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Pregled bibliografske jedinice broj: 393562

Genetic basis of Gilbert's syndrome


Nikolac, Nora
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)


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. studenog - 15. studenog 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


Projekt / tema
134-1340227-0200 - Upala i udio farmakogenetike u razvoju i ishodu akutnih i kroničnih bolesti (Ana-Maria Šimundić, )

Ustanove
KBC "Sestre Milosrdnice"

Autor s matičnim brojem:
Nora Nikolac, (266202)

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