TO
1 - 25 of 5
| Creator | Title | Description | Subject | Date | ||
|---|---|---|---|---|---|---|
| 1 |
 |
Lee, Hani | Post-traumatic headache: an opportunity to develop new preclinical models for better understanding of pathology and treatment | Post-traumatic headache (PTH) is identified as one of the most frequent symptoms following traumatic brain injury (TBI) (Faux & Sheedy, 2008). Despite the high prevalence, there are currently no treatments which specifically target PTH. Instead of etiology-specific treatments, individuals suffering ... | 2022 | |
| 2 |
 |
Nau, Adam | The role of heparan sulfate in maintaining stereotyped birdsong | Song learning in Zebra Finches (Taeniopygia guttata) occurs during a critical period between 30-90 post hatch days, and involves acquisition of an acoustic model and a sensorimotor period of increasingly improving imitation of this model. Young birds sing highly variable songs early during this pe... | Birdsongs - Research; Zebra finch - Research; Songbirds - Behavior; Heparan sulfate; Taeniopygia guttata; Neural circuitry | 2016-04 |
| 3 |
 |
Bernardo, Madeline F. | The Neural Mechanisms of Sexual Transformation in Thalassoma Bifasciatum, the Bluehead Wrasse | Thalassoma bifasciatum, the bluehead wrasse, is a protogynous sequential hermaphrodite and a commonly used model for studying environmental sex determination and adult sexual plasticity. Terminal phase (TP) male bluehead wrasses demonstrate characteristic behaviors and coloration changes when courti... | 2020 | |
| 4 |
 |
Wang, Zhirong | The role of the autism-associated gene kirrel3 in synapse formation | Alterations in the gene Kirrel3 are repeatedly associated with intellectual disability and autism. Kirrel3 regulates synapse formation in C. elegans but the role of Kirrel3 in synapse formation in the mammalian brain is unknown. In mice, Kirrel3 is expressed in specific cell types throughout the bra... | Autism -- Genetic aspects; Synapses; Kirrel3 gene; Synapse formation | 2015-04 |
| 5 |
 |
Auduong, Priscilla | Spinal muscular atrophy modeled in drosophila melanogaster | Spinal Muscular Atrophy (SMA) is the most commonly inherited cause of death in children (Park, Kariya, & Monani, 2010 for review). This disease is characterized by a loss of motor neurons which leads to muscle degeneration, paralysis, and eventual death by respiratory failure (Monani, 2005 for revie... | Spinal muscular atrophy - Research; Drosophila melanogaster - Researcher | 2012-05 |
1 - 25 of 5