Calvin S. Carter, Ph.D.

Affiliations: 
2014 Neuroscience University of Iowa, Iowa City, IA 
Area:
Neuroscience Biology, Medicine and Surgery, Human Development
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"Calvin Carter"
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Val C. Sheffield grad student 2014 University of Iowa
 (Characterizing the role of primary cilia in neural progenitor cell development and neonatal hydrocephalus.)
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Publications

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Carter CS, Huang SC, Searby CC, et al. (2022) Exposure to Static Magnetic and Electric Fields Treats Type 2 Diabetes. Cell Metabolism. 34: 1893
Stubbs T, Koemeter-Cox A, Bingman JI, et al. (2022) Disruption of dopamine receptor 1 localization to primary cilia impairs signaling in striatal neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Huang SC, Pak TK, Graber CP, et al. (2022) An open source and convenient method for the wide-spread testing of COVID-19 using deep throat sputum samples. Peerj. 10: e13277
Pak TK, Carter CS, Zhang Q, et al. (2021) A mouse model of Bardet-Biedl Syndrome has impaired fear memory, which is rescued by lithium treatment. Plos Genetics. 17: e1009484
Carter CS, Huang S, Searby C, et al. (2021) Response to: An alternative hypothesis for why exposure to static magnetic and electric fields treats type 2 diabetes. American Journal of Physiology. Endocrinology and Metabolism
Carter CS, Huang S, Searby C, et al. (2021) Counterpoint regarding an alternative hypothesis for why exposure to static magnetic and electric fields treat type 2 diabetes. American Journal of Physiology. Endocrinology and Metabolism
Carter CS, Huang SC, Searby CC, et al. (2020) Exposure to Static Magnetic and Electric Fields Treats Type 2 Diabetes. Cell Metabolism. 32: 1076
Carter CS, Huang SC, Searby CC, et al. (2020) Exposure to Static Magnetic and Electric Fields Treats Type 2 Diabetes. Cell Metabolism. 32: 561-574.e7
Weihbrecht K, Goar WA, Carter CS, et al. (2018) Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse model. Plos One. 13: e0192755
Zhang Q, Nishimura D, Vogel T, et al. (2013) BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking. Journal of Cell Science. 126: 2372-80
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