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PubMed 24376633 Association of levels of mannose-binding lectin and the MBL2 gene with type 2 diabetes and diabetic nephropathy. OBJECTIVE: To investigate the association of Mannose-binding lectin (MBL) and the MBL2 1.93 KB 2015-11-27 6 5
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PubMed 23560613 Association study of OPRM1 polymorphisms with Schizophrenia in Han Chinese population. BACKGROUND: The expression of μ-opioid receptor has important role in cognitive dysfunction in Schizophrenia (SZ) 2.23 KB 2015-11-26 6 14
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PubMed 23064873 HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Prostate cancer has a strong familial component but uncovering the 1.9 KB 2015-11-27 6 9
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PubMed 24086514 Association of polymorphisms in pharmacogenetic candidate genes (OPRD1, GAL, ABCB1, OPRM1) with opioid dependence in European population: a case-control study. It is becoming increasingly evident that 1.98 KB 2015-11-26 4 10
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PubMed 23383292 FADS gene polymorphisms confer the risk of coronary artery disease in a Chinese Han population through the altered desaturase activities: based on high-resolution melting analysis. OBJECTIVE: We explo 1.56 KB 2015-11-26 5 11
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PubMed 21545724 Serotonin transporter gene polymorphisms and brain function during emotional distraction from cognitive processing in posttraumatic stress disorder. BACKGROUND: Serotonergic system dysfunction has bee 2.33 KB 2015-11-26 6 6
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PubMed 22666313 Convergent evidence from mouse and human studies suggests the involvement of zinc finger protein 326 gene in antidepressant treatment response. OBJECTIVES: The forced swim test (FST) is a commonly use 1.86 KB 2015-03-13 5 5
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PubMed 23029260 p53 codon 72 polymorphism and hematological cancer risk: an update meta-analysis. BACKGROUND: Previous studies on the association of p53 codon 72 (Arg72Pro) polymorphism with hematological malignancie 1.63 KB 2015-11-26 4 16
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PubMed 23029558 Myocilin polymorphisms and primary open-angle glaucoma: a systematic review and meta-analysis. BACKGROUND: Glaucoma is the leading cause of irreversible blindness in the world. Recent evidence indicat 1.36 KB 2016-01-13 5 13
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PubMed 22419846 A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene. PURPOSE: Oguchi's disease is a rare autosomal recessive disease and known to be c 2.28 KB 2016-01-09 5 3
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