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Th a high negative predictive value, an 80 sensitivity and 74.7 specificity. Although its prognostic value was not independent of the presence/absence of obstructive CAD, adding CS and CTA data to clinical parameters improved the prediction of CVEV: the combined model had the highest AUC (0.888, 95 CI 0.789-0.987, p

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Receptors also modulate response to therapy [8,9], we also assessed, as a secondary aim of this study, the predictive value of DC-SCRIPT by using clinical benefit and progression-free survival (PFS) after first-line tamoxifen for advanced disease as the main endpoints.Materials and methodsPatientsdetermined by real-time reverse transcriptase-polymerase chain reaction (RT-PCR) [14,16,17]. Follow-up

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For assistance with writing the manuscript, and members of Peterlin laboratory for helpful discussions and continuous support. This work was supported by grants from the National Institutes of Health to B.M.P. (AI49104 and AI058708). T.L. was supported in part by a grant from the National Institutes of Health, University of California San Francisco ladstone Institute of Virology Immunology Cente