Yufei Zhu

发表

SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell

Xiangyin Kong, Landian Hu, Li Zhou, 2010, Journal of cellular and molecular medicine.

Screening of Kozak-motif-located SNPs and analysis of their association with human diseases.

Xiangyin Kong, Landian Hu, Li Zhou, 2010, Biochemical and biophysical research communications.

A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15

Xiangyin Kong, B. Li, Bo Li, 2007, Human Genetics.

Alternative splicing at GYNNGY 5′ splice sites: more noise, less regulation

M. Wang, Xiangyin Kong, Yuchao Zhang, 2014, Nucleic acids research.

C/EBPα deficiency in podocytes aggravates podocyte senescence and kidney injury in aging mice

N. Chen, Liwen Zhang, Weiming Wang, 2019, Cell Death & Disease.

The role of maternal immune activation in the immunological and neurological pathogenesis of autism

Xiangyin Kong, Yufei Zhu, Keqin Liu, 2022, Journal of Neurorestoratology.

Genes that Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving

L. Hurst, Xiangyin Kong, Yuchao Zhang, 2015, Molecular biology and evolution.

Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Xiangyin Kong, Bin Cui, Yu Xia, 2009, American journal of human genetics.

Uncovering the Rare Variants of DLC1 Isoform 1 and Their Functional Effects in a Chinese Sporadic Congenital Heart Disease Cohort

Xiangyin Kong, G. Ning, Yuchao Zhang, 2014, PloS one.

Genes that Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving

Araxi O. Urrutia, L. Hurst, Xiangyin Kong, 2015, Molecular biology and evolution.

Genes That Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving

L. Hurst, Xiangyin Kong, Yuchao Zhang, 2013, Molecular biology and evolution.

Integrative analysis reveals enhanced regulatory effects of human long intergenic non-coding RNAs in lung adenocarcinoma.

Xiangyin Kong, G. Hu, Yufang Shi, 2015, Journal of genetics and genomics = Yi chuan xue bao.

COL4A3 mutations cause focal segmental glomerulosclerosis.

Xiangyin Kong, K. Kiryluk, N. Chen, 2014, Journal of molecular cell biology.

Combined Analysis with Copy Number Variation Identifies Risk Loci in Lung Cancer

Xiangyin Kong, Xianfu Yi, G. Hu, 2014, BioMed research international.

Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer

Xiangyin Kong, Landian Hu, Yufei Zhu, 2021, Communications biology.

Single-cell RNA sequencing reveals the suppressive effect of PPP1R15A inhibitor Sephin1 in antitumor immunity

Ling-hua Meng, Yuchao Zhang, Wei Guo, 2023, iScience.

Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations

Zhimin Chen, Xiangyin Kong, Zhe Wang, 2015, Scientific Reports.

Altered Expression of Long Noncoding and Messenger RNAs in Diabetic Nephropathy following Treatment with Rosiglitazone

N. Chen, Liwen Zhang, Weiming Wang, 2020, BioMed research international.

Revisiting Non-BRCA1/2 Familial Whole Exome Sequencing Datasets Implicates NCK1 as a Cancer Gene

Xiangyin Kong, Landian Hu, Yufei Zhu, 2019, Front. Genet..

De novo Structure Variations of the Y Chromosome in a 47,XXY Female with Ovarian Failure: A Case Report

Xiangyin Kong, Landian Hu, Yufei Zhu, 2014, Cytogenetic and Genome Research.

Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer

Xiangyin Kong, Wei Guo, Landian Hu, 2021, Communications Biology.

Rare germline GLMN variants identified from blue rubber bleb nevus syndrome might impact mTOR signaling.

Kai Wu, Xiangyin Kong, Xiangyin Kong, 2019, Combinatorial chemistry & high throughput screening.

Progress and challenges of personalized neoantigens in the clinical treatment of tumors

Yuchao Zhang, Yufei Zhu, Dongliang Liu, 2020, Medicine in Drug Discovery.

Evidence for OTUD-6B Participation in B Lymphocytes Cell Cycle after Cytokine Stimulation

Xiangyin Kong, Landian Hu, Zhongping Xu, 2011, PloS one.

Length of the ORF, position of the first AUG and the Kozak motif are important factors in potential dual-coding transcripts

Xiangyin Kong, Ping Wang, Xiangyin Kong, 2010, Cell Research.

Nonsense-mediated decay targets have multiple sequence-related features that can inhibit translation

Yang Liu, Xiangyin Kong, L. Hurst, 2010, Molecular systems biology.

Characterization of the Blood and Cerebrospinal Fluid Microbiome in Children with Bacterial Meningitis and Its Potential Correlation with Inflammation

Xiangyin Kong, Yongli Guo, Landian Hu, 2021, mSystems.

Longitudinal immune profiling reveals dominant epitopes mediating long-term humoral immunity in COVID-19–convalescent individuals

Xiangyin Kong, Yuchao Zhang, Dongming Zhou, 2022, Journal of Allergy and Clinical Immunology.

ONECUT2 overexpression promotes RAS-driven lung adenocarcinoma progression

Xiangyin Kong, Hui Li, G. Hu, 2019, Scientific Reports.

COL4A3 mutations cause focal segmental glomerulosclerosis.

Xiangyin Kong, K. Kiryluk, N. Chen, 2015, Journal of molecular cell biology.

Escaping but not the inactive X-linked protein complex coding genes may achieve X-chromosome dosage compensation and underlie X chromosome inactivation-related diseases

Xiangyin Kong, Yuchao Zhang, Zhihao Xing, 2023, Heliyon.

Assessing the activity of nonsense-mediated mRNA decay in lung cancer

Xiangyin Kong, Landian Hu, Zhenguo Zhang, 2017, BMC Medical Genomics.

Genes That Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving

Araxi O. Urrutia, L. Hurst, Xiangyin Kong, 2013, Molecular biology and evolution.

Assessing the activity of nonsense-mediated mRNA decay in lung cancer

Xiangyin Kong, Landian Hu, Zhenguo Zhang, 2017, BMC Medical Genomics.