期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background The prognosis of pancreatic cancer is poor, with a 5-year survival rate of less than 10%. Studies have shown that chemokines in the tumour ......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background Although the relationship between inflammatory response and tumor has been gradually recognized, the potential implications of of inflammat......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background This study investigated the role of TP73 gene polymorphism, rs1801173on risk of gastric cancer. Methods We conducted a case-controlled stud......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
SMG9-deficiency syndrome, also known as heart and brain malformation syndrome, is a very rare congenital genetic disorder mainly characterized by brai......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background Increasing evidence has suggested an association between carotid atherosclerosis (CAS) and periodontitis (PD); however, the mechanisms have......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Objective Gastric carcinoma is the most common malignant tumour of the human digestive system worldwide. CD44 serves as a marker for several tumour st......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background: Among the most lethal cancers, pancreatic adenocarcinoma (PAAD) is an essential component of digestive system malignancies that still lack......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background Precision medicine has increased the accuracy of cancer diagnosis and treatment, especially in the era of cancer immunotherapy. Despite rec......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background Immunotherapy using immune checkpoint inhibitors (ICIs), such as antibody of programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) ha......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (SUPPL 2)
Background Non-invasive, especially the urine-based diagnosis of prostate cancer (PCa) remains challenging. Although prostate cancer antigen (PSA) is ......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background: Methamphetamine (METH) abuse causes serious health problems, including injury to the immune system, leading to increased incidence of infe......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background To investigate the genetic causes of hearing loss in patients with enlarged vestibular aqueduct (EVA), the SLC26A4-related genotypes and ph......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background Recurrent patellar dislocation is the result of anatomical alignment and imbalance of restraint of bone and soft tissue. We investigate the......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Background This study was to report a novel CREBBP mutation and phenotype in a child with Rubinstein-Taybi syndrome. Methods Case report of a 9-year-o......
期刊： BMC MEDICAL GENOMICS, 2022; 15 (1)
Objectives The purpose of this study was to investigate the association of PNPLA3 single nucleotide polymorphisms (SNPs) (rs738409 C > G, rs3747207......
