Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Sungkyoung Choi"'
Publikováno v:
BMC Nursing, Vol 23, Iss 1, Pp 1-10 (2024)
Abstract Background Physical restraint (PR) is used to ensure the safety of care recipients. However, this causes an ethical dilemma between the autonomy and dignity of the recipients and the provision of effective treatment by health workers. This s
Externí odkaz:
https://doaj.org/article/46d9393a0cd94574a9358fdebb1b6971
Publikováno v:
BMC Bioinformatics, Vol 25, Iss 1, Pp 1-27 (2024)
Abstract Background Genome-wide association studies have successfully identified genetic variants associated with human disease. Various statistical approaches based on penalized and machine learning methods have recently been proposed for disease pr
Externí odkaz:
https://doaj.org/article/cbfe60f1785c402bae0e11d76f409ba7
Autor:
Mina Baek, Minjae Kim, Hae In Choi, Bert Binas, Junho Cha, Kyoung Hwa Jung, Sungkyoung Choi, Young Gyu Chai
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0301663 (2024)
The multikinase inhibitor sorafenib is the standard first-line treatment for advanced hepatocellular carcinoma (HCC), but many patients become sorafenib-resistant (SR). This study investigated the efficacy of another kinase inhibitor, regorafenib (Re
Externí odkaz:
https://doaj.org/article/6e5f5b67370e4b4a8c90946bb9101951
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0290403 (2023)
The COVID-19 pandemic has sparked a rapid worldwide increase in the utilization of delivery services. This study delves into the experiences of delivery workers as one of the activley developed industries during the COVID-19 pandemic in South Korea a
Externí odkaz:
https://doaj.org/article/e3b7aac3d430409d841b7e5f5f7b7927
Autor:
Junho Cha, Sungkyoung Choi
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 15, p 12266 (2023)
Asthma is a complex heterogeneous disease caused by gene–environment interactions. Although numerous genome-wide association studies have been conducted, these interactions have not been systemically investigated. We sought to identify genetic fact
Externí odkaz:
https://doaj.org/article/0ce6b51c5d314c9ea536505f811dc84a
Publikováno v:
Journal of Educational Evaluation for Health Professions, Vol 19 (2022)
Purpose The purpose of this study was to evaluate the impact of synchronous online education on the patient safety competency (knowledge, attitudes, and skills) of nursing students in Korea and to explore what they thought about this educational meth
Externí odkaz:
https://doaj.org/article/7288c3e1d451498880bc967af42299d8
Autor:
Ji Yeon Kim, Sungkyoung Choi, Taesung Park, Seul Ki Kim, Yoon Suk Jung, Jung Ho Park, Hong Joo Kim, Yong Kyun Cho, Chong Il Sohn, Woo Kyu Jeon, Byung Ik Kim, Kyu Yong Choi, Dong Il Park
Publikováno v:
Intestinal Research, Vol 17, Iss 2, Pp 253-264 (2019)
Background/Aims Colorectal cancer incidence among patients aged ≤50 years is increasing. This study aimed to develop and validate an advanced colorectal neoplasm (ACRN) screening model for young adults aged
Externí odkaz:
https://doaj.org/article/628c03ba0357472fa4580549e8afee4e
Publikováno v:
BMC Bioinformatics, Vol 19, Iss S9, Pp 33-44 (2018)
Abstract Background Component-based structural equation modeling methods are now widely used in science, business, education, and other fields. This method uses unobservable variables, i.e., “latent” variables, and structural equation model relat
Externí odkaz:
https://doaj.org/article/8712ead067044b33bea4147e368318be
Publikováno v:
BMC Bioinformatics, Vol 19, Iss S4, Pp 25-34 (2018)
Abstract Background Identification of multi-markers is one of the most challenging issues in personalized medicine era. Nowadays, many different types of omics data are generated from the same subject. Although many methods endeavor to identify candi
Externí odkaz:
https://doaj.org/article/0ce7fadf0ae14bb6b7aa1ab8bc6ea88d
Pathway-based approach using hierarchical components of rare variants to analyze multiple phenotypes
Publikováno v:
BMC Bioinformatics, Vol 19, Iss S4, Pp 85-97 (2018)
Abstract Background As one possible solution to the “missing heritability” problem, many methods have been proposed that apply pathway-based analyses, using rare variants that are detected by next generation sequencing technology. However, while
Externí odkaz:
https://doaj.org/article/a0e86bd6ef8f4fc3b8239d76231eb2b6