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 *

141 related articles for article (PubMed ID: 8514049)

  • 21. 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]  

  • 22. Hepatic conversion of bilirubin monoglucuronide to diglucuronide in uridine diphosphate-glucuronyl transferase-deficient man and rat by bilirubin glucuronoside glucuronosyltransferase.
    Chowdhury JR; Jansen PL; Fischberg EB; Daniller A; Arias IM
    J Clin Invest; 1978 Jul; 62(1):191-6. PubMed ID: 96142
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
    Bosma PJ; Chowdhury JR; Bakker C; Gantla S; de Boer A; Oostra BA; Lindhout D; Tytgat GN; Jansen PL; Oude Elferink RP
    N Engl J Med; 1995 Nov; 333(18):1171-5. PubMed ID: 7565971
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Relationship between bilirubin UDP-glucuronosyl transferase polymorphism and neonatal jaundice].
    Sha B
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Oct; 9(5):510-3. PubMed ID: 17937877
    [No Abstract]   [Full Text] [Related]  

  • 25. Cell and gene therapy for inherited deficiency of bilirubin glucuronidation.
    Kim BH; Takahashi M; Tada K; Bosma PJ; Roy-Chowdhury J; Roy-Chowdhury N
    J Perinatol; 1996; 16(3 Pt 2):S67-72. PubMed ID: 8817442
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. Unconjugated bilirubin and an increased proportion of bilirubin monoconjugates in the bile of patients with Gilbert's syndrome and Crigler-Najjar disease.
    Fevery J; Blanckaert N; Heirwegh KP; Préaux AM; Berthelot P
    J Clin Invest; 1977 Nov; 60(5):970-9. PubMed ID: 409736
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The glucuronidation of exogenous and endogenous compounds by stably expressed rat and human UDP-glucuronosyltransferase 1.1.
    King CD; Green MD; Rios GR; Coffman BL; Owens IS; Bishop WP; Tephly TR
    Arch Biochem Biophys; 1996 Aug; 332(1):92-100. PubMed ID: 8806713
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The conjugation of bilirubin: clinico-experimental studies].
    Fevery J
    Verh K Acad Geneeskd Belg; 1980; 42(5-6):258-95. PubMed ID: 7020277
    [No Abstract]   [Full Text] [Related]  

  • 30. Genetic factors in neonatal hyperbilirubinemia and kernicterus.
    Sarici SU; Saldir M
    Turk J Pediatr; 2007; 49(3):245-9. PubMed ID: 17990575
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hereditary hyperbilirubinemias.
    Radlović N
    Srp Arh Celok Lek; 2014; 142(3-4):257-60. PubMed ID: 24839786
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
    Chalasani N; Chowdhury NR; Chowdhury JR; Boyer TD
    Gastroenterology; 1997 Jun; 112(6):2099-103. PubMed ID: 9178703
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gilbert's syndrome--a legitimate genetic anomaly?
    Schmid R
    N Engl J Med; 1995 Nov; 333(18):1217-8. PubMed ID: 7565981
    [No Abstract]   [Full Text] [Related]  

  • 34. Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?
    Strassburg CP
    Drug Metab Rev; 2010 Feb; 42(1):168-81. PubMed ID: 20070246
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic defects at the UGT1 locus associated with Crigler-Najjar type I disease, including a prenatal diagnosis.
    Ciotti M; Obaray R; Martín MG; Owens IS
    Am J Med Genet; 1997 Jan; 68(2):173-8. PubMed ID: 9028453
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Molecular biology of bilirubin metabolism.
    Jansen PL; Bosma PJ; Chowdhury JR
    Prog Liver Dis; 1995; 13():125-50. PubMed ID: 9224500
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Disruption of HNF1α binding site causes inherited severe unconjugated hyperbilirubinemia.
    van Dijk R; Mayayo-Peralta I; Aronson SJ; Kattentidt-Mouravieva AA; van der Mark VA; de Knegt R; Oruc N; Beuers U; Bosma PJ
    J Hepatol; 2015 Dec; 63(6):1525-9. PubMed ID: 26220753
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [The analysis of UGT1A1 gene mutations in hereditary unconjugated hyperbilirubinemia].
    Sun L; Zhang L; Li M; Teng XY; Qi LM; Zhou XG; Lang ZW; Wang P
    Zhonghua Gan Zang Bing Za Zhi; 2016 Nov; 24(11):863-866. PubMed ID: 27978934
    [No Abstract]   [Full Text] [Related]  

  • 40. Correction of the UDP-glucuronosyltransferase gene defect in the gunn rat model of crigler-najjar syndrome type I with a chimeric oligonucleotide.
    Kren BT; Parashar B; Bandyopadhyay P; Chowdhury NR; Chowdhury JR; Steer CJ
    Proc Natl Acad Sci U S A; 1999 Aug; 96(18):10349-54. PubMed ID: 10468611
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.