Serum transferrin microheterogeneity in cystis fibrosis

Result code in 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>

Alternative codes found

RIV/00179906:_____/09:10051637

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Serum transferrin microheterogeneity in cystis fibrosis

Original language description

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.

Czech name

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Czech description

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Type

C - Chapter in a specialist book

CEP classification

FG - Paediatrics

OECD FORD branch

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Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2009

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Book/collection name

Cystic Fibrosis: Etiology, Diagnosis and Treatments

ISBN

978-1-60741-833-7

Number of pages of the result

8

Pages from-to

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Number of pages of the book

275

Publisher name

Nova Science Publishers, Inc.

Place of publication

New York

UT code for WoS chapter

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