Tyler L. Perfitt - Publications

Affiliations: 
Molecular Physiology & Biophysics Vanderbilt University, Nashville, TN 
Area:
CaMKII, neuroscience

5/8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Yang Q, Perfitt TL, Quay J, Hu L, Lawson-Qureshi D, Colbran RJ. Clustering of Ca 1.3 L-type calcium channels by Shank3. Journal of Neurochemistry. PMID 37392026 DOI: 10.1111/jnc.15880  0.558
2020 Perfitt TL, Wang X, Dickerson MT, Stephenson JR, Nakagawa T, Jacobson DA, Colbran RJ. Neuronal L-Type Calcium Channel Signaling to the Nucleus Requires a Novel CaMKIIα-Shank3 Interaction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32019829 DOI: 10.1523/Jneurosci.0893-19.2020  0.713
2020 Perfitt TL, Stauffer PE, Spiess KL, Colbran RJ. CaMKIIα phosphorylation of Shank3 modulates ABI1-Shank3 interaction. Biochemical and Biophysical Research Communications. PMID 31983435 DOI: 10.1016/J.Bbrc.2020.01.089  0.661
2017 Wang X, Marks CR, Perfitt TL, Nakagawa T, Lee A, Jacobson DA, Colbran RJ. A novel mechanism for Ca(2+)/calmodulin-dependent protein kinase II targeting to L-type Ca(2+) channels that initiates long-range signaling to the nucleus. The Journal of Biological Chemistry. PMID 28916724 DOI: 10.1074/Jbc.M117.788331  0.72
2017 Stephenson JR, Wang X, Perfitt TL, Parrish WP, Shonesy BC, Marks CR, Mortlock DP, Nakagawa T, Sutcliffe JS, Colbran RJ. A novel human CAMK2A mutation disrupts dendritic morphology and synaptic transmission, and causes ASD-related behaviors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 28130356 DOI: 10.1523/Jneurosci.2068-16.2017  0.54
Low-probability matches (unlikely to be authored by this person)
2022 Huichalaf C, Perfitt TL, Kuperman A, Gooch R, Kovi RC, Brenneman KA, Chen X, Hirenallur-Shanthappa D, Ma T, Assaf BT, Pardo I, Franks T, Monarski L, Cheng TW, Le K, et al. overexpression of frataxin causes toxicity mediated by iron-sulfur cluster deficiency. Molecular Therapy. Methods & Clinical Development. 24: 367-378. PMID 35252470 DOI: 10.1016/j.omtm.2022.02.002  0.151
2023 Perfitt TL, Huichalaf C, Gooch R, Kuperman A, Ahn Y, Chen X, Ullas S, Hirenallur-Shanthappa D, Zhan Y, Otis D, Whiteley LO, Bulawa C, Martelli A. A modified mouse model of Friedreich's ataxia with conditional allele homozygosity delays onset of cardiomyopathy. American Journal of Physiology. Heart and Circulatory Physiology. PMID 38038720 DOI: 10.1152/ajpheart.00496.2023  0.127
2010 Perfitt T, Englert B. Megaphone: Fault tolerant, scalable, and trustworthy P2P microblogging 5th International Conference On Internet and Web Applications and Services, Iciw 2010. 469-477. DOI: 10.1109/ICIW.2010.77  0.01
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