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Apr 28, 2016 (publication date) through Nov 28, 2024
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Publication Name
World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Chandhok G, Horvath J, Aggarwal A, Bhatt M, Zibert A, Schmidt HH. Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines. World J Gastroenterol 2016; 22(16): 4109-4119 [PMID: 27122662 DOI: 10.3748/wjg.v22.i16.4109] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v22/i16/4109.htm |
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Niti Kumari, Aman Kumar, Babu Ram Thapa, Manish Modi, Arnab Pal, Rajendra Prasad. Characterization of mutation spectrum and identification of novel mutations in ATP7B
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Sarah Guttmann, Friedrich Bernick, Magdalena Naorniakowska, Ulf Michgehl, Sara Reinartz Groba, Piotr Socha, Andree Zibert, Hartmut H. Schmidt. Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease. Frontiers in Pediatrics 2018; 6 doi: 10.3389/fped.2018.00106
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Cortnie Hartwig, Stephanie A Zlatic, Melissa Wallin, Alysia Vrailas-Mortimer, Christoph J Fahrni, Victor Faundez. Trafficking mechanisms of P-type ATPase copper transporters. Current Opinion in Cell Biology 2019; 59: 24 doi: 10.1016/j.ceb.2019.02.009
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Roman S. Polishchuk, Elena V. Polishchuk. From and to the Golgi – defining the Wilson disease protein road map. FEBS Letters 2019; 593(17): 2341 doi: 10.1002/1873-3468.13575
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Biplab K. Maiti, José J. G. Moura. Diverse biological roles of the tetrathiomolybdate anion. Coordination Chemistry Reviews 2021; 429: 213635 doi: 10.1016/j.ccr.2020.213635
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Simona Allocca, Michela Ciano, Maria Camilla Ciardulli, Chiara D’Ambrosio, Andrea Scaloni, Daniela Sarnataro, Maria Gabriella Caporaso, Massimo D’Agostino, Stefano Bonatti. An αB-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population. International Journal of Molecular Sciences 2018; 19(7): 1892 doi: 10.3390/ijms19071892
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Julia Smirnova, Ekaterina Kabin, Ivar Järving, Olga Bragina, Vello Tõugu, Thomas Plitz, Peep Palumaa. Copper(I)-binding properties of de-coppering drugs for the treatment of Wilson disease. α-Lipoic acid as a potential anti-copper agent. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-19873-2
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Jie Chen, Wenming Yang, Ting Dong, Huaizhen Chen, Jing Zhang, Guocun Xu, Chenling Zhao, Jingyu Zeng, Lulu Tang. Quercetin ameliorates liver fibrosis in Wilson disease and EMT involving suppression of the Hedgehog signaling pathway. Arabian Journal of Chemistry 2024; 17(1): 105487 doi: 10.1016/j.arabjc.2023.105487
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Roman S. Polishchuk. Clinical and Translational Perspectives on WILSON DISEASE. 2019; : 45 doi: 10.1016/B978-0-12-810532-0.00006-9
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Michael Pöhler, Sarah Guttmann, Oksana Nadzemova, Malte Lenders, Eva Brand, Andree Zibert, Hartmut H. Schmidt, Vanessa Sandfort, Oleg Y. Dmitriev. CRISPR/Cas9-mediated correction of mutated copper transporter ATP7B. PLOS ONE 2020; 15(9): e0239411 doi: 10.1371/journal.pone.0239411
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Meng-Hsuan Wen, Xihong Xie, Pei-San Huang, Karen Yang, Tai-Yen Chen. Crossroads between membrane trafficking machinery and copper homeostasis in the nerve system. Open Biology 2021; 11(12) doi: 10.1098/rsob.210128
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