Zobrazeno 1 - 10
of 55
pro vyhledávání: '"JeeHee Yoon"'
Publikováno v:
Journal of Movement Disorders, Vol 15, Iss 2, Pp 132-139 (2022)
Objective The Montreal Cognitive Assessment (MoCA) is recommended for assessing general cognition in Parkinson’s disease (PD). Several cutoffs of MoCA scores for diagnosing PD with cognitive impairment (PD-CI) have been proposed, with varying sensi
Externí odkaz:
https://doaj.org/article/3b25e7421de24bba91a5204b62bb52a4
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundStudies regarding differentially expressed genes (DEGs) in Parkinson’s disease (PD) have focused on common upstream regulators or dysregulated pathways or ontologies; however, the relationships between DEGs and disease-related or cell typ
Externí odkaz:
https://doaj.org/article/5159180a91c547e8983df48d3ee9c019
Publikováno v:
International Journal of Thyroidology. 15:42-48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e0fa142edba24924ac32fdda6318b34
https://doi.org/10.11106/ijt.2022.15.1.42
https://doi.org/10.11106/ijt.2022.15.1.42
Publikováno v:
Journal of KIISE. 48:358-367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d33cc9dbafdcc2074b2d86c8a7b11399
https://doi.org/10.5626/jok.2021.48.3.358
https://doi.org/10.5626/jok.2021.48.3.358
Autor:
JaeMoon Shin, Junbeom Jeon, Dawoon Jung, Kiyong Kim, Yun Joong Kim, Dong-Hoon Jeong, JeeHee Yoon
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 6; Pages: 959
Precision medicine has been revolutionized by the advent of high-throughput next-generation sequencing (NGS) technology and development of various bioinformatic analysis tools for large-scale NGS big data. At the population level, biomedical studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce84870c9cd17b75170157e1e046e2ba
Autor:
Hyung Jun Park, Kyoungjune Pak, Jeehee Yoon, Chul Hyoung Lyoo, Jinwoo Lee, Na Yeon Jung, Myung Jun Lee, Jong Hun Kim, Jae Hyeok Lee, Yun Joong Kim
Publikováno v:
Neurology. 93:e665-e674
ObjectiveTo investigate the effect of polygenic load on the progression of striatal dopaminergic dysfunction in patients with Parkinson disease (PD).MethodsUsing data from 335 patients with PD in the Parkinson's Progression Markers Initiative (PPMI)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a504139dccd483ebe893f4c6a065fe22
https://doi.org/10.1212/wnl.0000000000007939
https://doi.org/10.1212/wnl.0000000000007939
Publikováno v:
Yonsei Medical Journal; Aug2022, Vol. 63 Issue 8, p724-734, 11p
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 14 (2020)
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundStudies regarding differentially expressed genes (DEGs) in Parkinson’s disease (PD) have focused on common upstream regulators or dysregulated pathways or ontologies; however, the relationships between DEGs and disease-related or cell typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086eb405dc628844499d73c44845fc64
http://europepmc.org/articles/PMC7775392
http://europepmc.org/articles/PMC7775392
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 18
International Journal of Molecular Sciences, Vol 21, Iss 6452, p 6452 (2020)
Volume 21
Issue 18
International Journal of Molecular Sciences, Vol 21, Iss 6452, p 6452 (2020)
RNA decay is an important regulatory mechanism for gene expression at the posttranscriptional level. Although the main pathways and major enzymes that facilitate this process are well defined, global analysis of RNA turnover remains under-investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04307dd1237fab368aed411ede8dceb1
Publikováno v:
Neurobiology of aging. 100
Increased burdens of rare coding variants in genes related to lysosomal storage disease or mitochondrial pathways were reported to be associated with idiopathic Parkinson's disease. Under a hypothesis that the burden of damaging rare coding variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2733f2ccb42467abf79f679650c2753
https://pubmed.ncbi.nlm.nih.gov/33423827
https://pubmed.ncbi.nlm.nih.gov/33423827