血液分析仪红细胞指数质控方法的探讨

目的 探讨血液分析仪红细胞指数的质控方法。方法 利用L-J质控空图和某全血质控物提供的有关数据,推理论证红细胞指数[MCV、MCH、MCHC]在控时对其有关测定参数值的新的质控要求。结果 红细胞指数有关测定参数值的质控范围应分别为HGB:(?)±1.7 s,HCT:(?)±1.06 s,RBC:(?)±1.06s。超出此范围判定为失控。结论 执行该质控判定标准可以实现对红细胞指数实施质控的目的。     

天津市城区成年居民坐高身高指数的调查

目的：探讨成年人坐高身高指数的规律。方法：按中国体育科学会体育研究会规定的方法，测量男性321名，女性324名成人的坐高和身高，每5周岁为一个年龄组，男女各10个年龄组，结果：坐高身高指数均值曲线在男性21－30岁，女性21－35岁年龄组呈递增趋势，提示成年人QD在此年龄组躯干仍存在生长的可能性，在男性56－70岁，女性61－70岁年龄组呈递减趋势，提示成年人在此年龄组脊柱在逐渐缩短，男女两性的指数曲线在30岁左右形成一个交叉点，在此交叉点前女性低于男性，交叉点之后男性低于女性，成人坐高身高指数均值显示男女两性均属躯干均衡型，结论：成年人坐高身高指数具有阶段性递增，递减规律。     

分子吸附再循环系统对冠心病并发重度脓毒症患者心率和动脉压的影响

目的研究分子吸附再循环系统(MARS)对冠心病并发重度脓毒症患者心率和动脉压的影响.方法对2002年11月至2004年2月在ICU治疗的冠心病并发重度脓毒症患者所进行的12次床边MARS治疗有关资料进行回顾性分析和探讨.结果MARS治疗4 h后患者心率显著减慢,收缩压、舒张压和平均动脉压明显升高.结论MARS可改善MODS患者血流动力学指标.     

D1S549等6个短串重复序列基因座在河南汉族群体的遗传多态性

目的　探讨河南汉族群体的D1S5 49、D3S175 4、D2 2S683和CSF1PO、TPOX、TH0 1基因座遗传多态性分布。方法　ACD抗凝血样采自 2 19名无血缘关系汉族个体 ,酚 氯仿法提取DNA ,应用复合扩增技术对D1S5 49等 6个短串重复序列 (STR)基因座进行扩增 ,采用高分辨率的聚丙烯酰胺凝胶电泳分离、银染法显影技术。统计各基因频率、计算杂合度、多态信息含量、个人识别概率及亲权否定概率。结果　 6个STR基因座基因频率的分布均符合Hardy Weinberg平衡 ,各基因座的杂合度分别为 0 .7964、0 .72 3 1、0 .815 9、0 .75 81、0 .65 2 3、0 .6816;非父排除概率为 0 .62 46、0 .4914、0 .65 0 1、0 .5 2 3 6、0 .40 98、0 .42 87;个人识别机率为 0 .8996、0 .8781、0 .92 3 1、0 .8896、0 .8167、0 .83 92 ;多态信息含量为 0 .72 16、0 .6994、0 .742 1、0 .7169、0 .65 17、0 .710 6。结论　D1S5 49等 6个STR基因座是一组高度多态性的遗传标记系统 ,在人类遗传学及法医学研究中具有重要意义     

脾脏切除对胸腺和淋巴结免疫功能的影响

报道脾脏切除（脾切）对动物胸腺和淋巴结免疫功能的影响，脾切后３ｗ大鼠胸腺细胞自发增殖及ＣｏｎＡ诱导增殖均无明显变化，ＣｏｎＡ诱导淋巴结细胞增殖脾切组明显高于假手术对照组，脾切后３ｗ再用ＳＲＢＣ免疫，５ｄ后小鼠腹腔淋巴结数量脾切明显高于对照组，用ＱＨＳ法测定淋巴结细胞对ＳＲＢＣ初次抗体产生脾切组则明显低于对照组。     

Analysis of clozapine response and polymorphisms of the dopamine D4 receptor gene (DRD4) in schizophrenic patients

We have examined the hypothesis that a variable number of tandem repeats in the third cytoplasmic loop of the dopamine D4 receptor influences clinical response to clozapine using a sample of 189 schizophrenic patients. Alleles of the 48-bp repeat, which range from two to ten copies in the normal human population, were analysed by the polymerase chain reaction using genomic DNA as template. Association between these alleles and response to clozapine was tested using the difference in pre-and post-treatment GAS scores as a measure of response. We found no statistically significant variation between genotypic groups and response by analysis of variance. We conclude that the variation of the number of 48-bp repeats alone does not determine response to clozapine. Larger studies are underway to determine if there is a more subtle relationship with sequence variation within the repeats or at other polymorphic sites within the gene that may provide evidence for a component of clozapine's action being at D4 receptors. © 1995 Wiley-Liss, Inc.     

Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosis.

The phenotype in the rd mouse is similar to the clinical presentation of Leber congenital amaurosis (LCA) in humans. Recently a nonsense mutation in the beta subunit of the cGMP phosphodiesterase (Pdeb) gene has been defined as the cause for the rd phenotype in the mouse and has raised the question as to whether mutations in the human PDEB gene might cause LCA. We have previously cloned and characterized the human homologue of the mouse Pdeb gene and have mapped it to chromosome 4p16.3. In this study, a total of 23 LCA families of various ethnic backgrounds have been investigated. Linkage analysis using highly polymorphic (CA)n microsatellites has excluded the PDEB gene as a cause for LCA in 6 families. In the remaining 17 families, we have searched for mutations in the 22 exons of the PDEB gene using single-strand gel electrophoresis (SSGE). Multiple exonic polymorphisms have been determined. However, no DNA changes in the PDEB gene have been identified in our study population which could be causative for the LCA phenotype.     

Inhibitory effect of human blood granulocyte glycosaminoglycans on colony-forming activity of bone marrow fibroblasts

Inhibitory effect of glycosaminoglycans isolated from peripheral blood granulocytes of patients with chronic myeloleukemia and normal subjects on increment in colony-forming units of fibroblasts in monolayer cultures of rat bone marrow is determined by the degree of sulfation of their main component chondroitin-4-sulfate and by increased content of heparan sulfate. Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 125, No. 3, pp. 319–322, March, 1998     

神经系统疾病患者血小板参数的变化及临床意义

目的 探讨神经系统疾病患者血小板参数的变化。方法 测定神经系统疾病患者血小板数(PLT)和平均血小板体积(MPV)，并与对照组作比较。结果 与对照组比较，脑梗死、椎-基底动脉供血不足患者PLT明显减少，MPV明显增大；脑出血组MPV、PLT均减少。结论 血小板参数的变化对神经系统疾病的诊断、预防和治疗有重要的参考价值。     

D4S1647、D6S2414基因座在中国汉族、蒙古族、藏族的遗传多态性

目的 调查D4S1647、D6S2414基因座在中国汉族、蒙古族、藏族群体中的遗传分布规律。方法 采集308份血及唾液标本应用PCR技术，扩增产物用非变性聚丙酰胺凝胶电泳分离，银染显色分析。结果 两位点各群体基因型频率分布均符合Hardy-Weinberg平衡，每一位点等位基因频率分布在各群体间无显著差异；通过对10个汉族家系的遗传模式分析，证实了两位点等位基因传递遵循孟德尔遗传规律。结论 D4S1647、D6S2414基因座在中国汉族，蒙古族，藏族群体均具有高度遗传多态性。