Xiangzhu Xiao

发表

Metastable contacts and structural disorder in the estrogen receptor transactivation domain

M. Chance, M. Buck, Wenwei Zheng, 2018 .

Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease

J. Laplanche, J. Langeveld, M. Moudjou, 2013, PLoS ONE.

Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy

J. Langeveld, M. Moudjou, Li Cui, 2021, Pathogens.

Isolation of soluble and insoluble PrP oligomers in the normal human brain.

W. Zou, Jue Yuan, Xiangzhu Xiao, 2012, Journal of visualized experiments : JoVE.

Transmission Characteristics of Variably Protease-Sensitive Prionopathy

J. Torres, P. Gambetti, Qingzhong Kong, 2014, Emerging infectious diseases.

PrP Conformational Transitions Alter Species Preference of a PrP-specific Antibody*

N. Greenspan, J. Langeveld, P. Mcgeer, 2010, The Journal of Biological Chemistry.

A novel human disease with abnormal prion protein sensitive to protease

T. Montine, K. Marder, D. Dickson, 2008, Annals of neurology.

Short Communication Failure to Detect the Presence of Prions in the Uterine and Gestational Tissues from a Gravida with Creutzfeldt-Jakob Disease

B. Ghetti, G. MacLennan, J. McGeehan, 2009 .

Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.

B. Ghetti, G. MacLennan, J. McGeehan, 2009, The American journal of pathology.

Characterization of physiochemical properties of caveolin-1 from normal and prion-infected human brains.

Li Cui, Jiachun Feng, Zhiqian Dong, 2017, Oncotarget.

Prions in Variably Protease-Sensitive Prionopathy: An Update

J. Langeveld, L. Pirisinu, P. Gambetti, 2013, Pathogens.

Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains*

J. McGeehan, G. Kneale, P. Gambetti, 2006, Journal of Biological Chemistry.

Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease

J. Laplanche, J. Langeveld, M. Moudjou, 2013, PloS one.

Protease-sensitive prions with 144-bp insertion mutations

P. Gambetti, Heming Wang, Qingzhong Kong, 2013, Aging.

Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein

B. Crain, D. Dickson, N. Cairns, 2010, Annals of neurology.

Structural attributes of mammalian prion infectivity: Insights from studies with synthetic prions

W. Surewicz, J. Bohon, J. Kiselar, 2018, The Journal of Biological Chemistry.

Sequence-dependent Prion Protein Misfolding and Neurotoxicity*

D. Rincon-Limas, S. Casas-Tintó, P. Fernandez-Funez, 2010, The Journal of Biological Chemistry.

Artificial strain of human prions created in vitro

W. Surewicz, Qingzhong Kong, Shugui Chen, 2018, Nature Communications.

Characterization of spontaneously generated prion-like conformers in cultured cells

M. Moudjou, H. Laude, R. Petersen, 2011, Aging.

Synthetic Aβ peptides acquire prion-like properties in the brain

Qingzhong Kong, H. Fujioka, G. Puoti, 2014, Oncotarget.

Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old

J. Morris, N. Cairns, R. Schmidt, 2014, Alzheimer disease and associated disorders.

Insoluble cellular prion protein and its association with prion and Alzheimer diseases

W. Zou, Jue Yuan, Xiangzhu Xiao, 2011, Prion.

Structural Determinants of Phenotypic Diversity and Replication Rate of Human Prions

Wei Chen, W. Surewicz, M. E. Kabir, 2015, PLoS pathogens.

Classification of sporadic Creutzfeldt-Jakob disease revisited.

R. Castellani, P. Gambetti, Piero Parchi, 2006, Brain : a journal of neurology.

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

W. Surewicz, Anuradha Bharara Singh, P. Gambetti, 2020, Acta Neuropathologica Communications.

Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments

B. Ghetti, W. Surewicz, P. Gambetti, 2019, Acta Neuropathologica Communications.

Recombinant Human Prion Protein Inhibits Prion Propagation in vitro

J. Steyaert, J. Castilla, W. Surewicz, 2013, Scientific Reports.

Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease

E. Uro-Coste, P. Brown, J. Ironside, 2014, Journal of clinical & cellular immunology.

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

W. Surewicz, Anuradha Bharara Singh, P. Gambetti, 2020, Acta Neuropathologica Communications.

Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments

B. Ghetti, W. Surewicz, P. Gambetti, 2019, Acta Neuropathologica Communications.

Post-translational modifications in PrP expand the conformational diversity of prions in vivo

C. Sigurdson, K. Nilsson, J. Castilla, 2017, Scientific Reports.

Alkylating Antitumor Drug Mechlorethamine Conceals A Structured PrP Domain and Inhibits in Vitro Prion Amplification

J. Wong, M. Shimoji, W. Zou, 2011, Journal of toxicology and environmental health. Part A.

Amyloid-β42 Interacts Mainly with Insoluble Prion Protein in the Alzheimer Brain*

Hyoung-Gon Lee, Xiongwei Zhu, Mark A. Smith, 2011, The Journal of Biological Chemistry.

A Metastable Contact and Structural Disorder in the Estrogen Receptor Transactivation Domain.

Prashansa Agrawal, Mark R. Chance, Matthias Buck, 2019, Structure.

Artificial strain of human prions created in vitro

W. Surewicz, Qingzhong Kong, Shugui Chen, 2018, Nature Communications.

Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

P. Mcgeer, W. Surewicz, J. McGeehan, 2008, Cellular and Molecular Life Sciences.

Sequence-dependent Prion Protein Misfolding and Neurotoxicity*

D. Rincon-Limas, S. Casas-Tintó, P. Fernandez-Funez, 2010, The Journal of Biological Chemistry.

Characterization of spontaneously generated prion-like conformers in cultured cells

M. Moudjou, H. Laude, R. Petersen, 2011, Aging.

A metastable contact and structural disorder in the estrogen receptor transactivation domain

M. Chance, M. Buck, Wenwei Zheng, 2018, bioRxiv.

Variant Creutzfeldt-Jakob Disease

Qingzhong Kong, M. Shimoji, W. Zou, 2010 .