Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Young Bin Hong"'
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
Autor:
Kyong-hwa Kang, Ji Eun Han, Hyunjin Kim, Sohee Kim, Young Bin Hong, Jeanho Yun, Soo Hyun Nam, Byung-Ok Choi, Hyongjong Koh
Publikováno v:
Biomedicines, Vol 11, Iss 3, p 832 (2023)
Charcot–Marie–Tooth disease (CMT) is a group of inherited peripheral nerve disorders characterized by progressive muscle weakness and atrophy, sensory loss, foot deformities and steppage gait. Missense mutations in the gene encoding the small hea
Externí odkaz:
https://doaj.org/article/91945eac65de41a08c5e7d68bb1b0ed9
Publikováno v:
Animal Cells and Systems, Vol 25, Iss 1, Pp 11-18 (2021)
Charcot-Marie-Tooth disease (CMT), a genetically heterogeneous group of diseases in the peripheral nervous system, is characterized by progressive and symmetrical distal weakness resulting in gait abnormality. The necessity of the diagnostic and prog
Externí odkaz:
https://doaj.org/article/fb34e66919fe417da246ec8bd9f871b9
Autor:
Hye Jin Kim, Sang Beom Kim, Hyun Su Kim, Hye Mi Kwon, Jae Hong Park, Ah Jin Lee, Si On Lim, Soo Hyun Nam, Young Bin Hong, Ki Wha Chung, Byung‐Ok Choi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Charcot–Marie–Tooth disease (CMT) is the most common hereditary peripheral neuropathy. Mutations in the neurofilament light polypeptide (NEFL) gene produce diverse clinical phenotypes, including demyelinating (CMT1F), axonal (CMT2E), and
Externí odkaz:
https://doaj.org/article/9f945a2ad238414dba32c1891b411b4c
Autor:
Young Hee Kim, Young Hye Kim, Yoon Kyung Shin, Young Rae Jo, Da Kyeong Park, Min‐Young Song, Byeol‐A. Yoon, Soo Hyun Nam, Jong Hyun Kim, Byung‐Ok Choi, Ha Young Shin, Seung Woo Kim, Se Hoon Kim, Young Bin Hong, Jong Kuk Kim, Hwan Tae Park
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1292-1301 (2019)
Abstract Objective Myelinated Schwann cells (SCs) in adult peripheral nerves dedifferentiate into immature cells in demyelinating neuropathies and Wallerian degeneration. This plastic SC change is actively involved in the myelin destruction and clear
Externí odkaz:
https://doaj.org/article/23616be5233c4928bc8403b413168468
Autor:
Young Yeon Kim, Jeong-Hyun Yoon, Jee-Hyun Um, Dae Jin Jeong, Dong Jin Shin, Young Bin Hong, Jong Kuk Kim, Dong Hyun Kim, Changsoo Kim, Chang Geon Chung, Sung Bae Lee, Hyongjong Koh, Jeanho Yun
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0257439 (2021)
[This corrects the article DOI: 10.1371/journal.pone.0239126.].
Externí odkaz:
https://doaj.org/article/24e85f5550e048afa8920d9a257d5b52
Autor:
Young Yeon Kim, Jeong-Hyun Yoon, Jee-Hyun Um, Dae Jin Jeong, Dong Jin Shin, Young Bin Hong, Jong Kuk Kim, Dong Hyun Kim, Changsoo Kim, Chang Geon Chung, Sung Bae Lee, Hyongjong Koh, Jeanho Yun
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0239126 (2020)
Paclitaxel is a representative anticancer drug that induces chemotherapy-induced peripheral neuropathy (CIPN), a common side effect that limits many anticancer chemotherapies. Although PINK1, a key mediator of mitochondrial quality control, has been
Externí odkaz:
https://doaj.org/article/f765cfb95b9c44a49c4cdb9c2bb1a631
Autor:
Ji-Su Lee, Eun Hyuk Chang, Ok Jae Koo, Dong Hwan Jwa, Won Min Mo, Geon Kwak, Hyo Won Moon, Hwan Tae Park, Young Bin Hong, Byung-Ok Choi
Publikováno v:
Neurobiology of Disease, Vol 100, Iss , Pp 99-107 (2017)
Charcot-Marie-Tooth disease (CMT) is a genetic disorder that can be caused by aberrations in >80 genes. CMT has heterogeneous modes of inheritance, including autosomal dominant, autosomal recessive, X-linked dominant, and X-linked recessive. Over 95%
Externí odkaz:
https://doaj.org/article/046a240c8f184ec19b972d729e7d7f0b
Autor:
Young Bin Hong, Jaesoon Joo, Young Se Hyun, Geon Kwak, Yu-Ri Choi, Ha Kyung Yeo, Dong Hwan Jwa, Eun Ja Kim, Won Min Mo, Soo Hyun Nam, Sung Min Kim, Jeong Hyun Yoo, Heasoo Koo, Hwan Tae Park, Ki Wha Chung, Byung-Ok Choi
Publikováno v:
PLoS Genetics, Vol 12, Iss 2, p e1005829 (2016)
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of peripheral neuropathies with diverse genetic causes. In this study, we identified p.I43N mutation in PMP2 from a family exhibiting autosomal dominant demyelinating CMT neuropathy by whole
Externí odkaz:
https://doaj.org/article/7d3a1c012e2d4792841fc3db70e1d610
Autor:
Ji-Yon Kim, So-Youn Woo, Young Bin Hong, Heesun Choi, Jisoo Kim, Hyunjung Choi, Inhee Mook-Jung, Nina Ha, Jangbeen Kyung, Soo Kyung Koo, Sung-Chul Jung, Byung-Ok Choi
Publikováno v:
Stem Cells International, Vol 2016 (2016)
The Charcot-Marie-Tooth disease 2F (CMT2F) and distal hereditary motor neuropathy 2B (dHMN2B) are caused by autosomal dominantly inherited mutations of the heat shock 27 kDa protein 1 (HSPB1) gene and there are no specific therapies available yet. He
Externí odkaz:
https://doaj.org/article/598d0fb127e142eb890052a98109342e