Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and ABCB11[original query] |
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| Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy. Pharmacogenetics 2004 Feb 14 (2): 91-102. Pauli-Magnus C, Lang T, Meier Y, Zodan-Marin T, Jung D, Breymann C, Zimmermann R, Kenngott S, Beuers U, Reichel C, Kerb R, Penger A, Meier PJ, Kullak-Ublick GA |
| Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease. Hepatology (Baltimore, Md.) 2006 Sep 44 (3): 650-7. Schafmayer Clemens, Tepel Jürgen, Franke Andre, Buch Stephan, Lieb Sören, Seeger Marcus, Lammert Frank, Kremer Bernd, Fölsch Ulrich R, Fändrich Fred, Schreiber Stefan, Hampe Joch |
| Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy. Gut 2009 Apr 58 (4): 537-44. Dixon P H, van Mil S W C, Chambers J, Strautnieks S, Thompson R J, Lammert F, Kubitz R, Keitel V, Glantz A, Mattsson L-A, Marschall H-U, Molokhia M, Moore G E, Linton K J, Williamson |
| Genetic determinants of serum lipid levels in Chinese subjects: a population-based study in Shanghai, China. European journal of epidemiology 2009 24 (12): 763-74. Andreotti Gabriella, Menashe Idan, Chen Jinbo, Chang Shih-Chen, Rashid Asif, Gao Yu-Tang, Han Tian-Quan, Sakoda Lori C, Chanock Stephen, Rosenberg Philip S, Hsing Ann |
| Role of common canalicular transporter gene variations in aetiology of idiopathic gallstones in childhood. Folia biologica 2010 56 (1): 9-13. Bronský J, Jirsa M, Nevoral J, Hrebícek |
| A common polymorphism in the ABCB11 gene is associated with advanced fibrosis in hepatitis C but not in non-alcoholic fatty liver disease. Clinical science (London, England : 1979) 2011 Apr 120 (7): 287-96. Iwata Rika, Baur Katharina, Stieger Bruno, Mertens Joachim C, Daly Ann K, Frei Pascal, Braun Julia, Vergopoulos Athanasios, Stickel Felix, Sabrane Karim, Martin Ina V, Schmitt Johannes, Goetze Oliver, Day Chris P, Müllhaupt Beat, Geier Andreas, |
| Genetic factors in the pathogenesis of cholangiocarcinoma. Digestive diseases (Basel, Switzerland) 2011 29 (1): 93-7. Wadsworth Christopher A, Dixon Peter H, Wong Jason H, Chapman Michael H, McKay Siobhan C, Sharif Amar, Spalding Duncan R, Pereira Stephen P, Thomas Howard C, Taylor-Robinson Simon D, Whittaker John, Williamson Catherine, Khan Shahid |
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
Diabetes 2011 Apr 60 (4): 1329-39. Kraja Aldi T, Vaidya Dhananjay, Pankow James S, Goodarzi Mark O, Assimes Themistocles L, Kullo Iftikhar J, Sovio Ulla, Mathias Rasika A, Sun Yan V, Franceschini Nora, Absher Devin, Li Guo, Zhang Qunyuan, Feitosa Mary F, Glazer Nicole L, Haritunians Talin, Hartikainen Anna-Liisa, Knowles Joshua W, North Kari E, Iribarren Carlos, Kral Brian, Yanek Lisa, O'Reilly Paul F, McCarthy Mark I, Jaquish Cashell, Couper David J, Chakravarti Aravinda, Psaty Bruce M, Becker Lewis C, Province Michael A, Boerwinkle Eric, Quertermous Thomas, Palotie Leena, Jarvelin Marjo-Riitta, Becker Diane M, Kardia Sharon L R, Rotter Jerome I, Chen Yii-Der Ida, Borecki Ingrid |
| Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Nature genetics 2011 Nov 43 (11): 1131-8. Chambers John C, Zhang Weihua, Sehmi Joban, Li Xinzhong, Wass Mark N, Van der Harst Pim, Holm Hilma, Sanna Serena, Kavousi Maryam, Baumeister Sebastian E, Coin Lachlan J, Deng Guohong, Gieger Christian, Heard-Costa Nancy L, Hottenga Jouke-Jan, Kühnel Brigitte, Kumar Vinod, Lagou Vasiliki, Liang Liming, Luan Jian'an, Vidal Pedro Marques, Mateo Leach Irene, O'Reilly Paul F, Peden John F, Rahmioglu Nilufer, Soininen Pasi, Speliotes Elizabeth K, Yuan Xin, Thorleifsson Gudmar, Alizadeh Behrooz Z, Atwood Larry D, Borecki Ingrid B, Brown Morris J, Charoen Pimphen, Cucca Francesco, Das Debashish, de Geus Eco J C, Dixon Anna L, Döring Angela, Ehret Georg, Eyjolfsson Gudmundur I, Farrall Martin, Forouhi Nita G, Friedrich Nele, Goessling Wolfram, Gudbjartsson Daniel F, Harris Tamara B, Hartikainen Anna-Liisa, Heath Simon, Hirschfield Gideon M, Hofman Albert, Homuth Georg, Hyppönen Elina, Janssen Harry L A, Johnson Toby, Kangas Antti J, Kema Ido P, Kühn Jens P, Lai Sandra, Lathrop Mark, Lerch Markus M, Li Yun, Liang T Jake, Lin Jing-Ping, Loos Ruth J F, Martin Nicholas G, Moffatt Miriam F, Montgomery Grant W, Munroe Patricia B, Musunuru Kiran, Nakamura Yusuke, O'Donnell Christopher J, Olafsson Isleifur, Penninx Brenda W, Pouta Anneli, Prins Bram P, Prokopenko Inga, Puls Ralf, Ruokonen Aimo, Savolainen Markku J, Schlessinger David, Schouten Jeoffrey N L, Seedorf Udo, Sen-Chowdhry Srijita, Siminovitch Katherine A, Smit Johannes H, Spector Timothy D, Tan Wenting, Teslovich Tanya M, Tukiainen Taru, Uitterlinden Andre G, Van der Klauw Melanie M, Vasan Ramachandran S, Wallace Chris, Wallaschofski Henri, Wichmann H-Erich, Willemsen Gonneke, Würtz Peter, Xu Chun, Yerges-Armstrong Laura M, , , , , , , , Abecasis Goncalo R, Ahmadi Kourosh R, Boomsma Dorret I, Caulfield Mark, Cookson William O, van Duijn Cornelia M, Froguel Philippe, Matsuda Koichi, McCarthy Mark I, Meisinger Christa, Mooser Vincent, Pietiläinen Kirsi H, Schumann Gunter, Snieder Harold, Sternberg Michael J E, Stolk Ronald P, Thomas Howard C, Thorsteinsdottir Unnur, Uda Manuela, Waeber Gérard, Wareham Nicholas J, Waterworth Dawn M, Watkins Hugh, Whitfield John B, Witteman Jacqueline C M, Wolffenbuttel Bruce H R, Fox Caroline S, Ala-Korpela Mika, Stefansson Kari, Vollenweider Peter, Völzke Henry, Schadt Eric E, Scott James, Järvelin Marjo-Riitta, Elliott Paul, Kooner Jaspal |
| A frequent variant in the human bile salt export pump gene ABCB11 is associated with hepatitis C virus infection, but not liver stiffness in a German population. BMC gastroenterology 2012 12 63. Müllenbach Roman, Weber Susanne N, Krawczyk Marcin, Zimmer Vincent, Sarrazin Christoph, Lammert Frank, Grünhage Fra |
| Genetic variations in bile acid homeostasis are not overrepresented in alcoholic cirrhosis compared to patients with heavy alcohol abuse and absent liver disease. Mutagenesis 2012 Sep 27 (5): 567-72. Many Natalie, Stickel Felix, Schmitt Johannes, Stieger Bruno, Soyka Michael, Frei Pascal, Götze Oliver, Müllhaupt Beat, Geier Andre |
| Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencing. Molecular medicine reports 2014 Sep 10 (3): 1264-74. Hu Guorui, He Ping, Liu Zhifeng, Chen Qian, Zheng Bixia, Zhang Qih |
| Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis. Hepatology research : the official journal of the Japan Society of Hepatology 2015 Jun . Goldschmidt Monique L, Mourya Reena, Connor Jessica, Dexheimer Phillip, Karns Rebekah, Miethke Alexander, Sheridan Rachel, Zhang Kejian, Bezerra Jorge |
| No contribution of the ABCB11 p.444A polymorphism in Japanese patients with drug-induced cholestasis. Drug metabolism and disposition: the biological fate of chemicals 2015 May 43 (5): 691-7. Kagawa Tatehiro, Hirose Shunji, Arase Yoshitaka, Oka Akira, Anzai Kazuya, Tsuruya Kota, Shiraishi Koichi, Orii Reiko, Ieda Satsuki, Nakazawa Takahide, Tomita Kengo, Hokari Ryota, Miura Soichiro, Ebinuma Hirotoshi, Saito Hidetsugu, Kitamura Tsuneo, Horie Yoshinori, Okuse Chiaki, Wasada Mitsuru, Inoko Hidetoshi, Tohkin Masahiro, Saito Yoshiro, Maekawa Keiko, Takikawa Hajime, Mine Tetsu |
| Triplex High-Resolution Melting Assay for the Simultaneous Assessment of IFNL3 rs12979860, ABCB11 rs2287622, and RNF7 rs16851720 Genotypes in Chronic Hepatitis C Patients. The Journal of molecular diagnostics : JMD 2017 9 19 (6): 857-869. Enache Elena L, Sin Anca, Enache Liviu S, Bancu Lig |
| Sequencing of FIC1, BSEP and MDR3 in a large cohort of patients with cholestasis revealed a high number of different genetic variants. Journal of hepatology 2017 12 67 (6): 1253-1264. Dröge Carola, Bonus Michele, Baumann Ulrich, Klindt Caroline, Lainka Elke, Kathemann Simone, Brinkert Florian, Grabhorn Enke, Pfister Eva-Doreen, Wenning Daniel, Fichtner Alexander, Gotthardt Daniel N, Weiss Karl Heinz, McKiernan Patrick, Puri Ratna Dua, Verma I C, Kluge Stefanie, Gohlke Holger, Schmitt Lutz, Kubitz Ralf, Häussinger Dieter, Keitel Vere |
| Molecular findings in children with inherited intrahepatic cholestasis. Pediatric research 2019 Aug . Wang Neng-Li, Lu Yi, Gong Jing-Yu, Xie Xin-Bao, Lin Jing, Abuduxikuer Kuerbanjiang, Zhang Mei-Hong, Wang Jian-S |
| Whole-exome sequencing reveals ANO8 as a genetic risk factor for intrahepatic cholestasis of pregnancy. BMC pregnancy and childbirth 2020 Sep 20 (1): 544. Liu Xianxian, Lai Hua, Zeng Xiaoming, Xin Siming, Nie Liju, Liang Zhenyi, Wu Meiling, Chen Yu, Zheng Jiusheng, Zou Ya |
| Common ABCB4 and ABCB11 Genotypes Are Associated with Idiopathic Chronic Cholestasis in Adults. Digestive diseases (Basel, Switzerland) 2021 8 40 (4): 489-496. Jüngst Christoph, Justinger Christina, Fischer Janett, Berg Thomas, Lammert Fra |
| ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes. The Journal of pediatrics 2021 4 236 113-123.e2. Al-Hussaini Abdulrahman, Lone Khurram, Bashir Muhammed Salman, Alrashidi Sami, Fagih Mosa, Alanazi Alanoud, AlYaseen Salem, Almayouf Abdulaziz, Alruwaithi Muhanad, Asery A |
| The role of p.Val444Ala variant in the ABCB11 gene and susceptibility to biliary atresia in Vietnamese patients. Medicine 2021 12 100 (47): e28011. Van Tung Nguyen, Lien Nguyen Thi Kim, Lan Nguyen Ngoc, Mai Nguyen Thi Phuong, Yen Pham Thi Hai, Hoa Nguyen Pham Anh, Hoang Nguyen H |
| Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1. Hepatology communications 2022 7 6 (10): 2654-2664. Nayagam Jeremy S, Foskett Pierre, Strautnieks Sandra, Agarwal Kosh, Miquel Rosa, Joshi Deepak, Thompson Richard |
| Association of Drug-Metabolizing Enzyme and Transporter Gene Polymorphisms and Lipid-Lowering Response to Statins in Thai Patients with Dyslipidemia. Pharmacogenomics and personalized medicine 2022 15 119-130. Vanwong Natchaya, Tipnoppanon Sayanit, Na Nakorn Chalitpon, Srisawasdi Pornpen, Rodcharoen Punyanuch, Medhasi Sadeep, Chariyavilaskul Pajaree, Siwamogsatham Sarawut, Vorasettakarnkij Yongkasem, Sukasem Chonlaph |
| Genetic issues in ICP. Obstetric medicine 2024 9 17 (3): 157-161. Julia Zöllner, Catherine Williamson, Peter H Dix |
| Genome-Wide Association Study (GWAS) for Left Displaced Abomasum in Highly Productive Russian Holstein Cattle. Animals : an open access journal from MDPI 2024 10 14 (19): . Kirill Plemyashov, Anna Krutikova, Angelina Belikova, Tatiana Kuznetsova, Boris Semen |
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