Remarkable increases of α1-antichymotrypsin in brain tissues of rodents during prion infection

Keywords

Colocalization, Scrapie, Biology, Immunohistochemistry, Microglia

References

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Cited by

• Significant enhanced expressions of aquaporin-1, -4 and -9 in the brains of various prion diseasesQi Shi, Yue-Zhang Wu, Xuehua Yang — 2019
• Global profiles of a cetylated proteins in the brains of scrapie agents 139A- and ME7-infected mice collected at mid-early, mid-late and terminal stageQi Shi, Dongdong Chen, Adalaiti Maimaitiming — 2020
• Association of α-1-antichymotrypsin expression with the development of conformational changes of Tau protein in Alzheimer's disease brain.Perla H. Horta‐López, Graciela Mendoza-Franco, Fanny Rodríguez‐Cruz — 2022
• Serpin Signatures in Prion and Alzheimer’s DiseasesMarco Zattoni, Marika Mearelli, Silvia Vanni — 2022
• Alpha-1-antichymotrypsin as a novel biomarker for diagnosis, prognosis, and therapy prediction in human diseasesYanxia Jin, Weidong Wang, Qiyun Wang — 2022
• Innovative Non-PrP-Targeted Drug Strategy Designed to Enhance Prion ClearanceArianna Colini Baldeschi, Marco Zattoni, Silvia Vanni — 2022
• Activation of Innate Immunity and Autophagy in Brain Tissues with Prion Disease and Degradation of Abnormal PrPs in Cells — China’s StudiesCao Chen, Qi Shi, Kang Xiao — 2022
• Molecules of senescent glial cells differentiate Alzheimer’s disease from ageingLinbin Dai, Feng Gao, Qiong Wang — 2023
• Accumulation of Prion Triggers the Enhanced Glycolysis via Activation of AMKP Pathway in Prion-Infected Rodent and Cell ModelsQin Fan, Kang Xiao, A Ruhan — 2023
• Diagnosis in Scrapie: Conventional Methods and New BiomarkersDiego Sola, Marina Betancor, P Lorente — 2023

Related papers

• TRANSGENIC MICE EXPRESSING HAMSTER PRION PROTEIN PRODUCE SPECIES -SPECIFIC SCRAPIE INFECTIVITY AND AMYLOID PLAQUES: 152Michael Scott, Dallas Foster, C. Mirenda — 1990
• Astrocyte‐specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapieAlex J. Raeber, Richard E. Race, Sebastian Brandner — 1997
• Long-Term Subclinical Carrier State Precedes Scrapie Replication and Adaptation in a Resistant Species: Analogies to Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease in HumansRichard Race, A Raines, Gregory J. Raymond — 2001
• An Alternative Pretreatment Procedure in Animal Transmissible Spongiform Encephalopathies Diagnosis Using PrPsc ImmunohistochemistryAnna Bencsik, Sabine Debeer, Thierry Baron — 2005
• IMMUNO-GOLD LABELING OF FILAMENTOUS STRUCTURES ANTIGENICALLY RELATED TO THE PRION PROTEIN WITH SCRAPIE INFECTED HAMSTER BRAINSClayton A. Wiley, P. G. Burrola, Michael J. Buchmeier — 1986
• Partitioning of human and sheep forms of the pathogenic prion protein during the purification of therapeutic proteins from human plasmaChristopher J. Stenland, Douglas C. Lee, Paul Brown — 2002
• Different isoforms of human FcRII distinguished by CDw32 antibodies.Kingsley Micklem, W P Stross, A.C. Willis — 1990
• Comparison of Immunohistochemistry and Two Rapid Tests for Detection of Abnormal Prion Protein in Different Brain Regions of Sheep with Typical ScrapieRosa Bolea, Eva Monleón, Irene Schiller — 2005