Candice Frances

Publications

Displaying 1 - 2 of 2
  • Tzekov, R., Quezada, A., Gautier, M., Biggins, D., Frances, C., Mouzon, B., Jamison, J., Mullan, M., & Crawford, F. (2014). Repetitive mild traumatic brain injury causes optic nerve and retinal damage in a mouse model. Journal of Neuropathology and Experimental Neurology, 73(4), 345-361. doi:10.1097/NEN.0000000000000059.

    Abstract

    There is increasing evidence that long-lasting morphologic and
    functional consequences can be present in the human visual system
    after repetitive mild traumatic brain injury (r-mTBI). The exact lo-
    cation and extent of the damage in this condition are not well un-
    derstood. Using a recently developed mouse model of r-mTBI, we
    assessed the effects on the retina and optic nerve using histology and
    immunohistochemistry, electroretinography (ERG), and spectral-
    domain optical coherence tomography (SD-OCT) at 10 and 13 weeks
    after injury. Control mice received repetitive anesthesia alone (r-sham).
    We observed decreased optic nerve diameters and increased cellularity
    and areas of demyelination in optic nerves in r-mTBI versus r-sham
    mice. There were concomitant areas of decreased cellularity in the
    retinal ganglion cell layer and approximately 67% decrease in brain-
    specific homeobox/POU domain protein 3AYpositive retinal ganglion
    cells in retinal flat mounts. Furthermore, SD-OCT demonstrated a de-
    tectable thinning of the inner retina; ERG demonstrated a decrease in
    the amplitude of the photopic negative response without any change in
    a- or b-wave amplitude or timing. Thus, the ERG and SD-OCT data
    correlated well with changes detected by morphometric, histologic,
    and immunohistochemical methods, thereby supporting the use of
    these noninvasive methods in the assessment of visual function and
    morphology in clinical cases of mTBI.
  • Nomi, J. S., Frances, C., Nguyen, M. T., Bastidas, S., & Troup, L. J. (2013). Interaction of threat expressions and eye gaze: an event-related potential study. NeuroReport, 24, 813-817. doi:10.1097/WNR.0b013e3283647682.

    Abstract

    he current study examined the interaction of fearful, angry,
    happy, and neutral expressions with left, straight, and
    right eye gaze directions. Human participants viewed
    faces consisting of various expression and eye gaze
    combinations while event-related potential (ERP) data
    were collected. The results showed that angry expressions
    modulated the mean amplitude of the P1, whereas fearful
    and happy expressions modulated the mean amplitude of
    the N170. No influence of eye gaze on mean amplitudes for
    the P1 and N170 emerged. Fearful, angry, and happy
    expressions began to interact with eye gaze to influence
    mean amplitudes in the time window of 200–400 ms.
    The results suggest early processing of expression
    influence ERPs independent of eye gaze, whereas
    expression and gaze interact to influence later
    ERPs.

Share this page