低温等离子体技术降解含氮硫废气的研究进展

论述了采用低温等离子体技术处理含氮硫废气以及恶臭气体的反应机理和研究现状，重点介绍了低温等离子体技术与催化、吸附、光催化等技术的联合技术，分析了低温等离子体联合技术存在的问题及发展方向。     

牛粪厌氧发酵的载体筛选试验研究

为了提高厌氧发酵装置的效率，人们研究了各种各样的方法和措施，其中应用填料或载体使生物菌能够延长驻留期是其中的方法之一，开展载体筛选及其结构设计在厌氧发酵装置中的试验，有助于对此问题的深入研究以及将其成果应用于生产实践。通过静态载体筛选试验选择了玻璃纤维作为载体、PVC塑料管作为载体骨架制成的装置在动态序批式厌氧发酵装置中进行了试验。结果表明：此载体骨架结构对于牛粪动态厌氧发酵具有明显的提高产气效率、改变产气质量和促进有机物转化为挥发性脂肪酸的作用。     

Pilot study for the neonatal screening of fragile X syndrome

An Erratum has been published for this article in Prenatal Diagnosis 23 (9), 2003, 771. Fragile X syndrome (SFX) is the commonest form of inherited mental retardation. Due to the highly variable phenotype clinical diagnosis is complicated. In nearly all cases, the disorder is caused by expansion of a CGG-repeat in the 5′-untranslated region of the FMR1 (fragile X mental retardation-1) gene. We have evaluated the feasibility, efficiency and costs of two methodologies in order to develop a simple test to screen large populations: PCR and fragile X mental retardation-1 protein (FMRP) immunodetection. We studied 100 newborn males using PCR and immunodetection (26.91 Euro). All but one amplified the CGG repeat of the FMR1 gene within the normal size range. The sample that failed to amplify showed only 28% of FMRP expression by immunodetection study; both results indicated an affected male. A further 100 males were studied only by polymerase chain reaction (PCR) (7.8 Euro); all of them amplified within the normal size range. Both methodologies, PCR and immunodetection, are feasible for screening large populations, PCR being the most suitable, economical and less time-consuming. However, it is advisable to keep slides for immunodetection when PCR fails or the external control shows no amplification. Early detection of SFX-affected individuals would represent a great benefit for their maximum social integration, due to appropriate treatment and early stimulation and would permit a cascade screening in their pedigree. Copyright © 2002 John Wiley & Sons, Ltd.     

Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin

Prenatal diagnosis of 5p deletion syndrome, or cri du chat, following an abnormally low measurement of a screening of serum human chorionic gonadotrophin (hCG), is reported. Karyotyping following amniocentesis revealed a terminal deletion in the short arm of one chromosome 5. The pregnancy was electively terminated. 5p deletion syndrome has been described with abnormally high hCG levels and normal hCG levels. This is the first report of its association with abnormally low levels. The association between chromosomal abnormalities and hCG is discussed. Copyright © 2003 John Wiley & Sons, Ltd.