This HTML5 document contains 55 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
n14http://linked.opendata.cz/resource/domain/vavai/riv/tvurce/
n17http://linked.opendata.cz/ontology/domain/vavai/
n10http://linked.opendata.cz/resource/domain/vavai/zamer/
shttp://schema.org/
skoshttp://www.w3.org/2004/02/skos/core#
n3http://linked.opendata.cz/ontology/domain/vavai/riv/
n2http://linked.opendata.cz/resource/domain/vavai/vysledek/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n4http://linked.opendata.cz/ontology/domain/vavai/riv/klicoveSlovo/
n13http://linked.opendata.cz/ontology/domain/vavai/riv/duvernostUdaju/
n15http://linked.opendata.cz/resource/domain/vavai/vysledek/RIV%2F00064165%3A_____%2F10%3A7785%21RIV11-MZ0-00064165/
xsdhhttp://www.w3.org/2001/XMLSchema#
n11http://linked.opendata.cz/ontology/domain/vavai/riv/aktivita/
n6http://linked.opendata.cz/ontology/domain/vavai/riv/jazykVysledku/
n16http://linked.opendata.cz/ontology/domain/vavai/riv/druhVysledku/
n12http://linked.opendata.cz/ontology/domain/vavai/riv/obor/
n9http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:RIV%2F00064165%3A_____%2F10%3A7785%21RIV11-MZ0-00064165
rdf:type
skos:Concept n17:Vysledek
dcterms:description
The international research team studied expression pattern of lysosomal membrane protein NCL7 in normal mouse. This protein is targeted to the lysosomal system. Its function is presumed to be associated with transport processes. When mutated it leads to very serious neurological disorder called neuronal ceroid lipofuscinosis type 7 featured by extensive lysosomal storage of hydrophobic proteins. The Prague participation was requested as we could provide comparative study of neuropathology in human cases. The international research team studied expression pattern of lysosomal membrane protein NCL7 in normal mouse. This protein is targeted to the lysosomal system. Its function is presumed to be associated with transport processes. When mutated it leads to very serious neurological disorder called neuronal ceroid lipofuscinosis type 7 featured by extensive lysosomal storage of hydrophobic proteins. The Prague participation was requested as we could provide comparative study of neuropathology in human cases.
dcterms:title
Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis
skos:prefLabel
Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis
skos:notation
RIV/00064165:_____/10:7785!RIV11-MZ0-00064165
n3:aktivita
n11:Z n11:I
n3:aktivity
I, Z(MSM0021620806)
n3:cisloPeriodika
22
n3:dodaniDat
n9:2011
n3:domaciTvurceVysledku
n14:9809163 n14:6138225
n3:druhVysledku
n16:J
n3:duvernostUdaju
n13:S
n3:entitaPredkladatele
n15:predkladatel
n3:idSjednocenehoVysledku
258514
n3:idVysledku
RIV/00064165:_____/10:7785
n3:jazykVysledku
n6:eng
n3:klicovaSlova
NCL7 protein; expression pattern; lysosomal targeting; wild type mouse; neurolysosomal storage in humans
n3:klicoveSlovo
n4:wild%20type%20mouse n4:lysosomal%20targeting n4:NCL7%20protein n4:neurolysosomal%20storage%20in%20humans n4:expression%20pattern
n3:kodStatuVydavatele
GB - Spojené království Velké Británie a Severního Irska
n3:kontrolniKodProRIV
[B7202C21DDDE]
n3:nazevZdroje
Human Molecular Genetics
n3:obor
n12:EB
n3:pocetDomacichTvurcuVysledku
2
n3:pocetTvurcuVysledku
15
n3:rokUplatneniVysledku
n9:2010
n3:svazekPeriodika
19
n3:tvurceVysledku
Lehesjoki, AE Gasnier, B. Ruivo, R. Morel, L. Elleder, Milan Darmon, M. Bellenchi, GC Debacker, C. Sagne, C. Hůlková, Helena Sharifi, A. El Mestikawy, S. Jalanko, A. Kyttala, A. Kousi, M.
n3:wos
000283673500018
n3:zamer
n10:MSM0021620806
s:issn
0964-6906
s:numberOfPages
18