四川省蚋亚属一新种（双翅目：蚋科）

本文记述四川省峨眉山蚋属Simulium蚋亚属Simulium一新种，以中国科学院院士胡经甫命名为经甫蚋S．（S．）jinfful sp．nov．该蚋与S．（S．）himalayense Purl，1930，S．（S．）taiwanicum Takaoka，1979．S．（S．）shanxlense Cai and An，2003，S．（S．）immortalls Cai and An，2003，S．（S．）chamlongi Takaoka and Suzuki，1984相似，但是，雌虫的生殖叉突具内突和外突，肛上板椭圆形，前腿基节、转节、股节棕黄色；生殖腹板板体短，其长约为顶端宽度的0．8倍，与上述蚋种明显不同。模式标本保存在北京军事医学科学院医学昆虫标本馆。     

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region

Primary congenital glaucoma (gene symbol: GLC3) is an ocular disorder that occurs for 0.01-0.04% of blind people. In the majority of familial cases reported so far, this condition is inherited as an autosomal recessive trait. We have recently used a group of 17 GLC3 families with a minimum of two affected offspring and consanguinity in most of the parental generation and mapped the first GLC3 locus (GLC3A) to the 2p21 region. Six families did not show any linkage to the GLC3A locus and thus provided evidence for genetic heterogeneity of this disorder. A total of eight families unlinked to the 2p21 region were used to search for the chromosomal location of the second GLC3 locus. Herein, we describe mapping of a new locus (designated GLC3B) for primary congenital glaucoma to the short arm of chromosome 1 (1p36.2-36.1) that is situated centromeric to the neuroblastoma and Charcot-Marie-Tooth type 2A (CMT2A) loci. A total of 17 DNA markers were genotyped from this region of chromosome 1. Four families showed no recombination with the two markers D1S2834 and D1S402 with a maximum lod score of 4.510 and 4.157 respectively. Pairwise and multipoint linkage analysis and inspection of the haplotypes revealed that the remaining four families are not linked to this part of chromosome 1, thus providing further evidence that at least one more locus for the autosomal recessive form of GLC3 must exist in the genome. Based on the recombination events, the overall linkage map of this region is: tel-D1S1192-D1S1635-D1S1193 - (D1S1597/-D1S489/D1S228)- [GLC3B/D1S2834/D1S402] - (D1S1176/D1S507/D1S407) - D1S2728-(MFAP2/D1S170) - D1S1368 - D1S436- D1S1592-cen.      

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2

Results from a genome-wide screen of 10 multiplex families ascertained through probands with nonsyndromic cleft lip with or without cleft palate (CL/P) in Mexico, Argentina, and the United States yielded suggestive evidence of linkage to chromosomes 2, 6, 17 and 18. Fine mapping excluded all regions except chromosome 2. Subsequent analysis was performed on the original 10 families plus an additional 16 families using 31 markers on chromosome 2. This analysis showed intriguing evidence of linkage to 2q (Zlr=2.26, empirical P-value=0.028 in a chromosome-wide analysis). Transmission disequilibrium tests also revealed evidence of linkage and disequilibrium for two markers in this region (D2S168 and D2S1400 with P-values=0.022 and 0.006, respectively). A subset of these 26 families provided additional evidence for a susceptibility gene for CL/P on 2q, suggesting that further studies of genes in this region are warranted.     

Isolation and characterization of species-specific DNA probes from Taenia solium and Taenia saginata and their use in an egg detection assay.

Cysticercosis results from ingestion of the eggs of the tapeworm Taenia solium. Reduction of the incidence of human and swine cysticercosis requires identification and treatment of individuals who carry the adult tapeworm. T. solium and Taenia saginata eggs cannot be differentiated on the basis of morphology; thus, in order to improve existing methods for the diagnosis of taeniasis, we have developed highly sensitive, species-specific DNA probes which differentiate T. solium and T. saginata. Recombinant clones containing repetitive DNA sequences which hybridize specifically with genomic DNAs from either species were isolated and characterized. T. solium-specific DNA sequences contained complete and truncated forms of a tandemly repeated 158-bp DNA sequence. An unrelated T. saginata DNA sequence was also characterized and shown to encode a portion of the mitochondrial cytochrome c oxidase I gene. T. solium- and T. saginata-specific DNA probes did not hybridize in dot blot assays either with genomic DNA from the platyhelminths Taenia hydatigena, Taenia pisiformis, Taenia taeniaeformis, Echinococcus granulosus, and Schistosoma mansoni or with genomic DNA from other eukaryotes, including Saccharomyces cerevisiae, Candida albicans, Cryptosporidium parvum, Entamoeba histolytica, Trypanosoma gambiense, Trypanosoma brucei, and Giardia lamblia, Caenorhabditis elegans, and human DNA. By using these T. solium and T. saginata DNA probes, a rapid, highly sensitive and specific dot blot assay for the detection of T. solium eggs was developed.     

评“McCall观察方法”——对一种色谱系统分配效果观察方法的商榷

本文通过理论分析和文献数据的分析,对McCall提出的色谱系统分配效果的观察方法提出了不同的看法,认为McCall方法中的所谓logK并不是常数。McCall的方法无论在理论上和实践上都是不妥的。     

美国医保支付制度改革对我国康复护理服务的启示

梳理了美国医保支付制度改革进程,总结了捆绑支付模式内涵及其对康复护理服务的影响。结合我国国情,借鉴美国医保支付制度改革经验,认为我国应建立基于价值评价的康复护理服务医保支付制度,充分发挥医保基金的引导和保障作用,健全多元化的复合型医保支付体系,创建“以人民的健康为中心”的连续型医疗服务保障体系。     

2015—2020年南通市中小学生食源性疾病特征分析

目的 分析南通市中小学生食源性疾病流行病学特征,为有效防控中小学生食源性疾病提供科学依据。方法 收集2015—2020年南通市哨点医院就诊的中小学生食源性疾病病例信息,并采集病例粪便标本进行病原体检测,运用χ²检验比较不同学段中小学生食源性疾病病例的分布。结果 共监测中小学生食源性疾病病例1 432例。不同可疑暴露食品的分类和进食场所的病例数有统计学差异（χ²= 73.421;χ² = 66.857,P均＜0.001）,可疑暴露食品主要为肉与肉制品（28.21%）和水产动物及其制品（17.86%）,可疑进食场所主要为家庭（57.60%）和学校食堂（12.69%）。疑似食源性疾病暴发事件主要发生在学校食堂。共采集标本214份,检出病原体22份,总体检出率为10.28%,阳性病原体以诺如病毒（3.74%）和副溶血性弧菌（3.27%）为主。结论 需面向家庭、学校和学生开展有针对性的食品安全知识宣传,加强中小学生食源性疾病的重点食品和场所的食品安全监测和监管,最大限度地减少中小学生食源性疾病的发生。     

益糖康通过抑制AGE/RAGE信号通路改善骨骼肌细胞凋亡的机制

目的：研究益糖康通过抑制糖基化终末产物(AGE)/糖基化终末产物受体(RAGE)信号通路纠正骨骼肌细胞过度凋亡进而改善胰岛素抵抗(IR)的作用机制。方法：(1)体外实验,制备益糖康含药血清,将C2C12细胞设置空白组、模型组、益糖康含药血清高、中、低剂量(40、20、10 g·kg^-1)组、RAGE抑制剂组,除空白组外,用棕榈酸诱导C2C12 IR模型细胞,然后分别采取相应的干预方式后检测各组细胞的活性及葡萄糖消耗量水平,用流式细胞术检测各组细胞凋亡率,实时荧光定量聚合酶链式反应(Real-time PCR)及蛋白免疫印迹法(Western blot)检测重要凋亡蛋白[B细胞淋巴瘤-2(Bcl-2)、Bcl-2相关X蛋白(Bax)、p53、胱天蛋白酶(Caspase)-3、Caspase-9]的mRNA及蛋白表达水平。(2)体内实验,将96只符合研究标准的Wistar大鼠设置空白组、对照组、益糖康高、中、低剂量组(40、20、10 g·kg^-1)、吡格列酮(1.35 mg·kg^-1)组,运用高糖高脂糖尿病模型诱导饲料联合...     

磁共振成像对前置胎盘的临床诊断价值

目的：探究磁共振成像（MRI）对前置胎盘的诊断价值。方法：选取2018年1月至2021年6月新疆生产建设兵团医院接诊的基于临床症状诊断为前置胎盘孕妇79例,所有孕妇均在手术前行盆腔MRI扫描,观察胎盘厚度、宫颈长度、胎盘T2低信号带、宫颈边缘窦、膀胱隆起、子宫肌层变薄信号,分析上述MRI征象、指标对前置胎盘的诊断价值。结果：79例孕妇中,最终经手术病理证实为前置胎盘的患者52例。MRI征象中的胎盘T2低信号带、宫颈边缘窦、膀胱隆起、子宫肌层变薄均可有效诊断前置胎盘（P <0.05）;检出率由高到低依次为：胎盘T2低信号带>宫颈边缘窦>子宫肌层变薄>膀胱隆起;胎盘厚度≥10 mm时,胎盘厚度与前置胎盘呈正相关（r=0.852,P=0.016）;胎盘厚度<10 mm时,胎盘厚度与前置胎盘无相关性（r=0.201,P=0.052）。宫颈长度≥30 mm时,宫颈长度与前置胎盘无相关性（r=0.376,P=0.071）;宫颈长度<30 mm时,宫颈长度与前置胎盘呈负相关（r=–0.721,P=0.036）。结论：MRI征象（胎盘T2低信号带、宫颈边缘窦、膀胱隆...     

COVID-19对学术交流的影响及学术出版机构的应对举措

【目的】 研究COVID-19疫情暴发给学术交流及学术出版带来的深远影响。【方法】 利用文献调研法和案例分析法挖掘COVID-19疫情带来的学术环境变化,并探讨学术出版的整体变化趋势和国内外出版机构的应对方式。【结果】 COVID-19疫情改变了当前的学术交流环境:加速推进开放科学进程,快速传播的预出版模式受到青睐,开放评审促进快速学术交流,多项基金项目助力COVID-19科学研究,中国科研人员应对COVID-19反应积极而迅速。出版机构顺应学术出版的整体趋势,为科学共同体提供大量免费服务,扩大知识服务的目标群体,提供海量知识及COVID-19快速发表通道,我国出版机构应对COVID-19也采取了大量积极举措。【结论】 国内外出版机构应对突发事件时应建立学术出版应急机制,增强知识服务能力,促进知识创新及传播,以适应一个全新的快速发展的学术环境。