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Statements

Subject Item
n2:RIV%2F00216224%3A14110%2F04%3A00010483%21RIV%2F2005%2FGA0%2F141105%2FN
rdf:type
skos:Concept n17:Vysledek
dcterms:description
Several studies suggest that abnormalities in nitric oxide (NO) synthesis may contribute to the development of pulmonary diseases. We have, therefore, performed a case-control study to investigate a plausible association between two promoter polymorphisms in the NOS3 gene and respiratory allergic diseases. Řada prací naznačuje, že se abnormality v syntéze oxidu dusnatého (NO) mohou podílet na vývoji plicních nemocí. V naší studii kontrol a případů jsme analyzovali možnou asociaci mezi dvěma promotorovými polymorfizmy v genu pro NOS3 a respiračními alergickými chorobami. Several studies suggest that abnormalities in nitric oxide (NO) synthesis may contribute to the development of pulmonary diseases. We have, therefore, performed a case-control study to investigate a plausible association between two promoter polymorphisms in the NOS3 gene and respiratory allergic diseases.
dcterms:title
Na pohlaví závislá asociace polymorfizmů v genu pro syntázu oxidu dusnatého typu 3 (NOS3) s atopickými chorobami v české populaci Gender-specific association of nitric oxide synthase-3 (NOS3) gene polymorphisms with atopic diseases in the Czech population Gender-specific association of nitric oxide synthase-3 (NOS3) gene polymorphisms with atopic diseases in the Czech population
skos:prefLabel
Na pohlaví závislá asociace polymorfizmů v genu pro syntázu oxidu dusnatého typu 3 (NOS3) s atopickými chorobami v české populaci Gender-specific association of nitric oxide synthase-3 (NOS3) gene polymorphisms with atopic diseases in the Czech population Gender-specific association of nitric oxide synthase-3 (NOS3) gene polymorphisms with atopic diseases in the Czech population
skos:notation
RIV/00216224:14110/04:00010483!RIV/2005/GA0/141105/N
n5:strany
51P
n5:aktivita
n20:P n20:Z
n5:aktivity
P(GP310/03/P045), Z(MSM 141100002)
n5:dodaniDat
n12:2005
n5:domaciTvurceVysledku
n6:8430322 n6:4592026 n6:1379097 n6:1993038 n6:9688498 n6:6918115 n6:1730908
n5:druhVysledku
n10:D
n5:duvernostUdaju
n21:S
n5:entitaPredkladatele
n19:predkladatel
n5:idSjednocenehoVysledku
565240
n5:idVysledku
RIV/00216224:14110/04:00010483
n5:jazykVysledku
n15:eng
n5:klicovaSlova
nitric oxide, atopic disease, polymorphism, gene
n5:klicoveSlovo
n14:nitric%20oxide n14:atopic%20disease n14:gene n14:polymorphism
n5:kontrolniKodProRIV
[F2ABA181FBE9]
n5:mistoKonaniAkce
Hradec Králové
n5:mistoVydani
Praha
n5:nazevZdroje
Physiol Res
n5:obor
n9:EC
n5:pocetDomacichTvurcuVysledku
7
n5:pocetTvurcuVysledku
7
n5:projekt
n11:GP310%2F03%2FP045
n5:rokUplatneniVysledku
n12:2004
n5:tvurceVysledku
Znojil, Vladimír Bučková, Dana Vašků, Anna Schüller, Marcel Izakovičová-Hollá, Lydie Stejskalová, Andrea Vácha, Jiří
n5:typAkce
n16:EUR
n5:zahajeniAkce
2004-01-01+01:00
n5:zamer
n13:MSM%20141100002
s:issn
0862-8408
s:numberOfPages
1
n18:hasPublisher
Praha: Academia
n7:organizacniJednotka
14110