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Tests of selection for PRND and PRNP genes.
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创建时间：
2016-05-26
相关数据集
In vivo base editing extends lifespan of a humanized mouse model of prion disease
Prion disease is a fatal neurodegenerative disease caused by the misfolding of prion protein (PrP) encoded by the PRNP gene. While there is currently no cure for the disease, depleting PrP in the brai
NIAID Data Ecosystem80
Additional file 7 of Contrasting genetic variation and positive selection followed the divergence of NBS-encoding genes in Asian and European pears
Additional file 7. Ka/Ks ratios of orthologous gene pairs between P. bretschneideri and P. communis. ‘NA’ means no values.
Figshare2020-11-19 更新30
PrP(Sc) Is Not Detected in Peripheral Blood Leukocytes of Scrapie-Infected Sheep: Determining the Limit of Sensitivity by Immunohistochemistry
Peripheral blood leukocytes (PBLs) from scrapie-infected sheep were evaluated for the presence of PrP(Sc) by using dissociated retropharyngeal lymph node (DRLN) cells and immunohistochemistry (IHC). P
PubMed Central20
The Features of Genetic Prion Diseases Based on Chinese Surveillance Program
ObjectiveTo identify the features of Chinese genetic prion diseases.MethodsSuspected Creutzfeldt-Jakob disease (CJD) cases that were reported under CJD surveillance were diagnosed and subtyped using t
Figshare2016-01-15 更新30
Additional file 5 of Dysregulated microRNAs in blood correlate with central nervous system neuropathology of prion disease
Additional file 5. Novel significantly dysregulated miRNAs in blood from preclinical scrapie sheep compared with healthy sheep.
DataCite Commons2025-07-02 更新20
