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American Journal of Cancer Research|August 6, 2021
Doxycycline potentiates the anti-proliferation effects of gemcitabine in pancreatic cancer cellsYong Weon Yi, Na Young Park, Joo-In Park, et al.
Animal Cells and Systems|March 15, 2021
Gait parameters as tools for analyzing phenotypic alterations of a mouse model of Charcot-Marie-Tooth diseaseSun Hee Hwang, Eun Hyuk Chang, Geon Kwak, et al.
The Journal of Toxicological Sciences|May 14, 2013
Correlations between BRCA1 defect and environmental factors in the risk of breast cancerHyo Jin Kang, Young Bin Hong, Yong Weon Yi, et al.
Journal of Clinical Neurology (Seoul, Korea)|October 1, 2021
A Compound Heterozygous Pathogenic Variant in <i>B4GALNT1</i> Is Associated With Axonal Charcot-Marie-Tooth DiseaseJi Man Hong, Hyeonjin Jeon, Young Chul Choi, et al.
Biochemical and Biophysical Research Communications|October 7, 2023
PINK1 and Parkin rescue motor defects and mitochondria dysfunction induced by a patient-derived HSPB3 mutant in Drosophila modelsJi Eun Han, Kyong-Hwa Kang, Hyunjin Kim, et al.
Experimental Neurobiology|May 30, 2019
miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22Ji-Su Lee, Geon Kwak, Hye Jin Kim, et al.
The Journal of Gene Medicine|February 16, 2005
Long-term expression of the human glucocerebrosidase gene in vivo after transplantation of bone-marrow-derived cells transformed with a lentivirus vectorEun Young Kim, Young Bin Hong, Zhennan Lai, et al.
Molecular Medicine Reports|November 20, 2013
Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutationBum Chun Suh, Young Bin Hong, Khriezhanuo Nakhro, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 12, 2021
p53-mediated regulation of mitochondrial dynamics plays a pivotal role in the senescence of various normal cells as well as cancer cellsYoung Yeon Kim, Jee-Hyun Um, Dong Jin Shin, et al.
Biochemical and Biophysical Research Communications|October 22, 2019
Human HSPB1 mutation recapitulates features of distal hereditary motor neuropathy (dHMN) in DrosophilaKyong-Hwa Kang, Ji Eun Han, Young Bin Hong, et al.
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