Yong‐Chul Jeon

Hallym University — South Korea

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index389citations19works0.02yr avg
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Research Topics

Prion Diseases and Protein Misfolding(11), S100 Proteins and Annexins(4), RNA regulation and disease(4), Neurological diseases and metabolism(4), Rheumatoid Arthritis Research and Therapies(3)

Publications19 total

Increased Expression of S100B and RAGE in a Mouse Model of Bile Duct Ligation-induced Liver Fibrosis
Journal of Korean Medical Science·2021· 8 citedOpen Access
Accumulation of citrullinated glial fibrillary acidic protein in a mouse model of bile duct ligation-induced hepatic fibrosis
PLoS ONE·2018· 16 citedOpen Access
Myelin Basic Protein Citrullination, a Hallmark of Central Nervous System Demyelination, Assessed by Novel Monoclonal Antibodies in Prion Diseases
Molecular Neurobiology·2017· 22 cited
Upregulation of Connexin 43 Expression Via  <i>C</i> -Jun N-Terminal Kinase Signaling in Prion Disease
Journal of Alzheimer s Disease·2015· 5 cited
Mass spectrometric identification of citrullination sites and immunohistochemical detection of citrullinated glial fibrillary acidic protein in Alzheimer's disease brains
Journal of Neuroscience Research·2015· 70 cited
Peptidylarginine deiminase modulates the physiological roles of enolase via citrullination
The FASEB Journal·2013
Pathological characterization of TgElk mice injected with brain homogenate from elk with chronic wasting disease
Journal of Veterinary Science·2013· 6 citedOpen Access
Familial Creutzfeldt–Jakob disease with a mutation at codon 180 presenting with an atypical phenotype
Journal of Clinical Neuroscience·2012· 13 citedOpen Access
Peptidylarginine deiminase modulates the physiological roles of enolase via citrullination: links between altered multifunction of enolase and neurodegenerative diseases
Biochemical Journal·2012· 37 cited
Dura Mater Graft-Associated Creutzfeldt-Jakob Disease: The First Case in Korea
Journal of Korean Medical Science·2011· 24 citedOpen Access
A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome
Human Molecular Genetics·2010· 19 citedOpen Access
Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment
Neuropathology and Applied Neurobiology·2010· 24 cited
Altered expression of type 1 inositol 1,4,5-trisphosphate receptor in the Ngsk Prnp deficient mice
Neuroscience·2010· 3 cited
Association of endothelial nitric oxide synthase and mitochondrial dysfunction in the hippocampus of scrapie‐infected mice
Hippocampus·2010· 33 cited
Involvement of peptidylarginine deiminase-mediated post-translational citrullination in pathogenesis of sporadic Creutzfeldt-Jakob disease
Acta Neuropathologica·2009· 65 cited
Spontaneous immortalization of oligodendroglial cells derived from an SV40 T antigen-positive human glioblastoma multiforme
Cancer Letters·2009· 3 cited
P4‐235: Altered expression of type 1 inositol 1,4,5 trisphosphate receptor in the Ngsk PRNP deficient mice
Alzheimer s & Dementia·2008
Clinical Usefulness of Proton Pump Inhibitor Intravenous Treatment in Bleeding Peptic Ulcer
Clinical Endoscopy·2007
Nonenzymatic Glycation at the N Terminus of Pathogenic Prion Protein in Transmissible Spongiform Encephalopathies
Journal of Biological Chemistry·2004· 41 citedOpen Access

Frequent Co-authors

Yong‐Sun Kim(13), Eun‐Kyoung Choi(11), Richard I. Carp(11), Byungki Jang(7), Akihito Ishigami(6), Jin-Kyu Choi(5), Byung‐Hoon Jeong(5), Naoki Maruyama(4), Jae‐Il Kim(3), Seok‐Joo Park(3), Hee‐Jun Kim(3), Jae‐Kwang Jin(2), Han Jeong Cho(2), Jeong‐Ho Park(2), Boe‐Hyun Kim(2), Hae‐Young Shin(2), Hae-Young Shin(2), Hyun‐Pil Lee(2), Sung Eun Kim(2), Ji Won Park(2)