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 *

416 related articles for article (PubMed ID: 15985997)

  • 21. Congenital nonhemolytic hyperbilirubinemias.
    Cichoz-Lach H; Celiński K; Słomka M
    Ann Univ Mariae Curie Sklodowska Med; 2004; 59(1):449-52. PubMed ID: 16146029
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
    Maruo Y; Poon KK; Ito M; Iwai M; Takahashi H; Mori A; Sato H; Takeuchi Y
    Clin Genet; 2003 Nov; 64(5):420-3. PubMed ID: 14616765
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.
    Sun L; Li M; Zhang L; Teng X; Chen X; Zhou X; Ma Z; Qi L; Wang P
    Medicine (Baltimore); 2017 Nov; 96(45):e8620. PubMed ID: 29137095
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Gene replacement therapy for genetic hepatocellular jaundice.
    van Dijk R; Beuers U; Bosma PJ
    Clin Rev Allergy Immunol; 2015 Jun; 48(2-3):243-53. PubMed ID: 25315738
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
    Sampietro M; Iolascon A
    Haematologica; 1999 Feb; 84(2):150-7. PubMed ID: 10091414
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.
    Zmetáková I; Ferák V; Minárik G; Ficek A; Poláková H; Feráková E; Kádasi L
    Gen Physiol Biophys; 2007 Dec; 26(4):306-10. PubMed ID: 18281749
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease.
    Ciotti M; Chen F; Rubaltelli FF; Owens IS
    Biochim Biophys Acta; 1998 Jul; 1407(1):40-50. PubMed ID: 9639672
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome.
    Aggarwal V; Seth A; Sharma S; Aneja S; Sammarco P; Fabiano C
    Pediatr Blood Cancer; 2010 Apr; 54(4):627-8. PubMed ID: 19953640
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Analysis of bilirubin UDP-glucuronosyltransferase gene mutations in an unusual Crigler-Najjar syndrome patient.
    Liu WL; Li F; He ZX; Jiang HY; Ai R; Chen XX; Huang K
    Mol Med Rep; 2012 Sep; 6(3):667-9. PubMed ID: 22710376
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.
    Dabke PS; Colah RB; Ghosh KK; Nadkarni AH
    Hematology; 2014 Oct; 19(7):388-92. PubMed ID: 24620945
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
    Udomuksorn W; Elliot DJ; Lewis BC; Mackenzie PI; Yoovathaworn K; Miners JO
    Pharmacogenet Genomics; 2007 Dec; 17(12):1017-29. PubMed ID: 18004206
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
    Huang CS
    J Biomed Sci; 2005; 12(3):445-50. PubMed ID: 15965581
    [TBL] [Abstract][Full Text] [Related]  

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

  • 34. Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1.
    Maruo Y; Topaloglu AK; Takahashi H; Mori A; Iwai M; Duzovali O; Yamamoto K; Matui K; Sato H; Takeuchi Y
    J Pediatr Gastroenterol Nutr; 2006 Feb; 42(2):236-9. PubMed ID: 16456422
    [No Abstract]   [Full Text] [Related]  

  • 35. A new type of defect in the gene for bilirubin uridine 5'-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I.
    Aono S; Yamada Y; Keino H; Sasaoka Y; Nakagawa T; Onishi S; Mimura S; Koiwai O; Sato H
    Pediatr Res; 1994 Jun; 35(6):629-32. PubMed ID: 7936809
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial unconjugated hyperbilirubinemia syndromes.
    Reichen J
    Semin Liver Dis; 1983 Feb; 3(1):24-35. PubMed ID: 6836332
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.
    Maruo Y; Behnam M; Ikushiro S; Nakahara S; Nouri N; Salehi M
    J Gastrointestin Liver Dis; 2015 Dec; 24(4):523-6. PubMed ID: 26697581
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
    Kaplan M
    J Perinatol; 2001 Dec; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Crigler-Najjar Syndrome Type II Diagnosed in a Patient with Jaundice Since Birth.
    Liaqat A; Shahid A; Attiq H; Ameer A; Imran M
    J Coll Physicians Surg Pak; 2018 Oct; 28(10):806-808. PubMed ID: 30266131
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 21.