12 research outputs found

    PSR J1926-0652: A Pulsar with Interesting Emission Properties Discovered at FAST

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    We describe PSR J1926-0652, a pulsar recently discovered with the Five-hundred-meter Aperture Spherical radio Telescope (FAST). Using sensitive single-pulse detections from FAST and long-term timing observations from the Parkes 64-m radio telescope, we probed phenomena on both long and short time scales. The FAST observations covered a wide frequency range from 270 to 800 MHz, enabling individual pulses to be studied in detail. The pulsar exhibits at least four profile components, short-term nulling lasting from 4 to 450 pulses, complex subpulse drifting behaviours and intermittency on scales of tens of minutes. While the average band spacing P3 is relatively constant across different bursts and components, significant variations in the separation of adjacent bands are seen, especially near the beginning and end of a burst. Band shapes and slopes are quite variable, especially for the trailing components and for the shorter bursts. We show that for each burst the last detectable pulse prior to emission ceasing has different properties compared to other pulses. These complexities pose challenges for the classic carousel-type models.Comment: 13pages with 12 figure

    Protein Profiling of Bladder Urothelial Cell Carcinoma

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    <div><p>This study aimed to detect protein changes that can assist to understand the underlying biology of bladder cancer. The data showed forty five proteins were found to be differentially expressed comparing tumors vs non-tumor tissues, of which EGFR and cdc2p34 were correlated with muscle invasion and histological grade. Ten proteins (Ăź-catenin, HSP70, autotaxin, Notch4, PSTPIP1, DPYD, ODC, cyclinB1, calretinin and EPO) were able to classify muscle invasive BCa (MIBC) into 2 distinct groups, with group 2 associated with poorer survival. Finally, 3 proteins (P2X7, cdc25B and TFIIH p89) were independent factors for favorable overall survival.</p></div

    Differentially expressed proteins in different T stages.

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    <p>a) The hexagonal array displays the changing patterns of the proteins expression from Ta to T4. Each hexagon represents a protein, the color of a hexagon reflects its level of expression in current T stage with respect to corresponding non-tumor tissue. b) The significantly expressed proteins between tumor and non-tumor tissues in different T stages were listed in their own circle which represents a specific stage. The proteins listed in the overlap area were shared by 2 adjacent stages. Proteins in red are upregulated and proteins in green are downregulated.</p

    Hierarchical clustering analysis of 11 differentially expressed proteins in 31 tumors (T) and 43 non-tumor (N) samples.

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    <p>The color scale showed the level of expression. Red indicates overexpression, green indicates underexpression, black indicates no change, and gray no expression. The number in each column represents the sample number. Each row represents a protein.</p
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