Human Genome Epidemiology Literature Finder
|
Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and NR1H4[original query] |
|---|
| 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 |
| Association of genetic variation in the NR1H4 gene, encoding the nuclear bile acid receptor FXR, with inflammatory bowel disease. BMC research notes 2012 Aug 5 (1): 1. Attinkara R, Mwinyi J, Truninger K, Regula J, Gaj P, Rogler G, Kullak-Ublick GA, Eloranta JJ |
| Polymorphisms in the organic anion transporting polypeptide genes influence liver parenchymal enhancement in gadoxetic acid-enhanced MRI. Pharmacogenomics 2013 Oct 14 (13): 1573-82. Okubo Hironao, Ando Hitoshi, Kokubu Shigehiro, Miyazaki Akihisa, Watanabe Sumio, Fujimura Ak |
| Mild Methylenetetrahydrofolate Reductase Deficiency Alters Inflammatory and Lipid Pathways in Liver. Molecular nutrition & food research 2018 Nov e1801001. Leclerc Daniel, Christensen Karen E, Cauvi Olivia, Yang Ethan, Fournelle Frédéric, Bahous Renata H, Malysheva Olga V, Deng Liyuan, Wu Qing, Zhou Zili, Gao Zu-Hua, Chaurand Pierre, Caudill Marie A, Rozen Ri |
| NR1H4 rs35724 G>C variant modulates liver damage in nonalcoholic fatty liver disease. Liver international : official journal of the International Association for the Study of the Liver 2021 Jul . Grimaudo Stefania, Dongiovanni Paola, Pihlajamäki Jussi, Eslam Mohammed, Yki-Järvinen Hannele, Pipitone Rosaria Maria, Baselli Guido, Cammà Calogero, Di Marco Vito, Enea Marco, Longo Miriam, Pennisi Grazia, Prati Daniele, Zito Rossella, Fracanzani Anna Ludovica, Craxì Antonio, George Jacob, Romeo Stefano, Valenti Luca, Petta Salvato |
| Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids. Hepatology communications 2022 Sep . Handelman Samuel K, Puentes Yindra M, Kuppa Annapurna, Chen Yanhua, Du Xiaomeng, Feitosa Mary F, Palmer Nicholette D, Speliotes Elizabeth |
| Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients. BMC medical genomics 2022 4 15 (1): 90. Lai Hua, Liu Xianxian, Xin Siming, Zheng Jiusheng, Liu Huai, Ouyang Yu, Yang Huoxiu, Zeng Yang, Zou Yang, Zeng Xiaomi |
| The Role of FXR-Signaling Variability in the Development and Course of Non-Alcoholic Fatty Liver Disease in Children. Acta medica (Hradec Kralove) 2023 2 65 (3): 105-111. Stepanov Yuriy, Zavhorodnia Natalia, Klenina Inna, Grabovska Olena, Yagmur Viktor |
| Genetic issues in ICP. Obstetric medicine 2024 9 17 (3): 157-161. Julia Zöllner, Catherine Williamson, Peter H Dix |
| Meta-analyses uncover the genetic architecture of Idiopathic Inflammatory Myopathies. Arthritis & rheumatology (Hoboken, N.J.) 2024 12 . Catherine Zhu, Younghun Han, Jinyoung Byun, Xiangjun Xiao, Simon Rothwell, Frederick W Miller, Ingrid E Lundberg, Peter K Gregersen, Jiri Vencovsky, Vikram R Shaw, Neil McHugh, Vidya Limaye, Albert Selva-O'Callaghan, Michael G Hanna, Pedro M Machado, Lauren M Pachman, Ann M Reed, Lisa G Rider, Øyvind Molberg, Olivier Benveniste, Timothy Radstake, Andrea Doria, Jan L De Bleecker, Boel De Paepe, Britta Maurer, William E Ollier, Leonid Padyukov, Lucy R Wedderburn, Hector Chinoy, Janine A Lamb, Christopher I Amos, |
- Page last reviewed:Feb 1, 2024
- Content source: