All Publications

  • Pernicious pathogens or expedient elements of inheritance: the significance of yeast prions. PLoS pathogens Byers, J. S., Jarosz, D. F. 2014; 10 (4)

    View details for DOI 10.1371/journal.ppat.1003992

    View details for PubMedID 24722628

  • Pernicious Pathogens or Expedient Elements of Inheritance: The Significance of Yeast Prions PLOS PATHOGENS Byers, J. S., Jarosz, D. F. 2014; 10 (4)
  • Neuroprotective Effects of Testosterone on Motoneuron and Muscle Morphology Following Spinal Cord Injury JOURNAL OF COMPARATIVE NEUROLOGY Byers, J. S., Huguenard, A. L., Kuruppu, D., Liu, N., Xu, X., Sengelaub, D. R. 2012; 520 (12): 2683-2696


    Treatment with testosterone is neuroprotective/neurotherapeutic after a variety of motoneuron injuries. Here we assessed whether testosterone might have similar beneficial effects after spinal cord injury (SCI). Young adult female rats received either sham or T9 spinal cord contusion injuries and were implanted with blank or testosterone-filled Silastic capsules. Four weeks later, motoneurons innervating the vastus lateralis muscle of the quadriceps were labeled with cholera toxin-conjugated horseradish peroxidase, and dendritic arbors were reconstructed in three dimensions. Soma volume, motoneuron number, lesion volume, and tissue sparing were also assessed, as were muscle weight, fiber cross-sectional area, and motor endplate size and density. Contusion injury resulted in large lesions, with no significant differences in lesion volume, percent total volume of lesion, or spared white or gray matter between SCI groups. SCI with or without testosterone treatment also had no effect on the number or soma volume of quadriceps motoneurons. However, SCI resulted in a decrease in dendritic length of quadriceps motoneurons in untreated animals, and this decrease was completely prevented by treatment with testosterone. Similarly, the vastus lateralis muscle weights and fiber cross-sectional areas of untreated SCI animals were smaller than those of sham-surgery controls, and these reductions were both prevented by testosterone treatment. No effects on motor endplate area or density were observed across treatment groups. These findings suggest that regressive changes in motoneuron and muscle morphology seen after SCI can be prevented by testosterone treatment, further supporting a role for testosterone as a neurotherapeutic agent in the injured nervous system.

    View details for DOI 10.1002/cne.23066

    View details for Web of Science ID 000306129400010

    View details for PubMedID 22314886

  • Analysis of a Hand1 Hypomorphic Allele Reveals a Critical Threshold for Embryonic Viability DEVELOPMENTAL DYNAMICS Firulli, B. A., McConville, D. P., Byers, J. S., Vincentz, J. W., Barnes, R. M., Firulli, A. B. 2010; 239 (10): 2748-2760


    Loss-of-function analysis of the basic helix-loop-helix (bHLH) transcription factor Hand1 indicates critical roles in development. In an effort to generate a Hand1 cDNA knock-in reporter mouse, we generated two hypomorphic alleles, which extend embryonic survival to between embryonic day (E) 10.5 and E12.5. Heart morphogenesis appears largely normal; however, hypomorphic mice display thin left ventricular myocardium and reduction in pharyngeal mesoderm. Caudal defects, large allantois, and thickened yolk sac are observed and consistent with systemic Hand1 gene deletion. Hand1 mRNA is expressed at 30% of wild-type littermates and known Hand1-dependent genes show intermediate expression compared with wild-type and Hand1 null mice. Interestingly, putative bHLH partners, Hand2 and Twist1, show altered expression in both Hand1 null and hypomorphic backgrounds and intercrossing the Hand1 hypomorphic mice onto the Hand2 systemic null background exacerbates the cardiac and lateral mesoderm phenotypes. Together, these data define a critical threshold of Hand1 expression that is necessary for embryonic survival.

    View details for DOI 10.1002/dvdy.22402

    View details for Web of Science ID 000283103500022

    View details for PubMedID 20737509

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