Add to ORKGTato bakalářská práce je zaměřena na prionová onemocnění. Cílem práce bylo shrnutí poznatků o těchto chorobách. Prionózy jsou v práci rozděleny do dvou skupin (humánní a animální) a jsou detailně popsány. Jednou z částí bakalářské práce je i kapitola zabývající se diagnostikou prionóz a možnostmi jejich léčby.This bachelor thesis is focused on prion diseases. The aim was to summarize knowledges about these diseases. In this thesis are diseases described in detail and divided into two groups (human diseases and animal diseases). One part of the thesis is chapter dealing with diagnosis and treatment of these diseases.Fakulta chemicko-technologick
scrapie, feline Protein prion pascatranslasi menjadilemba suatu chaperone. Dalam dua dekade terakhir...
Prion protein (PrPC) is connected with the origin of transmissive spongiform encephalopathies (TSEs)...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Choroby prionowe należą do grupy rzadkich, śmiertelnych zaburzeń neurodegeneracyjnych. Są one spowod...
Goveđa spongiformna encefalopatija i grebež najpoznatije su prionske bolesti od kojih obolijevaju ...
Choroby prionowe to grupa chorób ultrarzadkich – dotyczą zaledwie 1-2 osoby na milion. Choroby tego ...
Prioni (engl. proteinaceous infectious particle) su sitne, zarazne proteinske čestice koje uzrokuju ...
Prions are protein infectious particles in absence of nucleic acid, responsible for the fatal transm...
Human prion disease is divided into three broad classes: idiopathic, genetic and acquired, reflectin...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
W pracy omówiono problemy dotyczące nowego rodzaju zagrożeń biologicznych. Przedstawiono historię ba...
Charles University in Prague, Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
The article discusses the current views on the causes of various types of slow infections and their ...
A prion is a small infectious particle, which resist inactivation by procedures that modify nucleic ...
Abstract Prion diseases are transmissible neurodegenerative conditions affecting human and a wide ra...
scrapie, feline Protein prion pascatranslasi menjadilemba suatu chaperone. Dalam dua dekade terakhir...
Prion protein (PrPC) is connected with the origin of transmissive spongiform encephalopathies (TSEs)...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...
Choroby prionowe należą do grupy rzadkich, śmiertelnych zaburzeń neurodegeneracyjnych. Są one spowod...
Goveđa spongiformna encefalopatija i grebež najpoznatije su prionske bolesti od kojih obolijevaju ...
Choroby prionowe to grupa chorób ultrarzadkich – dotyczą zaledwie 1-2 osoby na milion. Choroby tego ...
Prioni (engl. proteinaceous infectious particle) su sitne, zarazne proteinske čestice koje uzrokuju ...
Prions are protein infectious particles in absence of nucleic acid, responsible for the fatal transm...
Human prion disease is divided into three broad classes: idiopathic, genetic and acquired, reflectin...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
W pracy omówiono problemy dotyczące nowego rodzaju zagrożeń biologicznych. Przedstawiono historię ba...
Charles University in Prague, Faculty of Pharmacy in Hradec Králové Department of Biological and Med...
The article discusses the current views on the causes of various types of slow infections and their ...
A prion is a small infectious particle, which resist inactivation by procedures that modify nucleic ...
Abstract Prion diseases are transmissible neurodegenerative conditions affecting human and a wide ra...
scrapie, feline Protein prion pascatranslasi menjadilemba suatu chaperone. Dalam dua dekade terakhir...
Prion protein (PrPC) is connected with the origin of transmissive spongiform encephalopathies (TSEs)...
Prion diseases are caused by a misfolded protein which have the uncanny ability to escape destructio...