Codon 129 Polymorphism Specific Cerebrospinal Fluid Proteome Pattern in Sporadic Creutzfeldt−Jakob Disease and the Implication of Glycolytic Enzymes in Prion-Induced Pathology
Author:
Affiliation:
1. National Reference Center for TSE Surveillance, Department of Clinical Chemistry, Department of Nephrology and Rheumatology, and Department of Neuropathology, Medical Center Georg-August University, Goettingen, Germany
Publisher
American Chemical Society (ACS)
Subject
General Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/pr1004604
Reference51 articles.
1. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
2. Sporadic and familial CJD: classification and characterisation
3. Proteome and proteomics: New technologies, new concepts, and new words
4. Abnormal Proteins in the Cerebrospinal Fluid of Patients with Creutzfeldt–Jakob Disease
5. The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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2. Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients;Biomolecules;2019-11-28
3. Cerebrospinal fluid in Creutzfeldt–Jakob disease;Cerebrospinal Fluid in Neurologic Disorders;2018
4. Prion Protein Interactome: Identifying Novel Targets in Slowly and Rapidly Progressive Forms of Alzheimer’s Disease;Journal of Alzheimer's Disease;2017-07-03
5. Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt–Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress;Molecular Neurobiology;2016-12-14
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