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Progress on low susceptibility mechanisms of transmissible spongiform encephalopathiesShadoo/PrP (Sprn(0/0) /Prnp(0/0) ) double knockout mice: more than zeroesAn overview of human prion diseasesPrion protein interaction with soil humic substances: environmental implicationsIs the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?The Malignant Protein Puzzle.Bovine Brain: An in vitro Translational Model in Developmental Neuroscience and Neurodegenerative ResearchPrion protein genotypes of sheep as determined from 3343 samples submitted from Ontario and other provinces of Canada from 2005 to 2012.A review of luteinising hormone and human chorionic gonadotropin when used in assisted reproductive technology.Lesion profiling and subcellular prion localization of cervid chronic wasting disease in domestic cats.Susceptibility of domestic cats to chronic wasting diseasePrion protein scrapie and the normal cellular prion proteinNetwork analysis of human post-mortem microarrays reveals novel genes, microRNAs, and mechanistic scenarios of potential importance in fighting huntington's disease.Could avian scavengers translocate infectious prions to disease-free areas initiating new foci of chronic wasting disease?Procedures for identifying infectious prions after passage through the digestive system of an avian species.A concise review of amyloidosis in animals.Proteolytic processing of the prion protein in health and disease.Significant reduction of the GLUT3 level, but not GLUT1 level, was observed in the brain tissues of several scrapie experimental animals and scrapie-infected cell lines.Functional genomics approach for identification of molecular processes underlying neurodegenerative disorders in prion diseases.Fixed differences in the 3'UTR of buffalo PRNP gene provide binding sites for miRNAs post-transcriptional regulationJellyfish collagen matrices conserve the chondrogenic phenotype in two- and three-dimensional collagen matrices.Shedding light on prion disease.Neuronal Vacuolization in Feline Panleukopenia Virus Infection.The mechanisms of humic substances self-assembly with biological molecules: The case study of the prion protein.Behind the potential evolution towards prion resistant species.Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
An overview of animal prion diseases.
@ast
An overview of animal prion diseases.
@en
type
label
An overview of animal prion diseases.
@ast
An overview of animal prion diseases.
@en
prefLabel
An overview of animal prion diseases.
@ast
An overview of animal prion diseases.
@en
P2860
P356
P1433
P1476
An overview of animal prion diseases.
@en
P2093
Muhammad Imran
Saqib Mahmood
P2860
P2888
P356
10.1186/1743-422X-8-493
P5008
P577
2011-11-01T00:00:00Z
P6179
1042911633