Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Eun Hyuk Chang"'
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:
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:
Eun Hyuk Chang, Istvan Adorjan, Bin Sun, Mayara Vieira Mundim, Maria Luz V Dizon, Francis G Szele
Publikováno v:
Frontiers in Neuroscience, Vol 10 (2016)
Traumatic brain injury (TBI) is common in both civilian and military life placing a large burden on survivors and society. However, with recognition of neural stem cells in adult mammals, including humans, came the possibility of harnessing these cel
Externí odkaz:
https://doaj.org/article/e8033b1ee1884fd8b3afa41f4ec82e5f
Autor:
Na Kyung Lee, Jehoon Yang, Eun Hyuk Chang, Sang Eon Park, Jeongmin Lee, Soo Jin Choi, Wonil Oh, Jong Wook Chang, Duk L Na
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155912 (2016)
Mesenchymal stem cells (MSCs) have a promising role as a therapeutic agent for neurodegenerative diseases such as Alzheimer's disease (AD). Prior studies suggested that intra-arterially administered MSCs are engrafted into the brain in stroke or trau
Externí odkaz:
https://doaj.org/article/5069380c3f5742108501660ab513df91
Autor:
Hyeonjin Jeon, Hye Jin Kim, Hyun Myung Doo, Eun Hyuk Chang, Geon Kwak, Won Min Mo, So Young Jang, Myoung Woo Lee, Byung-Ok Choi, Young Bin Hong
Publikováno v:
Biochemical and Biophysical Research Communications. 597:1-7
Demyelinating Charcot-Marie-Tooth disease (CMT) is caused by mutations in the genes that encode myelinating proteins or their transcription factors. Our study thus sought to assess the therapeutic effects of cytokines secreted from mesenchymal stem c
Publikováno v:
Animal Cells and Systems, Vol 25, Iss 1, Pp 11-18 (2021)
Animal Cells and Systems
article-version (VoR) Version of Record
Animal Cells and Systems
article-version (VoR) Version of Record
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
Autor:
Yoonkyung Lee, Duk L. Na, Jee Hoon Roh, Mahito Nakanishi, Minchul Kim, Ling Li, Wonyoung Koh, Hee Jin Kim, Suji Lee, Jong Wook Chang, Jihwan Song, Roger A. Barker, Eun Hyuk Chang
Publikováno v:
Experimental Neurobiology
Disease modeling of Alzheimer's disease (AD) has been hampered by the lack of suitable cellular models while animal models are mainly based on the overexpression of AD-related genes which often results in an overemphasis of certain pathways and is al
Autor:
Won Min Mo, Dong Hwan Jwa, Eun Hyuk Chang, Hwan Tae Park, Hyo Won Moon, Ok Jae Koo, Young Bin Hong, Ji-Su Lee, Byung-Ok Choi, Geon Kwak
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%
Autor:
Ji Su Lee, Won Min Mo, Eun Hyuk Chang, Byung Ok Choi, Hyun Myung Doo, Young Bin Hong, Hwan Tae Park
Publikováno v:
International Journal of Molecular Medicine
Mutations in myelin protein zero (MPZ) cause inherited peripheral neuropathies, including Charcot‑Marie‑Tooth disease (CMT) and Dejerine‑Sottas neuropathy. Mutant MPZ proteins have previously been reported to cause CMT via enhanced endoplasmic
Autor:
Eun Hyuk Chang, Jeong Min Lee, Duk L. Na, Jong Wook Chang, Ji-Hee Sung, Sang Eon Park, Jonghwa Kim
Publikováno v:
Archives of Pharmacal Research. 39:1171-1179
Alzheimer's disease (AD) is characterized by progressive loss of memory in addition to cortical atrophy. Cortical atrophy in AD brains begins in the parietal and temporal lobes, which are near the subventricular zone (SVZ). The aim of this study was