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Cited by in CrossRef
For: Simon I, Schaefer M, Reichert J, Stremmel W. Analysis of the human Atox 1 homologue in Wilson patients. World J Gastroenterol 2008; 14(15): 2383-2387 [PMID: 18416466 DOI: 10.3748/wjg.14.2383]
URL: https://www.wjgnet.com/1007-9327/full/v14/i15/2383.htm
Number Citing Articles
1
A Zarina, I Tolmane, Z Krumina, AI Tutane, L Gailite. Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in LatviaBalkan Journal of Medical Genetics 2019; 22(2): 37 doi: 10.2478/bjmg-2019-0023
2
Ana Sánchez-Monteagudo, Edna Ripollés, Marina Berenguer, Carmen Espinós. Wilson’s Disease: Facing the Challenge of Diagnosing a Rare DiseaseBiomedicines 2021; 9(9): 1100 doi: 10.3390/biomedicines9091100
3
Stefanie D. Boyd, Morgan S. Ullrich, Amelie Skopp, Duane D. Winkler. Copper Sources for Sod1 ActivationAntioxidants 2020; 9(6): 500 doi: 10.3390/antiox9060500
4
Rosanna Squitti, Mariacarla Ventriglia, Massimo Gennarelli, Nicola A. Colabufo, Imane Ghafir El Idrissi, Serena Bucossi, Stefania Mariani, Mauro Rongioletti, Orazio Zanetti, Chiara Congiu, Paolo M. Rossini, Cristian Bonvicini. Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer’s Disease: a Genetic Study of ATP7B FrequencyMolecular Neurobiology 2017; 54(1): 671 doi: 10.1007/s12035-015-9664-6
5
Dorothy A. Kieffer, Valentina Medici. Wilson disease: At the crossroads between genetics and epigenetics—A review of the evidenceLiver Research 2017; 1(2): 121 doi: 10.1016/j.livres.2017.08.003
6
Magdalena Araya, Monica Andrews, Fernando Pizarro, Miguel Arredondo. Chaperones CCS, ATOX and COXIV responses to copper supplementation in healthy adultsBioMetals 2012; 25(2): 383 doi: 10.1007/s10534-011-9511-9
7
I. Zh. Zhalsanova, E. A. Fonova, D. I. Zhigalina, N. A. Skryabin. The ATOX1 Gene Role in Copper Metabolism and the Pathogenesis of Copper-Induced DiseasesRussian Journal of Genetics 2023; 59(3): 242 doi: 10.1134/S1022795423030122
8
Radan Bruha, Libor Vitek, Zdenek Marecek, Lenka Pospisilova, Sona Nevsimalova, Pavel Martasek, Jaromir Petrtyl, Petr Urbanek, Alena Jiraskova, Ivana Malikova, Martin Haluzik, Peter Ferenci. Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptomsJournal of Inherited Metabolic Disease 2012; 35(3): 541 doi: 10.1007/s10545-011-9422-5
9
Louis C. Penning, Marina Berenguer, Anna Czlonkowska, Kay L. Double, Petr Dusek, Carmen Espinós, Svetlana Lutsenko, Valentina Medici, Wiebke Papenthin, Wolfgang Stremmel, Jose Willemse, Ralf Weiskirchen. A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and TreatmentBiomedicines 2023; 11(2): 420 doi: 10.3390/biomedicines11020420
10
Ayca Cankorur-Cetinkaya, Serpil Eraslan, Betul Kirdar. Transcriptomic response of yeast cells to ATX1 deletion under different copper levelsBMC Genomics 2016; 17(1) doi: 10.1186/s12864-016-2771-6
11
Radan Bruha, Zdenek Marecek, Lenka Pospisilova, Sona Nevsimalova, Libor Vitek, Pavel Martasek, Jiri Nevoral, Jaromir Petrtyl, Petr Urbanek, Alena Jiraskova, Peter Ferenci. Long‐term follow‐up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlationLiver International 2011; 31(1): 83 doi: 10.1111/j.1478-3231.2010.02354.x
12
L. Králík, E. Flachsová, H. Hansíková, V. Saudek, J. Zeman, Pavel Martásek. Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes DiseaseFolia Biologica 2017; 63(5-6): 165 doi: 10.14712/fb2017063050165
13
I. Zh. Zhalsanova, E. A. Fonova, D. I. Zhigalina, N. A. Skryabin. The <i>ATOX1</i> Gene Role in Copper Metabolism and in the Copper-Induced Diseases PathogenesisГенетика 2023; 59(3): 283 doi: 10.31857/S0016675823030128
14
Tomasz Litwin, Anna Członkowska. Choroba Wilsona – czynniki wpływające na obraz klinicznyNeurologia i Neurochirurgia Polska 2013; 47(2): 161 doi: 10.5114/ninp.2013.34397
15
Irene J. Chang, Si Houn Hahn. Wilson DiseaseHandbook of Clinical Neurology 2017; 142: 19 doi: 10.1016/B978-0-444-63625-6.00003-3
16
Niti Kumari, Aman Kumar, Amit Pal, Babu Ram Thapa, Manish Modi, Rajendra Prasad. In-silico analysis of novel p.(Gly14Ser) variant of ATOX1 gene: plausible role in modulating ATOX1–ATP7B interactionMolecular Biology Reports 2019; 46(3): 3307 doi: 10.1007/s11033-019-04791-x
17
Beom H. Lee, Joo H. Kim, Sun Y. Lee, Hye Y. Jin, Kwi-Joo Kim, Jin-Joo Lee, Jung-Young Park, Gu-Hwan Kim, Jin-Ho Choi, Kyung M. Kim, Han-Wook Yoo. Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohortLiver International 2011; 31(6): 831 doi: 10.1111/j.1478-3231.2011.02503.x
18
Nivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah, Saketh Kapoor, Vishwanath Kumble Bhat, Lakshminarayanapuram Gopal Viswanathan, Madhu Nagappa, Parayil S. Bindu, Arun B. Taly, Sanjib Sinha, Arun Kumar, Andreas R. Janecke. Genetic analysis of ATP7B in 102 south Indian families with Wilson diseasePLOS ONE 2019; 14(5): e0215779 doi: 10.1371/journal.pone.0215779
19
T. Litwin, G. Gromadzka, J. Samochowiec, A. Grzywacz, A. Członkowski, A. Członkowska. JIMD Reports - Case and Research Reports, 2012/5JIMD Reports 2012; 8: 73 doi: 10.1007/8904_2012_163
20
Anna Członkowska, Tomasz Litwin, Petr Dusek, Peter Ferenci, Svetlana Lutsenko, Valentina Medici, Janusz K. Rybakowski, Karl Heinz Weiss, Michael L. Schilsky. Wilson diseaseNature Reviews Disease Primers 2018; 4(1) doi: 10.1038/s41572-018-0018-3
21
May T. Maung, Alyssa Carlson, Monserrat Olea‐Flores, Lobna Elkhadragy, Kyle M. Schachtschneider, Napoleon Navarro‐Tito, Teresita Padilla‐Benavides. The molecular and cellular basis of copper dysregulation and its relationship with human pathologiesThe FASEB Journal 2021; 35(9) doi: 10.1096/fj.202100273RR
22
Relu Cocoş, Alina Şendroiu, Sorina Schipor, Laurenţiu Camil Bohîlţea, Ionuţ Şendroiu, Florina Raicu, Bart Dermaut. Genotype-Phenotype Correlations in a Mountain Population Community with High Prevalence of Wilson’s Disease: Genetic and Clinical HomogeneityPLoS ONE 2014; 9(6): e98520 doi: 10.1371/journal.pone.0098520
23
Karolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, Karolina Gramza, Anna Członkowska. Families with Wilson's disease in subsequent generations: Clinical and genetic analysisMovement Disorders 2014; 29(14): 1828 doi: 10.1002/mds.26057
24
Donghu Zhou, Siyu Jia, Liping Yi, Zhen Wu, Yi Song, Bei Zhang, Yanmeng Li, Xiaoxi Yang, Anjian Xu, Xiaojin Li, Wei Zhang, Weijia Duan, Zhenkun Li, Saiping Qi, Zhibin Chen, Qin Ouyang, Jidong Jia, Jian Huang, Xiaojuan Ou, Hong You. Identification of potential modifier genes in Chinese patients with Wilson diseaseMetallomics 2022; 14(5) doi: 10.1093/mtomcs/mfac024
25
Grażyna Gromadzka, Magdalena Rudnicka, Grzegorz Chabik, Adam Przybyłkowski, Anna Członkowska. Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson’s diseaseJournal of Hepatology 2011; 55(4): 913 doi: 10.1016/j.jhep.2011.01.030
26
Richard Kirk. Clinical and Translational Perspectives on WILSON DISEASE2019; : 143 doi: 10.1016/B978-0-12-810532-0.00014-8
27
Xiaoyan Wu, Elise R. den Boer, Manon Vos-Loohuis, Frank G. van Steenbeek, Glen R. Monroe, Isaäc J. Nijman, Peter. A. J. Leegwater, Hille Fieten. Investigation of Genetic Modifiers of Copper Toxicosis in Labrador RetrieversLife 2020; 10(11): 266 doi: 10.3390/life10110266
28
Elena Vasilievna Ovchinnikova, Mikhail Maksimovich Garbuz, Anna Aleksandrovna Ovchinnikova, Vadim Vladimirovich Kumeiko. Epidemiology of Wilson’s Disease and Pathogenic Variants of the ATP7B Gene Leading to Diversified Protein DisfunctionsInternational Journal of Molecular Sciences 2024; 25(4): 2402 doi: 10.3390/ijms25042402
29
Karl Heinz Weiss, Wolfgang Stremmel. Evolving Perspectives in Wilson Disease: Diagnosis, Treatment and MonitoringCurrent Gastroenterology Reports 2012; 14(1): 1 doi: 10.1007/s11894-011-0227-3
30
Muriel Bost, Guénaelle Piguet-Lacroix, François Parant, C.M.R. Wilson. Molecular analysis of Wilson patients: Direct sequencing and MLPA analysis in the ATP7B gene and Atox1 and COMMD1 gene analysisJournal of Trace Elements in Medicine and Biology 2012; 26(2-3): 97 doi: 10.1016/j.jtemb.2012.04.024
31
Angela Sabalic, Veronica Mei, Giuliana Solinas, Roberto Madeddu. The Role of Copper in Alzheimer’s Disease Etiopathogenesis: An Updated Systematic ReviewToxics 2024; 12(10): 755 doi: 10.3390/toxics12100755
32
Valentina Medici, Karl-Heinz Weiss. Wilson DiseaseHandbook of Clinical Neurology 2017; 142: 35 doi: 10.1016/B978-0-444-63625-6.00004-5
33
Petr Dusek, Daniela Zahorakova. Movement Disorder Genetics2015; : 293 doi: 10.1007/978-3-319-17223-1_14
34
Michelle Angela Camarata, Si Houn Hahn. Wilson Disease2019; : 105 doi: 10.1016/B978-0-12-811077-5.00009-8
35
Ronald Jan Corbee, Louis C. Penning. COMMD1 Exemplifies the Power of Inbred Dogs to Dissect Genetic Causes of Rare Copper-Related DisordersAnimals 2021; 11(3): 601 doi: 10.3390/ani11030601
36
S. Suresh Kumar, George Kurian, C. E. Eapen, Eve A. Roberts. Genetics of Wilson’s disease: a clinical perspectiveIndian Journal of Gastroenterology 2012; 31(6): 285 doi: 10.1007/s12664-012-0237-6
37
A. E. Postrigan, I. Zh. Zhalsanova, E. A. Fonova, N. A. Skryabin. Modifier Genes as a Cause of Wilson–Konovalov Disease Clinical PolymorphismRussian Journal of Genetics 2021; 57(5): 522 doi: 10.1134/S1022795421050094