897 research outputs found

    Domain general learning: Infants use social and non-social cues when learning object statistics.

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    Previous research has shown that infants can learn from social cues. But is a social cue more effective at directing learning than a non-social cue? This study investigated whether 9-month-old infants (N = 55) could learn a visual statistical regularity in the presence of a distracting visual sequence when attention was directed by either a social cue (a person) or a non-social cue (a rectangle). The results show that both social and non-social cues can guide infants' attention to a visual shape sequence (and away from a distracting sequence). The social cue more effectively directed attention than the non-social cue during the familiarization phase, but the social cue did not result in significantly stronger learning than the non-social cue. The findings suggest that domain general attention mechanisms allow for the comparable learning seen in both conditions

    The test stand system for the PHENIX iFVTX silicon detector

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    PHENIX is the largest of the four experiments currently taking data at the Relativistic Heavy Ion Collider (RHIC), and the iFVTX is a new pixel tracker which will be installed in the forward tracker region of PHENIX. Fermilab has developed a complete test stand system for the examination of FPix2.1 modules, hybrids, and pixel chips that will be installed in the iFVTX. The system is currently in use for chip, module, and wafer testing at Fermilab. The test stand architecture is flexible and can be adapted to new requirements. In this paper, the software and hardware integration will be discussed followed by an analysis of the advantages of choosing a modular approach for the system. Finally, a selection of tests supported by the system, along with sample results, will be presented and explained

    Early Assessment of Tumor Response to Radiation Therapy using High-Resolution Quantitative Microvascular Ultrasound Imaging

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    Measuring changes in tumor volume using anatomical imaging weeks to months post radiation therapy (RT) is currently the clinical standard for indicating treatment response to RT. For patients whose tumors do not respond successfully to treatment, this approach is suboptimal as timely modification of the treatment approach may lead to better clinical outcomes. We propose to use tumor microvasculature as a biomarker for early assessment of tumor response to RT. Acoustic angiography is a novel contrast ultrasound imaging technique that enables high-resolution microvascular imaging and has been shown to detect changes in microvascular structure due to cancer growth. Data suggest that acoustic angiography can detect longitudinal changes in the tumor microvascular environment that correlate with RT response

    An application using micro TCA for real-time event assembly

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    Bianchi I Quantum cosmology in the Bergmann-Wagoner theory

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    The Wheeler-DeWitt equation is considered in the context of generalized scalar-tensor theories of gravitation for Bianchi type I cosmology. Exact solutions are found for two selfinteracting potentials and arbitary coupling function. The WKB wavefunctions are obtained and a family of solutions satisfying the Hawking-Page regularity conditions of wormholes are found.Comment: 12 pages, Latex fil

    The Dkk3 gene encodes a vital intracellular regulator of cell proliferation

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    Members of the Dickkopf (Dkk) family of Wnt antagonists interrupt Wnt-induced receptor assembly and participate in axial patterning and cell fate determination. One family member, DKK3, does not block Wnt receptor activation. Loss of Dkk3 expression in cancer is associated with hyperproliferation and dysregulated ss-catenin signaling, and ectopic expression of Dkk3 halts cancer growth. The molecular events mediating the DKK3-dependent arrest of ss-catenin-driven cell proliferation in cancer cells are unknown. Here we report the identification of a new intracellular gene product originating from the Dkk3 locus. This Dkk3b transcript originates from a second transcriptional start site located in intron 2 of the Dkk3 gene. It is essential for early mouse development and is a newly recognized regulator of ss-catenin signaling and cell proliferation. Dkk3b interrupts nuclear translocation ss-catenin by capturing cytoplasmic, unphosphorylated ss-catenin in an extra-nuclear complex with ss-TrCP. These data reveal a new regulator of one of the most studied signal transduction pathways in metazoans and provides a novel, completely untapped therapeutic target for silencing the aberrant ss-catenin signaling that drives hyperproliferation in many cancers
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