Y. Jeon

发表

Creutzfeldt‐Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment

R. Carp, S.-J. Park, E. Choi, 2010, Neuropathology and applied neurobiology.

Myelin Basic Protein Citrullination, a Hallmark of Central Nervous System Demyelination, Assessed by Novel Monoclonal Antibodies in Prion Diseases

A. Ishigami, Yong-Sun Kim, E. Choi, 2018, Molecular Neurobiology.

Pathological characterization of TgElk mice injected with brain homogenate from elk with chronic wasting disease

J. Choi, R. Carp, Yong-Sun Kim, 2013, Journal of veterinary science.

Increased Expression of S100B and RAGE in a Mouse Model of Bile Duct Ligation-induced Liver Fibrosis

Se Jin Park, J. Park, D. J. Kim, 2021, Journal of Korean medical science.

Nonenzymatic Glycation at the N Terminus of Pathogenic Prion Protein in Transmissible Spongiform Encephalopathies*

R. Carp, Yong-Sun Kim, R. Rubenstein, 2004, Journal of Biological Chemistry.

Mass spectrometric identification of citrullination sites and immunohistochemical detection of citrullinated glial fibrillary acidic protein in Alzheimer's disease brains

A. Ishigami, N. Maruyama, Yong-Sun Kim, 2015, Journal of neuroscience research.

Involvement of peptidylarginine deiminase-mediated post-translational citrullination in pathogenesis of sporadic Creutzfeldt-Jakob disease

A. Ishigami, N. Maruyama, R. Carp, 2010, Acta Neuropathologica.

Spontaneous immortalization of oligodendroglial cells derived from an SV40 T antigen-positive human glioblastoma multiforme.

R. Carp, Yong-Sun Kim, Boe-Hyun Kim, 2009, Cancer letters.

Familial Creutzfeldt–Jakob disease with a mutation at codon 180 presenting with an atypical phenotype

Yong-Sun Kim, Seung-Hwan Lee, Sung-Hun Kim, 2013, Journal of Clinical Neuroscience.

Dura Mater Graft-Associated Creutzfeldt-Jakob Disease: The First Case in Korea

K. Kallenberg, I. Zerr, Y. Kim, 2011, Journal of Korean medical science.

A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.

Y. Koh, Hyun-pil Lee, J. Choi, 2010, Human molecular genetics.

Altered expression of type 1 inositol 1,4,5-trisphosphate receptor in the Ngsk Prnp deficient mice

Y. Kim, R. Carp, J. I. Kim, 2010, Neuroscience.

Peptidylarginine deiminase modulates the physiological roles of enolase via citrullination

A. Ishigami, N. Maruyama, J. Choi, 2012, The Biochemical journal.

Upregulation of Connexin 43 Expression Via C-Jun N-Terminal Kinase Signaling in Prion Disease.

R. Carp, Yong-Sun Kim, H. Choi, 2015, Journal of Alzheimer's disease : JAD.

Accumulation of citrullinated glial fibrillary acidic protein in a mouse model of bile duct ligation-induced hepatic fibrosis

J. Park, D. J. Kim, A. Ishigami, 2018, PloS one.

3D polycaprolactone scaffolds with controlled pore structure using a rapid prototyping system

Geunhyung Kim, Y. Koh, Sua Park, 2009, Journal of materials science. Materials in medicine.

Association of endothelial nitric oxide synthase and mitochondrial dysfunction in the hippocampus of scrapie‐infected mice

G. Wen, R. Carp, Yong-Sun Kim, 2011, Hippocampus.

A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.

Y. Koh, Hyun-pil Lee, J. Choi, 2010, Human Molecular Genetics.