Scott C Kelsey: Difference between revisions
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| image = Scott C Kelsey 2095.jpg | | image = Scott C Kelsey 2095.jpg | ||
| alt = Scott C. Kelsey | | alt = Scott C. Kelsey | ||
| residence = | | residence = Missouri, United States | ||
| nationality = American | |||
| fields = [[Molecular Cell Biology]] | |||
| workplaces = Missouri State University | |||
| alma_mater = Missouri State University | |||
| known_for = [[Electromagnetic Resonance]], [[DNA]] | | known_for = [[Electromagnetic Resonance]], [[DNA]] | ||
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'''Scott C. Kelsey''' is an American molecular cell biologist whose research has examined DNA repair and the effects of electromagnetic resonance on the telomeric regions of DNA. | |||
==Biography== | |||
Kelsey graduated with an emphasis in Molecular Cell Biology in 2008 from Missouri State University, where he then pursued a Master of Science in Cell and Molecular Biology in the Department of Biomedical Sciences. He completed his master's thesis, ''Qualification of Telomeric Maintenance and Elongation Due to Pulsed Electromagnetic Resonance Exposure'', in 2011 under the supervision of Joshua Smith. | |||
==Work== | |||
Kelsey's research focused on DNA repair techniques and the effects of extremely low frequency electromagnetic resonance on telomeric regions of primary cell lines in vitro. Using an oscillating circuit that generated an electromagnetic field with frequencies between 54 and 78 GHz, he exposed human astrocytoma cells and mouse (''Mus musculus'') primary cell cultures to daily electromagnetic resonance treatments. DNA from the exposed cells was isolated and analyzed for telomere length using singleplex quantitative PCR (qPCR) and the Southern blot technique, and compared against negative control cells of identical lineage. | |||
The singleplex qPCR data appeared to indicate telomeric maintenance, though supporting experiments using multiplex qPCR and Southern blot analysis remained to be performed at the time the thesis was completed. Kelsey framed the potential implications of the work in terms of aging mitigation and disease treatment. | |||
==External links== | |||
* [https://bearworks.missouristate.edu/theses/2835/ ''Qualification of Telomeric Maintenance and Elongation Due to Pulsed Electromagnetic Resonance Exposure'' (2011 thesis, BearWorks, Missouri State University)] | |||
[[Category:Scientist|Kelsey Scott]] | [[Category:Scientist|Kelsey Scott]] | ||
Revision as of 10:57, 17 July 2026
Scott C. Kelsey | |
|---|---|
 | |
| Residence | Missouri, United States |
| Nationality | American |
| Alma mater | Missouri State University |
| Known for | Electromagnetic Resonance, DNA |
| Scientific career | |
| Fields | Molecular Cell Biology |
| Institutions | Missouri State University |
Scott C. Kelsey is an American molecular cell biologist whose research has examined DNA repair and the effects of electromagnetic resonance on the telomeric regions of DNA.
Biography
Kelsey graduated with an emphasis in Molecular Cell Biology in 2008 from Missouri State University, where he then pursued a Master of Science in Cell and Molecular Biology in the Department of Biomedical Sciences. He completed his master's thesis, Qualification of Telomeric Maintenance and Elongation Due to Pulsed Electromagnetic Resonance Exposure, in 2011 under the supervision of Joshua Smith.
Work
Kelsey's research focused on DNA repair techniques and the effects of extremely low frequency electromagnetic resonance on telomeric regions of primary cell lines in vitro. Using an oscillating circuit that generated an electromagnetic field with frequencies between 54 and 78 GHz, he exposed human astrocytoma cells and mouse (Mus musculus) primary cell cultures to daily electromagnetic resonance treatments. DNA from the exposed cells was isolated and analyzed for telomere length using singleplex quantitative PCR (qPCR) and the Southern blot technique, and compared against negative control cells of identical lineage.
The singleplex qPCR data appeared to indicate telomeric maintenance, though supporting experiments using multiplex qPCR and Southern blot analysis remained to be performed at the time the thesis was completed. Kelsey framed the potential implications of the work in terms of aging mitigation and disease treatment.