Teresa M. Gunn
Affiliations: | 2001-2009 | Biomedical Sciences | Cornell University, Ithaca, NY, United States |
2009- | McLaughlin Research Institute, Great Falls, MT, United States |
Area:
Neuroscience Biology, Animal Physiology Biology, BiochemistryWebsite:
http://mclaughlinresearch.org/research-scientists/faculty/teresa-gunn/Google:
"Teresa M Gunn"Bio:
https://www.researchgate.net/profile/Teresa_Gunn
https://open.library.ubc.ca/cIRcle/collections/ubctheses/831/items/1.0087283
Mean distance: (not calculated yet)
Parents
Sign in to add mentorDiana M Juriloff | grad student | 1996 | UBC (GenetiTree) | |
(Genetic and developmental studies of abnormal neural tube closure in SELH/Bc mice.) | ||||
Gregory Barsh | post-doc | 1995-2001 | Stanford (GenetiTree) |
Children
Sign in to add traineePooneh Bagher | grad student | 2007 | Cornell |
Jian Jiao | grad student | 2008 | Cornell |
Kaihua Sun | grad student | 2008 | Cornell |
Seung-Woo Jung | grad student | 2009 | Cornell |
Will P. Walker | grad student | 2010 | Cornell |
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Publications
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Ratz-Mitchem ML, Leary G, Grindeland A, et al. (2023) Generation and characterization of a knock-in mouse model for spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM). Mammalian Genome : Official Journal of the International Mammalian Genome Society |
Ratz ML, Leary G, Grindeland A, et al. (2023) Generation and characterization of a knock-in mouse model for Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM). Research Square |
Kong JH, Young CB, Pusapati GV, et al. (2020) A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. Developmental Cell |
Gunn TM, Silvius D, Lester A, et al. (2019) Chronic and age-dependent effects of the spongiform neurodegeneration-associated MGRN1 E3 ubiquitin ligase on mitochondrial homeostasis. Mammalian Genome : Official Journal of the International Mammalian Genome Society |
Walker WP, Oehler A, Edinger AL, et al. (2016) Oligodendroglial deletion of ESCRT-I component TSG101 causes spongiform encephalopathy. Biology of the Cell / Under the Auspices of the European Cell Biology Organization |
Besio R, Maruelli S, Gioia R, et al. (2015) Lack of prolidase causes a bone phenotype both in human and in mouse. Bone. 72: 53-64 |
Anderson SR, Lee I, Ebeling C, et al. (2015) Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 26: 80-93 |
Gunn TM, Carlson GA. (2013) RML prions act through Mahogunin and Attractin-independent pathways. Prion. 7: 267-71 |
Jesty SA, Jung SW, Cordeiro JM, et al. (2013) Cardiomyocyte calcium cycling in a naturally occurring German shepherd dog model of inherited ventricular arrhythmia and sudden cardiac death. Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology. 15: 5-14 |
Silvius D, Pitstick R, Ahn M, et al. (2013) Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease. Plos One. 8: e55575 |