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METHODS: The authors studied a cohort of 229 Stage I nonsmall cell lung carcinoma (NSCLC) patients who had a minimum of 3 years follow-up and had been previously analyzed for 22 clinical, pathologic, and molecular features, of which 9 had been found to provide significant prognostic information in a Cox proportional hazards model.
This collection has been previously analyzed for mutants effecting meiotic chromosome segregation, spore formation, and ether resistance [21], [27].
A set of 67 phenotypic traits has been previously analyzed for QTL (pQTL) in this cross [16], [17].
All cases had been previously analyzed for MSI status [ 26].
Patient group 2 consisted of samples that had been previously analyzed for neuroborreliosis.
Both series have been previously analyzed for TP53 mutations [ 30, 32, 33].
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A majority (60.8%) of the individuals included in this study were previously analyzed for the chloroplast phylogenetic study [16] allowing for a direct comparison of the resulting patterns; the morphological character data analyzed in this study were also previously published [16].
These sequences were previously analyzed for their repeat content [ 39].
GSK3B was previously analyzed for association with PCOS susceptibility (13).
Each of these tumors was previously analyzed for gene expression using Affymetrix U133A arrays [ 15, 16].
Each tumor was previously analyzed for CHEK2 and TP53 mutation status.
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