Kathryn J. Jones

Testosterone treatment attenuates the effects of facial nerve transection on glial fibrillary acidic protein (GFAP) levels in the hamster facial motor nucleus.

Combination of gonadal steroid treatment and peripheral nerve grafting results in a peripheral motoneuron-like pattern of beta II-tubulin mRNA expression in axotomized hamster rubrospinal motoneurons.

Functional recovery after facial nerve crush is delayed in severe combined immunodeficient mice.

Ribosomal RNA transcriptional activation and processing in hamster rubrospinal motoneurons: effects of axotomy and testosterone treatment.

Use of a cell line to investigate olfactory ensheathing cell-enhanced axonal regeneration.

Androgen induced acceleration of functional recovery after rat sciatic nerve injury.

CD4+ T, but not CD8+ or B, lymphocytes mediate facial motoneuron survival after facial nerve transection.

Natural killer cells do not mediate facial motoneuron survival after facial nerve transection.

Glial fibrillary acidic protein expression in the hamster red nucleus: effects of axotomy and testosterone treatment.

Neurotherapeutic action of testosterone on hamster facial nerve regeneration: temporal window of effects.

CD4-positive T cell-mediated neuroprotection requires dual compartment antigen presentation.

Role of the immune system in the maintenance of mouse facial motoneuron viability after nerve injury.

Brain-derived neurotrophic factor supports facial motoneuron survival after facial nerve transection in immunodeficient mice.

Gonadal steroid attenuation of developing hamster facial motoneuron loss by axotomy: equal efficacy of testosterone, dihydrotestosterone, and 17-beta estradiol.

Motoneuron injury and repair: New perspectives on gonadal steroids as neurotherapeutics.

CD4+CD25+ regulatory T cells and CD1-restricted NKT cells do not mediate facial motoneuron survival after axotomy.

Immune-mediated neuroprotection of axotomized mouse facial motoneurons is dependent on the IL-4/STAT6 signaling pathway in CD4(+) T cells.

CD4(+) T cell-mediated facial motoneuron survival after injury: Distribution pattern of cell death and rescue throughout the extent of the facial motor nucleus.

Cellular localization of androgen and estrogen receptors in mouse-derived motoneuron hybrid cells and mouse facial motoneurons.

Phenotype of CD4+ T cell subsets that develop following mouse facial nerve axotomy.

Role of immunity in recovery from a peripheral nerve injury.

Effects of single versus combinatorial treatment strategies on beta II-tubulin gene expression in axotomized hamster rubrospinal motoneurons.

Androgen regulation of axon growth and neurite extension in motoneurons.

Androgen regulates neuritin mRNA levels in an in vivo model of steroid-enhanced peripheral nerve regeneration.

Accelerating functional recovery after rat facial nerve injury: Effects of gonadal steroids and electrical stimulation.

Electrical stimulation facilitates rat facial nerve recovery from a crush injury.

IL-1beta signaling initiates inflammatory hypernociception.

Neuroprotective actions of androgens on motoneurons.

Electrical stimulation and testosterone differentially enhance expression of regeneration-associated genes.

Comparison of extratemporal and intratemporal facial nerve injury models.

Effects of facial nerve axotomy on Th2- and Th1-associated chemokine expression in the facial motor nucleus of wild-type and presymptomatic mSOD1 mice.

Local delivery of a collagen-binding FGF-1 chimera to smooth muscle cells in collagen scaffolds for vascular tissue engineering.

Functional recovery and facial motoneuron survival are influenced by immunodeficiency in crush-axotomized mice.

Exacerbation of facial motoneuron loss after facial nerve axotomy in CCR3-deficient mice.

Effects of electrical stimulation and gonadal steroids on rat facial nerve regenerative properties.

Toll-like receptor 2 and facial motoneuron survival after facial nerve axotomy.

Effects of facial nerve axotomy on Th2-associated and Th1-associated chemokine mRNA expression in the facial motor nucleus of wild-type and presymptomatic SOD1 mice.

Differential actions of pituitary adenylyl cyclase-activating polypeptide and interferon gamma on Th2- and Th1-associated chemokine expression in cultured murine microglia.

Use of laser microdissection in the investigation of facial motoneuron and neuropil molecular phenotypes after peripheral axotomy.

Combinatorial treatments enhance recovery following facial nerve crush.

IL-10 within the CNS is necessary for CD4+ T cells to mediate neuroprotection.

Facial motor nuclei cell loss with intratemporal facial nerve crush injuries in rats.

Muscle matters--dendrites grow up.

Differential gene expression in the axotomized facial motor nucleus of presymptomatic SOD1 mice.

Immune cell-mediated neuroprotection is independent of estrogen action through estrogen receptor-alpha.

CD4+ T cell-mediated neuroprotection is independent of T cell-derived BDNF in a mouse facial nerve axotomy model.

Single session of brief electrical stimulation immediately following crush injury enhances functional recovery of rat facial nerve.

Androgen treatment and recovery of function following recurrent laryngeal nerve injury in the rat.

Electrical stimulation and testosterone enhance recovery from recurrent laryngeal nerve crush.

Axotomy-induced target disconnection promotes an additional death mechanism involved in motoneuron degeneration in amyotrophic lateral sclerosis transgenic mice.

Delayed functional recovery in presymptomatic mSOD1(G93A) mice following facial nerve crush axotomy.

The need for speed in rodent locomotion analyses.

SOD1(G93A) transgenic mouse CD4(+) T cells mediate neuroprotection after facial nerve axotomy when removed from a suppressive peripheral microenvironment.