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金纳米粒子增敏的SPRi技术应用于遗传性血栓疾病的检测 被引量:2
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作者 李伊凡 金尚忠 +3 位作者 姜丽 谭航彬 蒋彩玲 于自珍 《中国计量大学学报》 2022年第3期310-316,共7页
目的:基于表面等离子共振成像(SPRi)技术,欲对遗传性血栓疾病4种基因型实现高通量高灵敏的检测。方法:采用多聚腺苷酸(polyA)嵌块将探针简单快速地固定在金表面,制备了polyA-DNA-Au NPs作为增敏介质,结合SPRi技术的检测方法,对遗传性血... 目的:基于表面等离子共振成像(SPRi)技术,欲对遗传性血栓疾病4种基因型实现高通量高灵敏的检测。方法:采用多聚腺苷酸(polyA)嵌块将探针简单快速地固定在金表面,制备了polyA-DNA-Au NPs作为增敏介质,结合SPRi技术的检测方法,对遗传性血栓疾病中凝血酶原基因G20210A和凝血因子FV G1691A 4种DNA基因型进行了高通量定量检测。同时,对检测的可行性、灵敏度以及稳定性进行分析研究。结果:4种基因型的检测限可分别低至10.5 pmol/L,12.0 pmol/L,8.0 pmol/L和11.0 pmol/L。在超过16个检测周期后,信号强度仍然保持在98%以上,表明该检测技术的敏感性、重复性较好。结论:金纳米粒子增敏的SPRi技术可实现高通量高灵敏的遗传性血栓疾病标志物检测,并有望推广到更多DNA疾病的检测中。 展开更多
关键词 表面等离子共振成像技术 遗传性血栓疾病 高通量检测 金纳米粒子
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Risk factors of thrombosis in abdominal veins 被引量:2
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作者 Amit Kumar Dutta Ashok Chacko +3 位作者 Biju George Joseph Anjilivelil Joseph Sukesh Chandran Nair Vikram Mathews 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第28期4518-4522,共5页
AIM: To estimate the prevalence of inherited and acquired thrombophilic risk factors in patients with abdominal venous thrombosis and to compare the risk factor profiles between Budd-Chiari syndromes (BCS) and splanch... AIM: To estimate the prevalence of inherited and acquired thrombophilic risk factors in patients with abdominal venous thrombosis and to compare the risk factor profiles between Budd-Chiari syndromes (BCS) and splanchnic vein thrombosis (SVT). METHODS: In this retrospective study, 36 patients with abdominal venous thrombosis were studied. The patients were divided into Budd-Chiari group (hepatic vein, IVC thrombosis) and splanchnic venous thrombosis group (portal, splenic, superior mesenteric veins) based on the veins involved. Hereditary and acquired thrombophilic risk factors were evaluated in all patients. RESULTS: Twenty patients had SVT, 14 had BCS, and 2 had mixed venous thrombosis. Ten patients (28%) had hereditary and 10 patients (28%) acquired thrombophilic risk factors. The acquired risk factors were significantly more common in the SVT group (SVT vs BCS: 45% vs 7%, χ2 = 5.7, P = 0.02) while hereditary risk factors did not show significant differences between the two groups (SVT vs BCS: 25% vs 36%, χ2 = 0.46, P = 0.7). Multiple risk factors were present in one (7%) patient with BCS and in 3 patients (15%) with SVT. No risk factors were identified in 57% of patients with BCS and in 45% of patients with SVT. CONCLUSION: Hereditary and acquired risk factors play an important role in the etiopathogenesis of abdominal venous thrombosis. Acquired risk factorsare significantly more common in SVT patients while hereditary factors are similar in both groups. 展开更多
关键词 Budd Chiari syndrome Splanchnic vein thrombosis Risk factors HEREDITARY Risk comparison
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