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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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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Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article.
Medicine 2015 Jun 94 (22): e925. Oussalah Abderrahim, Bosco Paolo, Anello Guido, Spada Rosario, Guéant-Rodriguez Rosa-Maria, Chery Céline, Rouyer Pierre, Josse Thomas, Romano Antonino, Elia Maurizzio, Bronowicki Jean-Pierre, Guéant Jean-Lou |
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Extreme bilirubin levels as a causal risk factor for symptomatic gallstone disease.
JAMA internal medicine 2013 Jul 173 (13): 13. Stender S, Frikke-Schmidt R, Nordestgaard BG, Tybjærg-Hansen A |
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Gallstone disease in Swedish twins is associated with the Gilbert variant of UGT1A1.
Liver international : official journal of the International Association for the Study of the Liver 2013 Jul 33 (6): 904-8. Marschall Hanns-Ulrich, Krawczyk Marcin, Grünhage Frank, Katsika Despina, Einarsson Curt, Lammert Fra |
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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 |
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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 |
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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 |
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Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition.
Gastroenterology 2010 Dec 139 (6): 1942-1951.e2. Buch Stephan, Schafmayer Clemens, Völzke Henry, Seeger Marcus, Miquel Juan F, Sookoian Silvia C, Egberts Jan H, Arlt Alexander, Pirola Carlos J, Lerch Markus M, John Ulrich, Franke Andre, von Kampen Oliver, Brosch Mario, Nothnagel Michael, Kratzer Wolfgang, Boehm Bernhard O, Bröring Dieter C, Schreiber Stefan, Krawczak Michael, Hampe Joch |
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Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism is associated with choledocholithiasis in Taiwanese patients.
Journal of gastroenterology and hepatology 2009 Sep 24 (9): 1559-61. Chu Cheng-Hsin, Yang An-Ming, Kao Jia-Horng, Liu Chia-Yuan, Chang Wen-Hsiung, Yang Wei-Shiu |
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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 |
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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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Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population.
Genetic testing 2009 Jan . Tsezou A, Tzetis M, Giannatou E, Spanos I, Roma E, Fretzayas A, Kanavakis E, Kitsiou-Tzeli S |
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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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Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.
Hepatology (Baltimore, Md.) 2006 Apr 43 (4): 738-41. Wasmuth Hermann E, Keppeler Hildegard, Herrmann Ulrike, Schirin-Sokhan Ramin, Barker Michael, Lammert Fra |
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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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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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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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