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Biochemical and Biophysical Research Communications|April 12, 2012
Gs cascade regulates canonical transient receptor potential 5 (TRPC5) through cAMP mediated intracellular Ca2+ release and ion channel traffickingChansik Hong, Jinsung Kim, Jae-Pyo Jeon, et al.
Clinical and Translational Medicine|March 30, 2021
A novel modified RANKL variant can prevent osteoporosis by acting as a vaccine and an inhibitorYoung Jong Ko, Hong Moon Sohn, Yuria Jang, et al.
Molecular Medicine Reports|June 20, 2017
Scutellaria baicalensis Georgi induces caspase-dependent apoptosis via mitogen activated protein kinase activation and the generation of reactive oxygen species signaling pathways in MCF-7 breast cancer cellsJin Ryeong Park, Min Cheol Lee, Seong-Cheol Moon, et al.
Biochemical and Biophysical Research Communications|April 8, 2014
Reciprocal positive regulation between TRPV6 and NUMB in PTEN-deficient prostate cancer cellsSung-Young Kim, Chansik Hong, Jinhong Wie, et al.
The Journal of Biological Chemistry|March 30, 2012
Selective Gαi subunits as novel direct activators of transient receptor potential canonical (TRPC)4 and TRPC5 channelsJae-Pyo Jeon, Chansik Hong, Eun Jung Park, et al.
American Journal of Physiology. Cell Physiology|July 8, 2011
Molecular determinants of PKA-dependent inhibition of TRPC5 channelTae Sik Sung, Jae Pyo Jeon, Byung Joo Kim, et al.
Brain : a Journal of Neurology|July 3, 2015
Increased TRPC5 glutathionylation contributes to striatal neuron loss in Huntington's diseaseChansik Hong, Hyemyung Seo, Misun Kwak, et al.
Molecular Neurobiology|August 1, 2018
Contribution of Zinc-Dependent Delayed Calcium Influx via TRPC5 in Oxidative Neuronal Death and its Prevention by Novel TRPC AntagonistSang Eun Park, Ji Hoon Song, Chansik Hong, et al.
Molecular Neurobiology|December 14, 2018
Correction to: Contribution of Zinc-Dependent Delayed Calcium Influx via TRPC5 in Oxidative Neuronal Death and its Prevention by Novel TRPC AntagonistSang Eun Park, Ji Hoon Song, Chansik Hong, et al.
Annals of Neurology|September 1, 2017
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathyYongjin Yoo, Jane Jung, Yoo-Na Lee, et al.
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