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PubMed 9674978 Meta-analysis of DRD3 gene and schizophrenia: ethnic heterogeneity and significant association in Caucasians. The involvement of dopamine in the etiology of schizophrenia is suggested by a number of n 1.88 KB 2015-11-28 2 3
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PubMed 22534770 Differences in allele frequencies of autosomal dominant hypercholesterolemia SNPs in the Malaysian population. Hypercholesterolemia is caused by different interactions of lifestyle and genetic determi 1.85 KB 2015-11-26 4 11
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PubMed 19168133 Mendelian forms of Parkinson's disease. Over the last few years, genetic findings have changed our views on Parkinson's disease (PD), as mutations in a growing number of genes are found to cause monog 1.22 KB 2015-11-24 13 14
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PubMed 24796628 Tumor necrosis factor-β Nco1 polymorphism and susceptibility to sepsis following major elective surgery. BACKGROUND: Post-operative sepsis remains a substantial cause of morbidity and mortality. In in 2.75 KB 2015-11-27 5 6
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PubMed 12050219 Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome. Kallmann's syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia o 1.87 KB 2015-11-17 3 3
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PubMed 16317690 Oral adeno-associated virus-sTRAIL gene therapy suppresses human hepatocellular carcinoma growth in mice. The extracellular domain of the tumor necrosis factor-related apoptosis-inducing ligand (sTRAI 1.6 KB 2015-11-19 3 27
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PubMed 19850049 Analysis of angiogenesis induced by local IGF-1 expression after myocardial infarction using microSPECT-CT imaging. Insulin-like growth factor-1 (IGF-1) has been found to exert favorable effects on an 1.79 KB 2015-11-25 3 6
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PubMed 21164282 A proposed model for endometrial serous carcinogenesis. Endometrial serous carcinomas constitute no more than 10% of endometrial adenocarcinomas, but frequently present at an advanced stage and have a 1.68 KB 2015-11-25 3 7
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PubMed 16832093 Hyperekplexia in Kurdish families: a possible GLRA1 founder mutation. Autosomal recessive hyperekplexia is due to loss-of-function mutations in the GLRA1 gene. The authors describe six patients from t 394 Bytes 2015-11-19 3 5
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PubMed 25567759 CD22ΔE12 as a molecular target for corrective repair using RNA trans-splicing: anti-leukemic activity of a rationally designed RNA trans-splicing molecule. Our recent studies have demonstrated that th 1.65 KB 2016-01-19 4 39
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