Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Won Min Mo"'
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:
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:
Biomolecules & Therapeutics
Transcriptional co-activator with a PDZ-binding motif (TAZ) is an important factor in lysophosphatidic acid (LPA)-induced promotion of migration and proliferation of human mesenchymal stem cells (MSCs). The expression of TAZ significantly increased a
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:
Hyung Jun Park, Young Bin Hong, Young-Chul Choi, Jinho Lee, Eun Ja Kim, Ji-Su Lee, Won Min Mo, Soo Mi Ki, Hyo In Kim, Hye Jin Kim, Young Se Hyun, Hyun Dae Hong, Kisoo Nam, Sung Chul Jung, Sang-Beom Kim, Se Hoon Kim, Deok-Ho Kim, Ki-Wook Oh, Seung Hyun Kim, Jeong Hyun Yoo, Ji Eun Lee, Ki Wha Chung, Byung-Ok Choi
Publikováno v:
Annals of Neurology. 79:231-243
Autor:
Heasoo Koo, Ha Kyung Yeo, Sung Min Kim, Byung Ok Choi, Yu Ri Choi, Young Se Hyun, Soo Hyun Nam, Jaesoon Joo, Dong Hwan Jwa, Won Min Mo, Jeong Hyun Yoo, Geon Kwak, Hwan Tae Park, Ki Wha Chung, Eun Ja Kim, Young Bin Hong
Publikováno v:
PLoS Genetics, Vol 12, Iss 2, p e1005829 (2016)
PLOS GENETICS(12): 2
PLoS Genetics
PLOS GENETICS(12): 2
PLoS Genetics
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
Autor:
Hyung Jun, Park, Young Bin, Hong, Young-Chul, Choi, Jinho, Lee, Eun Ja, Kim, Ji-Su, Lee, Won Min, Mo, Soo Mi, Ki, Hyo In, Kim, Hye Jin, Kim, Young Se, Hyun, Hyun Dae, Hong, Kisoo, Nam, Sung Chul, Jung, Sang-Beom, Kim, Se Hoon, Kim, Deok-Ho, Kim, Ki-Wook, Oh, Seung Hyun, Kim, Jeong Hyun, Yoo, Ji Eun, Lee, Ki Wha, Chung, Byung-Ok, Choi
Publikováno v:
Annals of neurology. 79(2)
Distal myopathy is a heterogeneous group of muscle diseases characterized by predominant distal muscle weakness. A study was done to identify the underlying cause of autosomal recessive adolescent onset distal myopathy.Four patients from 2 unrelated
Autor:
Soon Chul Heo, Geun Ok Jeong, Jae Ho Kim, Il Ho Jang, Sang Mo Kwon, Yang Woo Kwon, Won Min Mo, Mi Jeong Lee, Jung Won Yoon, Jung Sub Lee
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. (12):2136-2144
Mesenchymal stem cells (MSCs) accelerate regeneration of ischemic or injured tissues by stimulation of angiogenesis through a paracrine mechanism. Tumor necrosis factor-α (TNF-α)-activated MSCs secrete pro-angiogenic cytokines, including IL-6 and I