Xia Wang

Subchronic Exposure to Low-Level Lanthanum, Cerium, and Yttrium Mixtures Altered Cell Cycle and Increased Oxidative Stress Pathways in Human LO-2 Hepatocytes but Did Not Cause Malignant Transformation

Systematic investigation of TetR-family transcriptional regulators and their roles on lignocellulosic inhibitor acetate tolerance in Zymomonas mobilis

Pangenome analysis provides insight into the evolution of the orange subfamily and a key gene for citric acid accumulation in citrus fruits

Effects of Fmr1 Gene Mutations on Sex Differences in Autism-Like Behavior and Dendritic Spine Development in Mice and Transcriptomic Studies

Benchmarking of long-read sequencing, assemblers and polishers for yeast genome

Fragile X Mental Retardation Protein Mediates the Effects of Androgen on Hippocampal PSD95 Expression and Dendritic Spines Density/Morphology and Autism-Like Behaviors Through miR-125a

A Decreased Absolute Number of Treg Cells in Patients with Active Rheumatoid Arthritis is Associated with Elevated Serum Osteopontin Levels with Disease Progression

Genomic basis of high-altitude adaptation in Tibetan Prunus fruit trees

Derivation of induced pluripotent stem cells from one child suffering Potocki-Lupski syndrome

Large-Scale Transgenic <i>Drosophila</i> Resource Collections for Loss- and Gain-of-Function Studies

Reanalysis of Clinical Exome Sequencing Data

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

Perspectives on gene expression regulation techniques in Drosophila

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

Phenotypic expansion in <i> <scp>DDX</scp> 3X </i> – a common cause of intellectual disability in females

An efficient and multiple target transgenic RNAi technique with low toxicity in Drosophila

Next-generation CRISPR/Cas9 transcriptional activation in <i>Drosophila</i> using flySAM

De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features

Use of Exome Sequencing for Infants in Intensive Care Units

Bug mapping and fitness testing of chemically synthesized chromosome X

Mutational spectrum of Barrett’s stem cells suggests paths to initiation of a precancerous lesion

Overexpression of HOXC8 is Associated With Poor Prognosis in Epithelial Ovarian Cancer

Expression of Sam68 Correlates With Cell Proliferation and Survival in Epithelial Ovarian Cancer

Molecular diagnostic experience of whole-exome sequencing in adult patients

Cloning and variation of ground state intestinal stem cells

Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort

<i>In vitro</i> and <i>in vivo</i> correlates of physiological and neoplastic human Fallopian tube stem cells

Enhanced Specificity and Efficiency of the CRISPR/Cas9 System with Optimized sgRNA Parameters in Drosophila

Collaborative Research: Frameworks: hpcGPT: Enhancing Computing Center User Support with HPC-enriched Generative AI

"RET Site" Research Experience for Teachers in Alternative Energy and Automotive Engineering (AEAE): Energizing K-12 Teaching and Learning

IRES: U.S.-China Collaboration on Fluid and Thermal Transport in Fuel Cells