Prusiner called that nonliving, infectious protein a “prion.” Does CWD threaten humans?

Each is photographed ... [+] separately. Prion diseases are rare but deadly neurodegenerative brain diseases that result from misfolding protein.

“FUS oncofusion protein condensates recruit mSWI/SNF chromatin remodeler via heterotypic interactions between prion-like domains.” The team showed

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Some prion diseases, such as Creutzfeldt-Jakob disease (CJD), can arise sporadically or from an inherited mutation in the prion protein.

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As chronic wasting disease continues to spread among deer farms and wild deer, the state agriculture agency has depopulated a farm in Antigo.

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Russia will pay ‘compensation’ for the devastation caused in Ukraine, President Volodymyr Zelensky has vowed.

The farm and its herd are under quarantine while an epidemiological investigation is conducted by the state department of agriculture and U.S.

Rep. Madison Cawthorn will have plenty of time to use that two-for-one VIP pass he picked up on his last vacation trip to Berchtesgaden.

Dana Milbank of the Washington Post calls our attention to a scarifying but necessary report produced by Institute for Research and Education on Hu

Whi3 is a mnemon (Whi3mnem), or in other words, a protein that stores information in individual cells by forming stable super-assemblies.

Recent research sheds light on the importance of p38 MAPKα in the neurodegenerative pathway of prion diseases.

With proliferation of advanced technologies in the diagnostics sector, early diagnosis of rare diseases such as human prion disease is no more a to

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The Genetic and Rare Disease Information Center from the National Center for Advancing Translational Sciences reports that “FFI is an inherited pri

Chronic Wasting Disease has been found in deer herds in two Canadian provinces.

A strange and highly communicable disease is spreading through the deer population in Canada.

Minnesota lawmakers will try to block new captive deer farms from opening in an attempt to stop or slow the spread of chronic wasting disease (CWD)

Almost two decades have passed since Stanley Prusiner proposed that the transmissible agent causing spongiform encephalopathies consists of a misfo

To view this video please enable JavaScript, and consider upgrading to a web browser that supports HTML5 video The 3D structure of an infectious pr

The researchers noted that the genetic forms of Creutzfeldt-Jakob disease generally would be identified using results of genetic testing for mutati

working to understand genetic variants of the prion protein in order to protect against prion disease The Utah Foundation for Biomedical Research: