For: | Farheen S, Sengupta S, Santra A, Pal S, Dhali GK, Chakravorty M, Majumder PP, Chowdhury A. 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. World J Gastroenterol 2006; 12(14): 2269-2275 [PMID: 16610035 DOI: 10.3748/wjg.v12.i14.2269] |
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URL: | https://www.wjgnet.com/1007-9327/full/v12/i14/2269.htm |
Number | Citing Articles |
1 |
Kuerbanjiang Abuduxikuer, Ling-Juan Fang, Li-Ting Li, Jing-Yu Gong, Jian-She Wang. UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children. Medicine 2018; 97(49): e13576 doi: 10.1097/MD.0000000000013576
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2 |
Tsai-Yuan Hsieh, Tzu-Yue Shiu, Shih-Ming Huang, Hsuan-Hwai Lin, Tai-Chi Lee, Peng-Jen Chen, Heng-Cheng Chu, Wei-Kuo Chang, King-Song Jeng, Michael M.C. Lai, You-Chen Chao. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter. Pharmacogenetics and Genomics 2007; 17(4): 229 doi: 10.1097/FPC.0b013e328012d0da
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3 |
Sanya Sachdeva, Ragini Bodade, Anand Bodade. A systemic review of association between UDP glucuronosyltransferase family 1 member A1 (UGT1A1) polymorphisms in Gilbert's syndrome in Sickle Cell Disease. Journal of Clinical and Scientific Research 2022; 11(2): 99 doi: 10.4103/jcsr.jcsr_56_21
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4 |
Jennifer M. Skierka, Katrina E. Kotzer, Susan A. Lagerstedt, Dennis J. O'Kane, Linnea M. Baudhuin. UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia. The Journal of Pediatrics 2013; 162(6): 1146 doi: 10.1016/j.jpeds.2012.11.042
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5 |
Selma D'Silva, Roshan B. Colah, Kanjaksha Ghosh, Malay B. Mukherjee. UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults. Gene 2013; 513(1): 36 doi: 10.1016/j.gene.2012.10.081
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6 |
Giulia Canu, Angelo Minucci, Cecilia Zuppi, Ettore Capoluongo. Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database. Blood Cells, Molecules, and Diseases 2013; 50(4): 273 doi: 10.1016/j.bcmd.2013.01.003
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7 |
Yuan Ming Di, Eli Chan, Ming Qian Wei, Jun-Ping Liu, Shu-Feng Zhou. Prediction of Deleterious Non-synonymous Single-Nucleotide Polymorphisms of Human Uridine Diphosphate Glucuronosyltransferase Genes. The AAPS Journal 2009; 11(3) doi: 10.1208/s12248-009-9126-z
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8 |
Marwa A. Kubba, Abeer Ali Marhoon, Rafed Abbas Kadhum. Study single nucleotide polymorphism in Promoter region of UGT1A1 Gene in Iraqi Patients with Gilbert's syndrome. Bionatura 2022; 7(1): 1 doi: 10.21931/RB/2022.07.01.31
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9 |
Oshan Shrestha, Alka Rani Khadwal, Manphool Singhal, Amita Trehan, Deepak Bansal, Richa Jain, Arnab Pal, Jasbir Kaur Hira, Sanjeev Chhabra, Pankaj Malhotra, Reena Das, Prashant Sharma. 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. Annals of Hematology 2020; 99(9): 2019 doi: 10.1007/s00277-020-04176-2
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10 |
May‐Jen Huang, Pei‐Lain Chen, Ching‐Shan Huang. Bilirubin metabolism andUDP‐glucuronosyltransferase1A1variants in Asians: Pathogenic implications and therapeutic response. The Kaohsiung Journal of Medical Sciences 2022; 38(8): 729 doi: 10.1002/kjm2.12579
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11 |
Christian P Strassburg. Pharmacogenetics of Gilbert‘s Syndrome. Pharmacogenomics 2008; 9(6): 703 doi: 10.2217/14622416.9.6.703
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12 |
Suad AlFadhli, Hassan Al-Jafer, Mays Hadi, Mashael Al-Mutairi, Rasheeba Nizam, Harriet Wikman. The Effect of UGT1A1 Promoter Polymorphism in the Development of Hyperbilirubinemia and Cholelithiasis in Hemoglobinopathy Patients. PLoS ONE 2013; 8(10): e77681 doi: 10.1371/journal.pone.0077681
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13 |
Robert S. Foti, Michael B. Fisher. Encyclopedia of Drug Metabolism and Interactions. 2012; : 1 doi: 10.1002/9780470921920.edm015
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14 |
Sushant Mane, Ashwini Ronghe. Gilbert Syndrome: A Case Series. Pediatric Oncall 2017; 14(2) doi: 10.7199/ped.oncall.2017.18
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15 |
Christian P. Strassburg. Gilbert-Meulengracht’s syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?. Drug Metabolism Reviews 2010; 42(1): 168 doi: 10.3109/03602530903209429
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16 |
Neha Gupta, Mercilena Benjamin, Anjana Kar, Sachin Dev Munjal, Aditya N. Sarangi, Ashwin Dalal, Rakesh Aggarwal, Sylvie Mazoyer. Identification of Promotor and Exonic Variations, and Functional Characterization of a Splice Site Mutation in Indian Patients with Unconjugated Hyperbilirubinemia. PLOS ONE 2015; 10(12): e0145967 doi: 10.1371/journal.pone.0145967
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17 |
P K Tiwari, A Bhutada, R Agarwal, S Basu, R Raman, A Kumar. UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns. Journal of Perinatology 2014; 34(2): 120 doi: 10.1038/jp.2013.140
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18 |
Pedro F. Paz, David E. Michalik. Newborn Infant With Prolonged Jaundice. Clinical Pediatrics 2011; 50(10): 981 doi: 10.1177/0009922811398965
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19 |
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20 |
Christian P. Strassburg, Sandra Kalthoff. Metabolism of Drugs and Other Xenobiotics. 2012; : 67 doi: 10.1002/9783527630905.ch3
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21 |
Zibi Yu, Kaichang Zhu, Li Wang, Ying Liu, Jianmei Sun. Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis. Medical Science Monitor 2015; 21: 3104 doi: 10.12659/MSM.894043
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22 |
Bibi Zubaida, Huma Arshad Cheema, Muhammad Almas Hashmi, Muhammad Naeem. Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemias. Clinical Biochemistry 2019; 69: 30 doi: 10.1016/j.clinbiochem.2019.05.012
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23 |
E. A. Losik, I. I. Yakushina, M. R. Skhirtladze, N. P. Balahonova, V. V. Kerchev, I. A. Garanina. Clinical case of combined genetic pathology in a patient. Terapevticheskii arkhiv 2020; 92(12): 180 doi: 10.26442/00403660.2020.12.200435
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24 |
Christian P. Strassburg, Sandra Kalthoff, Ursula Ehmer. Variability and Function of Family 1 Uridine-5′-Diphosphate Glucuronosyltransferases (UGT1A). Critical Reviews in Clinical Laboratory Sciences 2008; 45(6): 485 doi: 10.1080/10408360802374624
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25 |
Lufeng Li, Guohong Deng, Yi Tang, Qing Mao, Vinod Scaria. Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II. PLOS ONE 2015; 10(5): e0126263 doi: 10.1371/journal.pone.0126263
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26 |
Jon F. Watchko, Zhili Lin. Exploring the genetic architecture of neonatal hyperbilirubinemia. Seminars in Fetal and Neonatal Medicine 2010; 15(3): 169 doi: 10.1016/j.siny.2009.11.003
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27 |
Bernadett Faragó, Béla Melegh. Gilbert syndrome. Orvosi Hetilap 2008; 149(27): 1277 doi: 10.1556/oh.2008.28381
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28 |
Hassan Mehrad-Majd, Monir Sadat Haerian, Javad Akhtari, Yalda Ravanshad, Anoush Azarfar, Gholamali Mamouri. Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis. The Journal of Maternal-Fetal & Neonatal Medicine 2019; 32(10): 1575 doi: 10.1080/14767058.2017.1410789
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29 |
Selma D’Silva, Roshan B. Colah, Kanjaksha Ghosh, Malay B. Mukherjee. G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India. The Journal of Maternal-Fetal & Neonatal Medicine 2012; 25(9): 1833 doi: 10.3109/14767058.2011.644362
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30 |
Sneha P, Elaheh Ahmad Ebrahimi, Sara Ahmed Ghazala, Thirumal Kumar D, Siva R, George Priya Doss C, Hatem Zayed. Structural analysis of missense mutations in galactokinase 1 (GALK1) leading to galactosemia type‐2. Journal of Cellular Biochemistry 2018; 119(9): 7585 doi: 10.1002/jcb.27097
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31 |
Sunil K Agrawal, Praveen Kumar, Ritu Rathi, Neeraj Sharma, Reena Das, Rajendra Prasad, Anil Narang. UGT1A1 Gene Polymorphisms in North Indian Neonates Presenting with Unconjugated Hyperbilirubinemia. Pediatric Research 2009; 65(6): 675 doi: 10.1203/PDR.0b013e31819ed5de
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32 |
Ashish S. Chiddarwar, Selma Z. D'Silva, Roshan B. Colah, Kanjaksha Ghosh, Malay B. Mukherjee. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults. Annals of Human Genetics 2017; 81(1): 11 doi: 10.1111/ahg.12179
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33 |
Meng Zhang, Hongwu Wang, Yuancheng Huang, Xin Xu, Wei Liu, Qin Ning, Tao Chen, Junying Qi. Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert’s syndrome in Chinese Han people. Gene 2021; 781: 145526 doi: 10.1016/j.gene.2021.145526
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34 |
Jon F. Watchko, Zhili Lin, Reese H. Clark, Amy S. Kelleher, M. Whit Walker, Alan R. Spitzer. Complex Multifactorial Nature of Significant Hyperbilirubinemia in Neonates. Pediatrics 2009; 124(5): e868 doi: 10.1542/peds.2009-0460
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35 |
Ashish S. Chiddarwar, Selma Z. D’Silva, Roshan B. Colah, Kanjaksha Ghosh, Malay B. Mukherjee. Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India. Molecular Biology Reports 2018; 45(6): 2733 doi: 10.1007/s11033-018-4305-6
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36 |
Christian P. Strassburg, Tim O. Lankisch, Michael P. Manns, Ursula Ehmer. Family 1 uridine-5′-diphosphate glucuronosyltransferases (UGT1A): from Gilbert’s syndrome to genetic organization and variability. Archives of Toxicology 2008; 82(7): 415 doi: 10.1007/s00204-008-0314-x
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37 |
Vikrant Sood, Bikrant Bihari Lal, Shvetank Sharma, Rajeev Khanna, Manish K. Siloliya, Seema Alam. Gilbert’s Syndrome in Children with Unconjugated Hyperbilirubinemia – An Analysis of 170 Cases. The Indian Journal of Pediatrics 2021; 88(2): 154 doi: 10.1007/s12098-020-03271-6
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38 |
Arulraj Ramakrishnan, Grace L.‐H. Wong, Innocent K. Besigye. The Liver in Systemic Disease. 2023; : 31 doi: 10.1002/9781119802181.ch3
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39 |
Remco van Dijk, Isabel Mayayo-Peralta, Sem J. Aronson, Anja A. Kattentidt-Mouravieva, Vincent A. van der Mark, Rob de Knegt, Nevin Oruc, Ulrich Beuers, Piter J. Bosma. Disruption of HNF1α binding site causes inherited severe unconjugated hyperbilirubinemia. Journal of Hepatology 2015; 63(6): 1525 doi: 10.1016/j.jhep.2015.07.027
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40 |
Leilei Gu, Yue Han, Donghua Zhang, Qiming Gong, Xinxin Zhang. Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population. Molecular Genetics & Genomic Medicine 2022; 10(7) doi: 10.1002/mgg3.1958
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41 |
Hemant K Sharma, Shivani Prashar. Gilbert's Syndrome after Ritualistic Prolonged Fasting of Chhath Puja in Bihar, India: A Case Report and Literature Review. Indian Journal of Medical Biochemistry 2019; 23(3): 354 doi: 10.5005/jp-journals-10054-0127
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42 |
Piyush Ranjan, Sudha Kohli, Renu Saxena, Seema Thakur. Mutation Analysis in Crigler-Najjar Syndrome Type II—Case Report and Literature Review. Journal of Clinical and Experimental Hepatology 2011; 1(3): 204 doi: 10.1016/S0973-6883(11)60239-9
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43 |
Carina Rodrigues, Alice Santos-Silva, Elísio Costa, Elsa Bronze-da-Rocha. Performance of In Silico Tools for the Evaluation ofUGT1A1Missense Variants. Human Mutation 2015; 36(12): 1215 doi: 10.1002/humu.22903
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44 |
Shalini Datta, Abhijit Chowdhury, Malay Ghosh, Kaushik Das, Pankaj Jha, Roshan Colah, Mitali Mukerji, Partha P. Majumder. A Genome‐Wide Search for Non‐UGT1A1 Markers Associated with Unconjugated Bilirubin Level Reveals Significant Association with a Polymorphic Marker Near a Gene of the Nucleoporin Family. Annals of Human Genetics 2012; 76(1): 33 doi: 10.1111/j.1469-1809.2011.00688.x
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45 |
Tien-Thanh Nguyen, Wei Zhao, Xi Yang, Dan-Ni Zhong. The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns. Pediatric Research 2020; 88(6): 940 doi: 10.1038/s41390-020-0825-6
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46 |
Hui Yang, Fen Lin, Zi-kai Chen, Lin Zhang, Jia-Xin Xu, Yong-Hao Wu, Jing-Ying Gu, Yu-Bin Ma, Jian-Dong Li, Li-Ye Yang. UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC Pediatrics 2021; 21(1) doi: 10.1186/s12887-021-02726-9
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47 |
Min Wang, De-Feng Sun, Shuai Wang, Ying Qing, Shuo Chen, Dong Wu, Ying-Min Lin, Ji-Zhuang Luo, Yan-Qing Li, Hiromu Suzuki. Polymorphic Expression of UDP-Glucuronosyltransferase UGTlA Gene in Human Colorectal Cancer. PLoS ONE 2013; 8(2): e57045 doi: 10.1371/journal.pone.0057045
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48 |
Jackie Yao Liu, Kevin Qu, Anthony D. Sferruzza, Richard A. Bender. Distribution of the UGT1A1*28 polymorphism in Caucasian and Asian populations in the US: a genomic analysis of 138 healthy individuals. Anti-Cancer Drugs 2007; 18(6): 693 doi: 10.1097/CAD.0b013e32803a46fe
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