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Methylation of the TERT promoter and risk stratification of childhood brain tumours: an integrative genomic and molecular study
Using Multiplexed Assays of Oncogenic Drivers in Lung Cancers to Select Targeted Drugs
Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degenration in 332 subjets degeneration in 332 subjects.
Ensuring Biospeciment Quality
p16 gene CpG methylation in cervical squamous cell carcinoma and HPV16 infection in Uyghur women
Associations Between Polymorphisms in the Glucocorticoid-Receptor Gene and Cardiovascular Risk Factors in a Chinese Population
Patterns of DNA Mutations and ALK Rearrangement in Resected Node Negative Lung Adenocarcinoma
Haplotype association analysis of genes within the WNT signalling pathways in diabetic nephropathy
Association between CACNB2 gene polymorphisms and essential hypertension
Stathmin genotype is associated with reexperiencing symptoms of posttraumatic stress disorder in Chinese earthquake survivors