《Table 6 Modifying effect of diabetes mellitus on GST genotypes in relation to the risk of POAG》
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《GSTM1-null and GSTT1-active genotypes as risk determinants of primary open angle glaucoma among smokers》
OR:Odds ratio adjusted for age and gender.
Sample Collection and DNA Analysis Commercially available DNA kit(Qiagen,USA)was used to isolate DNA from blood leucocytes.The analysis of GSTM1 and GSTT1polymorphisms was carried out by polymerase chain reaction(PCR)using the multiplex PCR method[28].CYP1A1 was used as a housekeeping gene(Table 1).PCR protocol was as followed:denaturation at 94℃for 4min followed by94℃for 30s;annealing:59℃for 30s;extension:72℃for45s;number of cycles:30;final extension:72℃for 5min.The blinded samples for quality control were included to ensure the validation of procedures and steps in the genotype identification and the investigators who performed the multiplex PCR analysis were uninformed of the case-control status.The similarity of the results for the blinded samples was100%.
图表编号 | XD0023067200 严禁用于非法目的 |
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绘制时间 | 2018.09.18 |
作者 | Miroslav Stamenkovic、Vesna Lukic、Sonja Suvakov、Tatjana Simic、Ivan Sencanic、Marija Pljesa-Ercegovac、Vesna Jaksic、Sinisa Babovic、Marija Matic、Aleksandra Radosavljevic、Ana Savic-Radojevic、Tatjana Djukic |
绘制单位 | University Eye Clinic,Medical Center Zvezdara、Faculty of Special Education and Rehabilitation,University of Belgrade、University Eye Clinic,Medical Center Zvezdara、Institute of Medical and Clinical Biochemistry、Faculty of Medicine,University of Belgrade、In |
更多格式 | 高清、无水印(增值服务) |