Renowned Physicist Dr. Young Suh Kim Honored By Close Up Radio in the Field of Science
Close Up Radio honors one of our most respected guests, Dr. Young Suh Kim
BELTSVILLE, MD, UNITED STATES, April 21, 2025 / EINPresswire.com / -- How do the orbits of the hydrogen atom appear to you while you are in motion? Einstein asked this question in the 1950s. In 1978, Dr. Young Suh Kim answered. His paper, 'Representations of the Poincaré Group for Relativistic Extended Hadrons' was published by the Journal of Mathematical Physics in 1979. Dr. Kim reflects, 'It wasn't Einstein's fault. He didn't have access to high-energy accelerators—but fortunately, we do.'
Born in Sorae, Korea in 1935, Dr. Kim shares that the United States has been very good to him. 'I could never accomplish all I have in any other country except America.' Poverty, political unrest, and cultural norms would have made a life in academia impossible. 'Growing up in Korea during the 1950s gave me a solid work ethic. We attended the Sorae Church, which was founded by Horace Underwood, the first American Presbyterian missionary to come to Korea. My grandfather was a very good friend of Underwood's and took care of his properties while Underwood was traveling.' Kim explains.
This foundation is what Dr. Kim brought to America in 1954, where he attended Carnegie Institute of Technology (now Carnegie Mellon University). That's where Dr. Kim first learned about Albert Einstein.
'I just knew I had to meet Dr. Einstein, who had worked with Princeton University. In 1958, I was accepted to Princeton and my dream came true (as best it could),' explains Dr. Kim. 'Even though Einstein had passed in 1955, I was able to work with him through his research.'
That's when Dr. Kim learned that during the time Einstein formulated his Theory of Relativity in 1905, all particles were considered 'point particles,' or particles that do not take up space. Later, particles such as the hydrogen atom or the proton, were found to have very rich internal structures that do take up space. This discovery created a problem—how do particles appear when in motion?
Being so close to Dr. Einstein, Dr. Kim had to discover the answer. 'While at Princeton, I began studying Dr. Eugene Wigner's 1939 paper titled, 'On Unitary Representations of the Inhomogeneus Lorentz Group.' That's when I discovered a sort of dark period in scientific history.'
During the early years of the 20th Century, Niels Bohr was researching the hydrogen atom, while Einstein was studying how particles appear to moving observers. Although the two scientific icons met occasionally to discuss physics, they left no writings on whether or not they discussed how moving hydrogen atoms appear to observers at rest.
After 20 years (1966-1986) of continuous research, Dr. Kim discovered Wigner's 1939 mathematical paper is applicable to the internal space-time structure of particles. When Einstein formulated his theory of relativity in 1905, particles were considered to be 'point particles.' Later, particles such as the hydrogen atom or the proton, were found to have very rich internal structures. According to Dr. Kim, 'Wigner's 1939 paper allows us to extend Einstein's theory of relativity to the insides of those particles.'
While a graduate student and post-doc at Princeton, Dr. Kim met Professor Wigner. Both men are honored to now have a place in Einstein's genealogy as scientific leaders who made discoveries Einstein could not. Dr. Kim became known as Wigner's youngest student.
In 1962, Dr. Kim became an assistant professor of physics at the University of Maryland. After retiring from teaching duties in 2007, Dr. Kim is a Professor of Physics Emeritus at UMD where he has been focusing on research. A prolific author of several books and scientific articles, Dr. Kim most desires to expand Dr. Einstein's theories.
Although the competitive academic life has not always been easy for Dr. Kim, he is very happy to have created his very own Einstein-Wigner-Kim genealogy. 'I believe in what I believe,' concludes Dr. Kim. 'I endured a lot of hardship in delays in promotion to create this genealogy, and I succeeded. This is what makes me proud.'
So how do the orbits of the hydrogen atom appear to you while you are in motion? 'Spherical, of course,' Dr. Kim proudly replies.
Close Up Radio featured Dr. Young Suh Kim in an interview with Jim Masters on Friday, March 29th, 2024 at 2pm Eastern
Listen to His Show
For more information about Dr. Kim and the University of Maryland, please visit https://www.ysfine.com/ and https://www.terpconnect.umd.edu/~yskim//yspapers/index.html
Lou Ceparano
Close Up Television & Radio
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Soligenix is a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. Our Specialized BioTherapeutics business segment is developing and moving toward potential commercialization of HyBryte™ (SGX301 or synthetic hypericin) as a novel photodynamic therapy utilizing safe visible light for the treatment of cutaneous T-cell lymphoma (CTCL). With successful completion of the second Phase 3 study, regulatory approvals will be sought to support potential commercialization worldwide. Development programs in this business segment also include expansion of synthetic hypericin (SGX302) into psoriasis, our first-in-class innate defense regulator (IDR) technology, dusquetide for the treatment of inflammatory diseases, including oral mucositis in head and neck cancer (SGX942), and in Behçet's Disease (SGX945). Our Public Health Solutions business segment includes development programs for RiVax®, our ricin toxin vaccine candidate, as well as our vaccine programs targeting filoviruses (such as Marburg and Ebola) and CiVax™, our vaccine candidate for the prevention of COVID19 (caused by SARS-CoV-2). The development of our vaccine programs incorporates the use of our proprietary heat stabilization platform technology, known as ThermoVax®. To date, this business segment has been supported with government grant and contract funding from the National Institute of Allergy and Infectious Diseases (NIAID), the Defense Threat Reduction Agency (DTRA) and the Biomedical Advanced Research and Development Authority (BARDA). For further information regarding Soligenix, Inc., please visit the Company's website at and follow us on LinkedIn and Twitter at @Soligenix_Inc. This press release may contain forward-looking statements that reflect Soligenix's current expectations about its future results, performance, prospects and opportunities, including but not limited to, potential market sizes, patient populations, clinical trial enrollment. Statements that are not historical facts, such as "anticipates," "estimates," "believes," "hopes," "intends," "plans," "expects," "goal," "may," "suggest," "will," "potential," or similar expressions, are forward-looking statements. These statements are subject to a number of risks, uncertainties and other factors that could cause actual events or results in future periods to differ materially from what is expressed in, or implied by, these statements. Soligenix cannot assure you that it will be able to successfully develop, achieve regulatory approval for or commercialize products based on its technologies, particularly in light of the significant uncertainty inherent in developing therapeutics and vaccines against bioterror threats, conducting preclinical and clinical trials of therapeutics and vaccines, obtaining regulatory approvals and manufacturing therapeutics and vaccines, that product development and commercialization efforts will not be reduced or discontinued due to difficulties or delays in clinical trials or due to lack of progress or positive results from research and development efforts, that it will be able to successfully obtain any further funding to support product development and commercialization efforts, including grants and awards, maintain its existing grants which are subject to performance requirements, enter into any biodefense procurement contracts with the U.S. Government or other countries, that it will be able to compete with larger and better financed competitors in the biotechnology industry, that changes in health care practice, third party reimbursement limitations and Federal and/or state health care reform initiatives will not negatively affect its business, or that the U.S. Congress may not pass any legislation that would provide additional funding for the Project BioShield program. In addition, there can be no assurance as to the timing or success of any of its clinical/preclinical trials. Despite the statistically significant result achieved in the first HyBryte™ (SGX301) Phase 3 clinical trial for the treatment of cutaneous T-cell lymphoma or any other studies (including the open-label, investigator-initiated study), there can be no assurance that the second HyBryte™ (SGX301) Phase 3 clinical trial will be successful or that a marketing authorization from the FDA or EMA will be granted. Additionally, although the EMA has agreed to the key design components of the second HyBryte™ (SGX301) Phase 3 clinical trial, no assurance can be given that the Company will be able to modify the development path to adequately address the FDA's concerns or that the FDA will not require a longer duration comparative study. Notwithstanding the result in the first HyBryte™ (SGX301) Phase 3 clinical trial for the treatment of cutaneous T-cell lymphoma and the Phase 2a clinical trial of SGX302 for the treatment of psoriasis, there can be no assurance as to the timing or success of the clinical trials of SGX302 for the treatment of psoriasis. Additionally, despite the biologic activity observed in aphthous ulcers induced by chemotherapy and radiation, there can be no assurance as to the timing or success of the clinical trials of SGX945 for the treatment of Behçet's Disease. Further, there can be no assurance that RiVax® will qualify for a biodefense Priority Review Voucher (PRV) or that the prior sales of PRVs will be indicative of any potential sales price for a PRV for RiVax®. Also, no assurance can be provided that the Company will receive or continue to receive non-dilutive government funding from grants and contracts that have been or may be awarded or for which the Company will apply in the future. These and other risk factors are described from time to time in filings with the Securities and Exchange Commission (the "SEC"), including, but not limited to, Soligenix's reports on Forms 10-Q and 10-K. Unless required by law, Soligenix assumes no obligation to update or revise any forward-looking statements as a result of new information or future events. Corporate Communications IBN Austin, Texas 512.354.7000 Office Editor@ in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data