55 resultados para 198-1212
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目的 研究2 型糖尿病患者中线粒体tRNAL eu (UUR) 基因3243AöG 突变和NADH 脱氢酶亚 单位1 基因( ND1 ) 基因3316GöA 突变的发生频率及其与2 型糖尿病的相关性。方法 应用聚合酶链反 应及限制性片段长度多态性技术检测225 例中国云南2 型糖尿病患者和195 名无糖尿病家族史的健康对 照者有无3243AöG 突变和3316GöA 突变, 并经DNA 直接测序确证。结果 2 型糖尿病患者中3316GöA 突变者5 例(2. 22% ) , 195 例对照者中突变者2 例(1. 03% ) , 突变发生率在两组间差异无统计学意义(P = 0. 4576) ; 两组中无线粒体3243AöG 突变。结论 线粒体tRNAL eu (UUR) 基因3243AöG 突变在中国云南2 型 糖尿病人群中发生频率低, 可能不是云南人群中2 型糖尿病的常见病因。线粒体ND1 基因3316GöA 突变 可能仅为人群中线粒体基因组的正常多态。其他的遗传、环境及子宫内因素需要进一步研究。
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To investigate the genetic diversity of Tricholoma matsutake, we studied ITS and IGS1 sequences and PCR polymorphism of a retrotransposon in 56 fruit bodies collected from 13 counties of 9 regions in Yunnan Province. We found one and three haplotypes base
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Objective: To investigate the association of complement C4 null genes (C4QO, including C4AQO and C4BQO) and C2 gene with systemic lupus erythematosus (SLE) in southwest Han Chinese; 136 patients with SLE and 174 matched controls were genotyped. Methods: C4 null genes were determined by a polymerase chain reaction (PCR) procedure with sequence specific primers (PCR-SSP). The 2 bp insertion in exon 29, which was previously identified in non-Chinese populations and caused defective C4A genes, was directly typed by sequencing the whole exon 29 using exon specific primers. The exon 6 of complement C2 was also sequenced in both the patients and controls. Results: The frequency of homozygous C4AQO allele was 12.5% (17/136) in patients with SLE compared with 1.1% (2/174) in controls (p<0.001, odds ratio (OR)=12.286, 95% confidence interval (95% CI) 2.786 to 54.170). There was no significant difference for homozygous C4BQO allele between patients with SLE and controls (p=0.699). Patients with the C4AQO gene had an increased risk of acquiring renal disorder, serositis, and anti-dsDNA antibodies compared with those without C4AQO (for renal disorder, p=0.018, OR=8.951, 95% Cl 1.132 to 70.804; for serositis, p=0.011, OR 4.891, 95% CI 1.574 to 15.198; for anti-dsDNA, p=0.004, OR 7.630, 95%Cl 1.636 to 35.584). None of the patients or controls had the 2 bp insertion in exon 29 of the C4 gene. The type I C2 deficiency was not detected in the 3 10 samples. Conclusion: It is suggested that deficiency of C4A (not due to a 2 bp insertion in exon 29), but not C4B or C2, may be a risk factor for acquiring SLE in south west Han Chinese; this results in increased risk of renal disorder, serositis, and anti-dsDNA antibodies in patients with SLE. Racial differences seem to be relevant in susceptibility to SLE.
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线粒体 DNA (mtDNA)已被广泛用于动物群体遗传学和进化生物学的研究, 并取得了许多有意义的结果. 有效的 mtDNA 提取方法无疑是开展这方面研究的前提. 关于动物 mtDNA 的提取方法, 国内外已有不少报导. 概括起来, 可分为: 1)氯化铯超速离心法, 2)柱层析法, 3)DNase法, 4)碱变性法. 该文报道了一种改进的碱变性提取法, 与其它方法相比, 具有应用范围广、简便、经济等优点。
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Camptothecin (CPT), a traditional anti-tumor drug, has been shown to possess anti-HIV-1 activity. To increase the antiviral potency, the anti-HIV activities of two CPT derivatives, 10-hydroxy-CPT and 7-hydroxymethyl-CPT, were evaluated in vitro. The therapy index (TI) of CPT, 10-hydroxy-CPT and 7-hydroxymethyl-CPT against HIV-1(IIIB) in C8166 were 24.2, 4.2 and 198.1, and against clinical isolated strain HIV-1(KM018) in PBMC were 10.3, 3.5 and 66.0, respectively. While the TI of CPT, 10-hydroxy-CPT and 7-hydroxymethyl-CPT against HIV-2(CBL-20) were 34.5, 10.7 and 317.0, respectively, and the TI of the three compounds against HIV-2(ROD) showed the similar values. However, when the antiviral mechanisms were considered, we found there was no inhibition of 7-hydroxymethyl-CPT on viral cell-to-cell transmission, and was no inhibition on reverse transcriptase, protease or integrase in cell-free systems. 7-Hydroxymethyl-CPT showed no selective killing of chronically infected cells after 3 days of incubation. In conclusion, 7-hydroxymethyl-CPT showed more potent anti-HIV activity, while 10-hydroxy-CPT had less efficient activity, compared with the parent CPT. Though the antiviral mechanisms remain to be further elucidated; the modification of -OH residues at C-7 of CPT could enhance the antiviral activity, while of -OH residues at C-10 of CPT had decreased the antiviral activity, which provides the preliminary modification strategy for anti-viral activities enhancement of this compound.
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明纹花鼠是东南亚地区的特有种, 在中国有3 亚种(阿萨姆亚种、滇西亚种、滇南亚种) , 分布于 藏东南、云南西南部和南部。以往主要根据外部形态特征进行分类。为探讨3 亚种头骨性状的差异, 在测量15 个性状的基础上, 运用统计分析软件SPSS 1110 对其可测量性状进行多变量分析。结果及推测如下: ①明纹花 鼠3 个亚种的地位是确定的。②在头骨15 个性状中, 两两亚种之间具有显著差异的性状: 阿萨姆亚种与滇西亚 种有8 个(枕鼻长、吻宽、颧宽、眶间宽、后头宽、鼻骨宽、下齿列、下颌骨高) ; 阿萨姆亚种与滇西亚种有7 个(颅全长、枕鼻长、颧宽、眶间宽、后头宽、下颌高、下颌骨高) ; 滇西亚种与滇南亚种有4 个(吻宽、后头 宽、鼻骨宽、下颌高) 。③滇南亚种与滇西亚种之间的亲缘关系近于两者各自与阿萨姆亚种之间的亲缘关系。
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2008年5月,在广西壮族自治区靖两县禄洞村珠江水系采集到一批条鳅标本.经鉴定,为云南鳅属(Yunnanilus)-新种.新种靖西云南鳅(Yunnanilus jinxiensis)属于侧纹云南鳅种组(Yunnanilus pleurotaenis group).但新种全身除胸腹部外被有鳞片;侧线较长,具有15-20个侧线管孔;背鳍分枝鳍条8;胸鳍分枝鳍条13-14;鳔两室,后室发达;尾鳍凹形;体长为体高的3.9-_4.6倍,为头长的4.1-4.4倍,为尾柄高的7.5-9.0倍;头长为眼径的5.5-6.7倍,为眼间距的2.2-2.4倍等特征,可将新种与该种组内的其他种类相区分.
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《胞内共生与细胞研究》( 《Endocytobiosis and Cell Research》)是由国际胞内共生学会(International Society of Endocytobiology, ISE)主办的期刊, 它主要发表有关内共生物(endosy mbioses)和真核细胞的起源、发展、分化、进化和系统发育的研究论文. 在胞内共生和真核细胞的起源进化研究领域享有声誉. 去年该杂志发表了我国学者李靖炎先生的长篇论著“The primitive nucleus model and the origin of the cell nucleus(原始细胞核的模型与细胞核的起源)”(见1999, 13(1-3):1-86). 国外一家 SCI 收录的专业性刊物为中国学者发表一篇长达86页的 Review, 实不多见, 是我国学者在此领域的殊荣。