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| 1 | Extracellular superoxide dismutase in biology and medicine显示文摘 | Cheryl L F Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，3： | 1 |
| 2 | Extracenular superoxide dismutatse in biology and medicine 显示文摘 | Cheryl LF Lisa M S Tim Do | 2003 | Free Rad Bid Med2003，35，3： | 1 |
| 3 | Extracellular superoxide dismutase in biology and medicine显示文摘 | Cheryl LF Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，3： | 1 |
| 4 | Extracellular superoxide dismutase in biology and medicine显示文摘 | Cheryl LF Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，3： | 1 |
| 5 | Extrcellular superoxide dismutase in biology and medicine显示文摘 | Cheryl LF Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，3： | 1 |
| 6 | Extrcellular superoxide dismutase in bi- ology and medicine显示文摘 | Cheryl LF Lisa Tim DO | 2003 | Free Rad Biol Med2003，35，3： | 1 |
| 7 | Cationic membrane‐active peptides – anticancer and antifungal activity as well as penetration into human skin显示文摘 | Nhung Do Günther Weindl Lisa Grohmann Mario Salwiczek Beate Koksch Hans Christian Korting Monika Sch?fer‐Korting | 2014 | Exp Dermatol2014，，： | 1 |
| 8 | Extracellular superoxide dismutase in biology and medicine显示文摘 | Cheryl LF Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，： | 1 |
| 9 | Measurement of the ture affinity constant in solution of antigen-antibody complex by enzyme-linked immunosorbent assay显示文摘 | Friguent B Chaffatte AF Lisa DO | 1985 | Immunol Methods1985，77，2： | 1 |
| 10 | Extracellular superoxide dismutatse in biology and medicine显示文摘 | Lisa MS Tim Do | 2003 | Free Rad Bid Med2003，35，3： | 1 |
| 11 | Extracellular superoxide dismutase in biology and medicine显示文摘 | Cheryl LF Lisa MS Tim DO | 2003 | Free Rad Biol Med2003，35，： | 1 |
| 12 | 糖尿病管理的全科视角——运用评估工具问病史,全面而不遗漏显示文摘全科医生日常重要工作内容之一就是接诊慢性病患者、对慢性病患者进行管理与随访。本文将以LisaA.Kassenoff,DO老师接诊的一个糖尿病患者为例,阐述如何从全科视角来管理慢性病患者,如何运用评估工具将慢性病患者的接诊、随访工作做到全面而不遗漏。 | 王玲莉 裴宇慧 Lisa A.Kassenoff DO | 2018 | 医师在线2018，8，35： | 0 |
| 13 | Identification of a Target Region for Specific Molecular Diagnosis of Human Papillomavirus Subtype 16显示文摘Objective: To identify a target region for molecular diagnosis from the E6 region of the Human papillomavirus (HPV). Method: This was a quantitative data research. The sample was composed of sequences from the National Center for Biotechnology Information (NCBI), HPV subtype 16, E6 region, using the following search filters: viruses, genomic DNA/RNA. 3227 sequences were obtained, which were separated according to the country of origin. After selection, the total number of samples consisted of 22 sequences that were aligned in the Clustal/o program, available on the online platform at: http://gffzz7fe8ccc2a30242bfs0wf9fkppqv6c6uqc.ffgz.tsg.suse.edu.cn/Tools/msa/clustalo/ and reading it through the Jalview program to identify consensus regions. For the primer design, the FastPCR program was used and the data were attached to a spreadsheet in Microsoft Excel 2010. Results: The consensus sequence among the countries was selected according to the consensus region for the primer design, called the target region, with 95 nucleotides. FastPCR analyzed the sequence and defined 10 pairs of primers, 5 forward and 5 reverse. The primers were selected according to the percentage CG/AT ratio (50%-60%) and the specific temperature of 58 °C, resulting in 3 primer pairs. The pairs were analyzed in the BLAST program, obtaining a 100% identification and query score, identifying other sequences of HPV 16, region E6. Conclusion: The use of a primer with greater specificity will lead to the specific diagnosis of the virus, making possible the early diagnosis and the most effective treatment. | Ketly Rodrigues Barbosa dos Anjos Anderson Alves da Silva Bezerra Ana Lisa do Vale Gomes | 2019 | Journal of Pharmacy and Pharmacology2019，7，11： | 0 |
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