Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Cholestasis and ATP8B1[original query] |
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ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy. Gut 2005 Jun 54 (6): 829-34. Müllenbach R, Bennett A, Tetlow N, Patel N, Hamilton G, Cheng F, Chambers J, Howard R, Taylor-Robinson S D, Williamson |
Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy. European journal of human genetics : EJHG 2005 1 13 (4): 435-9. Painter Jodie N, Savander Miia, Ropponen Anne, Nupponen Nina, Riikonen Seija, Ylikorkala Olavi, Lehesjoki Anna-Elina, Aittomäki Kristii |
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 comprehensive analysis of common genetic variation around six candidate loci for intrahepatic cholestasis of pregnancy. The American journal of gastroenterology 2014 Jan 109 (1): 76-84. Dixon Peter H, Wadsworth Christopher A, Chambers Jennifer, Donnelly Jennifer, Cooley Sharon, Buckley Rebecca, Mannino Ramona, Jarvis Sheba, Syngelaki Argyro, Geenes Victoria, Paul Priyadarshini, Sothinathan Meera, Kubitz Ralf, Lammert Frank, Tribe Rachel M, Ch'ng Chin Lye, Marschall Hanns-Ulrich, Glantz Anna, Khan Shahid A, Nicolaides Kypros, Whittaker John, Geary Michael, Williamson Catheri |
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 |
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 |
The role of genetic mutations in intrahepatic cholestasis of pregnancy. Taiwanese journal of obstetrics & gynecology 2020 Sep 59 (5): 706-710. Ayd?n Gültekin Adana?, Özgen Gülten, Görükmez Orh |
Whole-Genome Sequencing Reveals Large ATP8B1 Deletion/Duplications as Second Mutations Missed by Exome-Based Sequencing. The Journal of molecular diagnostics : JMD 2021 9 23 (11): 1491-1499. Yang Ye, Zhang Jing, Li Li-Ting, Qiu Yi-Ling, Gong Jing-Yu, Zhang Mei-Hong, Li Cai-Hua, Wang Jian-S |
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 |
Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency. Hepatology (Baltimore, Md.) 2021 3 74 (2): 892-906. van Wessel Daan B E, Thompson Richard J, Gonzales Emmanuel, Jankowska Irena, Shneider Benjamin L, Sokal Etienne, Grammatikopoulos Tassos, Kadaristiana Agustina, Jacquemin Emmanuel, Spraul Anne, Lipi?ski Patryk, Czubkowski Piotr, Rock Nathalie, Shagrani Mohammad, Broering Dieter, Algoufi Talal, Mazhar Nejat, Nicastro Emanuele, Kelly Deirdre, Nebbia Gabriella, Arnell Henrik, Fischler Björn, Hulscher Jan B F, Serranti Daniele, Arikan Cigdem, Debray Dominique, Lacaille Florence, Goncalves Cristina, Hierro Loreto, Muñoz Bartolo Gema, Mozer-Glassberg Yael, Azaz Amer, Brecelj Jernej, Dezs?fi Antal, Luigi Calvo Pier, Krebs-Schmitt Dorothee, Hartleif Steffen, van der Woerd Wendy L, Wang Jian-She, Li Li-Ting, Durmaz Özlem, Kerkar Nanda, Hørby Jørgensen Marianne, Fischer Ryan, Jimenez-Rivera Carolina, Alam Seema, Cananzi Mara, Laverdure Noémie, Targa Ferreira Cristina, Ordonez Felipe, Wang Heng, Sency Valerie, Mo Kim Kyung, Chen Huey-Ling, Carvalho Elisa, Fabre Alexandre, Quintero Bernabeu Jesus, Alonso Estella M, Sokol Ronald J, Suchy Frederick J, Loomes Kathleen M, McKiernan Patrick J, Rosenthal Philip, Turmelle Yumirle, Rao Girish S, Horslen Simon, Kamath Binita M, Rogalidou Maria, Karnsakul Wikrom W, Hansen Bettina, Verkade Henkjan J, |
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 |
Progressive Familial Intrahepatic Cholestasis: Need for Genetic Analysis Before Liver Transplantation. Journal of clinical and experimental hepatology 2022 5 12 (2): 686-688. Lal Bikrant B, Sood Vikrant, Jain Kavita, Bihari Chhagan, Khanna Rajeev, Alam See |
Genetic issues in ICP. Obstetric medicine 2024 9 17 (3): 157-161. Julia Zöllner, Catherine Williamson, Peter H Dix |
- Page last reviewed:Feb 1, 2024
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