Zobrazeno 1 - 10
of 132
pro vyhledávání: '"Sung Min Chun"'
Autor:
Pil-Jong Kim, Hee Sang Hwang, Gyuheon Choi, Hyun-Jung Sung, Bokyung Ahn, Ji-Su Uh, Shinkyo Yoon, Deokhoon Kim, Sung-Min Chun, Se Jin Jang, Heounjeong Go
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract This study aimed to develop a deep learning (DL) model for predicting the recurrence risk of lung adenocarcinoma (LUAD) based on its histopathological features. Clinicopathological data and whole slide images from 164 LUAD cases were collect
Externí odkaz:
https://doaj.org/article/1b9c41ef9ac345f6b9f55479c8cd0a2e
Publikováno v:
Journal of Pathology and Translational Medicine, Vol 57, Iss 6, Pp 323-331 (2023)
Background Homologous recombination defect is an important biomarker of chemotherapy in certain tumor types, and the presence of pathogenic or likely pathogenic mutations involving BRCA1 or BRCA2 (p-BRCA) mutations is the most well-established marker
Externí odkaz:
https://doaj.org/article/fe436cdc6dda446981e3896de6ae0cf2
Autor:
Megan C Hanna, Christina Go, Christine Roden, Robert T Jones, Panisa Pochanard, Ahmed Yasir Javed, Awais Javed, Chandrani Mondal, Emanuele Palescandolo, Paul Van Hummelen, Charles Hatton, Adam J Bass, Sung Min Chun, Deuk Chae Na, Tae-Im Kim, Se Jin Jang, Raymond U Osarogiagbon, William C Hahn, Matthew Meyerson, Levi A Garraway, Laura E MacConaill
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74950 (2013)
It has been demonstrated for some cancers that the frequency of somatic oncogenic mutations may vary in ancestral populations. To determine whether key driver alterations might occur at different frequencies in colorectal cancer, we applied a high-th
Externí odkaz:
https://doaj.org/article/a4a1da8169604c15b81e8f98eabbb7dd
Autor:
Ji-Hye Oh, Sungyang Jo, Kye Won Park, Eun-Jae Lee, Seung Hyun Lee, Yun Su Hwang, Ha Ra Jeon, Yeonjin Ryu, Hee Jeong Yoon, Sung-Min Chun, Chong Jai Kim, Tae Won Kim, Chang Ohk Sung, Sehyun Chae, Sun Ju Chung
Publikováno v:
Experimental and Molecular Medicine, Vol 55, Iss 3, Pp 555-564 (2023)
Parkinson’s disease: genetic risk factors in a Korean population A whole-genome sequencing study of Korean individuals with Parkinson’s disease (PD) has identified several new genetic risk factors, ranging from single nucleotide variations (SNVs)
Externí odkaz:
https://doaj.org/article/427f9743ab9b42ca99fb560c6a692102
Autor:
Yeseul Kim, Bokyung Ahn, Shinkyo Yoon, Goeun Lee, Deokhoon Kim, Sung-Min Chun, Hyeong-Ryul Kim, Se Jin Jang, Hee Sang Hwang
Publikováno v:
PLoS ONE, Vol 18, Iss 6 (2023)
The Wnt/β-catenin pathway is known to be frequently dysregulated in various human malignancies. Alterations in the genes encoding the components of Wnt/β-catenin pathway have also been described in lung adenocarcinoma. Notably however, the clinical
Externí odkaz:
https://doaj.org/article/74acc74c01f648179fb7bb333f7e8de8
Autor:
Sung Min Chun, 宋旻駿
102
In this study we make use of the vertical alignment structure to replace the twisted nematic structure in the mixed-mode twisted nematic structure for creating the reflective liquid crystal display of having high contrast ratio of the VA adv
In this study we make use of the vertical alignment structure to replace the twisted nematic structure in the mixed-mode twisted nematic structure for creating the reflective liquid crystal display of having high contrast ratio of the VA adv
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/14644535936673284712
Autor:
Cheol-Kyu Park, Ha Ra Jun, Hyung-Joo Oh, Ji-Young Lee, Hyun-Ju Cho, Young-Chul Kim, Jeong Eun Lee, Seong Hoon Yoon, Chang Min Choi, Jae Cheol Lee, Sung Yong Lee, Shin Yup Lee, Sung-Min Chun, In-Jae Oh
Publikováno v:
Cells, Vol 12, Iss 9, p 1246 (2023)
This study aimed to investigate the feasibility of blood-based biomarkers, including blood tumor mutation burden (bTMB), to predict atezolizumab efficacy in relapsed and advanced non-small cell lung cancer (NSCLC). Stage IV NSCLC patients who had pre
Externí odkaz:
https://doaj.org/article/ba6e17b525b84cf6bb7ed91eb2eb274a
Publikováno v:
Haematologica, Vol 107, Iss 8 (2022)
Externí odkaz:
https://doaj.org/article/ef761d30ca3a4892bfca999c39ed338f
Autor:
Ji-Young Lee, Seyeon Jeon, Ha Ra Jun, Chang Ohk Sung, Se Jin Jang, Chang-Min Choi, Sung-Min Chun
Publikováno v:
Cancer Research & Treatment; Apr2024, Vol. 56 Issue 2, p484-501, 18p
Autor:
Se Jin Jang, Daehyun Baek, Gu Kong, Eunsil Yu, Charles Lee, Eunho Yang, Hye Yoon Jang, Wang-rim Jung, Jong-eun Lee, Sun Young Lee, Farhan Haq, Deokhoon Kim, Joon Seon Song, Ji-Young Lee, Yong-Hee Kim, Sang-We Kim, Eun Kyung Choi, Sung-Min Chun, Chang-min Choi, Sung-Min Ahn, Sukjun Kim, Jongkyu Kim, Chang Ohk Sung, Hyeong Ryul Kim, Seongmin Choi
Supplementary Tables 1 - 15. Supp. Table 1. Sequenced reads per tumor and normal sample. Supp. Table 2. Comparison of significantly mutated genes detected using various MuTect thresholds. Supp. Table 3. Comparison of the number and rate of substituti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a19e289f26461634da0108c85baff0
https://doi.org/10.1158/1078-0432.22458326
https://doi.org/10.1158/1078-0432.22458326