However, no statistical differences were detected between the untreated, ultra-fine ground and enzyme-hydrolysed OBC. The water-insoluble (WIS-OBC) and water-soluble (WS-OBC) fractions had opposite effects on the EF-based extrudates: 10 % addition of WIS-OBC fraction significantly decreased the expansion (163 %) and increased the hardness (313 N), whereas the addition of WS-OBC (10 or 20 %) enhanced the expansion (218-226 %) and resulted in less hard textures (131-146 N). The soluble fibres and low protein content

in WS-OBC fraction were hypothesised to cause the improved expansion and decreased hardness. The results demonstrated that extrudates with BIBF 1120 supplier acceptable expansion and hardness can be produced with defatted oat endosperm flour and oat bran fractions. However, the water-insoluble bran components had a negative effect on the textural properties of extrudates.”
“The present study is conducted to determine the potential mechanisms of Boron compounds, boric acid (BA) and borax (BX), on genotoxicity of zebrafish Danio rerio for 24, 48, 72 and 96-hours acute exposure

(level: 1, 4, 16, 64 mg/l BA and BX) in semi-static bioassay experiment. For that purpose, peripheral erythrocytes were drawn from caudal vein and Comet assay was applied to assess genotoxicity. Acute (96 hours) exposure and high concentrations of boric acid and borax increases % tail DNA and Olive tail moment. Genotoxicity was found for BA as concentration-dependent and BX as concentration and time dependent manner. Galardin mouse In general, significant effects (P smaller than 0,05) on both concentrations and exposure times were observed in experimental groups. DNA damage was highest at 96 h and 24 h for all BX and BA concentrations, respectively in peripheral blood of D. rerio. For the first time, our study demonstrates the effect of waterborne BA and BX exposure on genotoxicity at the molecular level, which

may contribute to understanding the mechanism of boric acid and borax-induced genotoxicity in fish.”
“Primary plasma cell leukemia (pPCL) is a rare, yet aggressive form of de novo plasma cell tumor, distinct from secondary PCL (sPCL) which represents a leukemic transformation of pre-existing multiple VX-770 myeloma (MM). Herein, we performed a comprehensive molecular analysis of a prospective series of pPCLs by means of FISH, single nucleotide polymorphism (SNP) array and gene expression profiling (GEP). IGH@ translocations were identified in 87% of pPCL cases, with prevalence of t(11;14) (40%) and t(14;16) (30.5%), whereas the most frequent numerical alterations involved 1p (38%), 1q (48%), 6q (29%), 8p (42%), 13q (74%), 14q (71%), 16q (53%), and 17p (35%). We identified a minimal biallelic deletion (1.5 Mb) in 8p21.2 encompassing the PPP2R2A gene, belonging to a family of putative tumor suppressors and found to be significantly down-regulated in deleted cases.