期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
Mutations around interferon sensitivity-determining region:A pilot resistance report of hepatitis C virus 1b in a Hong Kong population 被引量:3
1
作者 Xiao-Ming Zhou Paul Ks Chan john s tam 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第48期5317-5323,共7页
AIM: To explore mutations around the interferon sensitivity-determining region (ISDR) which are associated with the resistance of hepatitis C virus lb (HCV-lb) to interferon-α treatment. METHODS: Thirty-seven H... AIM: To explore mutations around the interferon sensitivity-determining region (ISDR) which are associated with the resistance of hepatitis C virus lb (HCV-lb) to interferon-α treatment. METHODS: Thirty-seven HCV-lb samples were obtained from Hong Kong patients who had completed the combined interferon-α/ribavirin treatment for more than one year with available response data. Nineteen of them were sustained virological responders, while 18 were non-responders. The amino acid sequences of the extended ISDR (eISDR) covering 64 amino acids upstream and 67 amino acids downstream from the previously reported ISDR were analyzed. RESULTS: One amino acid variation (I2268V, P = 0.023) was significantly correlated with treatment outcome in this pilot study with a limited number of patients, while two amino acid variations (R2260H, P = 0.05 and $2278T, P = 0.05) were weakly associated with treat- ment outcome. The extent of amino acid variations within the ISDR or eISDR was not correlated with treat- ment outcome as previously reported. CONCLUSION: Three amino acid mutations near but outside of ISDR may associate with interferon treatment resistance of HCV-lb patients in Hong Kong. 展开更多
关键词 Hepatitis C virus lb Extended interferon sen-sitivity-determining region Interferon-R RESISTANCE HONGKONG Mutation
下载PDF
荧光定量聚合酶链反应与分支链DNA信号扩增法检测血清HBV DNA的比较 被引量:3
2
作者 袁静 马为民 +3 位作者 周伯平 徐六妹 王火生 john s tam 《广东医学》 CAS CSCD 2000年第10期838-839,共2页
目的 了解荧光定量聚合酶链反应 (PCR)法与分支链DNA信号扩增 (bDNA)法在检测血清中HBVDNA含量上的优缺点。方法 分别用这两种方法平行检测 44份乙型肝炎患者的血清标本 ,并与定性PCR检测结果比较。同时用荧光定量PCR法观察 15例乙肝... 目的 了解荧光定量聚合酶链反应 (PCR)法与分支链DNA信号扩增 (bDNA)法在检测血清中HBVDNA含量上的优缺点。方法 分别用这两种方法平行检测 44份乙型肝炎患者的血清标本 ,并与定性PCR检测结果比较。同时用荧光定量PCR法观察 15例乙肝患者干扰素治疗期间HBVDNA含量变化。结果 ①荧光定量PCR法和bDNA法比较 ,○a前者测出的HBVDNA含量均值为 ( 3 5 0× 10 5± 3 3 6)copies/μl ;后者为 ( 3 0 7× 10 5± 12 9)copies/μl ,两者比较差异无显著性 (P >0 0 5 )。○b前者的HBVDNA阳性率 79 5 % ;后者及常规PCR定性法均为 5 9 1%。荧光定量PCR法的阳性检出率显著高于bDNA法及常规定性PCR法 (P <0 0 5 )。② 15例中 5例获完全应答的乙型肝炎患者其血清HBVDNA含量在治疗 16周内均逐渐下降至完全转阴。结论 荧光定量PCR法与bDNA法在检测血清HBVDNA含量上 ,结果大多一致 ,且敏感性强 ,检验也较简便、价廉 ,并能较好评价和检测乙肝患者抗病毒疗效 ,宜于临床推广。 展开更多
关键词 乙型肝炎 HBV-DNA bDNA法 荧光定量聚合酶链反应
下载PDF
Public Health Control Measures for the Co-circulation of Influenza and SARS-CoV-2 During Influenza Seasons
3
作者 john s tam Yuelong shu 《China CDC weekly》 2022年第2期22-26,共5页
SEASONAL INFLUENZA IN THE MIDST OF COVID-19 The World Health Organization(WHO)named the disease caused by severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)as coronavirus disease 2019(COVID-19)and declared th... SEASONAL INFLUENZA IN THE MIDST OF COVID-19 The World Health Organization(WHO)named the disease caused by severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)as coronavirus disease 2019(COVID-19)and declared the outbreak a Public Health Emergency of International Concern(PHEIC)on January 30,2020 and a pandemic on March 11,2020.Globally,there have been 239,437,517 confirmed cases of COVID-19 reported to WHO,including 4,879,235(2.1%)deaths as of October 15,2021(1).The COVID-19 pandemic continues to cause an unparalleled impact on global public health security and economic well-being in the context of previous influenza pandemics as well as other emerging infectious diseases in history(2).As the epidemiology,clinical presentations,and control measures for SARS-CoV-2 and influenza share many features,there is a need to develop strategies to address additional challenges arising in the continued surveillance,prevention,and clinical management of influenza in conjunction with COVID-19 pandemic responses. 展开更多
关键词 EPIDEMIOLOGY prevention ACUTE
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部