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GFP-labeled bacteria have been used in monitoring either single cells or a cell population in survival studies of E. coli in aquatic environments [8], in elucidating the spatial arrangement of Streptococcus species in biofilm structure [5], in tracing Vibrio parahaemolyticus in oysters [6], and in investigating survival and spatial location of Salmonella in alfalfa sprouts [7].
For survival studies of the LID mice and end-of-life pathology, total frequency and grade of lesions were compared between genotypes using a chi-square test.
For instance, if there are 3 RSA studies and 2 survival studies of the same PF combination, then there would be 6 possible combinations (3 × 2).
Population-based survival studies of BRC patients with regard to delivered treatment according to available Clinical Practice Guidelines (GPG) are scant.
For instance, if there are 3 RSA studies and 2 survival studies of the same PF, then there would be 6 possible combinations (3 times 2).
To test our method, we used two datasets publicly available: survival studies of neuroblastoma (Oberthuer et al., 2006) and breast cancer (Van De Vijver et al., 2002) patients.
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This question was tested in a survival study of tumor bearing mice.
A survival study of HIV-infected Koreans reported that 45% of deaths occurred within 6 months of HIV diagnosis [ 9], and suggested the presence of delayed diagnosis and antiretroviral therapy in Korea.
Remarkably, a long-term survival study of the Early Breast Cancer Trialists´ Group EBCTCGG) has notified that the ER status loses its predictive significance and that the long-term outcome of ER-positive and ER-negative tumors is not differential [ 30].
A late diagnosis was defined by a CD4+ T cell count <200 cells/mm3 at the time of diagnosis [ 9, 20, 21], according to KCDC guidelines and a survival study of HIV-infected Koreans.
Nevertheless, the quality of the survival studies and of the RSA studies showed only small effects on the association between migration and revision rate.
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