论文
| 论文题目 | 宣布年度 |
|---|---|
| m(6)A Modification Involves in Enriched Environment-Induced Neurogenesis and Cognition Enhancement | 2022 |
| A machine learning-assisted model for renal urate underexcretion with genetic and clinical variables among Chinese men with gout | 2022 |
| DNA polymerase η promotes nonhomologous end joining upon etoposide exposure dependent on the scaffolding protein Kap1 | 2022 |
| Global Quantification of Glutathione S-Transferases in Human Serum Using LC-MS/MS Coupled with Affinity Enrichment | 2022 |
| CRISPR/Cas9-based multiplex genome editing of BCL11A and HBG efficiently induces fetal hemoglobin expression | 2022 |
| Inherent single-cell bioelectrical parameters of thousands of neutrophils, eosinophils and basophils derived from impedance flow cytometry | 2022 |
| The transmission of human mitochondrial DNA in four-generation pedigrees | 2022 |
| Causal Inference of Genetic Variants and Genes in Amyotrophic Lateral Sclerosis | 2022 |
| Population Genomic Sequencing Delineates Global Landscape of Copy Number Variations that Drive Domestication and Breed Formation of in Chicken | 2022 |
| GMQN: A Reference-Based Method for Correcting Batch Effects and Probe Bias in HumanMethylation BeadChip | 2022 |
| Genetic evidence for facial variation being a composite phenotype of cranial variation and facial soft tissue thickness | 2022 |
| Pinpointing the animal origins of SARS-CoV-2: A genomic approach | 2022 |
| Transmembrane Protein ANTXR1 Regulates γ-Globin Expression by Targeting the Wnt/β-Catenin Signaling Pathway | 2022 |
| Diagnosis and Prediction of Endometrial Carcinoma Using Machine Learning and Artificial Neural Networks Based on Public Databases | 2022 |
| Identification of COVID-19-Associated DNA Methylation Variations by Integrating Methylation Array and scRNA-Seq Data at Cell-Type Resolution | 2022 |
| Decoding the multicellular ecosystem of vena caval tumor thrombus in clear cell？renal cell carcinoma by single-cell RNA sequencing | 2022 |
| Case Report: A Novel Compound Heterozygote Mutation of the？SCNN1B？Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia | 2022 |
| Identification of Potential Molecular Mechanism Related to Infertile Endometriosis | 2022 |
| CrisprVi: a software for visualizing and analyzing CRISPR sequences of prokaryotes | 2022 |
| MPoxVR – A comprehensive genomic resource for monkeypox virus variants surveillance | 2022 |
