Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Supplementary Materials of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (9972)
All Articles published online
|
Featured Article
|
Publishing Process of This Article
|
Apr 28, 2016 (publication date) through Jun 11, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
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] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v22/i16/4109.htm |
| Number | Citing Articles |
| 1 |
Dongkyu Kim, Su-Bin Kim, Jung Lim Ryu, Heesu Hong, Jin-Hyuk Chang, Tack-Jin Yoo, Xiong Jin, Han-Jin Park, Choongseong Han, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo, Jong-Hoon Kim, Dong-Hun Woo. Human Embryonic Stem Cell-Derived Wilson’s Disease Model for Screening Drug Efficacy. Cells 2020; 9(4): 872 doi: 10.3390/cells9040872
|
| 2 |
Niti Kumari, Aman Kumar, Babu Ram Thapa, Manish Modi, Arnab Pal, Rajendra Prasad. Characterization of mutation spectrum and identification of novel mutations in ATP7B
gene from a cohort of Wilson disease patients: Functional and therapeutic implications. Human Mutation 2018; 39(12): 1926 doi: 10.1002/humu.23614
|
| 3 |
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
|
| 4 |
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
|
| 5 |
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
|
| 6 |
Miao Wang, Ruoqi Zhang, Wim Dehaen, Yuyu Fang, Shan Qian, Yali Ren, Fang Cheng, Yuying Guo, Chuanjie Guo, Yuzhi Li, Yun Deng, Zhixing Cao, Cheng Peng. Specific recognition, intracellular assay and detoxification of fluorescent curcumin derivative for copper ions. Journal of Hazardous Materials 2021; 420: 126490 doi: 10.1016/j.jhazmat.2021.126490
|
| 7 |
Xiaojin Li, Wei Zhang, Donghu Zhou, Tingxia Lv, Anjian Xu, Hejing Wang, Xinyan Zhao, Bei Zhang, Yanmeng Li, Siyu Jia, Yu Wang, Xiaoming Wang, Zhen Wu, Weijia Duan, Qianyi Wang, Yuemin Nan, Jia Shang, Wei Jiang, Yongpeng Chen, Sujun Zheng, Mei Liu, Liying Sun, Hong You, Jidong Jia, Xiaojuan Ou, Jian Huang. Complex ATP7B
mutation patterns in Wilson disease and evaluation of a yeast model for functional analysis of variants. Human Mutation 2019; 40(5): 552 doi: 10.1002/humu.23714
|
| 8 |
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
|
| 9 |
Simona Allocca, Michela Ciano, Maria Ciardulli, Chiara D’Ambrosio, Andrea Scaloni, Daniela Sarnataro, Maria 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
|
| 10 |
Kelly C. Falls-Hubert, Aimee L. Butler, Kai Gui, Michael Anderson, Mengshi Li, Jeffrey M. Stolwijk, Samuel N. Rodman, Shane R. Solst, Ann Tomanek-Chalkley, Charles C. Searby, Val C. Sheffield, Vanessa Sandfort, Hartmut Schmidt, Michael L. McCormick, Brian R. Wels, Bryan G. Allen, Garry R. Buettner, Michael K. Schultz, Douglas R. Spitz. Disulfiram causes selective hypoxic cancer cell toxicity and radio-chemo-sensitization via redox cycling of copper. Free Radical Biology and Medicine 2020; 150: 1 doi: 10.1016/j.freeradbiomed.2020.01.186
|
| 11 |
Grażyna Gromadzka, Maria Bendykowska, Adam Przybyłkowski. Wilson’s Disease—Genetic Puzzles with Diagnostic Implications. Diagnostics 2023; 13(7): 1287 doi: 10.3390/diagnostics13071287
|
| 12 |
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
|
| 13 |
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
|
| 14 |
Roman S. Polishchuk. Clinical and Translational Perspectives on WILSON DISEASE. 2019; : 45 doi: 10.1016/B978-0-12-810532-0.00006-9
|
| 15 |
Ganna M. Shayakhmetova, Larysa B. Bondarenko, Alla K. Voronina, Valentina M. Kovalenko. Comparative investigation of methionine and novel formulation Metovitan protective effects in Wistar rats with testicular and epididymal toxicity induced by anti-tuberculosis drugs co-administration. Food and Chemical Toxicology 2017; 99: 222 doi: 10.1016/j.fct.2016.12.001
|
| 16 |
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
|
| 17 |
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
|
| 18 |
Mafalda Concilli, Raffaella Petruzzelli, Silvia Parisi, Federico Catalano, Francesco Sirci, Francesco Napolitano, Mario Renda, Luis J. V. Galietta, Diego Di Bernardo, Roman S. Polishchuk. Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7B. Proceedings of the National Academy of Sciences 2020; 117(51): 32453 doi: 10.1073/pnas.2006648117
|
| 19 |
Polarized trafficking and copper transport activity of ATP7B: A mutational approach to establish genotype–phenotype correlation in Wilson disease. Human Mutation 2022; 43(10): 1408 doi: 10.1002/humu.24428
|
| 20 |
Silvia Parisi, Elena V. Polishchuk, Simona Allocca, Michela Ciano, Anna Musto, Maria Gallo, Lucia Perone, Giusy Ranucci, Raffaele Iorio, Roman S. Polishchuk, Stefano Bonatti. Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-24717-0
|
| 21 |
Annu Aggarwal, Mohit Bhatt. Clinical and Translational Perspectives on WILSON DISEASE. 2019; : 195 doi: 10.1016/B978-0-12-810532-0.00018-5
|