Titlebook: Bovine Spongiform Encephalopathy; The BSE Dilemma Clarence J. Gibbs Book 1996 Springer-Verlag New York, Inc. 1996 BSE.biochemistry.genetics

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書目名稱Bovine Spongiform Encephalopathy影響因子(影響力)




書目名稱Bovine Spongiform Encephalopathy影響因子(影響力)學(xué)科排名




書目名稱Bovine Spongiform Encephalopathy網(wǎng)絡(luò)公開(kāi)度




書目名稱Bovine Spongiform Encephalopathy網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書目名稱Bovine Spongiform Encephalopathy被引頻次




書目名稱Bovine Spongiform Encephalopathy被引頻次學(xué)科排名




書目名稱Bovine Spongiform Encephalopathy年度引用




書目名稱Bovine Spongiform Encephalopathy年度引用學(xué)科排名




書目名稱Bovine Spongiform Encephalopathy讀者反饋




書目名稱Bovine Spongiform Encephalopathy讀者反饋學(xué)科排名

Additive

FLIP

鑲嵌細(xì)工

輕率看法

Experimental Transmission of Scrapie to Cattleof the National Renderers Association, the National Cattlemen’s Association, the National Milk Producers Federation, the American Sheep Industry Association, and the Food and Drug Administration, this project was undertaken to determine if the U.S. scrapie agent(s) could be transmitted to cattle and

火車車輪

Prion Strains and Neuromuscular Disease in PrP Transgenic Miceonal derivative of the normal prion protein isoform, PrP.(4). Beta-pleated sheet secondary structure predominates in PrP., with little, if any, found in PrP., and the two isoforms may differ only in their conformations (5, 6). PrP. is necessary, and probably sufficient, for transmission of scrapie.

compel

Book 1996entral nervous system and after fungi and bacteria had been incriminated in impor- tant chronic disorders of the nervous system such as torula and tuberculosis men- ingitis, we have been left, in neurology, with a wide range of subacute and chronic affections of the central nervous systems of unknow

預(yù)防注射

Basal-Ganglia

https://doi.org/10.1007/978-3-7985-1947-3 (FFI), transmissible mink encephalopathy (TME), chronic wasting disease (CWD), bovine spongiform encephalopathy (BSE)—transmissible cerebral amyloidosis. Normal aging of the brain, Alzheimer’s disease, and dementias of Down syndrome are nontransmissible amyloidoses based on a different precursor protein.

饑荒

Meinolf Bachmann,Andrada El-Akhraslosely related causative agents, these diseases are expected to differ clinically and neurohistologically. Defining them in terms of their similarities and differences would provide a clearer picture of their distinguishing features in comparative studies that include the related human diseases and all the experimental counterparts (3).