Prion Neurodegeneration

Prion diseases are fatal, transmissible, neurodegenerative diseases caused by the misfolding of the prion protein (prp). Here is the latest research on prion diseases.

January 19, 2022

Comparison of cerebrospinal fluid tau, ptau(181), synuclein, and 14-3-3 for the detection of Creutzfeldt-Jakob disease in clinical practice.

Journal of Neural Transmission
Martin FayolleConstance Delaby
January 17, 2022

Metal Ions Bound to Prion Protein Affect its Interaction with Plasminogen Activation System.

The Protein Journal
Maryam Borumand, Vincent Ellis
January 17, 2022

A case of fatal familial insomnia: diagnostic and therapeutic approaches.

Neurocase
Deborah K Rose, Andy J Liu
January 17, 2022

Ganglioside binding domains in proteins: Physiological and pathological mechanisms.

Advances in Protein Chemistry and Structural Biology
Fodil AzzazJacques Fantini
January 16, 2022

The modulation of neuroinflammation by inducible nitric oxide synthase.

Journal of Cell Communication and Signaling
Alberto Fernando Oliveira Justo, Claudia Kimie Suemoto
January 14, 2022
Review

Body-first Parkinson's disease and variant Creutzfeldt-Jakob disease - similar or different?

Neurobiology of Disease
Amanda L Woerman, Gültekin Tamgüney
January 14, 2022

Braiding Braak and Braak: Staging patterns and model selection in network neurodegeneration.

Network Neuroscience
Prama PutraAlain Goriely
January 14, 2022

A Creutzfeldt-Jakob disease patient with V180I mutation survived for 16.5 years after diagnosis.

Acta neurologica Belgica
Nayoung RyooSangYun Kim
January 14, 2022

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease.

Journal of Neurology, Neurosurgery, and Psychiatry
Akin NihatS. H. Mead
January 13, 2022
Review

Astrocyte in prion disease: a double-edged sword.

Neural Regeneration Research
Waqas TahirHermann M Schatzl
January 13, 2022
Open Access

Apparent stability masks underlying change in a mule deer herd with unmanaged chronic wasting disease.

Communications Biology
Mark C FisherMichael W Miller
January 13, 2022
Case Report

18FDG PET-CT in sporadic Creutzfeldt-Jakob disease, correlated with MRI and histology.

World Journal of Nuclear Medicine
Nicholas C D MorleyKevin M Bradley
January 12, 2022
Preprint
Open Access

The channel activities of the full-length prion and truncated proteins

BioRxiv : the Preprint Server for Biology
J. WuJinghui Luo
January 10, 2022

Prion-like α-synuclein pathology in the brain of infants with Krabbe disease.

Brain : a Journal of Neurology
Christopher HattonDaniel Erskine
January 11, 2022
Case Report

Rarely fast progressive memory loss diagnosed as Creutzfeldt-Jakob disease: A case report.

World Journal of Clinical Cases
Yong-Wei XuYun-Xia Li
January 11, 2022

Treatment of microglia with Anti-PrP monoclonal antibodies induces neuronal apoptosis in vitro.

Heliyon
Utpal Kumar AdhikariMourad Tayebi
January 8, 2022

Examination of the interaction between age-specific predation and chronic disease in the Greater Yellowstone Ecosystem.

The Journal of Animal Ecology
Ellen E BrandellPeter J Hudson
January 7, 2022

AEBP1 as a potential immune-related prognostic biomarker in glioblastoma: a bioinformatic analyses.

Annals of Translational Medicine
Mingjian LiuHanbing Shang
January 7, 2022
Review

Therapeutic strategies for identifying small molecules against prion diseases.

Cell and Tissue Research
Elisa UliassiGiuseppe Legname

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