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