Publications by authors named "Brian H Tran"

Charge detection mass spectrometry (CD-MS) is a powerful technique for the analysis of large, heterogeneous biomolecules. By directly measuring the charge states of individual ions, CD-MS can measure the masses from spectra where conventional deconvolution approaches fail due to the lack of isotopic resolution or distinguishable charge states. However, CD-MS is inherently slow because hundreds or thousands of spectra need to be collected to produce adequate ion statistics.

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Article Synopsis
  • - Charge detection mass spectrometry (CD-MS) allows for the analysis of large and complex analytes by examining individual ion signals, but it requires long analysis times due to the need for numerous scans to achieve reliable data.
  • - The slow speed of CD-MS presents challenges for integration with fast techniques like chromatography, as limited scans may not provide adequate ion statistics from a single injection.
  • - UniChromCD, a new module in the open-source UniDec package, simplifies the processing of CD-MS data by combining it with advanced demultiplexing methods, enhancing analysis and visualization of time-resolved data while supporting techniques like size-exclusion chromatography and ion mobility.
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Venous thromboembolism (VTE) is a potentially preventable disease that carries significant morbidity and mortality. Although malignancy is associated with increased risk for VTE, it varies according to cancer type. Despite the fact that breast cancer is the most common form of cancer in women, the incidence and risk factors associated with VTE in patients undergoing mastectomy have not been well characterized.

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GnRH, the central regulator of reproductive function, is produced by only approximately 800 highly specialized hypothalamic neurons. Previous studies identified a minimal promoter [GnRH minimal promoter (GnRH-P)] (-173/+1) and a neuron-specific enhancer [GnRH-enhancer (E)1] (-1863/-1571) as regulatory regions in the rat gene that confer this stringent specificity of GnRH expression to differentiated GnRH neurons. In transgenic mice, these two elements target only GnRH neurons but fail to drive expression in the entire population, suggesting the existence of additional regulatory regions.

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