Lista de obras - Shu Chen - Dominio Público Uruguay

Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease

artículo científico publicado en 2001

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

artículo científico publicado en 2000

Antibody to DNA detects scrapie but not normal prion protein

artículo científico publicado en 2004

Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2012

CD3 in Lewy pathology: does the abnormal recall of neurodevelopmental processes underlie Parkinson's disease

artículo científico publicado en 2010

Characterization of the prion protein in human urine

artículo científico publicado en 2010

Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein ⬇️

artículo científico publicado en 2005

Copper mediates dityrosine cross-linking of Alzheimer's amyloid-beta

artículo científico publicado en 2004

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

artículo científico publicado en 2005

Cryptic peptides of the kringle domains preferentially bind to disease-associated prion protein.

artículo científico publicado en 2009

Diagnostic value of skin RT-QuIC in Parkinson's disease: a two-laboratory study

artículo científico publicado en 2021

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

artículo científico publicado en 1998

Ectopic localization of FOXO3a protein in Lewy bodies in Lewy body dementia and Parkinson's disease

scientific article published on 23 July 2009

Exposure to the Functional Bacterial Amyloid Protein Curli Enhances Alpha-Synuclein Aggregation in Aged Fischer 344 Rats and Caenorhabditis elegans

scientific article published on 06 October 2016

Expression and structural characterization of the recombinant human doppel protein

artículo científico publicado en 2000

FadA from Fusobacterium nucleatum utilizes both secreted and nonsecreted forms for functional oligomerization for attachment and invasion of host cells

artículo científico publicado en 2007

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

artículo científico publicado en 1995

Genetic influence on the structural variations of the abnormal prion protein

scientific article published on August 2000

Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits

artículo científico publicado en 2006

Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson's disease

artículo científico publicado en 2014

Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.

artículo científico publicado en 2003

Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease

artículo científico publicado en 2003

Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice

artículo científico publicado en 2007

Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function

artículo científico publicado en 2001

Is nitric oxide a key target in the pathogenesis of brain lesions during the development of Alzheimer's disease?

artículo científico publicado en 2004

Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity

artículo científico publicado en 2012

LRRK2 in Parkinson's disease and dementia with Lewy bodies

artículo científico publicado en 2006

LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1

artículo científico publicado en 2012

LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's disease

artículo científico publicado en 2010

Leucine-rich repeat kinase 2 (LRRK2): a key player in the pathogenesis of Parkinson's disease

artículo científico publicado en 2009

Leucine-rich repeat kinase 2 colocalizes with alpha-synuclein in Parkinson's disease, but not tau-containing deposits in tauopathies

artículo científico publicado en 2008

Leucine-rich repeat kinase 2: relevance to Parkinson's disease

artículo científico publicado en 2006

Mitochondria DNA deletions in atherosclerotic hypoperfused brain microvessels as a primary target for the development of Alzheimer's disease

artículo científico publicado en 2004

Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats

artículo científico publicado en 2008

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

artículo científico publicado en 2001

Paradoxical role of prion protein aggregates in redox-iron induced toxicity

artículo científico publicado en 2010

Penicillin sulfone inhibitors of class D beta-lactamases

artículo científico publicado en 2010

Prion protein functions as a ferrireductase partner for ZIP14 and DMT1.

artículo científico publicado en 2015

Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine.

artículo científico publicado en 2004

Regional distribution of protease-resistant prion protein in fatal familial insomnia

artículo científico publicado en 1995

Regulation of DJ-1 by Glutaredoxin 1 in Vivo: Implications for Parkinson's Disease

artículo científico publicado en 2016

Selection and characterization of DNA aptamers against PrPSc

artículo científico publicado en 2011

Skin α-Synuclein Aggregation Seeding Activity as a Novel Biomarker for Parkinson Disease

scientific article published on 28 September 2020

Sporadic and familial CJD: classification and characterisation.

artículo científico publicado en 2003

Tau gene mutation in familial progressive subcortical gliosis

artículo científico publicado en 1999

The Parkinson's disease-associated protein, leucine-rich repeat kinase 2 (LRRK2), is an authentic GTPase that stimulates kinase activity

artículo científico publicado en 2007

The Roc domain of leucine-rich repeat kinase 2 is sufficient for interaction with microtubules

artículo científico publicado en 2008

Typing prion isoforms.

artículo científico publicado en 1997

Lista de obras de Shu Chen

Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

Antibody to DNA detects scrapie but not normal prion protein

Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob disease

CD3 in Lewy pathology: does the abnormal recall of neurodevelopmental processes underlie Parkinson's disease

Characterization of the prion protein in human urine

Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein ⬇️

Copper mediates dityrosine cross-linking of Alzheimer's amyloid-beta

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

Cryptic peptides of the kringle domains preferentially bind to disease-associated prion protein.

Diagnostic value of skin RT-QuIC in Parkinson's disease: a two-laboratory study

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

Ectopic localization of FOXO3a protein in Lewy bodies in Lewy body dementia and Parkinson's disease

Exposure to the Functional Bacterial Amyloid Protein Curli Enhances Alpha-Synuclein Aggregation in Aged Fischer 344 Rats and Caenorhabditis elegans

Expression and structural characterization of the recombinant human doppel protein

FadA from Fusobacterium nucleatum utilizes both secreted and nonsecreted forms for functional oligomerization for attachment and invasion of host cells

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

Genetic influence on the structural variations of the abnormal prion protein

Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits

Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson's disease

Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.

Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease

Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice

Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function

Is nitric oxide a key target in the pathogenesis of brain lesions during the development of Alzheimer's disease?

Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity

LRRK2 in Parkinson's disease and dementia with Lewy bodies

LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1

LRRK2-mediated neurodegeneration and dysfunction of dopaminergic neurons in a Caenorhabditis elegans model of Parkinson's disease

Leucine-rich repeat kinase 2 (LRRK2): a key player in the pathogenesis of Parkinson's disease

Leucine-rich repeat kinase 2 colocalizes with alpha-synuclein in Parkinson's disease, but not tau-containing deposits in tauopathies

Leucine-rich repeat kinase 2: relevance to Parkinson's disease

Mitochondria DNA deletions in atherosclerotic hypoperfused brain microvessels as a primary target for the development of Alzheimer's disease

Neuronal mitochondrial amelioration by feeding acetyl-L-carnitine and lipoic acid to aged rats

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

Paradoxical role of prion protein aggregates in redox-iron induced toxicity

Penicillin sulfone inhibitors of class D beta-lactamases

Prion protein functions as a ferrireductase partner for ZIP14 and DMT1.

Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine.

Regional distribution of protease-resistant prion protein in fatal familial insomnia

Regulation of DJ-1 by Glutaredoxin 1 in Vivo: Implications for Parkinson's Disease

Selection and characterization of DNA aptamers against PrPSc

Skin α-Synuclein Aggregation Seeding Activity as a Novel Biomarker for Parkinson Disease

Sporadic and familial CJD: classification and characterisation.

Tau gene mutation in familial progressive subcortical gliosis

The Parkinson's disease-associated protein, leucine-rich repeat kinase 2 (LRRK2), is an authentic GTPase that stimulates kinase activity

The Roc domain of leucine-rich repeat kinase 2 is sufficient for interaction with microtubules

Typing prion isoforms.