prion disease - Axtarish в Google
Прионы
Прио́ны — особый класс инфекционных патогенов, не содержащих нуклеиновых кислот. Прионы представляют собой белки с аномальной третичной структурой. Это положение лежит в основе прионной гипотезы, однако насчёт состава прионов существуют и другие... Википедия
МКБ-10 : A81
МКБ-11 : XN7AM
МКБ-9 : 046
Prions are responsible for prion diseases, known as transmissible spongiform encephalopathy (TSEs), which are fatal and transmissible neurodegenerative diseases ...
22 апр. 2024 г. · Prion diseases occur when proteins normally in the body misfold and cause illness. The misfolding leads to brain damage and other symptoms.
Prion diseases comprise several conditions. A prion is a type of protein that can trigger normal proteins in the brain to fold abnormally.
21 янв. 2024 г. · Prion disease is a group of rare, terminal neurodegenerative diseases. They happen when proteins in your brain turn into abnormal proteins ...
17 мая 2024 г. · Prion diseases are transmissible, untreatable, and fatal brain diseases of mammals. Their cause is highly unusual: The host's normal prion ...
Prion diseases are progressive, fatal, and untreatable degenerative brain disorders. Prominent types of prion diseases include. Creutzfeldt-Jakob disease (CJD) ...
16 дек. 2022 г. · Prion diseases are rare, fatal, degenerative brain disorders that are thought to occur worldwide in both humans and animals. They belong to the ...
Prion diseases are neurodegenerative diseases in which a malformed protein, the prion protein, accumulates in neurons and leads to their death. The ...
Prion diseases are caused by abnormal prions, microscopic infectious agents made of protein. Prions cause a number of diseases in a variety of mammals, ...
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