Shu G. Chen
Cited by
Cited by
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
P Parchi, R Castellani, S Capellari, B Ghetti, K Young, SG Chen, M Farlow, ...
Annals of neurology 39 (6), 767-778, 1996
Truncated forms of the human prion protein in normal brain and in prion diseases
SG Chen, DB Teplow, P Parchi, JK Teller, P Gambetti, L Autilio-Gambetti
Journal of Biological Chemistry 270 (32), 19173-19180, 1995
Sporadic and familial CJD: classification and characterisation
P Gambetti, Q Kong, W Zou, P Parchi, SG Chen
British medical bulletin 66 (1), 213-239, 2003
Copper mediates dityrosine cross-linking of Alzheimer's amyloid-β
CS Atwood, G Perry, H Zeng, Y Kato, WD Jones, KQ Ling, X Huang, ...
Biochemistry 43 (2), 560-568, 2004
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism
L Monari, SG Chen, P Brown, P Parchi, RB Petersen, J Mikol, F Gray, ...
Proceedings of the National Academy of Sciences 91 (7), 2839-2842, 1994
LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1
X Wang, MH Yan, H Fujioka, J Liu, A Wilson-Delfosse, SG Chen, G Perry, ...
Human molecular genetics 21 (9), 1931-1944, 2012
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans
GJ Raymond, J Hope, DA Kocisko, SA Priola, LD Raymond, A Bossers, ...
Nature 388 (6639), 285-288, 1997
Genetic influence on the structural variations of the abnormal prion protein
P Parchi, W Zou, W Wang, P Brown, S Capellari, B Ghetti, N Kopp, ...
Proceedings of the National Academy of Sciences 97 (18), 10168-10172, 2000
Typing prion isoforms
P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ...
Nature 386 (6622), 232-233, 1997
Aggregation and fibrillization of the recombinant human prion protein huPrP90− 231
W Swietnicki, M Morillas, SG Chen, P Gambetti, WK Surewicz
Biochemistry 39 (2), 424-431, 2000
Interaction between human prion protein and Amyloid-β (Aβ) oligomers role Of N-terminal residues
S Chen, SP Yadav, WK Surewicz
Journal of Biological Chemistry 285 (34), 26377-26383, 2010
Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models
Q Kong, S Huang, W Zou, D Vanegas, M Wang, D Wu, J Yuan, M Zheng, ...
Journal of Neuroscience 25 (35), 7944-7949, 2005
The Parkinson’s disease-associated protein, leucine-rich repeat kinase 2 (LRRK2), is an authentic GTPase thatstimulates kinase activity
L Guo, PN Gandhi, W Wang, RB Petersen, AL Wilson-Delfosse, SG Chen
Experimental cell research 313 (16), 3658-3670, 2007
Fatal familial insomnia and familial Creutzfeldt‐Jakob disease: clinical, pathological and molecular features
P Gambetti, P Parchi, RB Petersen, SG Chen, E Lugaresi
Brain pathology 5 (1), 43-51, 1995
Aberrant metal binding by prion protein in human prion disease
BS Wong, SG Chen, M Colucci, Z Xie, T Pan, T Liu, R Li, P Gambetti, ...
Journal of neurochemistry 78 (6), 1400-1408, 2001
Tau gene mutation in familial progressive subcortical gliosis
M Goedert, MG Spillantini, RA Crowther, SG Chen, P Parchi, M Tabaton, ...
Nature medicine 5 (4), 454-457, 1999
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann–Sträussler–Scheinker disease
P Parchi, SG Chen, P Brown, W Zou, S Capellari, H Budka, J Hainfellner, ...
Proceedings of the National Academy of Sciences 95 (14), 8322-8327, 1998
The Roc domain of leucine‐rich repeat kinase 2 is sufficient for interaction with microtubules
PN Gandhi, X Wang, X Zhu, SG Chen, AL Wilson‐Delfosse
Journal of neuroscience research 86 (8), 1711-1720, 2008
Regional distribution of protease‐resistant prion protein in fatal familial insomnia
P Parchi, R Castellani, P Cortelli, P Montagna, SG Chen, RB Petersen, ...
Annals of Neurology: Official Journal of the American Neurological …, 1995
Inherited prion diseases
Q Kong, WK Surewicz, RB Petersen, W Zou, SG Chen, P Gambetti, ...
The system can't perform the operation now. Try again later.
Articles 1–20