Rocco G. Gogliotti, Ph.D.
Affiliations: | 2012 | Integrated Graduate Program in the Life Sciences | Northwestern University, Evanston, IL |
Area:
Molecular Neuroscience, Motor Control, Neurobiology of DiseaseGoogle:
"Rocco Gogliotti"Mean distance: 35622
Parents
Sign in to add mentor| Christine Didonato | grad student | 2012 | Northwestern | |
| (Spinal Muscular Atrophy is a Cell Autonomous Disease of the Motor Neuron.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Cikowski J, Holt C, Arthur B, et al. (2022) Optimized Administration of the M PAM VU0467154 Demonstrates Broad Efficacy, but Limited Effective Concentrations in Mice. Acs Chemical Neuroscience |
| Vermudez SAD, Gogliotti RG, Arthur B, et al. (2021) Profiling beneficial and potential adverse effects of MeCP2 overexpression in a hypomorphic Rett syndrome mouse model. Genes, Brain, and Behavior |
| Fisher NM, AlHashim A, Buch AB, et al. (2021) A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes. Jci Insight |
| Gogliotti R, Fisher N, Stansley B, et al. (2018) Total RNA-sequencing of Rett Syndrome Autopsy Samples Identifies the M4 Muscarinic Receptor as a Novel Therapeutic Target. The Journal of Pharmacology and Experimental Therapeutics |
| Fisher NM, Gogliotti RG, Vermudez SAD, et al. (2017) Genetic Reduction or Negative Modulation of mGlu7 Does Not Impact Anxiety and Fear Learning Phenotypes in a Mouse Model of MECP2 Duplication Syndrome. Acs Chemical Neuroscience |
| Gogliotti RG, Klar R, Rook JM, et al. (2016) mGlu5 Positive Allosteric Modulation Normalizes Synaptic Plasticity Defects and Motor Phenotypes in a Mouse Model of Rett Syndrome. Human Molecular Genetics |
| Gogliotti RG, Cardona H, Singh J, et al. (2013) The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models. Human Molecular Genetics. 22: 4084-101 |
| Gogliotti RG, Quinlan KA, Barlow CB, et al. (2012) Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensory-motor defects are a consequence, not a cause, of motor neuron dysfunction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3818-29 |
| Gogliotti RG, Lutz C, Jorgensen M, et al. (2011) Characterization of a commonly used mouse model of SMA reveals increased seizure susceptibility and heightened fear response in FVB/N mice. Neurobiology of Disease. 43: 142-51 |
| Hammond SM, Gogliotti RG, Rao V, et al. (2010) Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late. Plos One. 5: e15887 |