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Yonsei Medical Journal|August 22, 2019
Coronary Artery Aneurysm after Second-Generation Drug-Eluting Stent ImplantationSung Jin Hong, Hyoeun Kim, Chul Min Ahn, et al.Stem Cell Research|July 24, 2025
Establishment of a homozygous LMNA knock-out human induced pluripotent stem cell line using CRISPR/Cas9 systemSo Hee Park, David Suh, Hyoeun Kim, et al.Journal of Lipid and Atherosclerosis|August 22, 2020
Lipid-Lowering Efficacy and Safety of a New Generic Rosuvastatin in Koreans: an 8-Week Randomized Comparative Study with a Proprietary RosuvastatinHyoeun Kim, Chan Joo Lee, Donghoon Choi, et al.Stem Cell Research|June 2, 2024
Generation of an induced pluripotent stem cell line from a patient with arrhythmogenic right ventricular cardiomyopathy harboring a TMEM43 splice-site variantSun-Ho Lee, Gibbeum Lim, Hyoeun Kim, et al.Neurotoxicology|May 23, 2026
A Critical Review of Potential Modifiers of Air Pollutant Associations with Dementia and Related OutcomesJeongWon Han, Yina Li, Sangji Lee, et al.The American Journal of Cardiology|September 9, 2019
Relation of Preprocedural Hemoglobin Level to Outcomes After Percutaneous Coronary InterventionByung Gyu Kim, Hyoeun Kim, Sung-Jin Hong, et al.Journal of Cardiovascular Ultrasound|November 3, 2017
Associates and Prognosis of Giant Left Atrium; Single Center ExperienceHyoeun Kim, Young-Ah Park, Sung Min Choi, et al.Stem Cell Research|August 2, 2022
An induced pluripotent stem cell line (YCMi006-A) generated from a patient with hypertrophic cardiomyopathy who carries the ACTA1 mutation p.Ile343MetHyoeun Kim, Hyeong-Jin Kim, Jaewon Oh, et al.Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|January 9, 2022
Association of Physical Activity With Risk of Liver Fibrosis, Sarcopenia, and Cardiovascular Disease in Nonalcoholic Fatty Liver DiseaseHo Soo Chun, Minjong Lee, Hye Ah Lee, et al.Stem Cell Research|February 21, 2023
Human induced pluripotent stem cell line YCMi007-A generated from a dilated cardiomyopathy patient with a heterozygous dominant c.613C > T (p. Arg205Trp) variant of the TNNT2 geneSae-Bom Jeon, Hyoeun Kim, Kyeong-Hyeon Chun, et al.Pageof 9