HuGE Literature Finder
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| Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ? haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort. Annals of hematology 2021 Feb . Batista Jéssica V G F, Arcanjo Gabriela S, Batista Thais H C, Sobreira Marcondes J, Santana Rodrigo M, Domingos Igor F, Hatzlhofer Betânia L, Falcão Diego A, Pereira-Martins Diego A, Oliveira Jéssica M, Araujo Amanda S, Laranjeira Luana P M, Medeiros Fernanda S, Albuquerque Flávia P, Albuquerque Dulcinéia M, Santos Magnun N, Hazin Manuela F, Dos Anjos Ana C, Costa Fernando F, Araujo Aderson S, Lucena-Araujo Antonio R, Bezerra Marcos |
| Effect of Genetic Polymorphisms on the Pharmacokinetics of Deferasirox in Healthy Chinese Subjects and an Artificial Neural Networks Model for Pharmacokinetic Prediction. European journal of drug metabolism and pharmacokinetics 2020 Sep . Chen Jinliang, Xu Yichao, Lou Honggang, Jiang Bo, Shao Rong, Yang Dandan, Hu Yin, Ruan Zouro |
| 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 ?-thalassemia. Annals of hematology 2020 7 99 (9): 2019-2026. Shrestha Oshan, Khadwal Alka Rani, Singhal Manphool, Trehan Amita, Bansal Deepak, Jain Richa, Pal Arnab, Hira Jasbir Kaur, Chhabra Sanjeev, Malhotra Pankaj, Das Reena, Sharma Prasha |
| Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana. PloS one 2020 9 15 (9): e0238691. Elenga Narcisse, Cuadro-Alvarez Emma, Martin Elise, Njuieyon Falucar, Defo Antoine, Maniassom Chimè |
| Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease? Molecular diagnosis & therapy 2017 May . de Azevedo Laura Alencastro, Bonazzoni Joyce, Wagner Sandrine Comparsi, Farias Mariela Granero, Bittar Christina M, Daudt Liane, de Castro Simone Marti |
| Genetic modulators of sickle cell disease in French Guiana: Markers of the slave trade. American journal of human biology : the official journal of the Human Biology Council 2016 Jun . Christine Simonnet, Narcisse Elanga, Philippe Joly, Tania Vaz, Mathieu Nach |
| Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan. BMC pediatrics 2016 16 (1): 144. Weng Yi-Hao, Chiu Ya-Wen, Cheng Shao-Wen, Yang Chun-Y |
| Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia. Pediatrics and neonatology 2015 Dec . Yang Hui, Wang Qian, Zheng Lei, Zheng Xiang-Bin, Lin Min, Zhan Xiao-Fen, Yang Li- |
| Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients. Hematology (Amsterdam, Netherlands) 2014 Oct 19 (7): 388-92. Dabke Pooja S, Colah Roshan B, Ghosh Kanjaksha K, Nadkarni Anita |
| Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes. American journal of hematology 2013 Jul 88 (7): 571-6. Sheehan Vivien A, Luo Zhaoyu, Flanagan Jonathan M, Howard Thad A, Thompson Bruce W, Wang Winfred C, Kutlar Abdullah, Ware Russell E, |
| Bilirubin concentrations in thalassemia heterozygotes in university students. European journal of haematology 2011 Apr 86 (4): 317-23. Huang Yang-Yang, Huang May-Jen, Wang Hai-Lung, Chan Cung-Cuan, Huang Ching-Sh |
| The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies. Clinical biochemistry 2010 Nov 43 (16-17): 1329-32. Italia Khushnooma Y, Jijina Farah F, Jain Dipty, Merchant Rashid, Nadkarni Anita H, Mukherjee Malay, Ghosh Kanjaksha, Colah Roshan |
| Association between promoter and coding region mutations of UDP-glucuronosyltransferase 1A1 and beta-thalassemia/Hb E with cholelithiasis. European journal of haematology 2008 Apr 80 (4): 351-5. Tankanitlert Jeeranut, Morales Noppawan P, Fucharoen Pranee, Fucharoen Suthat, Chantharaksri Ud |
| Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis. World journal of gastroenterology : WJG 2005 Sep 11 (36): 5710-3. Huang Yang-Yang, Huang Ching-Shui, Yang Sien-Sing, Lin Min-Shung, Huang May-Jen, Huang Ching-Sh |
| Gilbert syndrome associated with beta-thalassemia. Pediatric hematology and oncology 2001 Dec 18 (8): 477-84. Tzetis M, Kanavakis E, Tsezou A, Ladis V, Pateraki E, Georgakopoulou T, Kavazarakis E, Maragoudaki E, Karpathios T, Kitsiou-Tzeli |
| The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. Blood cells, molecules & diseases 0 31 (1): 98-101. Premawardhena A, Fisher C A, Liu Y T, Verma I C, de Silva S, Arambepola M, Clegg J B, Weatherall D |
| UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease. Annals of Saudi medicine 0 33 (4): 372-6. Hamad Zainab, Aljedai Abdullah, Halwani Rabih, AlSultan Abdulrahm |
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- Page last updated:Mar 30, 2023
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