Bilirubin

UDP glucuronosyltransferase family 1 member A1 ; Homo sapiens







405 Article(s)
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Pub. Year
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1 34625956 Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach. 2022 Feb 1
2 34807779 The relationship between UGT1A1 gene & various diseases and prevention strategies. 2022 Feb 2
3 35017453 Raltegravir-based Postnatal HIV Prophylaxis Therapy in a Neonate After in Utero Dolutegravir Exposure. 2022 Feb 1 1
4 35149777 UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. 2022 May 3
5 35192750 Dependence of blood biochemical parameters on various genotypes of the UGT1A1 gene associated with gilbert's syndrome. 2022 Feb 23 1
6 35241486 Inhibition of Human UDP-Glucuronosyltransferases1A1-Mediated Bilirubin Glucuronidation by the Popular Flavonoids Baicalein, Baicalin, and Hyperoside Is Responsible for Herb (Shuang-Huang-Lian)-Induced Jaundice. 2022 May 6
7 35281975 The Effects of Clofibrate on Neonatal Jaundice: A Systematic Review. 2022 1
8 35436954 Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity. 2022 Apr 18 1
9 35501760 Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population. 2022 May 2 1
10 35512135 Pharmacogenetics of dolutegravir plasma exposure among Southern Africans living with HIV. 2022 May 4 1
11 31339084 UGT1A1 mutations and psychoses: towards understanding the relationship with unconjugated bilirubin. 2021 Jun 1
12 33154041 Regulation of Intestinal UDP-Glucuronosyltransferase 1A1 by the Farnesoid X Receptor Agonist Obeticholic Acid Is Controlled by Constitutive Androstane Receptor through Intestinal Maturation. 2021 Jan 1
13 33604208 A Rare Case Report of Crigler Najjar Syndrome Type II. 2021 Jan 12 1
14 33631237 Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people. 2021 May 20 1
15 33685083 [Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome]. 2021 Feb 20 5
16 33901188 Tissue specificity-aware TWAS (TSA-TWAS) framework identifies novel associations with metabolic, immunologic, and virologic traits in HIV-positive adults. 2021 Apr 1
17 34007799 UGT1A1-related Bilirubin Encephalopathy/Kernicterus in Adults. 2021 Apr 28 1
18 34074250 UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. 2021 Jun 1 5
19 34093191 Pharmacogenetic Associations Between Atazanavir/UGT1A1*28 and Efavirenz/rs3745274 (CYP2B6) Account for Specific Adverse Reactions in Chilean Patients Undergoing Antiretroviral Therapy. 2021 1
20 34117260 A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals. 2021 Jun 11 2
21 34272713 Case Study 6: Deconvoluting Hyperbilirubinemia-Differentiating Between Hepatotoxicity and Reversible Inhibition of UGT1A1, MRP2, or OATP1B1 in Drug Development. 2021 2
22 34573035 Bilirubin Links HO-1 and UGT1A1*28 Gene Polymorphisms to Predict Cardiovascular Outcome in Patients Receiving Maintenance Hemodialysis. 2021 Aug 31 3
23 34609801 [Liver histologic changes in children with type 1 of Crigler-Najjar syndrome]. 2021 1
24 34814402 [Gilbert's syndrome: hyperbilirubinemia enemy or friend]. 2021 Oct 20 3
25 34866848 Gilbert's Syndrome, Bilirubin Level and UGT1A1∗28 Genotype in Men of North-West Region of Russia. 2021 Nov-Dec 5
26 34895177 Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong. 2021 Dec 11 2
27 34943103 Association of Serum Bilirubin and Functional Variants of Heme Oxygenase 1 and Bilirubin UDP-Glucuronosyl Transferase Genes in Czech Adult Patients with Non-Alcoholic Fatty Liver Disease. 2021 Dec 15 2
28 31342573 Regenerative cell therapy for the treatment of hyperbilirubinemic Gunn rats with fresh and frozen human induced pluripotent stem cells-derived hepatic stem cells. 2020 Jan 1
29 31495946 Disease burden of Crigler-Najjar syndrome: Systematic review and future perspectives. 2020 Apr 1
30 31602632 Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study. 2020 Mar 1
31 31888882 Influence of Uridine Diphosphate Glucuronosyltransferase Family 1 Member A1 and Solute Carrier Organic Anion Transporter Family 1 Member B1 Polymorphisms and Efavirenz on Bilirubin Disposition in Healthy Volunteers. 2020 Mar 5
32 31965023 Human liver stem cells express UGT1A1 and improve phenotype of immunocompromised Crigler Najjar syndrome type I mice. 2020 Jan 21 1
33 31980500 Differential Role of Liver X Receptor (LXR) α and LXRβ in the Regulation of UDP-Glucuronosyltransferase 1A1 in Humanized UGT1 Mice. 2020 Apr 1
34 32049823 Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome. 2020 Feb 1
35 32204767 [Research advances in neonatal hyperbilirubinemia and gene polymorphisms]. 2020 Mar 1
36 32237326 [Study on potential hepatotoxicity of rhein in Rhei Radix et Rhizoma based on liver metabolism]. 2020 Jan 1
37 32361755 Evaluation of the effect of UGT1A1 polymorphisms on the pharmacokinetics of oral and long-acting injectable cabotegravir. 2020 Aug 1 1
38 32433020 Down-regulation of SOX17, GATA4 and FoxA2 promotes differentiation potential of hepatocytes from human hematopoietic stem cells. 2020 Feb 1
39 32612873 An ultra-sensitive and easy-to-use assay for sensing human UGT1A1 activities in biological systems. 2020 Jun 2
40 32737884 Pharmacogenetic impact of UGT1A1 polymorphisms on pulmonary neuroendocrine tumours treated with metronomic irinotecan-based chemotherapy in Chinese populations. 2020 Nov 2
41 32796590 Prediction of Drug-Induced Hyperbilirubinemia by In Vitro Testing. 2020 Aug 11 2
42 32878631 Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses. 2020 Sep 3 1
43 32973940 Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report. 2020 Nov 1
44 33622990 Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency. 2020 1
45 33628187 Neobavaisoflavone Induces Bilirubin Metabolizing Enzyme UGT1A1 via PPARα and PPARγ. 2020 3
46 30385458 A Novel Pathogenic UGT1A1 Variant in a Sudanese Child with Type 1 Crigler-Najjar Syndrome. 2019 Jan 1
47 30588615 Induction of Mild Hyperbilirubinemia: Hype or Real Therapeutic Opportunity? 2019 Sep 1
48 30594625 Inhibition of UGT1A1 by natural and synthetic flavonoids. 2019 Apr 1 4
49 30820183 Significance of UGT1A1*28 Genotype in Patients with Advanced Liver Injury Caused By Chronic Hepatitis C. 2019 Mar 1
50 31017737 Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome. 2019 Jul 2