We developed a human mitochondria-focused gene database (hMiDas) and customized cDNA microarray chip (hMitChip) to help biomedical research in mitochondrial genomics. The current version of hMiDas contains 1,242 gene entries (including mtDNA genes, nuclear genes related to mitochondria structure and junctions, predicted loci and experimental genes), organized in 15 categories and 24 subcategories. The database interface allows keyword-based searches as well as advanced field and/or case-sensitive searches. Each gene record includes 19 fields, mostly hyperlinked to the corresponding source. Moreover, for each gene, the user is given the option to run literature search using PubMed, and gene/protein homology search using BLAST and FASTA. The hMitChip was constructed using hMiDas as a reference. Currently, it contains a selection of 501 mitochondria-related nuclear genes and 192 control elements, all spotted in duplicate on glass slides. Slide quality was checked by microarray hybridization with 50 /spl mu/g of Cy3-labeled sample cDNA and Cy5-labeled comparing cDNA, followed by array scan and image analysis. The hMitChip was tested in vitro using RNA extracted from cancer cell lines. Gene expression changes detected by hMitChip were confirmed by quantitative real-time RT-PCR analysis.
This chapter summarizes key requirements and recommendations for design and detailing of reinforced concrete components in regions of high seismic hazard as put forward by the European Committee for Standardization (CEN) and applied in European practice by means of Eurocodes 2 and 8. Seismic design according to the Eurocodes (specifically EN1998) is based on two different performance objectives, aiming to provide life safety in a rare seismic event and limit damage in a more frequent one. While lower design forces are used to design the higher ductility class buildings, better reinforcement details required for the higher ductility class buildings provide higher deformation capacities in critical regions. The lower design forces would lead to an expectation of greater damage in critical regions during moderate earthquakes compared with the lower ductility class buildings that are designed for higher design forces.
The aim of the present study was to examine the associations of obesity, percentage body fat and visceral fat mass with body Fe status in a representative sample of 1493 schoolchildren aged 9–13 years. Anthropometric, body composition, biochemical, clinical (Tanner stage, age of menarche) and dietary intake data were collected. Fe deficiency (ID) was defined as transferrin saturation (TS) < 16 %; and Fe-deficiency anaemia (IDA) as ID with Hb < 120 g/l. Obese boys and girls and those in the highest quartiles of percentage body fat mass had significantly higher levels of serum ferritin ( P ≤ 0·05) compared to their normal-weight peers and those in the corresponding lowest quartiles. Similarly, obese boys and girls and those in the highest quartiles of percentage body fat and visceral fat mass had significantly lower levels of TS ( P ≤ 0·05) compared to normal-weight children and those in the corresponding lowest quartiles. The prevalence of ID and IDA was significantly higher in boys and girls in the highest quartiles of percentage body fat than in peers in the lowest quartile. Higher quartiles of percentage body fat and visceral fat mass were the main significant predictors of ID in boys, after controlling for other important confounders, with OR of 2·48 (95 % CI, 1·26, 4·88) and 2·12 (95 % CI, 1·07, 4·19), respectively. Similar significant associations were observed for girls. In conclusion, percentage body fat and visceral fat mass were positively associated with ID in both sexes of preadolescents. These associations might be attributed to the chronic inflammation induced by excess adiposity.
No abstract is provided for this article.
The corticotropin-releasing hormone (CRH) family, CRH, CRH-related peptides and their receptors (R) play major roles in coordinating the behavioral, endocrine, autonomic, and immune responses to stress. The wide influence of the CRH system on physiologic processes in both brain and periphery implicates the respective peptides in the pathophysiology of numerous disorders characterized by dysregulated stress responses. CRH peptides and their receptors are being explored as therapeutic targets for intervention in stress-related disorders. Selective antagonists have been used experimentally to elucidate the role of CRH-related peptides in disease processes, such as anxiety and depression, sleep disorders, addictive disorders, inflammatory disorders, acute and chronic neurodegeneration and preterm labor. The development of effective antagonists with no significant side effects remains a challenge.