<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-7M1L98AK/4fb99a4f-e371-4d9c-a4ee-cef36378a256/PDF"><dcterms:extent>351 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-7M1L98AK/5a87ddf4-8af5-423d-a787-17701d8403d3/TEXT"><dcterms:extent>30 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1994-2025"><edm:begin xml:lang="en">1994</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:doc-7M1L98AK"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-46R7GGHL" /><dcterms:issued>2008</dcterms:issued><dc:creator>Gazić, Barbara</dc:creator><dc:creator>Popović, Mara</dc:creator><dc:format xml:lang="sl">številka:4</dc:format><dc:format xml:lang="sl">letnik:47</dc:format><dc:format xml:lang="sl">str. 391-402</dc:format><dc:identifier>ISSN:0025-8121</dc:identifier><dc:identifier>COBISSID:25579481</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-7M1L98AK</dc:identifier><dc:language>sl</dc:language><dc:publisher xml:lang="sl">Medicinski razgledi</dc:publisher><dcterms:isPartOf xml:lang="sl">Medicinski razgledi</dcterms:isPartOf><dc:subject xml:lang="sl">Alzheimerjeva bolezen</dc:subject><dc:subject xml:lang="en">Alzheimer'S Disease</dc:subject><dc:subject xml:lang="sl">Amiloidoza</dc:subject><dc:subject xml:lang="sl">Amiotrofična, lateralna skleroza</dc:subject><dc:subject xml:lang="en">Amyloidosis</dc:subject><dc:subject xml:lang="en">Amyotrophic Lateral Sclerosis</dc:subject><dc:subject xml:lang="sl">degenerativne bolezni</dc:subject><dc:subject xml:lang="en">Nerve Degeneration</dc:subject><dc:subject xml:lang="en">Paraproteinemias</dc:subject><dc:subject xml:lang="sl">Paraproteinemije</dc:subject><dc:subject xml:lang="en">Parkinson Disease</dc:subject><dc:subject xml:lang="sl">Parkinsonova bolezen</dc:subject><dc:subject xml:lang="sl">proteinopatije</dc:subject><dc:subject xml:lang="sl">živčevje</dc:subject><dc:subject xml:lang="sl">Živec, degeneracija</dc:subject><dc:subject rdf:resource="http://www.wikidata.org/entity/Q9404" /><dcterms:temporal rdf:resource="1994-2025" /><dc:title xml:lang="sl">Proteinopatije - bolezni odlaganja napačno zvitih beljakovin| Proteinopathies - diseases involving deposition of misfolded proteins|</dc:title><dc:description xml:lang="sl">Proteinopathies are protein deposition diseases caused by misfolded proteins. Molecules of misfolded proteins are prone to aggregate and damage the tissue, and eventually they may kill the patient if a vital organ is affected. There are many causes of protein misfolding, including gene mutations, failure in gene transcription or post-translational protein folding despite normal primary structure, protein overproduction and aberrant proteolysis. Risk factors for non-genetic proteinopathies are ageing, certain chronic diseases, certain tumors and dialysis. Misfolded protein could be deposited in the extracellular matrix or inside the cells, forming different inclusions. So far, more than 25 proteins have been identified to be prone to misfold and cause the disease. Based on the structural and tinctorial properties of misfolded protein aggregates, proteinopathies are divided to amyloidoses and non-amyloid proteinopathies. Proteinopathies can be systemic or localized, when several or only one organ is involved, respectively. The most frequent systemic proteinopathy is systemic amyloidosis which involves the deposition of immunoglobulin light chains, and the most frequent localised proteinopathy is Alzheimer's disease. Proteinopathies can be named by the misfolded proteins: monoclonal immunoglobulin deposition disease, tauopathies, synucleinopathies, prionopathies etc. Proteinopathies are progressive diseases, but most of them are so far incurable</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:doc-7M1L98AK"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:doc-7M1L98AK" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:doc-7M1L98AK/4fb99a4f-e371-4d9c-a4ee-cef36378a256/PDF" /><edm:rights rdf:resource="http://rightsstatements.org/vocab/InC/1.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Društvo Medicinski razgledi</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:doc-7M1L98AK/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:doc-7M1L98AK" /></ore:Aggregation></rdf:RDF>