Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Lyoung Hyo, Kim"'
Autor:
In Ki Baek, Hyun Sub Cheong, Seok Namgoong, Jeong-Hyun Kim, Seok-Gu Kang, Seon-Jin Yoon, Se Hoon Kim, Jong Hee Chang, Lyoung Hyo Kim, Hyoung Doo Shin
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Gliomas are the most common primary tumors in the brain and spinal cord. In previous GWASs, SNPs in epidermal growth factor receptor (EGFR) have been reported as risk loci for gliomas. However, EGFR variants associated with gliomas in the Ko
Externí odkaz:
https://doaj.org/article/608d6cdeebba46408e6febe592c15a67
Autor:
Jung Yeon Seo, Joong-Gon Shin, Byeong Ju Youn, Suhg Namgoong, Hyun Sub Cheong, Lyoung Hyo Kim, Ji On Kim, Hyoung Doo Shin, Yoon Jun Kim
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Hepatitis B is known to cause several forms of liver diseases including chronic hepatitis B (CHB), and hepatocellular carcinoma. Previous genome-wide association study of CHB risk has demonstrated that rs12614 of complement factor
Externí odkaz:
https://doaj.org/article/476139068a624ba8bf86f99971abf056
Autor:
Byeong Ju Youn, Hyun Sub Cheong, Suhg Namgoong, Lyoung Hyo Kim, In Ki Baek, Jeong-Hyun Kim, Seon-Jin Yoon, Eui Hyun Kim, Se Hoon Kim, Jong Hee Chang, Sun Ho Kim, Hyoung Doo Shin
Publikováno v:
Molecular Biology Reports. 49:10339-10346
Previous genomewide association studies (GWASs), single nucleotide polymorphisms (SNPs) on cyclin-dependent kinase inhibitor 2 A (CDKN2A), cyclin-dependent kinase inhibitor 2B (CDKN2B), and cyclin-dependent kinase inhibitor 2B antisense RNA1 (CDKN2B-
Autor:
Suhg Namgoong, Hyun Sub Cheong, Jeong-Hyun Kim, Lyoung Hyo Kim, Jung Yeon Seo, Seok-Gu Kang, Seon-Jin Yoon, Se Hoon Kim, Jong Hee Chang, Hyoung Doo Shin
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0207660 (2018)
Previous studies have identified multiple loci for inherited susceptibility to glioma development, including the regulator of telomere elongation helicase 1 (RTEL1). However, the association between RTEL1 variants and risk of glioma has not been well
Externí odkaz:
https://doaj.org/article/0337a88e28e24a7ba68bf51bf5ed714a
Autor:
Suhg Namgoong, Lyoung Hyo Kim, Ji On Kim, Jung Yeon Seo, Yoon Jun Kim, Hyoung Doo Shin, Byeong Ju Youn, Joong Gon Shin, Hyun Sub Cheong
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Hepatitis B is known to cause several forms of liver diseases including chronic hepatitis B (CHB), and hepatocellular carcinoma. Previous genome-wide association study of CHB risk has demonstrated that rs12614 of complement factor B (CFB)
Autor:
Jeong Hyun Kim, Hyoung Doo Shin, Jong Hee Chang, Seon Jin Yoon, Lyoung Hyo Kim, Se Hoon Kim, Suhg Namgoong, Eui Hyun Kim, Hyun Sub Cheong, Sun Ho Kim
Publikováno v:
Journal of Neuro-Oncology. 142:223-229
Previous studies have revealed that PHLDB1 single-nucleotide polymorphisms (SNPs) are associated with glioma risk. Nonetheless, the association between PHLDB1 SNPs and the risk of pituitary adenoma has not been studied. The present study evaluated th
Autor:
Seung-Woo Shin, Byung Lae Park, HunSoo Chang, Jong Sook Park, Da-Jeong Bae, Hyun-Ji Song, Inseon S Choi, Mi-Kyeong Kim, Hea-Sim Park, Lyoung Hyo Kim, Suhg Namgoong, Ji On Kim, Hyoung Doo Shin, Choon-Sik Park
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111887 (2014)
Aspirin-exacerbated respiratory disease (AERD) is one phenotype of asthma, often occurring in the form of a severe and sudden attack. Due to the time-consuming nature and difficulty of oral aspirin challenge (OAC) for AERD diagnosis, non-invasive bio
Externí odkaz:
https://doaj.org/article/e9d1f5fb86114a2b9187797d37a0a239
Autor:
Jung Yeon Seo, Joong Gon Shin, Byeong Ju Youn, Suhg Namgoong, Hyun Sub Cheong, Lyoung Hyo Kim, Ji On Kim, Hyoung Doo Shin, Yoon Jun Kim
Background: Hepatitis B is known to cause several forms of liver diseases including chronic hepatitis B (CHB), and hepatocellular carcinoma. Previous genome-wide association study of CHB risk has demonstrated that rs12614 of complement factor B (CFB)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::248b09d55350c535c8a14bb82c58bfcf
https://doi.org/10.21203/rs.3.rs-48397/v1
https://doi.org/10.21203/rs.3.rs-48397/v1
Autor:
Seo, Jung Yeon, Joong-Gon Shin, Youn, Byeong Ju, Suhg Namgoong, Cheong, Hyun Sub, Lyoung Hyo Kim, Kim, Ji On, Shin, Hyoung Doo, Kim, Yoon Jun
Additional file 8: Supplementary Table 4. Combined genetic effects of eleven CHB susceptible loci.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f7e06afa4a19909f84d591e77f19b6b
Autor:
Seo, Jung Yeon, Joong-Gon Shin, Youn, Byeong Ju, Suhg Namgoong, Cheong, Hyun Sub, Lyoung Hyo Kim, Kim, Ji On, Shin, Hyoung Doo, Kim, Yoon Jun
Additional file 7: Supplementary Table 3. Association analysis of rs12614 using the Training and Test sets.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d31faa7f999c6b0d8a1a4f48b36314bd