Aberrant DNA methylation occurs early in oncogenesis, is stable, and can be assayed in tissues and body fluids. Therefore, genes with aberrant methylation can provide clues for understanding tumor pathways and are attractive candidates for detection of early neoplastic events. Identification of sequences that optimally discriminate cancer from other diseased and healthy tissues is needed to advance both approaches.
View Article and Find Full Text PDFComb Chem High Throughput Screen
December 2005
The objective of this work was the application of peptidomics technologies for the detection and identification of reliable and robust biomarkers for Alzheimer's disease (AD) contributing to facilitate and further improve the diagnosis of AD. Using a new method for the comprehensive and comparative profiling of peptides, the differential peptide display (DPD), 312 cerebrospinal fluid (CSF) samples from AD patients, cognitively unimpaired subjects and from patients suffering from other primary dementia disorders were analysed as four independent analytical sets. By combination with a cross validation procedure, candidates were selected from a total of more than 6,000 different peptide signals based on their discriminating power.
View Article and Find Full Text PDFNew markers measuring an imbalance of the bone modeling process have been established in research and in clinical studies, but not yet within the routine laboratories. The improvement of clinical utility by both better interlaboratory comparability as well as minimization of assay influences would facilitate the acceptance in the routine laboratory. Using two specifically developed monoclonal antibodies, a new osteocalcin assay in an Enzymun-Test format has become capable to measure intact as well as the stable N-Mid fragment of osteocalcin.
View Article and Find Full Text PDFFrom a panel of 4 murine monoclonal antibodies directed against keratin 19 various antibody combinations were evaluated in solid-phase enzyme-linked sandwich immunoassays for detection of soluble keratin 19 fragments in patient sera. One of these antibody combinations, comprised of the monoclonal antibodies Ks 19.1 and BM 19.
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