Serum transferrin microheterogeneity in cystis fibrosis

Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F09%3A10051637" target="_blank" >RIV/00216208:11150/09:10051637 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00179906:_____/09:10051637
Výsledek na webu
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DOI - Digital Object Identifier
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Jazyk výsledku
angličtina
Název v původním jazyce
Serum transferrin microheterogeneity in cystis fibrosis
Popis výsledku v původním jazyce
Glycosylation degree of serum transferrin and the type of its protein variants in patients with cystic fibrosis (CF) were recorded by isoelectric focusing and possible relation to the CFTR genotype, P. aeruginosa infection, respiratory capacity and pancreatic (in)sufficiency was checked. Our results did not confirm some earlier findings of Tf hypoglycosylation in CF, however, we observed significant mean increase (p=0.001) of Tf C2 allele frequency in the patients when compared to controls.
Název v anglickém jazyce
Serum transferrin microheterogeneity in cystis fibrosis
Popis výsledku anglicky
Glycosylation degree of serum transferrin and the type of its protein variants in patients with cystic fibrosis (CF) were recorded by isoelectric focusing and possible relation to the CFTR genotype, P. aeruginosa infection, respiratory capacity and pancreatic (in)sufficiency was checked. Our results did not confirm some earlier findings of Tf hypoglycosylation in CF, however, we observed significant mean increase (p=0.001) of Tf C2 allele frequency in the patients when compared to controls.

Rok uplatnění
2009
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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