HuGE Literature Finder
Records 1-25
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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 |
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Deferasirox pharmacogenetic influence on pharmacokinetic, efficacy and toxicity in a cohort of pediatric patients.
Pharmacogenomics 2017 Mar . Allegra Sarah, De Francia Silvia, Cusato Jessica, Arduino Arianna, Massano Davide, Longo Filomena, Piga Antonio, D'Avolio Anton |
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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 |
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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 |
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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, |
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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 |
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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 |
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 |
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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 |
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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 |
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Cholelithiasis in thalassemia major.
European journal of haematology 2009 Jan 82 (1): 22-5. Origa Raffaella, Galanello Renzo, Perseu Lucia, Tavazzi Dario, Domenica Cappellini M, Terenzani Laura, Forni Gian Luca, Quarta Giovanni, Boetti Tatiana, Piga Anton |
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UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
American journal of hematology 2008 Oct 83 (10): 800-3. Carpenter Shannon L, Lieff Susan, Howard Thad A, Eggleston Barry, Ware Russell |
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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 |
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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 |
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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 |
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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 |
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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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UGT1A1 variation and gallstone formation in sickle cell disease.
Blood 2005 Feb 105 (3): 968-72. Haverfield Eden V, McKenzie Colin A, Forrester Terrence, Bouzekri Nourdine, Harding Rosalind, Serjeant Graham, Walker Thomas, Peto Tim E A, Ward Ryk, Weatherall David |
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Thalassemia minor, the Gilbert mutation, and the risk of gallstones.
Haematologica 2003 Oct 88 (10): 1106-9. Borgna-Pignatti Caterina, Rigon Francesca, Merlo Luciano, Chakrok Roksana, Micciolo Rocco, Perseu Luciana, Galanello Ren |
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UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemia.
The Journal of laboratory and clinical medicine 2003 Apr 141 (4): 279-82. Heeney Matthew M, Howard Thad A, Zimmerman Sherri A, Ware Russell |
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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 |
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Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Journal of pediatric hematology/oncology 2001 Oct 23 (7): 448-51. Passon R G, Howard T A, Zimmerman S A, Schultz W H, Ware R |
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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.
Blood cells, molecules & diseases 0 31 (1): 38-42. Kalotychou Vassiliki, Antonatou Katerina, Tzanetea Revekka, Terpos Evaggelos, Loukopoulos Dimitris, Rombos Yann |
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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 |
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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:Sep 23, 2020
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