Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Gallstones and UGT1A1[original query] |
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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 |
| 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 |
| 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 |
| 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 |
Genome-wide association meta-analysis for total serum bilirubin levels.
Human molecular genetics 2009 Jul 18 (14): 2700-10. Johnson Andrew D, Kavousi Maryam, Smith Albert V, Chen Ming-Huei, Dehghan Abbas, Aspelund Thor, Lin Jing-Ping, van Duijn Cornelia M, Harris Tamara B, Cupples L Adrienne, Uitterlinden Andre G, Launer Lenore, Hofman Albert, Rivadeneira Fernando, Stricker Bruno, Yang Qiong, O'Donnell Christopher J, Gudnason Vilmundur, Witteman Jacqueline |
| 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 |
| 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 |
| 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 |
| 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 |
| Polymorphisms in UGT1A1 Gene Predispose South Indians to Pigmentous Gallstones. Journal of clinical and experimental hepatology 2016 Sep 6 (3): 216-223. Ravikanth Vishnubhotla Venkata, Rao Guduru Venkat, Govardhan Bale, Sasikala Mitnala, Subramanyam Chivukula, Vivekananda Murthy H V, Siva Prasad Siddapuram, Deepika G, Pradeep Rebala, Nageshwar Reddy Duvvu |
| 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 |
| Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria. BMC medical genetics 2019 Oct 20 (1): 160. Olatunya Oladele Simeon, Albuquerque Dulcineia Martins, Akanbi Ganiyu Olusola, Aduayi Olufunso Simisola, Taiwo Adekunle Bamidele, Faboya Opeyemi Ayodeji, Kayode Tolorunju Segun, Leonardo Daniela Pinheiro, Adekile Adekunle, Costa Fernando Ferrei |
| 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 |
| Common variant p.D19H of the hepatobiliary sterol transporter ABCG8 increases the risk of gallstones in children. Liver international : official journal of the International Association for the Study of the Liver 2022 Feb . Krawczyk Marcin, Niewiadomska Olga, Jankowska Irena, Jankowski Krzysztof, Wi?ckowski Sebastian, Lebensztejn Dariusz, Wi?cek Sabina, Gozdowska Jolanta, Ku?aga Zbigniew, Weber Susanne N, Lütjohann Dieter, Lammert Frank, Socha Pio |
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