Zobrazeno 1 - 10 of 16 pro vyhledávání: '"Na-Yoon Lee"'
1
Akademický článek
Nanoplasmonic immunosensor for the detection of SCG2, a candidate serum biomarker for the early diagnosis of neurodevelopmental disorder
Autor: So-Hee Lim, Yun-Ju Sung, Narae Jo, Na-Yoon Lee, Kyoung-Shim Kim, Da Yong Lee, Nam-Soon Kim, Jeehun Lee, Ju-Young Byun, Yong-Beom Shin, Jae-Ran Lee
Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The neural circuits of the infant brain are rapidly established near 6 months of age, but neurodevelopmental disorders can be diagnosed only at the age of 2–3 years using existing diagnostic methods. Early diagnosis is very important to al
Externí odkaz: https://doaj.org/article/c6d97dc35d924530bfecbe6899a38c80
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3
Akademický článek
Autosomal dominant transmission of complicated hereditary spastic paraplegia due to a dominant negative mutation of KIF1A, SPG30 gene
Autor: Chong Kun Cheon, So-Hee Lim, Yoo-Mi Kim, Doyoun Kim, Na-Yoon Lee, Tae-Sung Yoon, Nam-Soon Kim, Eunjoon Kim, Jae-Ran Lee
Publikováno v: Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract KIF1A is a brain-specific anterograde motor protein that transports cargoes towards the plus-ends of microtubules. Many variants of the KIF1A gene have been associated with neurodegenerative diseases and developmental delay. Homozygous mutat
Externí odkaz: https://doaj.org/article/900c8ddcf499428b9be3ca0b91865770
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5
Phosphoproteome profiling of hippocampal synaptic plasticity
Autor: So-Hee Lim, Na-Yoon Lee, Ju Yeon Ryu, Jin Hua An, Ga Seul Lee, Sun Seek Min, Jeonghee Moon, Jae-Ran Lee
Publikováno v: Biochemical and Biophysical Research Communications. 626:92-99
The balance between the actions of protein kinases and phosphatases is crucial for neuronal functions, including synaptic plasticity. Although the phosphorylation and dephosphorylation of neuronal proteins are regulated by synaptic plasticity, no sys
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::428a7f699371f8702476fb81da03e29e
https://doi.org/10.1016/j.bbrc.2022.07.051
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8
1860. Streptococcus mitis/oralis sepsis in patients with neutropenia after chemotherapy
Autor: Na Yoon Lee, Hyun Mi Kang, Dae Chul Jeong, Seong Koo Kim, Jae Wook Lee, Nack-Gyun Chung, Bin Cho
Publikováno v: Open Forum Infectious Diseases. 9
Background Streptococci are the dominant species in the human oral cavity and upper respiratory tract. Oral mucositis affects 30–40% of the patients receiving chemotherapy and 80% undergoing HSCT. During episode of oral mucositis, patients are at a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9129e4c0aba9b25d1ad7548936ff4e74
https://doi.org/10.1093/ofid/ofac492.1489
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9
Nanoplasmonic immunosensor for the detection of SCG2, a candidate serum biomarker for the early diagnosis of neurodevelopmental disorder
Autor: Yun-Ju Sung, Jae-Ran Lee, Jeehun Lee, Narae Jo, Ju-Young Byun, So-Hee Lim, Nam-Soon Kim, Da Yong Lee, Kyoung-Shim Kim, Na-Yoon Lee, Yong-Beom Shin
Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports
The neural circuits of the infant brain are rapidly established near 6 months of age, but neurodevelopmental disorders can be diagnosed only at the age of 2–3 years using existing diagnostic methods. Early diagnosis is very important to alleviate l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f03f49f6279741f9ccf6f5a05fb4fd
https://doi.org/10.1038/s41598-021-02262-7
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10
Autosomal dominant transmission of complicated hereditary spastic paraplegia due to a dominant negative mutation of KIF1A, SPG30 gene
Autor: Yoo-Mi Kim, Jae-Ran Lee, Doyoun Kim, Eunjoon Kim, Tae-Sung Yoon, Na-Yoon Lee, Chong Kun Cheon, Nam-Soon Kim, So-Hee Lim
Publikováno v: Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Scientific Reports
SCIENTIFIC REPORTS(7)
KIF1A is a brain-specific anterograde motor protein that transports cargoes towards the plus-ends of microtubules. Many variants of the KIF1A gene have been associated with neurodegenerative diseases and developmental delay. Homozygous mutations of K
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::232fcbae1f76952f197649e123bb908f
https://doaj.org/article/900c8ddcf499428b9be3ca0b91865770
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