These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 23485750)

  • 1. [Not Available].
    Aeschlimann AG
    Praxis (Bern 1994); 2013 Mar; 102(6):315. PubMed ID: 23485750
    [No Abstract]   [Full Text] [Related]  

  • 2. [Not Available].
    Vavricka S
    Praxis (Bern 1994); 2013 Mar; 102(6):315-6. PubMed ID: 23547323
    [No Abstract]   [Full Text] [Related]  

  • 3. [Meulengracht disease].
    Zeitz J; Schmidinger I; Rentsch K; Rogler G; Vavricka S
    Praxis (Bern 1994); 2013 Jan; 102(3):129-35. PubMed ID: 23384981
    [No Abstract]   [Full Text] [Related]  

  • 4. Gilbert's syndrome phenotypically expressed as Crigler-Najjar syndrome type II.
    Seo YS; Keum B; Park S; Kim du R; Kwon YD; Kim YS; Jeen YT; Chun HJ; Um SH; Kim CD; Ryu HS
    Scand J Gastroenterol; 2007 Apr; 42(4):540-1. PubMed ID: 17454871
    [No Abstract]   [Full Text] [Related]  

  • 5. UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis.
    Fretzayas A; Kitsiou S; Tsezou A; Alexaki A; Nicolaidou P
    Scand J Infect Dis; 2006; 38(6-7):537-40. PubMed ID: 16798708
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gilbert's syndrome--clinical and pharmacological implications.
    Radu P; Atsmon J
    Isr Med Assoc J; 2001 Aug; 3(8):593-8. PubMed ID: 11519385
    [No Abstract]   [Full Text] [Related]  

  • 7. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.
    Costa E
    Blood Cells Mol Dis; 2006; 36(1):77-80. PubMed ID: 16386929
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage between A(TA)7TAA and -3279T>G mutations in UGT1A1 is not essential for pathogenesis of Gilbert syndrome.
    Jirsa M; Petrasek J; Vitek L
    Liver Int; 2006 Dec; 26(10):1302-3. PubMed ID: 17105600
    [No Abstract]   [Full Text] [Related]  

  • 9. [Gilbert syndrome].
    Faragó B; Melegh B
    Orv Hetil; 2008 Jul; 149(27):1277-82. PubMed ID: 18579467
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects.
    Te Morsche RH; Zusterzeel PL; Raijmakers MT; Roes EM; Steegers EA; Peters WH
    Hepatology; 2001 Mar; 33(3):765. PubMed ID: 11230763
    [No Abstract]   [Full Text] [Related]  

  • 11. Melting temperature assay for a UGT1A gene variant in Gilbert syndrome.
    Marziliano N; Pelo E; Minuti B; Passerini I; Torricelli F; Da Prato L
    Clin Chem; 2000 Mar; 46(3):423-5. PubMed ID: 10702534
    [No Abstract]   [Full Text] [Related]  

  • 12. Gilbert syndrome associated with beta-thalassemia.
    Tzetis M; Kanavakis E; Tsezou A; Ladis V; Pateraki E; Georgakopoulou T; Kavazarakis E; Maragoudaki E; Karpathios T; Kitsiou-Tzeli S
    Pediatr Hematol Oncol; 2001 Dec; 18(8):477-84. PubMed ID: 11764096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gilbert syndrome: the UGT1A1*28 promoter polymorphism as a biomarker of multifactorial diseases and drug metabolism.
    Gil J; Sąsiadek MM
    Biomark Med; 2012 Apr; 6(2):223-30. PubMed ID: 22448797
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of double gradient denaturing gradient gel electrophoresis to detect (AT)n polymorphisms in the UDP-glucuronosyltransferase 1 gene promoter associated with Gilbert's syndrome.
    Gürtler V; Parkin JD; Mayall BC
    Electrophoresis; 1999 Oct; 20(14):2841-3. PubMed ID: 10546817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern Italy.
    Iolascon A; Perrotta S; Coppola B; Carbone R; Miraglia Del Giudice E
    Haematologica; 2000 Mar; 85(3):335-6. PubMed ID: 10702836
    [No Abstract]   [Full Text] [Related]  

  • 16. Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler-Najjar syndromes.
    Costa E; Vieira E; Martins M; Saraiva J; Cancela E; Costa M; Bauerle R; Freitas T; Carvalho JR; Santos-Silva E; Barbot J; Dos Santos R
    Blood Cells Mol Dis; 2006; 36(1):91-7. PubMed ID: 16269258
    [TBL] [Abstract][Full Text] [Related]  

  • 17. TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome.
    Costa E; Vieira E; Santos-Silva E; Barbot J; dos Santos R
    Haematologica; 2002 Apr; 87(4):ELT21. PubMed ID: 11940506
    [No Abstract]   [Full Text] [Related]  

  • 18. Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.
    Aiso M; Yagi M; Tanaka A; Miura K; Miura R; Arizumi T; Takamori Y; Nakahara S; Maruo Y; Takikawa H
    Intern Med; 2017; 56(6):661-664. PubMed ID: 28321066
    [TBL] [Abstract][Full Text] [Related]  

  • 19. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
    Khan S; Irfan M; Sher G; Zubaida B; Alvi MA; Yasinzai M; Naeem M
    Ann Hum Genet; 2013 Nov; 77(6):482-7. PubMed ID: 23992562
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in
    Jiang J; Wang HG; Wu WL; Peng XX
    Chin Med J (Engl); 2017 Apr; 130(8):1003-1005. PubMed ID: 28397734
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.