120 related articles for article (PubMed ID: 15388579)
1. UGT1A1 variation and gallstone formation in sickle cell disease.
Haverfield EV; McKenzie CA; Forrester T; Bouzekri N; Harding R; Serjeant G; Walker T; Peto TE; Ward R; Weatherall DJ
Blood; 2005 Feb; 105(3):968-72. PubMed ID: 15388579
[TBL] [Abstract][Full Text] [Related]
2. Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria.
Olatunya OS; Albuquerque DM; Akanbi GO; Aduayi OS; Taiwo AB; Faboya OA; Kayode TS; Leonardo DP; Adekile A; Costa FF
BMC Med Genet; 2019 Oct; 20(1):160. PubMed ID: 31619193
[TBL] [Abstract][Full Text] [Related]
3. Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Passon RG; Howard TA; Zimmerman SA; Schultz WH; Ware RE
J Pediatr Hematol Oncol; 2001 Oct; 23(7):448-51. PubMed ID: 11878580
[TBL] [Abstract][Full Text] [Related]
4. The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.
Vasavda N; Menzel S; Kondaveeti S; Maytham E; Awogbade M; Bannister S; Cunningham J; Eichholz A; Daniel Y; Okpala I; Fulford T; Thein SL
Br J Haematol; 2007 Jul; 138(2):263-70. PubMed ID: 17593033
[TBL] [Abstract][Full Text] [Related]
5. Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Chaar V; Kéclard L; Diara JP; Leturdu C; Elion J; Krishnamoorthy R; Clayton J; Romana M
Haematologica; 2005 Feb; 90(2):188-99. PubMed ID: 15710570
[TBL] [Abstract][Full Text] [Related]
6. UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Carpenter SL; Lieff S; Howard TA; Eggleston B; Ware RE
Am J Hematol; 2008 Oct; 83(10):800-3. PubMed ID: 18756540
[TBL] [Abstract][Full Text] [Related]
7. Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.
Chaouch L; Talbi E; Moumni I; Ben Chaabene A; Kalai M; Chaouachi D; Mallouli F; Ghanem A; Abbes S
Dis Markers; 2013; 35(2):67-72. PubMed ID: 24167350
[TBL] [Abstract][Full Text] [Related]
8. UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.
Hamad Z; Aljedai A; Halwani R; AlSultan A
Ann Saudi Med; 2013; 33(4):372-6. PubMed ID: 24060717
[TBL] [Abstract][Full Text] [Related]
9. Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.
Chaouch L; Kalai M; Chaouachi D; Mallouli F; Hafsia R; Ben Ammar S; Abbes S
Tunis Med; 2015 Apr; 93(4):237-41. PubMed ID: 26375741
[TBL] [Abstract][Full Text] [Related]
10. Influence of UGT1A1 promoter polymorphism, α-thalassemia and β
Batista JVGF; Arcanjo GS; Batista THC; Sobreira MJ; Santana RM; Domingos IF; Hatzlhofer BL; Falcão DA; Pereira-Martins DA; Oliveira JM; Araujo AS; Laranjeira LPM; Medeiros FS; Albuquerque FP; Albuquerque DM; Santos MN; Hazin MF; Dos Anjos AC; Costa FF; Araujo AS; Lucena-Araujo AR; Bezerra MA
Ann Hematol; 2021 Apr; 100(4):903-911. PubMed ID: 33523291
[TBL] [Abstract][Full Text] [Related]
11. Bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1) gene promoter polymorphisms and HPRT, glycophorin A, and micronuclei mutant frequencies in human blood.
Grant DJ; Hall IJ; Eastmond DA; Jones IM; Bell DA
Mutat Res; 2004 May; 560(1):1-10. PubMed ID: 15099818
[TBL] [Abstract][Full Text] [Related]
12. [Influence of Gilbert's syndrome on serum bilirubin levels and gallstone formation in children with chronic hemolytic disease].
Costa E; Pinto R; Vieira E; Polo S; Sarmento AM; Oliveira I; Pimenta R; Dos Santos R; Barbot J
An Esp Pediatr; 2002 Dec; 57(6):529-33. PubMed ID: 12466075
[TBL] [Abstract][Full Text] [Related]
13. A cross-sectional clinic-based study exploring whether variants within the glutathione S-transferase, haptoglobin and uridine 5'-diphospho-glucuronosyltransferase 1A1 genes are associated with interindividual phenotypic variation in sickle cell anaemia in Jamaica.
Howell S; Marshall K; Reid M; McFarlane-Anderson N; McKenzie C
Eur J Haematol; 2018 Feb; 100(2):147-153. PubMed ID: 29114966
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism.
Martins R; Morais A; Dias A; Soares I; Rolão C; Ducla-Soares JL; Braga L; Seixas T; Nunes B; Olim G; Romão L; Lavinha J; Faustino P
J Hum Genet; 2008; 53(6):524-528. PubMed ID: 18392554
[TBL] [Abstract][Full Text] [Related]
16. Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia.
Chaouch L; Said Y; Moumni I; Mahjoubi I; Chaabene AB; Darragi I; Ghanem A; Abbes S
Ann Biol Clin (Paris); 2012; 70(6):702-6. PubMed ID: 23207817
[TBL] [Abstract][Full Text] [Related]
17. Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.
Wasmuth HE; Keppeler H; Herrmann U; Schirin-Sokhan R; Barker M; Lammert F
Hepatology; 2006 Apr; 43(4):738-41. PubMed ID: 16557566
[TBL] [Abstract][Full Text] [Related]
18. Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease.
Kalotychou V; Antonatou K; Tzanetea R; Terpos E; Loukopoulos D; Rombos Y
Blood Cells Mol Dis; 2003; 31(1):38-42. PubMed ID: 12850481
[TBL] [Abstract][Full Text] [Related]
19. A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia.
Shrestha O; Khadwal AR; Singhal M; Trehan A; Bansal D; Jain R; Pal A; Hira JK; Chhabra S; Malhotra P; Das R; Sharma P
Ann Hematol; 2020 Sep; 99(9):2019-2026. PubMed ID: 32676731
[TBL] [Abstract][Full Text] [Related]
20. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
Hsieh TY; Shiu TY; Huang SM; Lin HH; Lee TC; Chen PJ; Chu HC; Chang WK; Jeng KS; Lai MM; Chao YC
Pharmacogenet Genomics; 2007 Apr; 17(4):229-36. PubMed ID: 17496722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
