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Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms
Cell competition is driven by Xrp1-mediated phosphorylation of eukaryotic initiation factor 2α
Pharmacogenomic Single Nucleotide Polymorphism (SNP) Variants As Predictors of Toxicity Phenotypes in the Treatment of Acute Childhood Leukemia
Associations of MCM8 rs3761873 and rs16991617 variants with abnormal uterine bleeding induced by copper intrauterine device
Advanced glycation end‐products (AGEs) are lower in prostate tumor tissue and inversely related to proportion of West African ancestry
FYB Methylation in Peripheral Blood as A Potential Marker for the Early-stage Lung Cancer: A Case-control Study in Chinese Population
MALDI MS-Based Investigations for SARS-CoV-2 Detection
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
Genetic Variant of PP2A Subunit Gene Confers an Increased Risk of Primary Liver Cancer in Chinese
Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
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