| P2093 | author name string | Suad AlFadhli | |
| | Mashael Al-Mutairi | |
| | Rasheeba Nizam | |
| | Hassan Al-Jafer | |
| | Mays Hadi | |
| P2860 | cites work | Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population. | Q53647539 |
| | Incidence of cholelithiasis in sickle cell anemia using the ultrasonic gray-scale technique | Q71188527 |
| | Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects | Q72996734 |
| | Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects | Q73568231 |
| | 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 | Q73634240 |
| | Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias | Q74066972 |
| | Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population | Q77822775 |
| | Genotyping by"cold single-strand conformation polymorphism" of the UGT1A1 promoter polymorphism in Mexican mestizos | Q78035808 |
| | UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians | Q79463926 |
| | Validation of rapid polymerase chain reaction-based detection of all length polymorphisms in the UGT 1A1 gene promoter | Q80243161 |
| | Rare TA repeats in promoter TATA box of the UDP glucuronosyltranferase (UGT1A1) gene in Croatian subjects | Q80832597 |
| | Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study | Q80979261 |
| | Neonatal jaundice and bilirubin UDP-glucuronosyl transferase 1A1 gene polymorphism in Turkish patients | Q83175329 |
| | Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population | Q83524552 |
| | Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? | Q24670527 |
| | Inherited disorders of bilirubin metabolism | Q28217356 |
| | Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man | Q28244675 |
| | Gall stones in Jamaican children with homozygous sickle cell disease | Q30495050 |
| | The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease | Q33288909 |
| | Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes. | Q33544891 |
| | Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene | Q33867195 |
| | Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene | Q33920356 |
| | Frequent co-occurrence of the TATA box mutation associated with Gilbert’s syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians | Q33965830 |
| | The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome | Q34057969 |
| | Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome | Q34374626 |
| | Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans | Q35258583 |
| | Hepatobiliary system in sickle cell disease. | Q39731859 |
| | Management of sickle cell disease; lessons from the Jamaican Cohort Study | Q40780919 |
| | Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans | Q40895512 |
| | Cholelithiasis in Jamaican patients with homozygous sickle cell disease | Q42153888 |
| | Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels. | Q43636885 |
| | UGT1A1 genetic polymorphisms, endogenous estrogen exposure, soy food intake, and endometrial cancer risk | Q44209224 |
| | UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemia | Q44391446 |
| | The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications | Q44506208 |
| | Glucose-6-phosphate dehydrogenase (G6PD) mutations and UDP-glucuronosyltransferase promoter polymorphism among G6PD deficient Kuwaitis | Q44583458 |
| | UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia | Q45254705 |
| | Transcriptional regulation of human UGT1A1 gene expression through distal and proximal promoter motifs: implication of defects in the UGT1A1 gene promoter | Q46825278 |
| | Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil | Q47582860 |
| | Bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1) gene promoter polymorphisms and HPRT, glycophorin A, and micronuclei mutant frequencies in human blood | Q47728093 |
| | Variability at the uridine diphosphate glucuronosyltransferase 1A1 promoter in human populations and primates. | Q47903526 |
| | Cholecystectomy in sickle cell anemia patients: perioperative outcome of 364 cases from the National Preoperative Transfusion Study. Preoperative Transfusion in Sickle Cell Disease Study Group. | Q50158439 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bilirubin metabolic disorder | Q390475 |
| | hemoglobinopathy | Q1642147 |
| | gallstone | Q272714 |
| P304 | page(s) | e77681 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients | |
| P478 | volume | 8 | |