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31.
The localization of HIV-1 proviruses in compositional DNA fractions from 27 AIDS patients during the chronic phase of the disease with depletion of CD4+ and different levels of viremia showed the following. (1) At low viremia, proviruses are predominantly localized in the GC-richest isochores, which are characterized by an open chromatin structure; this result mimics findings on HIV-1 integration in early infected cells in culture. (2) At higher viremia, an increased distribution of proviruses in GC-poor isochores (which match the GC poorness of HIV-1) was found; this suggests a selection of cells in which the isopycnic localization leads to a higher expression of proviruses and, in turn, to higher viremia. (3) At the highest viremia, integrations in GC-rich isochores are often predominant again, but generally not at the same level as in (1); this may be the consequence of new integrations from the extremely abundant RNA copies.Received 21 November 2003; received after revision 13 January 2004: accepted 15 January 2004  相似文献   
32.
3种白斑综合征病毒膜蛋白(VP39、VP124和VP187)各自特异性抗血清用于体外中和试验,研究它们是否参与病毒的感染,进一步用定量PCR检测中和试验中病毒的感染情况.结果表明,WSSV的感染能够被抗VP124抗体中和,VP124在病毒的感染中有起作用.  相似文献   
33.
目的:探讨新生儿捂热综合症的血糖及临床意义;方法:回顾性分析32例新生儿捂热综合症的临床资料,跟踪随访患儿预后;结果:新生儿捂热综合症血糖明显增高时死亡率及神经系统后遗症发生率明显增加;结论:新生儿捂热综合症应严密监测血糖,维持内环境的稳定对疾病的恢复是极其重要的.  相似文献   
34.
Melkersson-Rosenthal综合征3例临床分析   总被引:1,自引:0,他引:1  
Melkersson-Rosenthal综合征,是一种罕见的神经,皮肤粘膜综合征,临床以间歇性面瘫,再发性唇面肿胀及皱襞舌为三主症,激素治疗有显著疗效,但国内报道极少,早期诊断困难,易被诊,本文报道我院近十年来收治的3例完全型MRS病人及随访资料,结合国内外文献,就其病因,发病机制,临床特征及近年来研究进展进行分析,认为该病发病机理可能与免疫功能异常所致组织炎性肉芽肿有关。  相似文献   
35.
研究结合中年女性生理特点,通过两年的大众艺术体操锻炼实验,分析健康中年女性的体质指数、心率、血压、血糖、血脂等与代谢综合征密切相关的生理生化指标在实验前后的变化,探讨长期参加大众艺术体操锻炼对代谢综合征的预防作用。结果表明两年的大众艺术体操锻炼使健康中年女性保持原正常的BMI、HR、DBP、BS、TG、TC、HDL-C、LDL-C水平,降低了SBP水平,有效减缓了各项指标向不利于健康方向发展的趋势,对代谢综合征的预防起到一定的作用。  相似文献   
36.
一种(71,36,11) QR码的快速代数译码算法   总被引:2,自引:2,他引:0  
在平方剩余(quadratic residue,QR)码的译码过程中,当接收码字中出现的错误个数较多时,未知校正子的计算非常困难,计算量与复杂度都很高,因此增加了解码过程所需要的时间.鉴于此,在(71,36,11)QR码的错误模式权重为4时,通过对牛顿恒等式的数学推导,在不需要计算未知校正子的情况下,导出了其错误位置多项式的系数,简化了(71,36,11)QR码中出现4个错误时的判断条件,并对所有可纠错的错误图案进行了穷举验证.仿真结果表明,提出的算法在解4个错与5个错时,分别提高了56.12%与18.19%的解码效率,验证了算法的正确性与有效性.  相似文献   
37.
Inhaled nitric oxide (NO) is used to treat various cardiopulmonary disorders associated with pulmonary hypertension. The rationale is based on the fact that NO, given by inhalation, only dilates those pulmonary vessels that perfuse well-ventilated lung units. As a result, pulmonary gas exchange is improved while pulmonary vascular resistance is reduced and pulmonary blood flow is increased. Inhaled NO has been succesfully applied to treat persistent pulmonary hypertension of the newborn, reducing the need for extracorporeal life support. Although pulmonary hypertension and altered vasoreactivity contribute to profound hypoxaemia in adult and paediatric acute respiratory distress syndrome (ARDS), the benefit of inhaled NO still remains to be established in patients with ARDS. ARDS is a complex response of the lung to direct or indirect insults, leading to pulmonary vasoconstriction and various inflammatory responses. Recent randomized trials suggest that inhaled NO only causes a transient improvement in oxygenation. Whether this effect is important in the long-term management of ARDS remains to be established. NO, measured in the exhaled breath, is an elegant and non-invasive means to monitor inflammation of the upper and lower respiratory tract. In the normal upper airways, the bulk of exhaled NO originates from the paranasal sinuses. Exhaled NO is increased in nasal allergy and decreased in cystic fibrosis, nasal polyposis and chronic sinusitis. That NO production is increased in asthmatic airways is also well established. However, several questions still need to be addressed, in particular evaluation of the sensitivity and specificity of the measurement techniques, and assessment of the bronchodilator action of endogenous NO.  相似文献   
38.
以自制 ND- EDS二联油苗为主进行免疫试验 ,并以同种二联油苗、ND和 EDS单油苗作对照 ,测定各种疫苗免疫后 ND、EDSHI抗体消涨规律 ,并进行强毒攻击试验。在此基础上 ,用自制二联苗实地免疫产前蛋鸡 2 6 830只 ,进行田间免疫试验。结果表明 :自制二联苗免疫效果良好 ,免疫期为 36 0 d左右 ,免疫期内对 ND和 EDS强毒攻击的保护率分别为 10 0 %和 95.8%  相似文献   
39.
EpidemicPredictionofHemorrhagicFeverwithRenalSyndromeUsingGreyMultivariableModelGENGJianping(Firstteam,FourthMilitaryMedicalU...  相似文献   
40.
Objective: To explore the relationship between genetic polymorphisms in methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR), the central enzymes in folate metabolism that affects DNA methylation and synthesis, and the risk of Down syndrome in China. Methods: Genomic DNA was isolated from the peripheral lymphocytes of 64 mothers of children with Down syndrome and 70 age matched control subjects. Polymerase chain reaction and restriction fragment length polymorphism were used to examine the polymorphisms of MTHFR 677C→T, MTRR 66A→G and the relationship between these genotypes and the risk of Down syndrome was analyzed. Results: The results show that the MTHFR 677C→T polymorphism is more prevalent among mothers of children with Down syndrome than among control mothers, with an odds ratio of 3.78 (95% confidence interval (CI), 1.78-8.47). In addition, the homozygous MTRR 66A→G polymorphism was independently associated with a 5.2-fold increase in estimated risk (95% CI, 1.90-14.22). The combined presence of both polymorphisms was associated with a greater risk of Down syndrome than the presence of either alone, with an odds ratio of 6.0 (95% CI, 2.058-17.496). The two polymorphisms appear to act without a multiplicative interaction. Conclusion: MTHFR and MTRR gene mutation alleles are related to Down syndrome, and CT, TT and GG gene mutation types increase the risk of Down syndrome.  相似文献   
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