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Nitric oxide synthase 1 as a potential modifier gene of decline in lung function in patients with cystic fibrosis

Methods: Dinucleotide GT repeat polymorphism was studied in the 5' untranslated region of the NOS1 gene, immediately upstream from the transcription initiation site, in 59 patients with CF and 59 healthy controls. Results: Nineteen alleles of the NOS1 gene were identified according to the numbe...

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Bibliografski detalji
Glavni autori: Texereau, J, Marullo, S, Hubert, D, Coste, J, Dusser, D, Dall'Ava-Santucci, J, Dinh-Xuan, A
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2004
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1746921/
https://ncbi.nlm.nih.gov/pubmed/14760158
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thorax.2003.006718
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