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Statements

Subject Item
n2:RIV%2F00216208%3A11120%2F06%3A00000993%21RIV09-MSM-11120___
rdf:type
skos:Concept n16:Vysledek
dcterms:description
Amyloidosis represents a group of diseases with the common feature of extracellular deposition of insoluble patologic proteinaceous substance - amyloid - in tissues. Amyloid deposits can be formed by proteins of different origin and nature, the prerequisite is the ability of these proteins to form cross-beta-pleated sheet conformation. Special staining with Congo red is used to identify amyloid deposits. Progressive extracellular accummulation of amyloid within the tissues produces atrophy of adjacent cells and interference with blood supply play a significant role in organ derangement. Amyloidosis represents a group of diseases with the common feature of extracellular deposition of insoluble patologic proteinaceous substance - amyloid - in tissues. Amyloid deposits can be formed by proteins of different origin and nature, the prerequisite is the ability of these proteins to form cross-beta-pleated sheet conformation. Special staining with Congo red is used to identify amyloid deposits. Progressive extracellular accummulation of amyloid within the tissues produces atrophy of adjacent cells and interference with blood supply play a significant role in organ derangement. Amyloidóza představuje skupinu onemocnění, jejichž společnou vlastností je extracelulární ukládání nerozpustné patologické proteiní substance - amyloidu - ve tkáních. Amyloidní depozita mohou být tvořena proteiny různého původu, jejichž společnou vlastností je schopnost vytvářet beta strukturu. Specielní barvení kongočervení je používáno k identifikaci amyloidních depozit. Progresivní extracelulární akumulace amyloidu ve tkáních vede k jejich atrofii a k cirkulačním poruchám, které mohou vyústit v poškození orgánů.
dcterms:title
Amyloidosis from starch to molecular pathology Amyloidóza: Od škrobu k molekulární patologii Amyloidosis from starch to molecular pathology
skos:prefLabel
Amyloidosis from starch to molecular pathology Amyloidosis from starch to molecular pathology Amyloidóza: Od škrobu k molekulární patologii
skos:notation
RIV/00216208:11120/06:00000993!RIV09-MSM-11120___
n5:aktivita
n13:S
n5:aktivity
S
n5:cisloPeriodika
2
n5:dodaniDat
n8:2009
n5:domaciTvurceVysledku
n12:7449186
n5:druhVysledku
n14:J
n5:duvernostUdaju
n9:S
n5:entitaPredkladatele
n17:predkladatel
n5:idSjednocenehoVysledku
464737
n5:idVysledku
RIV/00216208:11120/06:00000993
n5:jazykVysledku
n15:eng
n5:klicovaSlova
amyloidosis; amyloidogenous proteins; beta structure; organ damage
n5:klicoveSlovo
n6:amyloidosis n6:beta%20structure n6:organ%20damage n6:amyloidogenous%20proteins
n5:kodStatuVydavatele
CZ - Česká republika
n5:kontrolniKodProRIV
[7052CE631FF8]
n5:nazevZdroje
Folia Gastroenterologica et Hepatologica
n5:obor
n10:FP
n5:pocetDomacichTvurcuVysledku
1
n5:pocetTvurcuVysledku
1
n5:rokUplatneniVysledku
n8:2006
n5:svazekPeriodika
4
n5:tvurceVysledku
Mandys, Václav
s:issn
1214-4088
s:numberOfPages
3
n11:organizacniJednotka
11120