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Biochemical analytes were compared between those homozygous for Gc1f-1f vs. other Gc variants (Gc1f-1s, Gc1f-2s, Gc1f-2, Gc1s-2 & Gc2-2) using DataDesk 6.3.1 (Data Description Inc, Ithaca, NY, USA) with Student's 2-sample t-tests.
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For each measurement, the concentration and the peak area of the analytes were compared with those of the internal standard.
The mean serum concentrations for individual analytes were compared between patients with breast cancer and those without breast cancer.
Other serum and urine biochemical analytes were measured on the Beckman DXC880i analyzer (Beckman Coulter, Woerden, The Netherlands).
The hemodynamic and biochemical parameters were compared.
Their biochemical and immunological properties were compared with intact gp120.
Analyte assay concentrations were compared.
Using this approach, values of the analytes in each subgroup were compared to another, e.g., controls vs. LRRK2 PD patients.
Ce and Sm were used as analytes and signal intensities were compared.
Clinical and biochemical characteristics and cytokine levels were compared.
Multiple analyte immunoassay (MAIA) results for two sets of three different analytes, one employing polyclonal and the other monoclonal capture antibodies, were compared with results for identical analytes performed in a single-analyte immunoassay (SAIA) format.
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