Toward more predictive genetic mouse models of Alzheimer’s disease

gan Onos, Kristen D., Sukoff Rizzo, Stacey J., Howell, Gareth R., Sasner, Michael
Cyhoeddwyd yn Brain Res Bull (2015)

Continuous Glucose Monitoring in Female NOD Mice Reveals Daily Rhythms and a Negative Correlation With Body Temperature

gan Korstanje, Ron, Ryan, Jennifer L., Savage, Holly S., Lyons, Bonnie L., Kane, Kevin G., Sukoff Rizzo, Stacey J.
Cyhoeddwyd yn Endocrinology (2017)

Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy

gan Sayed-Zahid, Ambreen A, Sher, Roger B, Sukoff Rizzo, Stacey J, Anderson, Laura C, Patenaude, Kathryn E, Cox, Gregory A
Cyhoeddwyd yn Hum Mol Genet (2019)

Improving preclinical to clinical translation in Alzheimer's disease research

gan Sukoff Rizzo, Stacey J., Masters, Andi, Onos, Kristen D., Quinney, Sara, Sasner, Michael, Oblak, Adrian, Lamb, Bruce T., Territo, Paul R
Cyhoeddwyd yn Alzheimers Dement (N Y) (2020)

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

gan Asinof, Samuel K., Sukoff Rizzo, Stacey J., Buckley, Alexandra R., Beyer, Barbara J., Letts, Verity A., Frankel, Wayne N., Boumil, Rebecca M.
Cyhoeddwyd yn PLoS Genet (2015)

Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism

gan Silverman, Jill L., Smith, Daniel G., Sukoff Rizzo, Stacey J., Karras, Michael N., Turner, Sarah M., Tolu, Seda S., Bryce, Dianne K., Smith, Deborah L., Fonseca, Kari, Ring, Robert H., Crawley, Jacqueline N.
Cyhoeddwyd yn Sci Transl Med (2012)

Behavioral Characterization of A53T Mice Reveals Early and Late Stage Deficits Related to Parkinson’s Disease

gan Paumier, Katrina L., Sukoff Rizzo, Stacey J., Berger, Zdenek, Chen, Yi, Gonzales, Cathleen, Kaftan, Edward, Li, Li, Lotarski, Susan, Monaghan, Michael, Shen, Wei, Stolyar, Polina, Vasilyev, Dmytro, Zaleska, Margaret, D. Hirst, Warren, Dunlop, John
Cyhoeddwyd 2013

Enhancing face validity of mouse models of Alzheimer’s disease with natural genetic variation

gan Onos, Kristen D., Uyar, Asli, Keezer, Kelly J., Jackson, Harriet M., Preuss, Christoph, Acklin, Casey J., O’Rourke, Rita, Buchanan, Rebecca, Cossette, Travis L., Sukoff Rizzo, Stacey J., Soto, Ileana, Carter, Gregory W., Howell, Gareth R.
Cyhoeddwyd yn PLoS Genet (2019)

Analysis of sleep traits in knockout mice from the large-scale KOMP2 population using a non-invasive, high-throughput piezoelectric system

gan Sethi, Mansi, Joshi, Shreyas S, Striz, Martin, Cole, Neil, Ryan, Jennifer, Lhamon, Michael E, Agarwal, Anuj, Sukoff Rizzo, Stacey J, Denegre, James M, Braun, Robert E, Fardo, David W, Donohue, Kevin D, Chesler, Elissa J, Svenson, Karen L, O'Hara, Bruce F
Cyhoeddwyd yn BMC Bioinformatics (2015)

Characterization of PF-6142, a Novel, Non-Catecholamine Dopamine Receptor D1 Agonist, in Murine and Nonhuman Primate Models of Dopaminergic Activation

gan Kozak, Rouba, Kiss, Tamás, Dlugolenski, Keith, Johnson, David E., Gorczyca, Roxanne R., Kuszpit, Kyle, Harvey, Brian D., Stolyar, Polina, Sukoff Rizzo, Stacey J., Hoffmann, William E., Volfson, Dmitri, Hajós, Mihaly, Davoren, Jennifer E., Abbott, Amanda L., Williams, Graham V., Castner, Stacy A., Gray, David L.
Cyhoeddwyd yn Front Pharmacol (2020)

Acarbose improves health and lifespan in aging HET3 mice

gan Harrison, David E., Strong, Randy, Alavez, Silvestre, Astle, Clinton Michael, DiGiovanni, John, Fernandez, Elizabeth, Flurkey, Kevin, Garratt, Michael, Gelfond, Jonathan A. L., Javors, Martin A., Levi, Moshe, Lithgow, Gordon J., Macchiarini, Francesca, Nelson, James F., Sukoff Rizzo, Stacey J., Slaga, Thomas J., Stearns, Tim, Wilkinson, John Erby, Miller, Richard A.
Cyhoeddwyd yn Aging Cell (2019)

Model organism development and evaluation for late‐onset Alzheimer's disease: MODEL‐AD

gan Oblak, Adrian L., Forner, Stefania, Territo, Paul R., Sasner, Michael, Carter, Gregory W., Howell, Gareth R., Sukoff‐Rizzo, Stacey J., Logsdon, Benjamin A., Mangravite, Lara M., Mortazavi, Ali, Baglietto‐Vargas, David, Green, Kim N., MacGregor, Grant R., Wood, Marcelo A., Tenner, Andrea J., LaFerla, Frank M., Lamb, Bruce T.
Cyhoeddwyd yn Alzheimers Dement (N Y) (2020)

Phosphodiesterase 11A in brain is enriched in ventral hippocampus and deletion causes psychiatric disease-related phenotypes

gan Kelly, Michele P., Logue, Sheree F., Brennan, Julie, Day, Jonathon P., Lakkaraju, Subha, Jiang, Lixin, Zhong, Xiaotian, Tam, May, Sukoff Rizzo, Stacey J., Platt, Brian J., Dwyer, Jason M., Neal, Sarah, Pulito, Virginia L., Agostino, Michael J., Grauer, Steven M., Navarra, Rachel L., Kelley, Cody, Comery, Thomas A., Murrills, Richard J., Houslay, Miles D., Brandon, Nicholas J.
Cyhoeddwyd 2010

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

gan Diggle, Christine P., Sukoff Rizzo, Stacey J., Popiolek, Michael, Hinttala, Reetta, Schülke, Jan-Philip, Kurian, Manju A., Carr, Ian M., Markham, Alexander F., Bonthron, David T., Watson, Christopher, Sharif, Saghira Malik, Reinhart, Veronica, James, Larry C., Vanase-Frawley, Michelle A., Charych, Erik, Allen, Melanie, Harms, John, Schmidt, Christopher J., Ng, Joanne, Pysden, Karen, Strick, Christine, Vieira, Päivi, Mankinen, Katariina, Kokkonen, Hannaleena, Kallioinen, Matti, Sormunen, Raija, Rinne, Juha O., Johansson, Jarkko, Alakurtti, Kati, Huilaja, Laura, Hurskainen, Tiina, Tasanen, Kaisa, Anttila, Eija, Marques, Tiago Reis, Howes, Oliver, Politis, Marius, Fahiminiya, Somayyeh, Nguyen, Khanh Q., Majewski, Jacek, Uusimaa, Johanna, Sheridan, Eamonn, Brandon, Nicholas J.
Cyhoeddwyd yn Am J Hum Genet (2016)

Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy

gan Peng, Yanyan, Shinde, Deepali N, Valencia, C Alexander, Mo, Jun-Song, Rosenfeld, Jill, Truitt Cho, Megan, Chamberlin, Adam, Li, Zhuo, Liu, Jie, Gui, Baoheng, Brockhage, Rachel, Basinger, Alice, Alvarez-Leon, Brenda, Heydemann, Peter, Magoulas, Pilar L, Lewis, Andrea M, Scaglia, Fernando, Gril, Solange, Chong, Shuk Ching, Bower, Matthew, Monaghan, Kristin G, Willaert, Rebecca, Plona, Maria-Renee, Dineen, Rich, Milan, Francisca, Hoganson, George, Powis, Zoe, Helbig, Katherine L, Keller-Ramey, Jennifer, Harris, Belinda, Anderson, Laura C, Green, Torrian, Sukoff Rizzo, Stacey J, Kaylor, Julie, Chen, Jiani, Guan, Min-Xin, Sellars, Elizabeth, Sparagana, Steven P, Gibson, James B, Reinholdt, Laura G, Tang, Sha, Huang, Taosheng
Cyhoeddwyd yn Hum Mol Genet (2017)