Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo
Lee, Ji-Su, Chang, Eun Hyuk, Koo, Ok Jae, Jwa, Dong Hwan, Mo, Won Min, Kwak, Geon, Moon, Hyo Won, Park, Hwan Tae, Hong, Young Bin, Choi, Byung-Ok
Published in Neurobiology of disease (01.04.2017)
Published in Neurobiology of disease (01.04.2017)
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A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy
Hong, Young Bin, Joo, Jaesoon, Hyun, Young Se, Kwak, Geon, Choi, Yu-Ri, Yeo, Ha Kyung, Jwa, Dong Hwan, Kim, Eun Ja, Mo, Won Min, Nam, Soo Hyun, Kim, Sung Min, Yoo, Jeong Hyun, Koo, Heasoo, Park, Hwan Tae, Chung, Ki Wha, Choi, Byung-Ok
Published in PLoS genetics (01.02.2016)
Published in PLoS genetics (01.02.2016)
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ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy
Park, Hyung Jun, Hong, Young Bin, Choi, Young-Chul, Lee, Jinho, Kim, Eun Ja, Lee, Ji-Su, Mo, Won Min, Ki, Soo Mi, Kim, Hyo In, Kim, Hye Jin, Hyun, Young Se, Hong, Hyun Dae, Nam, Kisoo, Jung, Sung Chul, Kim, Sang-Beom, Kim, Se Hoon, Kim, Deok-Ho, Oh, Ki-Wook, Kim, Seung Hyun, Yoo, Jeong Hyun, Lee, Ji Eun, Chung, Ki Wha, Choi, Byung-Ok
Published in Annals of neurology (01.02.2016)
Published in Annals of neurology (01.02.2016)
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Tumor necrosis factor-α-activated mesenchymal stem cells promote endothelial progenitor cell homing and angiogenesis
Kwon, Yang Woo, Heo, Soon Chul, Jeong, Geun Ok, Yoon, Jung Won, Mo, Won Min, Lee, Mi Jeong, Jang, Il-Ho, Kwon, Sang Mo, Lee, Jung Sub, Kim, Jae Ho
Published in Biochimica et biophysica acta (01.12.2013)
Published in Biochimica et biophysica acta (01.12.2013)
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Cytokines secreted by mesenchymal stem cells reduce demyelination in an animal model of Charcot-Marie-Tooth disease
Jeon, Hyeonjin, Kim, Hye Jin, Doo, Hyun Myung, Chang, Eun Hyuk, Kwak, Geon, Mo, Won Min, Jang, So Young, Lee, Myoung Woo, Choi, Byung-Ok, Hong, Young Bin
Published in Biochemical and biophysical research communications (15.03.2022)
Published in Biochemical and biophysical research communications (15.03.2022)
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ADSSL 1 mutation relevant to autosomal recessive adolescent onset distal myopathy
Park, Hyung Jun, Hong, Young Bin, Choi, Young‐Chul, Lee, Jinho, Kim, Eun Ja, Lee, Ji‐Su, Mo, Won Min, Ki, Soo Mi, Kim, Hyo In, Kim, Hye Jin, Hyun, Young Se, Hong, Hyun Dae, Nam, Kisoo, Jung, Sung Chul, Kim, Sang‐Beom, Kim, Se Hoon, Kim, Deok‐Ho, Oh, Ki‐Wook, Kim, Seung Hyun, Yoo, Jeong Hyun, Lee, Ji Eun, Chung, Ki Wha, Choi, Byung‐Ok
Published in Annals of neurology (01.02.2016)
Published in Annals of neurology (01.02.2016)
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A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy: e1005829
Hong, Young Bin, Joo, Jaesoon, Hyun, Young Se, Kwak, Geon, Choi, Yu-Ri, Yeo, Ha Kyung, Jwa, Dong Hwan, Kim, Eun Ja, Mo, Won Min, Nam, Soo Hyun, Kim, Sung Min, Yoo, Jeong Hyun, Koo, Heasoo, Park, Hwan Tae, Chung, Ki Wha, Choi, Byung-Ok
Published in PLoS genetics (01.02.2016)
Published in PLoS genetics (01.02.2016)
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