang, Weiwei, Ma, Dingyuan, Chen, Jun
Publicado 2020

A high-throughput Gaussia luciferase reporter assay for screening potential gasdermin E activators against pancreatic cancer

por Liu, Yang, Zhang, Xiaowei, Zhang, Ping, He, Tingting, Zhang, Weitao, Ma, Dingyuan, Li, Ping, Chen, Jun
Publicado 2023

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

Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population

por Wang, Xin, Wang, Yanyun, Ma, Dingyuan, Zhang, Zhilei, Li, Yahong, Yang, Peiying, Sun, Yun, Jiang, Tao
Publicado 2021

Neonatal screening and genotype-phenotype correlation of hyperphenylalaninemia in the Chinese population

por Wang, Xin, Wang, Yanyun, Ma, Dingyuan, Zhang, Zhilei, Li, Yahong, Yang, Peiying, Sun, Yun, Jiang, Tao
Publicado 2021

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

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

por Zhang, Jingjing, Ma, Dingyuan, Liu, Gang, Wang, Yuguo, Liu, An, Li, Li, Luo, Chunyu, Hu, Ping, Xu, Zhengfeng
Publicado 2019

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy

por Zhou, Jing, Tan, Jianxin, Ma, Dingyuan, Zhang, Jingjing, Cheng, Jian, Luo, Chunyu, Liu, Gang, Wang, Yuguo, Xu, Zhengfeng
Publicado 2018

A novel splice site mutation in the UBE2A gene leads to aberrant mRNA splicing in a Chinese patient with X‐linked intellectual disability type Nascimento

por Ma, Dingyuan, Tan, Jianxin, Zhou, Jing, Zhang, Jingjing, Cheng, Jian, Luo, Chunyu, Liu, Gang, Wang, Yuguo, Xu, Zhengfeng
Publicado 2019

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies

por Ji, Xiuqing, Pan, Qiong, Wang, Yan, Wu, Yun, Zhou, Jing, Liu, An, Qiao, Fengchang, Ma, Dingyuan, Hu, Ping, Xu, Zhengfeng
Publicado 2018

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson’s disease: a case report

por Liu, Gang, Ma, Dingyuan, Cheng, Jian, Zhang, Jingjing, Luo, Chunyu, Sun, Yun, Hu, Ping, Wang, Yuguo, Jiang, Tao, Xu, Zhengfeng
Publicado 2018

A Novel Whole Gene Deletion of BCKDHB by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine Disease

por Liu, Gang, Ma, Dingyuan, Hu, Ping, Wang, Wen, Luo, Chunyu, Wang, Yan, Sun, Yun, Zhang, Jingjing, Jiang, Tao, Xu, Zhengfeng
Publicado 2018

Modification of Cyclic NGR Tumor Neovasculature-Homing Motif Sequence to Human Plasminogen Kringle 5 Improves Inhibition of Tumor Growth

por Jiang, Weiwei, Jin, Guanghui, Ma, Dingyuan, Wang, Feng, Fu, Tong, Chen, Xiao, Chen, Xiwen, Jia, Kunzhi, Marikar, Faiz M. M. T., Hua, Zichun
Publicado 2012

Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect

por Zhang, Jingjing, Ma, Dingyuan, Wang, Yan, Cao, Li, Wu, Yun, Qiao, Fengchang, Liu, An, Li, Li, Lin, Ying, Liu, Gang, Liu, Cuiyun, Hu, Ping, Xu, Zhengfeng
Publicado 2015

Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA

por Ma, Dingyuan, Yuan, Yuan, Luo, Chunyu, Wang, Yaoshen, Jiang, Tao, Guo, Fengyu, Zhang, Jingjing, Chen, Chao, Sun, Yun, Cheng, Jian, Hu, Ping, Wang, Jian, Yang, Huanming, Yi, Xin, Wang, Wei, Asan, Xu, Zhengfeng
Publicado 2017