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Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models
The association of CASC16 variants with breast Cancer risk in a northwest Chinese female population
Promoter aberrant methylation status of ADRA1A is associated with hepatocellular carcinoma
Proofreading of single nucleotide insertion/deletion replication errors analyzed by MALDI-TOF mass spectrometry assay
Germline polymorphisms in the Von Hippel-Lindau and Hypoxia-inducible factor 1-alpha genes, gene-environment and gene-gene interactions and renal cell cancer
Interaction between early environment and genetic predisposition instigates the metabolically obese, normal weight phenotype in children: findings from the BCAMS study
Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach
Establishment and Characterisation by Expression Microarray of Patient-Derived Xenograft Panel of Human Pancreatic Adenocarcinoma Patients
Endoplasmic reticulum aminopeptidase 1 (ERAP1) polymorphisms and psoriasis susceptibility: A systematic review and meta-analysis
Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study
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