background genome-wide association studies have shown that rs738491, rs2143571, and rs3761472 in the sorting and assembly machinery component 50 homolog (samm50) gene are significantly associated with susceptibility to nonalcoholic fatty liver disease (nafld). conclusions we first demonstrated that the rs738491 t allele, rs2143571 a allele, and rs3761472 g allele in the samm50 gene created susc...

background coronary artery disease (cad) is the most common cause of death worldwide. mef2a directly regulates target genes in the process of muscle development. this gene product is a transcription factor. mef2a protein in homodimer or heterodimer forms binds to a/t-rich cis elements with conserved sequence in promoter, regulator, and enhancer of many genes, which are determining in evolution ...

the snp (rs11209026, arg381gln, r381q) in the il-23 receptor (il23r) confers protection against multiple inflammatory diseases, representing one of the most significant human genetic polymorphisms in inflammatory diseases. we, therefore, investigated the association between il-23 r r381q gene polymorphism and asthma.this case-control study was performed on 209 patients, and 200 healthy controls...

Impressum Forschungsberichte der FHDW Hannover – Veröffentlichungen aus dem Bereich Forschung und Entwicklung der FHDW Hannover. Abstract. The paper extends single-pushout graph transformation by poly-morphism, a key concept in object-oriented design. The notions sub-rule and remainder, well-known in single-pushout rewriting, are applied to model dynamic rule extension and type dependent rule a...

background: despite extensive progress in ivf techniques, one of the most difficult problems is the variability in the response to controlled ovarian hyperstimulation (coh). recent studies show the effects of individual genetic variability on coh outcome. objective: to evaluate the correlation between lhβ g1502a polymorphisms in exon 3 of the lh gene and ovarian response to coh. materials and m...

results no significant difference was found between the groups regarding bmht rs3797546 gene polymorphism. the c allele was not associated with ns-cl/p (or = 1.27, 95% ci = 0.85-2.79, p = 0.690). conclusions our data suggested that bmht rs3797546 gene polymorphism was not associated with risk/ protection for ns-cl/p in a sample of iranian population. larger studies are required to validate our ...

For the Kirillov–Poisson structure on the vector space g∗, where g is a finite-dimensional Lie algebra, it is known at least two canonical deformations quantization of this structure: they are the M.Kontsevich universal formula [K], and the formula, arising from the classical Campbell–Baker–Hausdorff formula [Ka]. It was proved in [Ka] that the last formula is exactly the part of Kontsevich’s f...