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PubMed 20143913 Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient. Apparent homozygosity for the mutation p.R315X present on exon 5 of 1.09 KB 2015-11-25 51 0 2021-12-23
PubMed 15814629 The number of lymph node metastases in gastric cancer correlates with the angiotensin I-converting enzyme gene insertion/deletion polymorphism. PURPOSE: In the present study, we aimed to substantiate 1.72 KB 2015-11-19 26 0 2021-12-23
PubMed 24442316 Cultured mycelium Cordyceps sinensis protects liver sinusoidal endothelial cells in acute liver injured mice. Cultured mycelium Cordyceps sinensis (CMCS) was widely used for a variety of diseases incl 2.64 KB 2016-01-16 27 1 2021-12-23
PubMed 26900322 CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome. PURPOSE: Complement factor I (CFI) plays an important role in complement activation pathways and is known to affect the devel 1.95 KB 2017-09-04 26 0 2021-12-23
PubMed 18779591 Identification of a gain-of-function mutation of the prolactin receptor in women with benign breast tumors. There is currently no known genetic disease linked to prolactin (Prl) or its receptor (PrlR) 1.71 KB 2015-11-24 27 3 2021-12-23
PubMed 25622904 Inactivation of Sag/Rbx2/Roc2 e3 ubiquitin ligase triggers senescence and inhibits kras-induced immortalization. Our recent study showed that SAG/RBX2 E3 ubiquitin ligase regulates apoptosis and vascu 1.7 KB 2016-01-18 27 0 2021-12-23
PubMed 23069675 Critical role of neuronal pentraxin 1 in mitochondria-mediated hypoxic-ischemic neuronal injury. Developing brain is highly susceptible to hypoxic-ischemic (HI) injury leading to severe neurological d 2.39 KB 2016-01-12 29 0 2021-12-23
PubMed 17083016 Genetic polymorphism of the binding domain of surfactant protein-A2 increases susceptibility to meningococcal disease. BACKGROUND: Meningococcal disease occurs after colonization of the nasopharynx wi 1.72 KB 2015-11-23 29 0 2021-12-23
PubMed 17065198 Analysis of skin cancer risk factors in immunosuppressed renal transplant patients shows high levels of UV-specific tandem CC to TT mutations of the p53 gene. Immunosuppressed renal transplant recipie 1.78 KB 2015-11-23 27 0 2021-12-23
PubMed 1848636 Debrisoquine phenotype and the pharmacokinetics and beta-2 receptor pharmacodynamics of metoprolol and its enantiomers. The metabolism of the cardioselective beta-blocker metoprolol is under genetic c 1.78 KB 2015-12-07 32 0 2021-12-23