Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review

por Deng, Cechuan, Liu, Shanling
Publicado 2022

Expression of V-domain immunoglobulin suppressor of T cell activation is associated with the advanced stage and presence of lymph node metastasis in ovarian cancer

por Liao, Hong, Zhu, Hongmei, Liu, Shanling, Wang, He
Publicado 2018

Fibronectin Regulates the Dynamic Formation of Ovarian Cancer Multicellular Aggregates and the Expression of Integrin Receptors

por Gong, Lin, Zheng, Ying, Liu, Shanling, Peng, Zhilan
Publicado 2018

Chromosomal microarray analysis for the detection of chromosome abnormalities in fetuses with echogenic intracardiac focus in women without high-risk factors

por He, Min, Zhang, Zhu, Hu, Ting, Liu, Shanling
Publicado 2020

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis

por Liu, Xijing, Liu, Shanling, Wang, He, Hu, Ting
Publicado 2022

Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansio...

por Zhou, Cong, Wei, Xing, Xiao, Yuanyuan, Liu, Shanling, Wang, Jing
Publicado 2023

Enhanced antifungal activity of bovine lactoferrin-producing probiotic Lactobacillus casei in the murine model of vulvovaginal candidiasis

por Liao, Hong, Liu, Shanling, Wang, He, Su, Hang, Liu, Zhenjun
Publicado 2019

Integrative single-cell analysis of transcriptome, DNA methylome and chromatin accessibility in mouse oocytes

por Gu, Chan, Liu, Shanling, Wu, Qihong, Zhang, Lin, Guo, Fan
Publicado 2018

A novel variant in ALMS1 in a patient with Alström syndrome and prenatal diagnosis for the fetus in the family: A case report and literature review

por Zhou, Cong, Xiao, Yuanyuan, Xie, Hanbing, Liu, Shanling, Wang, Jing
Publicado 2020

A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report

por Zhou, Cong, Xiao, Yuanyuan, Xie, Hanbing, Liu, Shanling, Wang, Jing
Publicado 2021

Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family

por Zhou, Cong, Xiao, Yuanyuan, Xie, Hanbing, Wang, Jing, Liu, Shanling
Publicado 2021

HIV-1-related factors interact with p53 to influence cellular processes

por Liu, Shanling, Guo, Ting, Hu, Jinwei, Huang, Weiliang, She, Pengfei, Wu, Yong
Publicado 2023

Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm

por Zhang, Zhu, Hu, Ting, Wang, Jiamin, Li, Qinqin, Wang, He, Liu, Shanling
Publicado 2019

A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report

por Hu, Qian, Mai, Jingqun, Xiang, Qinqin, Zhou, Bin, Liu, Shanling, Wang, Jing
Publicado 2022

NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism

por Xiao, Yuanyuan, Zhou, Cong, Xie, Hanbing, Huang, Shuang, Wang, Jing, Liu, Shanling
Publicado 2022

A Clinicopathologic Analysis of Decidual Polyps: A Potentially Problematic Diagnosis

por Zou, Juan, He, Ying, Chen, Huiling, Wang, Peng, Xiao, Xue, Liu, Shanling
Publicado 2022

Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case report

por Yang, Yue, Jiang, Nan, Mai, Jing Qun, Yang, Shuo, Xiao, Yuanyuan, Liu, Shanling
Publicado 2023

Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7

por Zhou, Cong, Zhu, Hongmei, Xiang, Qinqin, Mai, Jingqun, Wang, Xihan, Wang, Jing, Liu, Shanling
Publicado 2023

A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease

por Zhao, Qianying, Tan, Yu, Xiao, Xiao, Xiang, Qinqin, Yang, Mei, Wang, He, Liu, Shanling
Publicado 2023

Genomic amplification of the human telomerase gene (hTERC) associated with human papillomavirus is related to the progression of uterine cervical dysplasia to invasive cancer

por Liu, Hongqian, Liu, Shanling, Wang, He, Xie, Xiaoyan, Chen, Xinlian, Zhang, Xuemei, Zhang, Youcheng
Publicado 2012