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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 5
  • Printing - »õâ
    Synonyms :
  • Prion Diseases - »õâ A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
    Synonyms : Encephalopathies, Spongiform, Transmissible, Human Transmissible Spongiform Encephalopathies, Inherited, Inherited Human Transmissible Spongiform Encephalopathies, Prion Protein Diseases, Prion-Induced Disorder, Transmissible Spongiform Encephalopathies
  • Prions - »õâ Small proteinaceous infectious particles which resist inactivation by procedures that modify NUCLEIC ACIDS and contain an abnormal isoform of a cellular protein which is a major and necessary component. The abnormal (scrapie) isoform is PrPSc (PRPSC PROTEINS) and the cellular isoform PrPC (PRPC PROTEINS). The primary amino acid sequence of the two isoforms is identical. Human diseases caused by prions include CREUTZFELDT-JAKOB SYNDROME; GERSTMANN-STRAUSSLER SYNDROME; and INSOMNIA, FATAL FAMILIAL.
    Synonyms : Encephalopathy Virus, Mink
  • Prisoners - »õâ
    Synonyms : Hostage, Prisoner
  • Prisons - »õâ Penal institutions, or places of confinement for war prisoners.
    Synonyms : Prison
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 5
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