Pregled bibliografske jedinice broj: 393562
Genetic basis of Gilbert's syndrome
Genetic basis of Gilbert's syndrome // Clinical Chemistry and Laboratory Medicine / Siest, Gerard (ur.).
Berlin: Walter de Gruyter, 2008. str. A240-A240 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 393562 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic basis of Gilbert's syndrome
Autori
Nikolac, Nora
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Clinical Chemistry and Laboratory Medicine
/ Siest, Gerard - Berlin : Walter de Gruyter, 2008, A240-A240
Skup
3. Slovenian Congress of Clinical Chemistry and the 18th International Symposium of Slovenian Association for Clinical Chemistry and Croatian Society of Medical Biochemists
Mjesto i datum
Ljubljana, Slovenija, 13.11.2008. - 15.11.2008
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
polymorphism; Gilbert's syndrome
Sažetak
Gilbert’ s syndrome is a chronic or recurrent mild unconjugated hyperbilirubinemia caused by decreased activity of UDP glucuronosyltranferase (UGT1A1). The most common cause of Gilbert’ s syndrome in Caucasians is homozygous variant of the A(TA)7TAA promoter polymorphism. Alleles with five or eight TA repeats have also been described, but they are very rare in Caucasian populations.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
134-1340227-0200 - Upala i udio farmakogenetike u razvoju i ishodu akutnih i kroničnih bolesti (Šimundić, Ana-Maria, MZOS ) ( CroRIS)
Ustanove:
KBC "Sestre Milosrdnice"
Profili:
Nora Nikolac
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE