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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 |
| Correlates of gallbladder stones among patients with sickle cell disease: A meta-analysis. JGH open : an open access journal of gastroenterology and hepatology 2021 9 5 (9): 997-1003. Mohamed Sagad O O, Ibrahim Omer A O, Mohammad Dahlia A A, Ali Almigdad H |
| 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 |
| Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population. Journal of clinical and experimental hepatology 2018 Dec 8 (4): 362-366. Bale Govardhan, Avanthi Urmila S, Padaki N Rao, Sharma Mithun, Duvvur N Reddy, Vishnubhotla V Ravi Kan |
| 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 link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1. Hematology (Amsterdam, Netherlands) 2015 Jul . Chaouch Leila, Kalai1 Miniar, Darragi Imen, Boudrigua Imen, Chaouachi Dorra, Ammar Slim Ben, Mellouli F, Bjaoui M, Abbes Sal |
| Early complication in Sickle Cell Anemia children due to A(TA)<formula>_n</formula> TAA polymorphism at the promoter of UGT1A1 gene. Disease markers 2013 Apr . Chaouch Leila, Talbi Emna, Moumni Imen, Ben Chaabene Arij, Kalai Miniar, Chaouachi Dorra, Mallouli Fethi, Ghanem Abderraouf, Abbes Sal |
| Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene. Disease markers 2013 35 (2): 67-72. Chaouch Leila, Talbi Emna, Moumni Imen, Ben Chaabene Arij, Kalai Miniar, Chaouachi Dorra, Mallouli Fethi, Ghanem Abderraouf, Abbes Sal |
| The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients. PloS one 2013 8 (10): e77681. AlFadhli Suad, Al-Jafer Hassan, Hadi Mays, Al-Mutairi Mashael, Nizam Rashee |
| Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia. Annales de biologie clinique 2012 Dec 70 (6): 6. Chaouch L, Said Y, Moumni I, Mahjoubi I, Chaabene AB, Darragi I, Ghanem A, Abbes S |
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PloS one 2012 7 (4): e34741. Milton Jacqueline N, Sebastiani Paola, Solovieff Nadia, Hartley Stephen W, Bhatnagar Pallav, Arking Dan E, Dworkis Daniel A, Casella James F, Barron-Casella Emily, Bean Christopher J, Hooper W Craig, DeBaun Michael R, Garrett Melanie E, Soldano Karen, Telen Marilyn J, Ashley-Koch Allison, Gladwin Mark T, Baldwin Clinton T, Steinberg Martin H, Klings Elizabeth |
| Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population. Genetic testing and molecular biomarkers 2009 Feb 13 (1): 1. Tsezou A, Tzetis M, Giannatou E, Spanos I, Roma E, Fretzayas A, Kanavakis E, Kitsiou-Tzeli S |
| 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 |
| Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism. Journal of human genetics 2008 53 (6): 524-8. Martins Rute, Morais Anabela, Dias Alexandra, Soares Isabel, Rolão Cristiana, Ducla-Soares J L, Braga Lígia, Seixas Teresa, Nunes Baltazar, Olim Gabriel, Romão Luísa, Lavinha João, Faustino Pau |
| The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease. British journal of haematology 2007 Jul 138 (2): 263-70. Vasavda Nisha, Menzel Stephan, Kondaveeti Sheila, Maytham Emma, Awogbade Moji, Bannister Sybil, Cunningham Juliette, Eichholz Andrew, Daniel Yvonne, Okpala Iheanyi, Fulford Tony, Thein Swee L |
| 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 |
| Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia. Haematologica 2005 Feb 90 (2): 188-99. Chaar Vicky, Kéclard Lysiane, Diara Jean Pierre, Leturdu Claudine, Elion Jacques, Krishnamoorthy Rajagopal, Clayton John, Romana Ma |
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- Page last updated:Mar 22, 2023
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