Jessica Erin Poort

Cynthia Jordan	grad student	2014	Michigan State
(Pathology at the neuromuscular junction in mouse models of spinal bulbar muscular atrophy.)

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Poort JE, Rheuben MB, Marc Breedlove S, et al. (2016) Neuromuscular junctions are pathological but not denervated in two mouse models of spinal bulbar muscular atrophy. Human Molecular Genetics
Halievski K, Henley CL, Domino L, et al. (2015) Androgen-dependent loss of muscle BDNF mRNA in two mouse models of SBMA. Experimental Neurology. 269: 224-32
Oki K, Halievski K, Vicente L, et al. (2015) Contractile dysfunction in muscle may underlie androgen-dependent motor dysfunction in spinal bulbar muscular atrophy. Journal of Applied Physiology (Bethesda, Md. : 1985). 118: 941-52
Smith MR, Hamson DK, Poort JE, et al. (2012) Ontogeny of androgen receptor expression in spinal nucleus of the bulbocavernosus motoneurons and their target muscles in male mice. Neuroscience Letters. 513: 119-23
Zuloaga DG, Poort JE, Jordan CL, et al. (2011) Male rats with the testicular feminization mutation of the androgen receptor display elevated anxiety-related behavior and corticosterone response to mild stress. Hormones and Behavior. 60: 380-8
Ottem EN, Poort JE, Wang H, et al. (2010) Differential expression and regulation of brain-derived neurotrophic factor (BDNF) mRNA isoforms in androgen-sensitive motoneurons of the rat lumbar spinal cord. Molecular and Cellular Endocrinology. 328: 40-6