12 research outputs found

    Noise Performance of the CrIS Instrument

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    The Cross-track Infrared Sounder (CrIS) is a spaceborne Fourier transform spectrometer (FTS) that was launched into orbit on 28 October 2011 onboard the Suomi National Polar-orbiting Partnership satellite. CrIS is a sophisticated sounding sensor that accurately measures upwelling infrared radiance at high spectral resolution. Data obtained from this sensor are used for atmospheric profiles retrieval and assimilation by numerical weather prediction models. Optimum vertical sounding resolution is achieved with high spectral resolution and multiple spectral channels; however, this can lead to increased noise. The CrIS instrument is designed to overcome this problem. Noise Equivalent Differential Radiance (NEdN) is one of the key parameters of the Sensor Data Record product. The CrIS on-orbit NEdN surpassesmission requirements with margin and has comparable or better performance when compared to heritage hyperspectral sensors currently on orbit. This paper describes CrIS noise performance through the characterization of the sensor’s NEdN and compares it to calibration data obtained during ground test. In addition, since FTS sensors can be affected by vibration that leads to spectrally correlated noise on top of the random noise inherent to infrared detectors, this paper also characterizes the CrIS NEdN with respect to the correlated noise contribution to the total NEdN. Lastly, the noise estimated from the imaginary part of the complex FTS spectra is extremely useful to assess andmonitor in-flight FTS sensor health. Preliminary results on the imaginary spectra noise analysis are also presented

    Role of early second-trimester uterine artery Doppler screening to predict small-for-gestational-age babies in nulliparous women

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    Background Trophoblastic invasion of the uterine spiral arteries substantially increases compliance to accommodate increased blood flow to the placenta. Failure of this process impedes uterine artery blood flow, and this may be detected by uterine artery Doppler flow studies. However, the clinical utility of uterine artery Doppler flow studies in the prediction of adverse pregnancy outcomes in a general population remains largely unknown. Objective We sought to determine the utility of early second-trimester uterine artery Doppler studies as a predictor of small-for-gestational-age neonates. Study Design Nulliparous women with a viable singleton pregnancy were recruited during their first trimester into an observational prospective cohort study at 8 institutions across the United States. Participants were seen at 3 study visits during pregnancy and again at delivery. Three indices of uterine artery Doppler flow (resistance index, pulsatility index, and diastolic notching) were measured in the right and left uterine arteries between 16 weeks 0 days’ and 22 weeks 6 days’ gestation. Test characteristics for varying thresholds in the prediction of small for gestational age (defined as birthweight <5th percentile for gestational age [Alexander growth curve]) were evaluated. Results Uterine artery Doppler indices, birthweight, and gestational age at birth were available for 8024 women. Birthweight <5th percentile for gestational age occurred in 358 (4.5%) births. Typical thresholds for the uterine artery Doppler indices were all associated with birthweight <5th percentile for gestational age (P < .0001 for each), but the positive predictive values for these cutoffs were all <15% and areas under receiver operating characteristic curves ranged from 0.50-0.60. Across the continuous scales for these measures, the areas under receiver operating characteristic curves ranged from 0.56-0.62. Incorporating maternal age, early pregnancy body mass index, race/ethnicity, smoking status prior to pregnancy, chronic hypertension, and pregestational diabetes in the prediction model resulted in only modest improvements in the areas under receiver operating characteristic curves ranging from 0.63-0.66. Conclusion In this large prospective cohort, early second-trimester uterine artery Doppler studies were not a clinically useful test for predicting small-for-gestational-age babies

    Pleural innate response activator B cells protect against pneumonia via a GM-CSF-IgM axis

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    Pneumonia is a major cause of mortality worldwide and a serious problem in critical care medicine, but the immunophysiological processes that confer either protection or morbidity are not completely understood. We show that in response to lung infection, B1a B cells migrate from the pleural space to the lung parenchyma to secrete polyreactive emergency immunoglobulin M (IgM). The process requires innate response activator (IRA) B cells, a transitional B1a-derived inflammatory subset which controls IgM production via autocrine granulocyte/macrophage colony-stimulating factor (GM-CSF) signaling. The strategic location of these cells, coupled with the capacity to produce GM-CSF–dependent IgM, ensures effective early frontline defense against bacteria invading the lungs. The study describes a previously unrecognized GM-CSF-IgM axis and positions IRA B cells as orchestrators of protective IgM immunity

    Synthetic Lethal and Convergent Biological Effects of Cancer-Associated Spliceosomal Gene Mutations

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    Mutations affecting RNA splicing factors are the most common genetic alterations in myelodysplastic syndrome (MDS) patients and occur in a mutually exclusive manner. The basis for the mutual exclusivity of these mutations and how they contribute to MDSis not well understood. Here we report that although different spliceosome gene mutations impart distinct effects on splicing, they are negatively selected for when co-expressed due to aberrant splicing and downregulation of regulators of hematopoietic stem cell survival and quiescence. In addition to this synthetic lethal interaction, mutations in the splicing factors SF3B1 and SRSF2 shareconvergent effects on aberrant splicing of mRNAs that promote nuclear factor kB signaling. These data identify shared consequences of splicing-factor mutations and the basis for their mutual exclusivity
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