Zobrazeno 1 - 10
of 342
pro vyhledávání: '"Byung Ok Choi"'
Autor:
Byeol-A Yoon, Young Hee Kim, Soo Hyun Nam, Hye-Jin Lee, Seong-il Oh, Namhee Kim, Kyeong-Hee Kim, Young Rae Jo, Jong Kuk Kim, Byung-Ok Choi, Hwan Tae Park
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Autophagy is a self-degradation system for recycling to maintain homeostasis. p62/sequestosome-1 (p62) is an autophagy receptor that accumulates in neuroglia in neurodegenerative diseases. The objective of this study was to determine the ele
Externí odkaz:
https://doaj.org/article/60ab188d4287449ab1de0957e4b8a4d9
Autor:
Dong-Min Lee, Minki Kang, Inah Hyun, Byung-Joon Park, Hye Jin Kim, Soo Hyun Nam, Hong-Joon Yoon, Hanjun Ryu, Hyun-moon Park, Byung-Ok Choi, Sang-Woo Kim
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-11 (2023)
Abstract Bioresorbable bioelectronics, with their natural degradation properties, hold significant potential to eliminate the need for surgical removal. Despite notable achievements, two major challenges hinder their practical application in medical
Externí odkaz:
https://doaj.org/article/55ee47c12b4c491984f20817a29279fb
Autor:
Byung Kwon Pi, Yeon Hak Chung, Hyun Su Kim, Soo Hyun Nam, Ah Jin Lee, Da Eun Nam, Hyung Jun Park, Sang Beom Kim, Ki Wha Chung, Byung-Ok Choi
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 12, p 6378 (2024)
Mutations in the SACS gene are associated with autosomal recessive spastic ataxia of Charlevoix-Saguenay disease (ARSACS) or complex clinical phenotypes of Charcot-Marie-Tooth disease (CMT). This study aimed to identify SACS mutations in a Korean CMT
Externí odkaz:
https://doaj.org/article/9c9da76b44204be1bdc0b13d40326986
Publikováno v:
Genes, Vol 15, Iss 4, p 485 (2024)
Autosomal recessive Nonaka distal myopathy is a rare autosomal recessive genetic disease characterized by progressive degeneration of the distal muscles, causing muscle weakness and decreased grip strength. It is primarily associated with mutations i
Externí odkaz:
https://doaj.org/article/bbdd34f20ba44dd3bb0dea2fcdae83d4
Autor:
Yunjeong Lee, In Seo Yeo, Namhee Kim, Dong-Keun Lee, Kyung-Tai Kim, Jiyoung Yoon, Jawoon Yi, Young Bin Hong, Byung-Ok Choi, Yoichi Kosodo, Daesoo Kim, Jihwan Park, Mi-Ryoung Song
Publikováno v:
eLife, Vol 12 (2023)
The fidelity of motor control requires the precise positional arrangement of motor pools and the establishment of synaptic connections between them. During neural development in the spinal cord, motor nerves project to specific target muscles and rec
Externí odkaz:
https://doaj.org/article/7de075f0991d4a55a288f4bdc034560c
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract We aimed to derive comprehensive MRI parameters that reflect intramuscular fat infiltration severity for designated lower extremity levels, based on semiquantitative analyses in Charcot-Marie-Tooth disease type 1A (CMT1A) patients. We review
Externí odkaz:
https://doaj.org/article/f9e9a257ee4c4c8c8e4f96829bb434b1
Autor:
Yu Hwa Nam, Saeyoung Park, Yoonji Yum, Soyeon Jeong, Hyo Eun Park, Ho Jin Kim, Jaeseung Lim, Byung-Ok Choi, Sung-Chul Jung
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3334 (2023)
Charcot–Marie–Tooth disease (CMT) is a hereditary disease with heterogeneous phenotypes and genetic causes. CMT type 1A (CMT1A) is a type of disease affecting the peripheral nerves and is caused by the duplication of the peripheral myelin protein
Externí odkaz:
https://doaj.org/article/c9fe0194592845558a5d74cb717cd5b4
Autor:
Jihyun Park, So Young Joo, Byung-Ok Choi, Dae-Hyun Kim, Jong Bum Park, Jong Weon Lee, Deog Young Kim
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 10, p 1473 (2023)
The aim of this study was to evaluate the characteristics of gait patterns in Charcot-Marie-Tooth disease type 1A (CMT1A) patients according to disease severity. Twenty-two CMT1A patients were enrolled and classified into two groups, according to the
Externí odkaz:
https://doaj.org/article/326e46e87d9c48c09ac7ca1fe3f6e300
Autor:
Hyun Su Kim, Ji Hyun Lee, Young Cheol Yoon, Min Jae Cha, Soo Hyun Nam, Hye Mi Kwon, Seonwoo Kim, Hojeong Won, Byung-Ok Choi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The objectives of this study were to assess the fat fraction (FF) and cross-sectional area (CSA) of the sciatic nerve in Charcot-Marie-Tooth disease type 1A (CMT1A) patients using Dixon-based proton density fat quantification MRI and to eluc
Externí odkaz:
https://doaj.org/article/826fbea9acd040d7aa6284b880f49b5b
Autor:
Na-Young Park, Geon Kwak, Hyun-Myung Doo, Hye-Jin Kim, So-Young Jang, Yun-Il Lee, Byung-Ok Choi, Young-Bin Hong
Publikováno v:
Current Issues in Molecular Biology, Vol 43, Iss 3, Pp 2011-2021 (2021)
Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous disease affecting the peripheral nervous system that is caused by either the demyelination of Schwann cells or degeneration of the peripheral axon. Currently, there are no treatment opt
Externí odkaz:
https://doaj.org/article/0d05dcbda8e348daa3bf9ee143eff943