Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Seul Kee Byeon"'
Autor:
Linsey E. Jackson, Jennifer L. Tomlinson, Roberto Alva-Ruiz, Lindsey A. Gregory, Seul Kee Byeon, Amro M. Abdelrahman, Dong-Gi Mun, Caroline W. Grant, Zachary C. Fogarty, Chen Wang, Lewis R. Roberts, Rondell P. Graham, Mitesh J. Borad, Sumera I. Ilyas, Gregory J. Gores, Akhilesh Pandey, Arjun P. Athreya, Rory L. Smoot
Publikováno v:
JHEP Reports, Vol 6, Iss 6, Pp 101068- (2024)
Background & Aims: Metabolomic and lipidomic analyses provide an opportunity for novel biological insights. Cholangiocarcinoma (CCA) remains a highly lethal cancer with limited response to systemic, targeted, and immunotherapeutic approaches. Using a
Externí odkaz:
https://doaj.org/article/2c99399c263347e3bad6c6dcc1769f86
Autor:
Guang Lin, Burak Tepe, Geoff McGrane, Regine C Tipon, Gist Croft, Leena Panwala, Amanda Hope, Agnes JH Liang, Zhongyuan Zuo, Seul Kee Byeon, Lily Wang, Akhilesh Pandey, Hugo J Bellen
Publikováno v:
eLife, Vol 12 (2023)
Infantile neuroaxonal dystrophy (INAD) is caused by recessive variants in PLA2G6 and is a lethal pediatric neurodegenerative disorder. Loss of the Drosophila homolog of PLA2G6, leads to ceramide accumulation, lysosome expansion, and mitochondrial def
Externí odkaz:
https://doaj.org/article/e4633d77eb604aa29a4117eee3456289
Publikováno v:
Journal of Mass Spectrometry and Advances in the Clinical Lab, Vol 22, Iss , Pp 43-49 (2021)
Lipidomics is an important component of most multi-Omics systems biology studies and is largely driven by mass spectrometry (MS). Because lipids are tight regulators of multiple cellular functions, including energy homeostasis, membrane structures an
Externí odkaz:
https://doaj.org/article/7c4e217bab354228baa6b482a814bda0
Autor:
Se Mi Park, Seul Kee Byeon, Hojun Lee, Hyerim Sung, Il Yong Kim, Je Kyung Seong, Myeong Hee Moon
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Tumour suppressor p53 is known to be associated with the maintenance of mitochondrial functional properties in the skeletal muscles. As deactivation or mutation of p53 can affect the synthesis of lipids, investigating the relationship betwee
Externí odkaz:
https://doaj.org/article/facac261b9ba49f09d8b834261b91636
Autor:
Seul Kee Byeon, Anil K Madugundu, Kishore Garapati, Madan Gopal Ramarajan, Mayank Saraswat, Praveen Kumar-M, Travis Hughes, Rameen Shah, Mrinal M Patnaik, Nicholas Chia, Susan Ashrafzadeh-Kian, Joseph D Yao, Bobbi S Pritt, Roberto Cattaneo, Mohamed E Salama, Roman M Zenka, Benjamin R Kipp, Stefan K G Grebe, Ravinder J Singh, Amir A Sadighi Akha, Alicia Algeciras-Schimnich, Surendra Dasari, Janet E Olson, Jesse R Walsh, A J Venkatakrishnan, Garrett Jenkinson, John C O'Horo, Andrew D Badley, Akhilesh Pandey
Publikováno v:
The Lancet Digital Health. 4:e632-e645
COVID-19 is a multi-system disorder with high variability in clinical outcomes among patients who are admitted to hospital. Although some cytokines such as interleukin (IL)-6 are believed to be associated with severity, there are no early biomarkers
Autor:
Guang Lin, Burak Tepe, Geoff McGrane, Regine C Tipon, Gist Croft, Leena Panwala, Amanda Hope, Agnes JH Liang, Zhongyuan Zuo, Seul Kee Byeon, Lily Wang, Akhilesh Pandey, Hugo J Bellen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5737f82bb244b9dc487fd1679729501d
https://doi.org/10.7554/elife.82555.sa2
https://doi.org/10.7554/elife.82555.sa2
Autor:
Ewout Muylle, Huafang Jiang, Christin Johnsen, Seul Kee Byeon, Wasantha Ranatunga, Kishore Garapati, Roman M. Zenka, Graeme Preston, Akhilesh Pandey, Tamas Kozicz, Fang Fang, Eva Morava
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 45(6)
TRIT1 defect is a rare, autosomal-recessive disorder of transcription, initially described as a condition with developmental delay, myoclonic seizures, and abnormal mitochondrial function. Currently, only 13 patients have been reported. We reviewed t
Autor:
Liping Wang, Guang Lin, Zhongyuan Zuo, Yarong Li, Seul Kee Byeon, Akhilesh Pandey, Hugo J. Bellen
Publikováno v:
Science Advances. 8
Recessive variants in GBA1 cause Gaucher disease, a prevalent form of lysosome storage disease. GBA1 encodes a lysosomal enzyme that hydrolyzes glucosylceramide (GlcCer) into glucose and ceramide. Its loss causes lysosomal dysfunction and increased l
Autor:
Kishore Garapati, Seul Kee Byeon, Jesse R Walsh, Garrett Jenkinson, Roberto Cattaneo, John C O'Horo, Andrew D Badley, Akhilesh Pandey
Publikováno v:
The Lancet Digital Health. 5:e57
Autor:
Syed Jafar Raza Rizvi, Amy L Piazza, Seul Kee Byeon, Nabidul H. Chowdhury, Tarik Hasan, Sayedur Rahman, Piero Rinaldo, Akhilesh Pandey, Salahuddin Ahmed, Kwang Pyo Kim, Abdullah H Baqui, Rasheda Khanam, Rubhana Raqib, Madan Gopal Ramarajan, Anil K. Madugundu, Jae Hun Jung
Publikováno v:
Molecular Omics. 17:956-966
To discover lipidomic alterations during pregnancy in mothers who subsequently delivered small for gestational age (SGA) neonates and identify predictive lipid markers that can help recognize and manage these mothers, we carried out untargeted lipido